Lista de obras - Jan Lubiński - Dominio Público Uruguay

11q13 is a susceptibility locus for hormone receptor positive breast cancer

artículo científico publicado en 2012

A Lowering of Breast and Ovarian Cancer Risk in Women with a BRCA1 Mutation by Selenium Supplementation of Diet

artículo científico publicado en 2006

A Range of Cancers Is Associated with the rs6983267 Marker on Chromosome 8

A case of carotid body paraganglioma and haemangioblastoma of the spinal cord in a patient with the N131K missense mutation in the VHL gene

artículo científico publicado en 2011

A combination of the immunohistochemical markers CK7 and SATB2 is highly sensitive and specific for distinguishing primary ovarian mucinous tumors from colorectal and appendiceal metastases

scientific article published on 25 June 2019

A common missense variant in BRCA2 predisposes to early onset breast cancer

artículo científico publicado en 2005

A common nonsense mutation of the BLM gene and prostate cancer risk and survival

artículo científico publicado en 2013

A common variant of CDKN2A (p16) predisposes to breast cancer

artículo científico publicado en 2005

A comparison of ovarian cancer mortality in women with BRCA1 mutations undergoing annual ultrasound screening or preventive oophorectomy

scientific article published on 26 September 2019

A deletion in CHEK2 of 5,395 bp predisposes to breast cancer in Poland

artículo científico publicado en 2006

A genome-wide analysis of populations from European Russia reveals a new pole of genetic diversity in northern Europe

artículo científico publicado en 2013

A genome-wide association study for extremely high intelligence.

artículo científico publicado en 2017

A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.

artículo científico publicado en 2009

A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23

artículo científico publicado en 2011

A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.

artículo científico publicado en 2010

A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium

artículo científico publicado en 2011

A high frequency of BRCA2 gene mutations in Polish families with ovarian and stomach cancer

artículo científico publicado en 2003

A high proportion of founder BRCA1 mutations in Polish breast cancer families

artículo científico publicado en 2004

A large germline deletion in the Chek2 kinase gene is associated with an increased risk of prostate cancer

artículo científico publicado en 2006

A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium

artículo científico publicado en 2013

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population

artículo científico publicado en 2010

A low selenium level is associated with lung and laryngeal cancers

artículo científico publicado en 2013

A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease

artículo científico publicado en 2012

A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

artículo científico publicado en 2020

A nonsense mutation (E1978X) in the ATM gene is associated with breast cancer

article

A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers

artículo científico publicado en 2012

A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndrome

scientific article published on 12 July 2016

A novel founder CHEK2 mutation is associated with increased prostate cancer risk

artículo científico publicado en 2004

A personalised approach to prostate cancer screening based on genotyping of risk founder alleles

artículo científico publicado en 2013

A prior diagnosis of breast cancer is a risk factor for breast cancer in BRCA1 and BRCA2 carriers

artículo científico publicado en 2014

A protein truncating BRCA1 allele with a low penetrance of breast cancer

artículo científico publicado en 2004

A rare truncating BRCA2 variant and genetic susceptibility to upper aerodigestive tract cancer

artículo científico publicado en 2015

A sex-specific association between a 15q25 variant and upper aerodigestive tract cancers

artículo científico publicado en 2011

A six-nucleotide deletion in the CASP8 promoter is not associated with a susceptibility to breast and prostate cancers in the Polish population

artículo científico publicado en 2007

A survey of preventive measures among BRCA1 mutation carriers from Poland

scientific article published on 01 February 2007

A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

artículo científico publicado en 2018

A variant in FTO shows association with melanoma risk not due to BMI

artículo científico publicado en 2013

AIDIT and IMPACT: building research collaborations in targeted prostate cancer screening

artículo científico publicado en 2006

ARLTS1 Trp149Stop Mutation and the Risk of Ovarian Cancer

scientific article published on 01 May 2007

AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a consortium of investigators of modifiers of BRCA1/2 study

artículo científico publicado en 2007

Abdominal integument atrophy after operative procedures

artículo científico publicado en 2012

Abnormalities of chromosome 5q correlate with morphologic features of better prognosis in clear cell renal carcinomas

artículo científico publicado en 1995

Absence or reduction of Fhit expression in most clear cell renal carcinomas.

artículo científico publicado en 1998

Abstract LB-159: Methylation of BRCA1 gene in blood is not inherited via maternal germ line and may predispose to triple-negative or medullary breast cancer

article

Activity of trabectedin in germline BRCA1/2-mutated metastatic breast cancer: results of an international first-in-class phase II study

scientific article published on 01 April 2014

Acute myeloid leukemia in a 38-year-old hemodialyzed patient with von Hippel-Lindau disease

artículo científico publicado en 2013

Adult body mass index and risk of ovarian cancer by subtype: a Mendelian randomization study

artículo científico

Adult height is associated with increased risk of ovarian cancer: a Mendelian randomisation study.

artículo científico publicado en 2018

Age at diagnosis of cancer as predictor of mutation occurrence in families suspected of HNPCC

artículo científico publicado el 1 de enero de 2001

Age at diagnosis to discriminate those patients for whom constitutional DNA sequencing is appropriate in sporadic unilateral retinoblastoma

artículo científico publicado en 1998

Age at first birth and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers

article

Age at first full-term birth and breast cancer risk in BRCA1 and BRCA2 mutation carriers

scientific article published on 17 May 2018

Age at menarche and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers

article

Age of diagnosis of colorectal cancer in HNPCC patients is more complex than that predicted by R72P polymorphism in TP53.

artículo científico publicado en 2006

Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers

artículo científico publicado en 2016

Age-specific ovarian cancer risks among women with a BRCA1 or BRCA2 mutation

scientific article published on 21 May 2018

Age-specific risks of incident, contralateral and ipsilateral breast cancer among 1776 Polish BRCA1 mutation carriers

scientific article published on 05 January 2019

Alcohol consumption and the risk of breast cancer among BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2010

Allelic modification of breast cancer risk in women with an NBN mutation

scientific article published on 13 August 2019

An Assessment of Serum Selenium Concentration in Women with Endometrial Cancer

artículo científico publicado en 2022

An Assessment of Serum Selenium Concentration in Women with Ovarian Cancer

artículo científico publicado en 2023

An evaluation of the polymorphisms Ins16bp and Arg72Pro in p53 as breast cancer risk modifiers in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2008

An inherited NBN mutation is associated with poor prognosis prostate cancer

artículo científico publicado en 2012

An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression

artículo científico publicado en 2016

An international survey of surveillance schemes for unaffected BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2016

An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

artículo científico publicado en 2015

Analysis of germline variants in CDH1, IGFBP3, MMP1, MMP3, STK15 and VEGF in familial and sporadic renal cell carcinoma

artículo científico publicado en 2009

Analysis of over 10,000 Cases finds no association between previously reported candidate polymorphisms and ovarian cancer outcome

artículo científico publicado en 2013

Anthropometric Measures and Risk of Ovarian Cancer Among BRCA1 and BRCA2 Mutation Carriers

article

Antigens HLA-G, sHLA- G and sHLA- class I in reproductive failure

scientific article published on 01 January 2007

Are two-centimeter breast cancers large or small?

artículo científico publicado en 2013

Arsenic (As) and breast cancer risk.

artículo científico publicado en 2012

Aryl hydrocarbon receptor interacting protein(AIP) gene mutation analysis in children and adolescents with sporadic pituitary adenomas

article

Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

artículo científico publicado en 2015

Assessing the genetic architecture of epithelial ovarian cancer histological subtypes

artículo científico publicado en 2016

Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer

artículo científico publicado en 2016

Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

artículo científico publicado en 2018

Association analysis identifies 65 new breast cancer risk loci.

artículo científico publicado en 2017

Association between early-onset breast and laryngeal cancers.

artículo científico publicado en 2005

Association of MMP8 gene variation with an increased risk of malignant melanoma

artículo científico publicado en 2011

Association of PHB 1630 C>T and MTHFR 677 C>T polymorphisms with breast and ovarian cancer risk in BRCA1/2 mutation carriers: results from a multicenter study

artículo científico publicado en 2012

Association of breast cancer risk with genetic variants showing differential allelic expression: Identification of a novel breast cancer susceptibility locus at 4q21.

scientific article published on 21 October 2016

Association of common WRAP 53 variant with ovarian cancer risk in the Polish population

artículo científico publicado en 2012

Association of genetic susceptibility variants for type 2 diabetes with breast cancer risk in women of European ancestry

artículo científico publicado en 2016

Association of germline genetic variants with breast cancer-specific survival in patient subgroups defined by clinic-pathological variables related to tumor biology and type of systemic treatment

artículo científico publicado en 2021

Association of p16 expression with prognosis varies across ovarian carcinoma histotypes: an Ovarian Tumor Tissue Analysis consortium study

artículo científico publicado en 2018

Association of recurrent mutations in BRCA1, BRCA2, RAD51C, PALB2, and CHEK2 with the risk of borderline ovarian tumor

artículo científico publicado en 2022

Association of type and location of BRCA1 and BRCA2 mutations with risk of breast and ovarian cancer

artículo científico publicado en 2015

Association of vitamin D levels and risk of ovarian cancer: a Mendelian randomization study

artículo científico publicado en 2016

Association of zinc level and polymorphism in MMP-7 gene with prostate cancer in Polish population

artículo científico publicado en 2018

Associations of breast cancer risk factors with tumor subtypes: a pooled analysis from the Breast Cancer Association Consortium studies

artículo científico publicado en 2010

Associations of common breast cancer susceptibility alleles with risk of breast cancer subtypes in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2014

Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium

artículo científico publicado en 2011

Associations of obesity and circulating insulin and glucose with breast cancer risk: a Mendelian randomization analysis

article by Xiang Shu et al published 1 October 2018 in International Journal of Epidemiology

Attitudes toward preventive oophorectomy among BRCA1 mutation carriers in Poland

artículo científico publicado en 2004

Aurora-A and Cyclin D1 polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer.

artículo científico publicado en 2008

Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

scholarly article published in Nature Genetics

Author Correction: Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

scholarly article published in Nature Genetics

Average risks of breast and ovarian cancer associated with BRCA1 or BRCA2 mutations detected in case Series unselected for family history: a combined analysis of 22 studies

artículo científico publicado en 2003

BARD1 and breast cancer in Poland.

artículo científico publicado en 2007

BARD1 is A Low/Moderate Breast Cancer Risk Gene: Evidence Based on An Association Study of the Central European p.Q564X Recurrent Mutation

artículo científico publicado en 2019

BRCA1 founder mutations and ovarian cancer in Belarus.

artículo científico publicado en 2015

BRCA1 founder mutations compared to ovarian cancer in Belarus

artículo científico publicado en 2014

BRCA1 founder mutations do not contribute to increased risk of gastric cancer in the Polish population

artículo científico publicado en 2016

BRCA1 mutations and colorectal cancer in Poland.

artículo científico publicado en 2010

BRCA1 mutations and prostate cancer in Poland

artículo científico publicado en 2008

BRCA1 promoter methylation in peripheral blood is associated with the risk of triple-negative breast cancer

scientific article published on 29 September 2019

BRCA1 testing

scientific article published on 15 June 2008

BRCA1-associated breast and ovarian cancer risks in Poland: no association with commonly studied polymorphisms

artículo científico publicado en 2009

BRCA1-positive breast cancers in young women from Poland.

artículo científico publicado en 2006

BRCA1-related gene signature in breast cancer: the role of ER status and molecular type

artículo científico publicado en 2011

BRCA1/2 mutations are not a common cause of malignant melanoma in the Polish population

artículo científico publicado en 2018

BRCA1/2-negative hereditary triple-negative breast cancers exhibit BRCAness

artículo científico publicado en 2016

BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer

artículo científico publicado en 2017

BRCA2 Polymorphic Stop Codon K3326X and the Risk of Breast, Prostate, and Ovarian Cancers

artículo científico publicado en 2015

BRCA2 gene mutations in families with aggregations of breast and stomach cancers

artículo científico publicado en 2002

Bilateral Oophorectomy and Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

artículo científico publicado en 2016

Blood and serum samples collection and storage for further selenium measurements

artículo científico publicado en 2012

Blood arsenic levels and the risk of familial breast cancer in Poland

artículo científico publicado en 2019

Blood cadmium levels as a marker for early lung cancer detection

scientific article published on 12 November 2020

Body mass index and breast cancer survival: a Mendelian randomization analysis

artículo científico publicado en 2017

Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk

artículo científico publicado en 2020

Breast and ovarian cancer risks to carriers of the BRCA1 5382insC and 185delAG and BRCA2 6174delT mutations: a combined analysis of 22 population based studies

artículo científico publicado en 2005

Breast cancer genetics: 20 years later

artículo científico publicado en 2013

Breast cancer predisposing alleles in Poland

artículo científico publicado en 2005

Breast cancer risk following bilateral oophorectomy in BRCA1 and BRCA2 mutation carriers: an international case-control study.

artículo científico publicado en 2005

Breast cancer risk reduction associated with the RAD51 polymorphism among carriers of the BRCA1 5382insC mutation in Poland ⬇️

artículo científico publicado el 1 de mayo de 2003

Breast cancer risk variants at 6q25 display different phenotype associations and regulate ESR1, RMND1 and CCDC170.

artículo científico publicado en 2016

Breast cancer susceptibility genes

article

Breast-feeding and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers.

artículo científico publicado en 2004

Breastfeeding and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2012

Breastfeeding and the risk of epithelial ovarian cancer among women with a BRCA1 or BRCA2 mutation

scientific article published on 30 September 2020

CDH1 gene mutations do not contribute in hereditary diffuse gastric cancer in Poland

artículo científico publicado en 2010

CDKN2A and CDK4 variants in Latvian melanoma patients: analysis of a clinic-based population

article

CDKN2A common variant and multi-organ cancer risk--a population-based study

artículo científico publicado en 2006

CDKN2A common variants and their association with melanoma risk: a population-based study.

artículo científico publicado en 2005

CDKN2A-positive breast cancers in young women from Poland.

artículo científico publicado en 2006

CHAPTER 22. Selenium and Cancer

artículo científico publicado en 2015

CHEK2 germline mutations correlate with recurrence rate in patients with superficial bladder cancer

scientific article published on 01 January 2008

CHEK2 is a multiorgan cancer susceptibility gene

artículo científico publicado en 2004

CHEK2 mutations and HNPCC-related colorectal cancer.

artículo científico publicado en 2010

CHEK2 mutations and the risk of papillary thyroid cancer.

artículo científico publicado en 2015

CHEK2 mutations as markers for high risk of breast cancer

artículo científico publicado en 2012

CHEK2 variants predispose to benign, borderline and low-grade invasive ovarian tumors

artículo científico publicado en 2006

CHEK2-positive breast cancers in young Polish women

scientific article published on 01 August 2006

CYP1B1 and predisposition to breast cancer in Poland

article

Can Serum Iron Concentrations in Early Healthy Pregnancy Be Risk Marker of Pregnancy-Induced Hypertension?

artículo científico publicado en 2019

Can selenium be a modifier of cancer risk in CHEK2 mutation carriers?

artículo científico publicado en 2013

Can selenium levels act as a marker of colorectal cancer risk?

artículo científico publicado en 2013

Cancer Familial Aggregation (CFA) and G446A polymorphism in ARLTS1 gene

artículo científico publicado en 2006

Cancer Predisposition Genes in Cancer-Free Families

artículo científico publicado en 2020

Cancer risks in first degree relatives of BRCA1 mutation carriers: effects of mutation and proband disease status

artículo científico publicado en 2005

Cancer risks in first-degree relatives of CHEK2 mutation carriers: effects of mutation type and cancer site in proband

artículo científico publicado en 2009

Cancer variation associated with the position of the mutation in the BRCA2 gene

artículo científico publicado en 2004

Candidate genetic modifiers for breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2014

Case report of a woman with monoclonal gammapathy and papillary thyroid carcinoma, diagnosed because of detection of CHEK2 (I157T) mutation in genetic examinations.

artículo científico publicado en 2010

Changes in body weight and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2005

Characterization of a familial RCC-associated t(2;3)(q33;q21) chromosome translocation

artículo científico publicado en 2001

Characterization of the c.190T>C missense mutation in BRCA1 codon 64 (Cys64Arg).

artículo científico publicado en 2009

Chemotherapy-induced amenorrhea in patients with breast cancer with a BRCA1 or BRCA2 mutation

scientific article published on 26 August 2013

Chromosome 8q23.3, 10p14 and 11q23.1 variants modify colorectal cancer risk in Lynch syndrome – a combined analysis of the Australian, Dutch and Polish Lynch syndrome cohorts

article

Chromosome aberrations, spontaneous SCE, and growth kinetics in PHA-stimulated lymphocytes of five cases with Sézary syndrome ⬇️

artículo científico publicado el 1 de agosto de 1995

Cis-eQTL analysis and functional validation of candidate susceptibility genes for high-grade serous ovarian cancer

artículo científico publicado en 2015

Cisplatin in breast cancer treatment in BRCA1 carriers

Clinical and epidemiological features of familial laryngeal cancer in Poland

article

Clinical characteristics of breast cancer in patients with an NBS1 mutation.

artículo científico publicado en 2013

Clinical characteristics of hereditary ovarian cancer (HOC) in Poland

scientific article published on 01 September 2002

Clinical characteristics of laryngeal cancer in BRCA-1 mutation carriers

artículo científico publicado en 2009

Clinical characteristics of tumors derived from colorectal cancer patients who harbor the tumor necrosis factor alpha-1031T/T and NOD2 3020insC polymorphism.

artículo científico publicado en 2009

Clinical features of familial ovarian cancer lacking mutations in BRCA1 or BRCA2

artículo científico publicado en 2004

Clinical genetic services for familial breast cancer in Poland

artículo científico publicado en 1999

Clinical outcomes in women with breast cancer and a PALB2 mutation: a prospective cohort analysis

artículo científico publicado en 2015

Coffee consumption and breast cancer risk amongBRCA1 andBRCA2 mutation carriers

article

Colorectal cancer susceptibility loci on chromosome 8q23.3 and 11q23.1 as modifiers for disease expression in Lynch syndrome

artículo científico publicado en 2010

Combined analysis of three lynch syndrome cohorts confirms the modifying effects of 8q23.3 and 11q23.1 in MLH1 mutation carriers

artículo científico publicado en 2012

Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients

artículo científico publicado en 2009

Combined iPLEX and TaqMan assays to screen for 45 common mutations in Lynch syndrome and FAP patients

artículo científico publicado en 2011

Common Genetic Variation In Cellular Transport Genes and Epithelial Ovarian Cancer (EOC) Risk

artículo científico publicado en 2015

Common Genetic Variation in Circadian Rhythm Genes and Risk of Epithelial Ovarian Cancer (EOC).

artículo científico publicado en 2015

Common alleles at 6q25.1 and 1p11.2 are associated with breast cancer risk for BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2011

Common alleles in candidate susceptibility genes associated with risk and development of epithelial ovarian cancer

artículo científico publicado en 2011

Common breast cancer susceptibility alleles and the risk of breast cancer for BRCA1 and BRCA2 mutation carriers: implications for risk prediction

artículo científico publicado en 2010

Common genetic variation at BARD1 is not associated with breast cancer risk in BRCA1 or BRCA2 mutation carriers

artículo científico publicado en 2011

Common germline polymorphisms associated with breast cancer-specific survival

artículo científico publicado en 2015

Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium

artículo científico publicado en 2014

Common regions of deletion in chromosome regions 3p12 and 3p14.2 in primary clear cell renal carcinomas

artículo científico publicado en 1994

Common variants at 12p11, 12q24, 9p21, 9q31.2 and in ZNF365 are associated with breast cancer risk for BRCA1 and/or BRCA2 mutation carriers

artículo científico publicado en 2012

Common variants at 19p13 are associated with susceptibility to ovarian cancer

artículo científico publicado en 2010

Common variants at the 19p13.1 and ZNF365 loci are associated with ER subtypes of breast cancer and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2012

Common variants at the CHEK2 gene locus and risk of epithelial ovarian cancer

artículo científico publicado en 2015

Common variants of DNA repair genes and malignant melanoma

artículo científico publicado en 2007

Common variants of ZNF750, RPTOR and TRAF3IP2 genes and psoriasis risk

scientific article published on 05 September 2013

Common variants of xeroderma pigmentosum genes and prostate cancer risk

artículo científico publicado en 2014

Comparison of Alu-PCR, microsatellite instability, and immunohistochemical analyses in finding features characteristic for hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2001

Comparison of DNA gains and losses in primary renal clear cell carcinomas and metastatic sites: importance of 1q and 3p copy number changes in metastatic events

artículo científico

Comparison of genomic abnormalities between BRCAX and sporadic breast cancers studied by comparative genomic hybridization

artículo científico publicado en 2005

Confirmation of 5p12 as a susceptibility locus for progesterone-receptor-positive, lower grade breast cancer

artículo científico publicado en 2011

Consortium analysis of gene and gene-folate interactions in purine and pyrimidine metabolism pathways with ovarian carcinoma risk

artículo científico publicado en 2014

Constitutional CHEK2 mutations are associated with a decreased risk of lung and laryngeal cancers

artículo científico publicado en 2008

Constitutional methylation of cancer-related and selenoprotein coding genes in breast carcinoma in Polish population

artículo científico publicado en 2012

Constitutional variants in POT1, TERF2IP, and ACD genes in patients with melanoma in the Polish population

scientific article published on 24 September 2020

Contribution of Germline Mutations in the RAD51B, RAD51C, and RAD51D Genes to Ovarian Cancer in the Population

artículo científico publicado en 2015

Copper as diagnostic marker of cancers.

artículo científico publicado en 2015

Correction to: Survival from breast cancer in women with a BRCA2 mutation by treatment

artículo científico publicado en 2023

Correction: A Genome-Wide Association Study of Upper Aerodigestive Tract Cancers Conducted within the INHANCE Consortium.

artículo científico publicado en 2011

Correction: A Low Selenium Level Is Associated with Lung and Laryngeal Cancers

artículo científico publicado en 2013

Correction: Genetic Structure of Europeans: A View from the North–East.

artículo científico publicado en 2010

Correction: Serum selenium levels and the risk of progression of laryngeal cancer.

artículo científico publicado en 2018

Corrigendum re “Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma” [Eur Urol 2017;72:747–54]

scholarly article published in European Urology

Corrigendum: Germline RECQL mutations are associated with breast cancer susceptibility

artículo científico publicado en 2016

Coverage of the genetic background of breast cancer in the polish population

artículo científico publicado en 2006

Cumulative Small Effect Genetic Markers and the Risk of Colorectal Cancer in Poland, Estonia, Lithuania, and Latvia

artículo científico publicado en 2015

Cumulative effects of genetic markers and the detection of advanced colorectal neoplasias by population screening

artículo científico publicado en 2014

Cumulative small effect genetic markers and the detection of advanced colorectal neoplasias by population screening.

artículo científico publicado en 2012

Cytogenetic and molecular findings in 75 clear cell renal cell carcinomas

artículo científico publicado en 2005

DNA glycosylases involved in base excision repair may be associated with cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2014

DNA repair gene polymorphisms and risk of early onset colorectal cancer in Lynch syndrome

artículo científico publicado en 2012

DNA testing for variants conferring low or moderate increase in the risk of cancer

artículo científico publicado en 2008

DNA variation in MSR1, RNASEL and E-cadherin genes and prostate cancer in Poland

scientific article published on 01 January 2007

Detection of germline mutations in the BRCA1 gene by RNA-based sequencing

artículo científico publicado en 2001

Detection of specific genetic alterations in cancer cells.

artículo científico publicado en 1996

Development and validation of the gene-expression Predictor of high-grade-serous Ovarian carcinoma molecular subTYPE (PrOTYPE)

scientific article published on 17 June 2020

Diabetes and breast cancer among women with BRCA1 and BRCA2 mutations

artículo científico publicado en 2010

Different CHEK2 germline mutations are associated with distinct immunophenotypic molecular subtypes of breast cancer

artículo científico publicado en 2011

Direct-to-patient BRCA1 testing: the Twoj Styl experience

artículo científico publicado en 2006

Do BRCA1 modifiers also affect the risk of breast cancer in non-carriers?

artículo científico publicado en 2008

Do founder mutations characteristic of some cancer sites also predispose to pancreatic cancer?

artículo científico publicado en 2016

Does preventive oophorectomy increase the risk of depression in BRCA mutation carriers?

artículo científico publicado en 2020

Does the age of breast cancer diagnosis in first-degree relatives impact on the risk of breast cancer in BRCA1 and BRCA2 mutation carriers?

artículo científico publicado en 2015

Dose-Response Association of CD8+ Tumor-Infiltrating Lymphocytes and Survival Time in High-Grade Serous Ovarian Cancer.

artículo científico publicado en 2017

Double heterozygotes among breast cancer patients analyzed for BRCA1, CHEK2, ATM, NBN/NBS1, and BLM germ-line mutations

artículo científico publicado en 2014

Dupuytren's disease and the risk of malignant neoplasms

artículo científico publicado en 2014

Duration of tamoxifen use and the risk of contralateral breast cancer in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2014

Early radiation exposures and BRCA1-associated breast cancer in young women from Poland

artículo científico publicado en 2008

Effect of CHEK2 missense variant I157T on the risk of breast cancer in carriers of other CHEK2 or BRCA1 mutations.

artículo científico publicado en 2008

Effect of aspirin or resistant starch on colorectal neoplasia in the Lynch syndrome

artículo científico publicado en 2008

Effect of pregnancy as a risk factor for breast cancer in BRCA1/BRCA2 mutation carriers

artículo científico publicado en 2005

Electro-oculogram in patients with neurofibromatosis type 1.

artículo científico publicado en 2001

Electro-oculographic and electroretinographic studies in HNPCC gene mutation carriers

artículo científico publicado en 2003

Electroretinographic Changes in Eyes of Patients with BRCA1 Gene Mutation ⬇️

artículo científico publicado el 1 de mayo de 2003

Electroretinographic changes in the inner retinal layers of the retained eyes of patients with sporadic unilateral retinoblastoma

artículo científico publicado en 2002

Elevated level of 8-oxo-7,8-dihydro-2'-deoxyguanosine in leukocytes of BRCA1 mutation carriers compared to healthy controls.

artículo científico publicado en 2009

Endolymphatic sac tumours and von Hippel-Lindau disease - case report, molecular analysis and histopathological characterization.

artículo científico publicado en 2009

Enhanced GAB2 Expression Is Associated with Improved Survival in High-Grade Serous Ovarian Cancer and Sensitivity to PI3K Inhibition

artículo científico publicado en 2015

Enrichment of putative PAX8 target genes at serous epithelial ovarian cancer susceptibility loci

artículo científico publicado en 2017

Environmental factors may regulate BCL2 associated lymphomagenesis: a very low incidence of BCL2-MBR translocation in Poland

artículo científico publicado en 1995

Epigenetic analysis leads to identification of HNF1B as a subtype-specific susceptibility gene for ovarian cancer

artículo científico publicado en 2013

Epistatic relationship between the cancer susceptibility genes CHEK2 and p27

scientific article published on 01 March 2007

Epithelial-Mesenchymal Transition (EMT) Gene Variants and Epithelial Ovarian Cancer (EOC) Risk

artículo científico publicado en 2015

Erratum: Corrigendum: Common variants at 19p13 are associated with susceptibility to ovarian cancer

scholarly article published in Nature Genetics

Erratum: Corrigendum: Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer

scholarly article published in Nature Genetics

Erratum: Germline CHEK2 mutations and colorectal cancer risk: different effects of a missense and truncating mutations?

artículo científico publicado en 2007

Estrogen receptor beta rs1271572 polymorphism and invasive ovarian carcinoma risk: pooled analysis within the Ovarian Cancer Association Consortium

artículo científico publicado en 2011

Estrogen receptor status in CHEK2-positive breast cancers: implications for chemoprevention

artículo científico publicado en 2008

Evaluating the ovarian cancer gonadotropin hypothesis: a candidate gene study

artículo científico publicado en 2014

Evaluation of Polygenic Risk Scores for Breast and Ovarian Cancer Risk Prediction in BRCA1 and BRCA2 Mutation Carriers

artículo científico publicado en 2017

Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation

artículo científico publicado en 2014

Evidence that the 5p12 Variant rs10941679 Confers Susceptibility to Estrogen-Receptor-Positive Breast Cancer through FGF10 and MRPS30 Regulation

scientific article published on 03 September 2016

Exome genotyping arrays to identify rare and low frequency variants associated with epithelial ovarian cancer risk

artículo científico publicado en 2016

Exploring the link between germline and somatic genetic alterations in breast carcinogenesis

artículo científico publicado en 2010

FGF receptor genes and breast cancer susceptibility: results from the Breast Cancer Association Consortium

artículo científico publicado en 2014

Factors influencing ovulation and the risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2014

Familial adenomatous polyposis of the colon

artículo científico publicado en 2013

Familial association of laryngeal, lung, stomach and early-onset breast cancer

Family History of Cancer and Cancer Risks in Women with BRCA1 or BRCA2 Mutations

article by K. Metcalfe et al published 23 November 2010 in Journal of the National Cancer Institute

Fast diagnostic test for the identification of an increased genetic predisposition to colon cancer (exemplified on a DNA test for recurrent mutations of the gene MMR).

artículo científico publicado en 2012

Fhit protein expression in endometrial cancers: no correlation with histological grade.

artículo científico publicado en 2001

Fhit protein expression in hereditary and sporadic colorectal cancers

artículo científico publicado en 2001

Fine mapping of genetic susceptibility loci for melanoma reveals a mixture of single variant and multiple variant regions

artículo científico publicado en 2014

Fine scale mapping of the 17q22 breast cancer locus using dense SNPs, genotyped within the Collaborative Oncological Gene-Environment Study (COGs).

artículo científico publicado en 2016

Fine-Mapping of the 1p11.2 Breast Cancer Susceptibility Locus

artículo científico publicado en 2016

Fine-Scale Mapping at 9p22.2 Identifies Candidate Causal Variants That Modify Ovarian Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

artículo científico publicado en 2016

Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression

artículo científico publicado en 2013

Fine-mapping identifies multiple prostate cancer risk loci at 5p15, one of which associates with TERT expression.

artículo científico publicado en 2013

Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2.

artículo científico publicado en 2015

Fine-mapping of 150 breast cancer risk regions identifies 178 high confidence target genes

article

Fine-mapping of 150 breast cancer risk regions identifies 191 likely target genes

artículo científico publicado en 2020

Fine-mapping of prostate cancer susceptibility loci in a large meta-analysis identifies candidate causal variants.

artículo científico publicado en 2018

Fine-scale mapping of 8q24 locus identifies multiple independent risk variants for breast cancer

artículo científico publicado en 2016

Fine-scale mapping of the 4q24 locus identifies two independent loci associated with breast cancer risk

artículo científico publicado en 2015

Fine-scale mapping of the 5q11.2 breast cancer locus reveals at least three independent risk variants regulating MAP3K1.

artículo científico publicado en 2014

Fine-scale mapping of the FGFR2 breast cancer risk locus: putative functional variants differentially bind FOXA1 and E2F1.

artículo científico publicado en 2013

First Trimester Microelements and their Relationships with Pregnancy Outcomes and Complications

artículo científico publicado en 2020

First Trimester Serum Copper or Zinc Levels, and Risk of Pregnancy-Induced Hypertension

scientific article published on 16 October 2019

First recurrent large genomic rearrangement in the BRCA1 gene found in Poland.

artículo científico publicado en 2014

Folic acid and breast cancer risk.

artículo científico publicado en 2012

Folic acid and cancer risk in BRCA1 carriers.

artículo científico publicado en 2012

Founder Mutations for Early Onset Melanoma as Revealed by Whole Exome Sequencing Suggests That This is Not Associated with the Increasing Incidence of Melanoma in Poland.

artículo científico publicado en 2018

Founder mutations in the BRCA1 gene in Polish families with breast-ovarian cancer

artículo científico publicado en 2000

Founder mutations in the BRCA1 gene in west Belarusian breast-ovarian cancer families

artículo científico publicado en 2001

Founder mutations of BRCA1 and BRCA2 in North American families of Polish origin that are affected with breast cancer

artículo científico publicado en 2001

Frequency and nature of germline Rb-1 gene mutations in a series of patients with sporadic unilateral retinoblastoma

artículo científico publicado en 1999

Frequency and nature of hMSH6 germline mutations in Polish patients with colorectal, endometrial and ovarian cancers

artículo científico publicado en 2006

Frequency of BRCA1 and BRCA2 causative founder variants in ovarian cancer patients in South-East Poland.

artículo científico publicado en 2018

Frequency of BRCA1 and BRCA2 mutations in ovarian cancer patients in South-East Poland

artículo científico publicado en 2022

Frequency of mutations related to hereditary haemochromatosis in northwestern Poland

artículo científico publicado en 2008

Functional annotation of the 2q35 breast cancer risk locus implicates a structural variant in influencing activity of a long-range enhancer element

artículo científico publicado en 2021

Functional mechanisms underlying pleiotropic risk alleles at the 19p13.1 breast-ovarian cancer susceptibility locus

artículo científico publicado en 2016

Functional screening identifies miRNAs influencing apoptosis and proliferation in colorectal cancer

artículo científico publicado en 2014

Functional variants at the 11q13 risk locus for breast cancer regulate cyclin D1 expression through long-range enhancers

artículo científico publicado en 2013

GWAS meta-analysis and replication identifies three new susceptibility loci for ovarian cancer

artículo científico publicado en 2013

Gene Expression Profiling in Hereditary, BRCA1-linked Breast Cancer: Preliminary Report

artículo científico publicado en 2006

Gene expression signature of hereditary breast cancer.

artículo científico publicado en 2005

Gene rearrangements detected by nonradioactive digoxigenin-labeled DNA probes

artículo científico publicado el 1 de junio de 1991

Genetic Polymorphisms in Xenobiotic Clearance Genes and Their Influence on Disease Expression in Hereditary Nonpolyposis Colorectal Cancer Patients

artículo científico publicado en 2006

Genetic Variants Related to Longer Telomere Length are Associated with Increased Risk of Renal Cell Carcinoma ⬇️

artículo científico publicado en 2017

Genetic characterization of northeastern Italian population isolates in the context of broader European genetic diversity

artículo científico publicado en 2012

Genetic contribution to all cancers: the first demonstration using the model of breast cancers from Poland stratified by age at diagnosis and tumour pathology

article

Genetic epidemiology studies in hereditary non-polyposis colorectal cancer

artículo científico publicado en 2009

Genetic heterogeneity of 8q24 region in susceptibility to cancer.

artículo científico publicado en 2009

Genetic polymorphisms may influence the vertical growth rate of melanoma

article published in 2018

Genetic predisposition to ductal carcinoma in situ of the breast

artículo científico publicado en 2016

Genetic predisposition to in situ and invasive lobular carcinoma of the breast

artículo científico publicado en 2014

Genetic structure of Europeans: a view from the North-East

artículo científico publicado en 2009

Genetic testing and common disorders in a public health framework: how to assess relevance and possibilities. Background Document to the ESHG recommendations on genetic testing and common disorders

artículo científico publicado en 2011

Genetic variation at 9p22.2 and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2010

Genetic variation at CYP3A is associated with age at menarche and breast cancer risk: a case-control study

artículo científico publicado en 2014

Genetic variation in insulin-like growth factor 2 may play a role in ovarian cancer risk

artículo científico publicado en 2011

Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade

artículo científico publicado en 2014

Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium

artículo científico publicado en 2015

Genetically Predicted Body Mass Index and Breast Cancer Risk: Mendelian Randomization Analyses of Data from 145,000 Women of European Descent

artículo científico publicado en 2016

Genome-Wide Meta-Analyses of Breast, Ovarian, and Prostate Cancer Association Studies Identify Multiple New Susceptibility Loci Shared by at Least Two Cancer Types

artículo científico publicado en 2016

Genome-wide Analysis Identifies Novel Loci Associated with Ovarian Cancer Outcomes: Findings from the Ovarian Cancer Association Consortium

artículo científico publicado en 2015

Genome-wide association analysis identifies three new breast cancer susceptibility loci

artículo científico publicado en 2012

Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer

artículo científico publicado en 2015

Genome-wide association and transcriptome studies identify target genes and risk loci for breast cancer

article

Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility

artículo científico publicado en 2020

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

artículo científico publicado en 2013

Genome-wide association study identifies 32 novel breast cancer susceptibility loci from overall and subtype-specific analyses

scientific article published on 18 May 2020

Genome-wide association study identifies multiple risk loci for renal cell carcinoma ⬇️

artículo científico publicado en 2017

Genome-wide association study identifies three loci associated with melanoma risk

scientific article published on 05 July 2009

Genome-wide association study identifies three new melanoma susceptibility loci

artículo científico publicado en 2011

Genome-wide association study in BRCA1 mutation carriers identifies novel loci associated with breast and ovarian cancer risk

artículo científico publicado en 2013

Genome-wide association study of germline variants and breast cancer-specific mortality

artículo científico publicado en 2019

Genome-wide association study of prostate cancer-specific survival

artículo científico publicado en 2015

Genome-wide association study of renal cell carcinoma identifies two susceptibility loci on 2p21 and 11q13.3

scientific journal article

Genome-wide association study of subtype-specific epithelial ovarian cancer risk alleles using pooled DNA.

artículo científico publicado en 2013

Genome-wide meta-analysis identifies five new susceptibility loci for cutaneous malignant melanoma ⬇️

artículo científico publicado en 2015

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic dissection of bipolar disorder and schizophrenia including 28 subphenotypes

artículo científico publicado en 2017

Genotypic analysis of DNA isolated from fine needle aspiration biopsies

artículo científico publicado en 1988

Genotyping by induced Förster Resonance Energy Transfer(iFRET) mechanism and simultaneous mutation scanning

artículo científico

Germline 657del5 mutation in the NBS1 gene in breast cancer patients

artículo científico publicado en 2003

Germline 657del5 mutation in the NBS1 gene in patients with malignant melanoma of the skin.

artículo científico publicado en 2003

Germline BRCA1 and BRCA2 mutations and the risk of bladder or kidney cancer in Poland

artículo científico publicado en 2022

Germline CHEK2 mutations and colorectal cancer risk: different effects of a missense and truncating mutations?

artículo científico publicado en 2006

Germline HOXB13 mutation p.G84E do not confer an increased bladder or kidney cancer risk in polish population

artículo científico publicado en 2022

Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk

artículo científico publicado en 2020

Germline MSH2 and MLH1 mutational spectrum in HNPCC families from Poland and the Baltic States

artículo científico publicado en 2002

Germline MSH2 and MLH1 mutational spectrum including large rearrangements in HNPCC families from Poland (update study)

artículo científico publicado en 2005

Germline RECQL mutations are associated with breast cancer susceptibility

artículo científico publicado en 2015

Germline deletions in the EPCAM gene as a cause of Lynch syndrome - literature review

artículo científico publicado en 2013

Germline fumarate hydratase mutations in patients with ovarian mucinous cystadenoma

artículo científico publicado en 2006

Germline mutation and large deletion analysis of the CDKN2A and ARF genes in families with multiple melanoma or an aggregation of malignant melanoma and breast cancer

artículo científico publicado en 2004

Germline mutations in the von Hippel-Lindau (VHL) gene in patients from Poland: disease presentation in patients with deletions of the entire VHL gene

artículo científico publicado en 2002

Germline mutations in theCHEK2 kinase gene are associated with an increased risk of bladder cancer

artículo científico publicado en 2007

Germline variants and breast cancer survival in patients with distant metastases at primary breast cancer diagnosis

artículo científico publicado en 2021

HFE gene mutations in patients with alcoholic liver disease. A prospective study from northwestern Poland.

artículo científico publicado en 2010

HLA-G polymorphism and in vitro fertilization failure in a Polish population.

artículo científico publicado en 2009

HLA-G polymorphism in a Polish population and reproductive failure

artículo científico publicado en 2007

HNPCC (Lynch Syndrome): Differential Diagnosis, Molecular Genetics and Management - a Review

HOXB13 mutations and prostate cancer in Poland.

artículo científico publicado en 2012

Haemochromatosis HFE gene polymorphisms as potential modifiers of hereditary nonpolyposis colorectal cancer risk and onset age.

artículo científico publicado en 2009

Haplotype of the C61G BRCA1 mutation in Polish and Jewish individuals

artículo científico publicado en 2009

Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2011

Haplotypes of the I157T CHEK2 germline mutation in ethnically diverse populations.

artículo científico publicado en 2009

Height and Body Mass Index as Modifiers of Breast Cancer Risk in BRCA1/2 Mutation Carriers: A Mendelian Randomization Study

artículo científico publicado en 2019

Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization

artículo científico publicado en 2015

Hereditary Cancer in Clinical Practice transfers to BioMed Central.

artículo científico publicado en 2009

Hereditary breast and ovarian cancer

artículo científico publicado en 2008

Hereditary breast cancer

artículo científico publicado en 1998

Hereditary ovarian cancer in Poland.

artículo científico publicado en 2003

Hereditary ovarian cancer: summary of 5 years of experience

artículo científico publicado en 1998

High Resolution Melting analysis as a rapid and efficient method of screening for small mutations in the STK11 gene in patients with Peutz-Jeghers syndrome.

artículo científico publicado en 2013

High incidence of 4153delA BRCA1 gene mutations in Lithuanian breast- and breast-ovarian cancer families

artículo científico publicado en 2005

Higher antitumor activity of trabectedin in germline BRCA2 carriers with advanced breast cancer as compared to BRCA1 carriers: A subset analysis of a dedicated phase II trial

artículo científico publicado en 2017

Hippel-Lindau disease

artículo científico publicado en 1998

Hormone Replacement Therapy After Oophorectomy and Breast Cancer Risk Among BRCA1 Mutation Carriers

artículo científico publicado en 2018

Hormone Replacement Therapy Appears to Be Safe After Prophylactic Adnexectomy in Premenopausal BRCA1/BRCA2 Mutation Carriers. Reaction to the 'Letter to readers' in Hereditary Cancer in Clinical Practice, 2005, 3 (2)

Hormone replacement therapy after menopause and risk of breast cancer in BRCA1 mutation carriers: a case-control study

artículo científico publicado en 2016

Hormone replacement therapy and the risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers.

artículo científico publicado en 2005

Hormone therapy and the risk of breast cancer in BRCA1 mutation carriers

artículo científico publicado en 2008

IGF1 is a modifier of disease risk in hereditary non-polyposis colorectal cancer

artículo científico publicado en 2008

IMPACT and AIDIT: Strengthening Research Ties in Eastern Europe

artículo científico publicado en 2006

Identification and characterization of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk

artículo científico publicado en 2014

Identification and molecular characterization of a new ovarian cancer susceptibility locus at 17q21.31.

artículo científico publicado en 2013

Identification of 23 new prostate cancer susceptibility loci using the iCOGS custom genotyping array

artículo científico publicado en 2013

Identification of Familial Hodgkin Lymphoma Predisposing Genes Using Whole Genome Sequencing

artículo científico publicado en 2020

Identification of four novel susceptibility loci for oestrogen receptor negative breast cancer

artículo científico publicado en 2016

Identification of independent association signals and putative functional variants for breast cancer risk through fine-scale mapping of the 12p11 locus

artículo científico publicado en 2016

Identification of novel genetic markers of breast cancer survival

artículo científico publicado en 2015

Identification of patients at high risk of negative psychological consequences associated with BRCA1 mutation

artículo científico publicado en 2012

Identification of patients at high risk of psychological distress after BRCA1 genetic testing

artículo científico publicado en 2009

Identification of six new susceptibility loci for invasive epithelial ovarian cancer

artículo científico publicado en 2015

Identification of ten variants associated with risk of estrogen-receptor-negative breast cancer

artículo científico publicado en 2017

Immunophenotypic predictive profiling of BRCA1-associated breast cancer

artículo científico publicado en 2010

Impact of BRCA1 mutation on survival after early onset breast cancer.

artículo científico publicado en 2012

Impact of oophorectomy on cancer incidence and mortality in women with a BRCA1 or BRCA2 mutation

artículo científico publicado en 2014

Importance of microsatellite instability (MSI) in colorectal cancer: MSI as a diagnostic tool

artículo científico publicado en 2004

Incidence of colorectal cancer in BRCA1 and BRCA2 mutation carriers: results from a follow-up study

artículo científico publicado en 2013

Incorporating progesterone receptor expression into the PREDICT breast prognostic model

artículo científico publicado en 2022

Increased incidence of visceral metastases in scottish patients with BRCA1/2-defective ovarian cancer: an extension of the ovarian BRCAness phenotype

artículo científico publicado en 2010

Increased rates of chromosome breakage in BRCA1 carriers are normalized by oral selenium supplementation

artículo científico publicado en 2005

Increased risk of breast cancer in relatives of malignant melanoma patients from families with strong cancer familial aggregation

artículo científico publicado en 2003

Infertility, treatment of infertility, and the risk of breast cancer among women with BRCA1 and BRCA2 mutations: a case-control study

artículo científico publicado en 2008

Inflammatory response gene polymorphisms and their relationship with colorectal cancer risk

artículo científico publicado en 2008

Influence of selected lifestyle factors on breast and ovarian cancer risk in BRCA1 mutation carriers from Poland

artículo científico publicado en 2006

Influence of the Levels of Arsenic, Cadmium, Mercury and Lead on Overall Survival in Lung Cancer

artículo científico publicado en 2021

Influence of the selenium level on overall survival in lung cancer

artículo científico publicado en 2019

Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women

artículo científico publicado en 2016

Inherited NBN Mutations and Prostate Cancer Risk and Survival

scientific article published on 13 December 2018

Inherited Variants in BLM and the Risk and Clinical Characteristics of Breast Cancer

artículo científico publicado en 2019

Inherited variants affecting RNA editing may contribute to ovarian cancer susceptibility: results from a large-scale collaboration

artículo científico publicado en 2016

Inherited variants in XRCC2 and the risk of breast cancer

scientific article published on 28 August 2019

Inherited variants in the inner centromere protein (INCENP) gene of the chromosomal passenger complex contribute to the susceptibility of ER-negative breast cancer

artículo científico publicado en 2015

Inhibition of cell cycle and induction of apoptosis by sulforaphane in cell lines carrying various inherited BRCA1 mutations.

artículo científico publicado en 2005

Iniparib in metastatic triple-negative breast cancer

artículo científico publicado en 2011

Integrated Proteogenomic Characterization of Clear Cell Renal Cell Carcinoma

artículo científico publicado en 2019

Integrated Proteogenomic Characterization of Clear Cell Renal Cell Carcinoma

scientific article published on 01 January 2020

Integrated proteogenomic deep sequencing and analytics accurately identify non-canonical peptides in tumor immunopeptidomes

artículo científico publicado en 2020

Integrin beta3 Leu33Pro polymorphism increases BRCA1-associated ovarian cancer risk

artículo científico publicado en 2007

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

artículo científico publicado en 2022

Interim Results from the IMPACT Study: Evidence for Prostate-specific Antigen Screening in BRCA2 Mutation Carriers

artículo científico publicado en 2019

International Lung Cancer Consortium: coordinated association study of 10 potential lung cancer susceptibility variants

artículo científico publicado en 2010

International rates of breast reconstruction after prophylactic mastectomy in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2013

International trends in the uptake of cancer risk reduction strategies in women with a BRCA1 or BRCA2 mutation

scientific article published on 11 April 2019

International variation in rates of uptake of preventive options in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2008

Interplay between BRCA1 and RHAMM regulates epithelial apicobasal polarization and may influence risk of breast cancer

artículo científico publicado en 2011

Investigation of Exomic Variants Associated with Overall Survival in Ovarian Cancer

artículo científico publicado en 2016

Iron and breast cancer risk

artículo científico publicado en 2012

Iron as diagnostic marker of cancer.

artículo científico publicado en 2015

Iron levels, genes involved in iron metabolism and antioxidative processes and lung cancer incidence

artículo científico publicado en 2019

Is there any relationship between BRCA1 gene mutation and pancreatic cancer development?

artículo científico publicado en 2008

LDL-R and Apo-B-100 gene mutations in Polish familial hypercholesterolemias

artículo científico publicado en 1998

Lack of association between genetic polymorphisms in cytokine genes and disease expression in patients with hereditary non-polyposis colorectal cancer

artículo científico publicado en 2007

Lactase persistence and ovarian carcinoma risk in Finland, Poland and Sweden

artículo científico publicado en 2005

Large BRCA1 and BRCA2 genomic rearrangements in Polish high-risk breast and ovarian cancer families

artículo científico publicado en 2013

Large deletion causing von Hippel-Lindau disease and hereditary breast cancer syndrome

artículo científico publicado en 2014

Large-Scale Genomic Analyses Link Reproductive Aging to Hypothalamic Signaling, Breast Cancer Susceptibility, and BRCA1-Mediated DNA Repair

artículo científico publicado en 2015

Large-scale genomic analyses link reproductive aging to hypothalamic signaling, breast cancer susceptibility and BRCA1-mediated DNA repair

artículo científico publicado en 2015

Large-scale genotyping identifies 41 new loci associated with breast cancer risk

artículo científico publicado en 2013

Long polymerase chain reaction in detection of germline deletions in the von Hippel-Lindau tumour suppressor gene

artículo científico publicado en 1999

Long-term effect of aspirin on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

artículo científico publicado en 2011

Long-term effect of resistant starch on cancer risk in carriers of hereditary colorectal cancer: an analysis from the CAPP2 randomised controlled trial

article

Long-term outcomes following a diagnosis of ovarian cancer at the time of preventive oophorectomy among BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2020

Loss or reduction of Fhit expression in renal neoplasias: correlation with histogenic class

scientific article published on 01 November 1999

Losses at 3p common deletion sites in subtypes of kidney tumours: histopathological correlations

artículo científico publicado en 1996

Low penetrance breast cancer susceptibility loci are associated with specific breast tumor subtypes: findings from the Breast Cancer Association Consortium

artículo científico publicado en 2011

Low prevalence of CDKN2A/ARF mutations among early-onset cancers of breast, pancreas and malignant melanoma in Poland

artículo científico publicado en 2008

Low-risk Genes and Multi-organ Cancer Risk in the Polish Population

artículo científico publicado en 2006

Lung Cancer Occurrence-Correlation with Serum Chromium Levels and Genotypes

scientific article published on 09 July 2020

Lung cancer susceptibility locus at 5p15.33

artículo científico publicado en 2008

Lynch syndrome (HNPCC).

artículo científico publicado en 2008

Lynch syndrome mutations in Poland and the Baltic States.

artículo científico publicado en 2015

Lynch syndrome mutations shared by the Baltic States and Poland.

artículo científico publicado en 2013

MC1R common variants, CDKN2A and their association with melanoma and breast cancer risk

artículo científico publicado en 2006

MDM2 SNP309 T>G alone or in combination with theTP53 R72P polymorphism does not appear to influence disease expression and age of diagnosis of colorectal cancer in HNPCC patients

artículo científico publicado en 2006

MSH2 and MLH1 testing

artículo científico publicado en 2008

MSH6 syndrome

artículo científico publicado en 2008

MTHFR 677 C>T and 1298 A>C polymorphisms and the age of onset of colorectal cancer in hereditary nonpolyposis colorectal cancer

artículo científico publicado en 2009

Magnesium as a diagnostic marker of cancer.

artículo científico publicado en 2015

Male breast cancer in BRCA1 and BRCA2 mutation carriers: pathology data from the Consortium of Investigators of Modifiers of BRCA1/2.

artículo científico publicado en 2016

Male to female ratio among offspring of BRCA1 mutation carriers.

artículo científico publicado en 2005

Mammography screening and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers: a prospective study

article

Management of ovarian and endometrial cancers in women belonging to HNPCC carrier families: review of the literature and results of cancer risk assessment in Polish HNPCC families

artículo científico publicado en 2015

Mapping genomic loci implicates genes and synaptic biology in schizophrenia

artículo científico publicado en 2022

Meeting abstracts from the Annual Conference on Hereditary Cancers 2015: Szczecin, Poland. 24-25 September, 2015.

artículo científico publicado en 2017

Meeting abstracts from the Annual Conference on Hereditary Cancers 2016: Szczecin, Poland. 14-15 September 2016.

artículo científico publicado en 2017

Mendelian randomisation study of height and body mass index as modifiers of ovarian cancer risk in 22,588 BRCA1 and BRCA2 mutation carriers

scientific article published on 19 June 2019

Mendelian randomisation study of smoking exposure in relation to breast cancer risk

artículo científico publicado en 2021

Methylation of the BRCA1 promoter in peripheral blood DNA is associated with triple-negative and medullary breast cancer

artículo científico publicado en 2014

Methylenetetrahydrofolate reductase polymorphisms modify BRCA1-associated breast and ovarian cancer risks

scientific article published on 25 October 2006

MiRNA-362-3p induces cell cycle arrest through targeting of E2F1, USF2 and PTPN1 and is associated with recurrence of colorectal cancer

artículo científico publicado en 2013

MicroRNA related polymorphisms and breast cancer risk

artículo científico publicado en 2014

Microelements as diagnostic markers of pancreatic cancer.

artículo científico publicado en 2015

Microelements as risk factors for cancer of the lung and larynx.

artículo científico publicado en 2012

Mitochondrial NADH-dehydrogenase subunit 3 (ND3) polymorphism (A10398G) and sporadic breast cancer in Poland

artículo científico publicado en 2009

Mitochondrial genotype and breast cancer predisposition

article

Modest association of malignant melanoma with the rs910873 and rs1885120 markers on chromosome 20: a population-based study

artículo científico publicado en 2010

Molecular basis of inherited predispositions for tumors.

artículo científico publicado en 2002

Molecular diagnosis of pituitary adenoma predisposition caused by aryl hydrocarbon receptor-interacting protein gene mutations

artículo científico publicado en 2007

Molecular evidence for derivation of metastatic cells from minor subclones of primary clear renal cell carcinomas

scientific article published on 01 January 1999

Molecular genetic analysis in the diagnosis of lymphoma in fine needle aspiration biopsies. I. Lymphomas versus benign lymphoproliferative disorders

artículo científico publicado en 1988

Molecular genetic analysis in the diagnosis of lymphoma in fine needle aspiration biopsies. II. Lymphomas versus nonlymphoid malignant tumors

artículo científico publicado en 1988

Multiple independent variants at the TERT locus are associated with telomere length and risks of breast and ovarian cancer

artículo científico publicado en 2013

Mutation analysis of MLH1 and MSH2 genes performed by denaturing high-performance liquid chromatography

artículo científico publicado en 2002

Mutation analysis of hypoxia-inducible factors HIF1A and HIF2A in renal cell carcinoma

article

Mutational Signature Analysis Reveals NTHL1 Deficiency to Cause a Multi-tumor Phenotype

scientific article published on 01 February 2019

Mutational Spectrum in a Worldwide Study of 29,700 Families with BRCA1 or BRCA2 Mutations

artículo científico publicado en 2018

Mutations and polymorphisms of genes moderate increase in gastric cancer risk.

artículo científico publicado en 2012

Mutations in ATM, NBN and BRCA2 predispose to aggressive prostate cancer in Poland

artículo científico publicado en 2020

Mutations in the von hippel-lindau tumour suppressor gene in central nervous system hemangioblastomas

artículo científico

Mutations predisposing to breast cancer in 12 candidate genes in breast cancer patients from Poland.

artículo científico publicado en 2014

Mutations spectrum in hereditary disorders predisposing to occurrence of intestine polyposis in Poland.

artículo científico publicado en 2012

MyD88 and TLR4 Expression in Epithelial Ovarian Cancer.

artículo científico publicado en 2018

NBS1 Mutation and prognosis of prostate cancer

NBS1 is a prostate cancer susceptibility gene

artículo científico publicado en 2004

NOD2 variants and the risk of malignant melanoma

artículo científico publicado en 2005

Neoadjuvant chemotherapy with Cisplatin in BRCA1 mutation carriers – results of treatment

artículo científico publicado en 2012

Neoadjuvant therapy with cisplatin in BRCA1-positive breast cancer patients

Network-Based Integration of GWAS and Gene Expression Identifies a HOX-Centric Network Associated with Serous Ovarian Cancer Risk

artículo científico publicado en 2015

New EPCAM founder deletion in Polish population

artículo científico publicado en 2017

No Evidence That Genetic Variation in the Myeloid-Derived Suppressor Cell Pathway Influences Ovarian Cancer Survival

artículo científico publicado en 2016

No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer.

artículo científico publicado en 2015

No evidence that protein truncating variants in BRIP1 are associated with breast cancer risk: implications for gene panel testing

scientific article published on 26 February 2016

Non-isotopic procedure with silver staining of polyacrylamide gels in detection of genomic abnormalities in tumors using microsatellites

artículo científico

Non-random transmission of mutant alleles to female offspring of BRCA1 carriers in Poland

artículo científico publicado en 2003

Nonalcoholic fatty liver disease and HFE gene mutations: a Polish study

artículo científico publicado en 2010

Novel RB1 gene constitutional mutations found in Polish patients with familial and/or bilateral retinoblastoma

artículo científico publicado en 2001

Novel germline mutations in the adenomatous polyposis coli gene in Polish families with familial adenomatous polyposis

artículo científico publicado en 2004

Novel mutations in the LKB1/STK11 gene in Dutch Peutz-Jeghers families

artículo científico publicado en 1999

Nuclear Pedigree Criteria for the Identification of Individuals Suspected to be at Risk of an Inherited Predisposition to Renal Cancer

artículo científico publicado en 2005

Nuclear Pedigree Criteria of Suspected HNPCC.

artículo científico publicado en 2003

Nuclear pedigree criteria for the identification of individuals suspected to be at risk of an inherited predisposition to gastric cancer

artículo científico publicado en 2004

Obesity, Aspirin, and Risk of Colorectal Cancer in Carriers of Hereditary Colorectal Cancer: A Prospective Investigation in the CAPP2 Study

artículo científico publicado en 2015

On the origin and diffusion of BRCA1 c.5266dupC (5382insC) in European populations

artículo científico publicado en 2010

Oophorectomy after menopause and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2012

Oophorectomy and risk of contralateral breast cancer among BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2019

Optimization of experimental conditions for RNA-based sequencing of MLH1 and MSH2 genes

artículo científico publicado en 2001

Optimizing recruitment to a prostate cancer surveillance program among male BRCA1 mutation carriers: invitation by mail or by telephone

scientific article published on 10 December 2013

Oral contraceptives and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2002

Ovarian cancer of endometrioid type as part of the MSH6 gene mutation phenotype

artículo científico publicado en 2002

Ovarian cancer risk in Polish BRCA1 mutation carriers is not associated with the prohibitin 3' untranslated region polymorphism

artículo científico publicado en 2008

Ovarian cancer susceptibility alleles and risk of ovarian cancer in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2012

Ovarian cystadenoma as a characteristic feature of families with hereditary ovarian cancers unassociated with BRCA1 and BRCA2 mutations.

artículo científico publicado en 2004

Overexpression of cyclin E protein is closely related to the mutator phenotype of colorectal carcinoma

artículo científico publicado en 2002

PALB2 mutations and prostate cancer risk and survival

artículo científico publicado en 2021

PALB2, CHEK2 and ATM rare variants and cancer risk: data from COGS

artículo científico publicado en 2016

PARP-1 expression in breast cancer including BRCA1-associated, triple negative and basal-like tumors: possible implications for PARP-1 inhibitor therapy

artículo científico publicado en 2011

PARS PLANA VITRECTOMY IN ADVANCED CASES OF VON HIPPEL-LINDAU EYE DISEASE.

artículo científico publicado en 2015

PHIP - a novel candidate breast cancer susceptibility locus on 6q14.1.

artículo científico publicado en 2017

Pathologic complete response rates in young women with BRCA1-positive breast cancers after neoadjuvant chemotherapy

artículo científico publicado en 2009

Pathologic complete response to neoadjuvant cisplatin in BRCA1-positive breast cancer patients

artículo científico publicado en 2014

Pathological complete response after cisplatin neoadjuvant therapy is associated with the downregulation of DNA repair genes in BRCA1-associated triple-negative breast cancers

artículo científico publicado en 2016

Pathological complete response to neoadjuvant cisplatin in BRCA1-positive breast cancer patients.

artículo científico publicado en 2015

Pathology of Tumors Associated With Pathogenic Germline Variants in 9 Breast Cancer Susceptibility Genes

artículo científico publicado en 2022

Pathology of breast cancer in women with constitutional CHEK2 mutations

artículo científico publicado en 2005

Patient survival and tumor characteristics associated with CHEK2:p.I157T - findings from the Breast Cancer Association Consortium

artículo científico publicado en 2016

Pedigree based DNA sequencing pipeline for germline genomes of cancer families

artículo científico publicado en 2016

Phase II, open-label, randomized, multicenter study comparing the efficacy and safety of olaparib, a poly (ADP-ribose) polymerase inhibitor, and pegylated liposomal doxorubicin in patients with BRCA1 or BRCA2 mutations and recurrent ovarian cancer

scientific article published on 27 December 2011

Phenocopies in breast cancer 1 (BRCA1) families: implications for genetic counselling

artículo científico publicado en 2007

Physical activity during adolescence and young adulthood and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2018

Plasma folate, vitamin B-6, and vitamin B-12 and breast cancer risk in BRCA1- and BRCA2-mutation carriers: a prospective study

artículo científico publicado en 2016

Plasma micronutrients, trace elements, and breast cancer in BRCA1 mutation carriers: an exploratory study

scientific article published on 11 May 2012

Pleomorphic adenoma of salivary glands does not appear to be a BRCA-1-dependent tumour in a Polish cohort.

artículo científico publicado en 2008

Poly(ADP)-ribose polymerase inhibition: frequent durable responses in BRCA carrier ovarian cancer correlating with platinum-free interval

artículo científico publicado en 2010

Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes

artículo científico publicado en 2019

Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants

artículo científico publicado en 2020

Polymorphic variants in VAX1 gene (rs7078160) and BMP4 gene (rs762642) and the risk of non-syndromic orofacial clefts in the Polish population

artículo científico publicado en 2014

Polymorphism in the P-glycoprotein drug transporter MDR1 gene in colon cancer patients.

artículo científico publicado en 2005

Polymorphism of GSTM1 gene in patients with colorectal cancer and colonic polyps

artículo científico publicado en 1999

Polymorphisms in MMP-1, MMP-2, MMP-7, MMP-13 and MT2A do not contribute to breast, lung and colon cancer risk in polish population

scientific article published on 31 July 2020

Polymorphisms in a Putative Enhancer at the 10q21.2 Breast Cancer Risk Locus Regulate NRBF2 Expression

artículo científico publicado en 2015

Polymorphisms in nucleotide excision repair genes and susceptibility to colorectal cancer in the Polish population

artículo científico publicado en 2014

Population Screening of CHEK2 Mutations in Poland

artículo científico publicado en 2006

Population screening for cancer family syndromes in the west pomeranian region of poland

artículo científico publicado en 2006

Population-based targeted sequencing of 54 candidate genes identifies PALB2 as a susceptibility gene for high-grade serous ovarian cancer

artículo científico publicado en 2020

Possible association of the BRCA2 gene C5972T variant with gastric cancer: a study on Polish population

artículo científico publicado en 2015

Pre-Pregnancy Obesity vs. Other Risk Factors in Probability Models of Preeclampsia and Gestational Hypertension

scientific article published on 02 September 2020

Prediction and clinical utility of a contralateral breast cancer risk model

scientific article published on 17 December 2019

Prediction of breast cancer risk based on profiling with common genetic variants

artículo científico publicado en 2015

Prediction of contralateral breast cancer: external validation of risk calculators in 20 international cohorts

scientific article published on 11 April 2020

Prediction of individual genetic risk to prostate cancer using a polygenic score

artículo científico publicado en 2015

Predictors of contralateral prophylactic mastectomy in women with a BRCA1 or BRCA2 mutation: the Hereditary Breast Cancer Clinical Study Group

artículo científico publicado en 2008

Predictors of survival for breast cancer patients with a BRCA1 mutation

artículo científico publicado en 2017

Prevalence and spectrum of MLH1, MSH2, and MSH6 pathogenic germline variants in Pakistani colorectal cancer patients

artículo científico publicado en 2019

Prevalence of BRCA1 and BRCA2 germline mutations in patients with triple-negative breast cancer

artículo científico publicado en 2015

Prevalence of Germline Mutations in Genes Engaged in DNA Damage Repair by Homologous Recombination in Patients with Triple-Negative and Hereditary Non-Triple-Negative Breast Cancers

artículo científico publicado en 2015

Prevalence of Recurrent Mutations Predisposing to Breast Cancer in Early-Onset Breast Cancer Patients from Poland

artículo científico publicado en 2020

Prevalence of germline TP53 variants among early-onset breast cancer patients from Polish population

artículo científico publicado en 2020

Prevalence of the BLM nonsense mutation, p.Q548X, in ovarian cancer patients from Central and Eastern Europe

artículo científico publicado en 2015

Prevalence of the E318K and V320I MITF germline mutations in Polish cancer patients and multiorgan cancer risk-a population-based study

artículo científico publicado en 2014

Prevalence of the NOD2 3020insC mutation in aggregations of breast and lung cancer

artículo científico publicado en 2005

Principles of genetic predisposition to malignancies

artículo científico publicado en 2008

Prognostic gene expression signature for high-grade serous ovarian cancer

artículo científico publicado en 2020

Prospective clinical trials on correlations between macro-/ microelements and vitamins and cancer risk

artículo científico publicado en 2012

Prospective evaluation of alcohol consumption and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers

scientific article published on 03 May 2015

Prospective evaluation of body size and breast cancer risk among BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2018

Prospective observation of breast/ovarian cancer risk in BRCA1 carriers depending on serum selenium level optimized with diet

artículo científico publicado en 2012

Prostate cancer screening based on genotyping for high risk founder alleles

Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition

artículo científico publicado en 2018

Prostate-specific antigen velocity in a prospective prostate cancer screening study of men with genetic predisposition.

artículo científico publicado en 2018

Proteogenomic insights into the biology and treatment of HPV-negative head and neck squamous cell carcinoma

artículo científico publicado en 2021

Psoriasis vulgaris and familial cancer risk- a population-based study.

artículo científico publicado en 2013

Publisher Correction: Evidence that breast cancer risk at the 2q35 locus is mediated through IGFBP5 regulation.

artículo científico publicado en 2018

Publisher Correction: Shared heritability and functional enrichment across six solid cancers

scientific article published on 23 September 2019

RAD51 135G-->C modifies breast cancer risk among BRCA2 mutation carriers: results from a combined analysis of 19 studies

artículo científico publicado en 2007

RAD51B in Familial Breast Cancer

artículo científico publicado en 2016

Rare variants of large effect in BRCA2 and CHEK2 affect risk of lung cancer

scientific journal article

Rarity of germline 1100delC mutation in CHK2 in patients with malignant melanoma of the skin

artículo científico publicado en 2004

Re: Roles of Radiation Dose, Chemotherapy, and Hormonal Factors in Breast Cancer Following Hodgkin's Disease ⬇️

artículo científico publicado el 15 de octubre de 2003

Recommendations to improve identification of hereditary and familial colorectal cancer in Europe.

artículo científico publicado en 2009

Recurrent Mutations in BRCA1, BRCA2, RAD51C, PALB2 and CHEK2 in Polish Patients with Ovarian Cancer

artículo científico publicado en 2021

Recurrent PALB2 mutations and the risk of cancers of bladder or kidney in Polish population

artículo científico publicado en 2021

Recurrent mutations of BRCA1 and BRCA2 in Poland: an update

artículo científico publicado en 2014

Recurrent mutations of BRCA1, BRCA2 and PALB2 in the population of breast and ovarian cancer patients in Southern Poland

artículo científico publicado en 2016

Refined histopathological predictors of BRCA1 and BRCA2 mutation status: a large-scale analysis of breast cancer characteristics from the BCAC, CIMBA, and ENIGMA consortia

artículo científico publicado en 2014

Reply to 'Mutations in RECQL are not associated with breast cancer risk in an Australian population'

scientific article published on 01 October 2018

Reproductive and hormonal factors, and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers: results from the International BRCA1/2 Carrier Cohort Study

artículo científico publicado en 2009

Reproductive risk factors for ovarian cancer in carriers of BRCA1 or BRCA2 mutations: a case-control study

article

Response to neo-adjuvant chemotherapy in women with BRCA1-positive breast cancers

artículo científico publicado en 2007

Response to neoadjuvant therapy with cisplatin in BRCA1-positive breast cancer patients

artículo científico publicado en 2008

Results of a phase II open-label, non-randomized trial of cisplatin chemotherapy in patients with BRCA1-positive metastatic breast cancer

artículo científico publicado en 2012

Retinal dysfunction in eyes of patients with BRCA1 gene mutation

artículo científico publicado en 2005

Retinal function in the von Hippel-Lindau disease

artículo científico publicado el 1 de mayo de 2003

Risk factors for endometrial cancer among women with a BRCA1 or BRCA2 mutation: a case control study

artículo científico publicado en 2015

Risk of breast cancer after a diagnosis of ovarian cancer in BRCA mutation carriers: Is preventive mastectomy warranted?

artículo científico publicado en 2017

Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer

artículo científico publicado en 2011

Risk of ovarian cancer and the NF-κB pathway: genetic association with IL1A and TNFSF10

artículo científico publicado en 2013

Role of germline aberrations affecting CTNNA1, MAP3K6 and MYD88 in gastric cancer susceptibility.

artículo científico publicado en 2018

Salpingo-oophorectomy and the risk of ovarian, fallopian tube, and peritoneal cancers in women with a BRCA1 or BRCA2 Mutation.

artículo científico publicado en 2006

Screening mammography and risk of breast cancer in BRCA1 and BRCA2 mutation carriers: a case-control study.

artículo científico publicado en 2006

Screening with Magnetic Resonance Imaging in women at low and intermediate risk of breast Cancer

Screening with magnetic resonance imaging, mammography and ultrasound in women at average and intermediate risk of breast cancer

scientific article published on March 2017

Selected features of breast and peritoneal cancers diagnosed in BRCA1 carriers after risk-reducing salpingo-oophorectomy

Selenium (Se) and breast cancer risk

Selenium (Se) and the risk of breast, ovarian and prostate cancers

artículo científico publicado en 2012

Selenium and cancer risk in CHEK2 mutation carriers

Selenium and gastrointestinal cancers risk

artículo científico publicado en 2012

Selenium and risk of bladder cancer

Selenium and the risk of cancer in BRCA1 carriers

artículo científico publicado en 2011

Selenium and the risk of cancer of the lung and larynx. A case-control study from a region with low selenium.

artículo científico publicado en 2012

Selenium and the risk of cancers of the colon, pancreas and stomach

artículo científico publicado en 2012

Selenium as a marker of cancer risk and of selection for control examinations in surveillance

artículo científico publicado en 2015

Selenium as diagnostic marker of cancers.

artículo científico publicado en 2015

Selenium as marker for cancer risk and prevention

artículo científico publicado en 2012

Selenium supplementation reduced oxidative DNA damage in adnexectomized BRCA1 mutations carriers

artículo científico publicado en 2009

Serum 25(OH)D concentration, common variants of the VDR gene and lung cancer occurrence

artículo científico publicado en 2017

Serum Concentrations of Selenium and Copper in Patients Diagnosed with Pancreatic Cancer

artículo científico publicado en 2015

Serum Microelements in Early Pregnancy and their Risk of Large-for-Gestational Age Birth Weight

scientific article published on 24 March 2020

Serum Selenium Level in Early Healthy Pregnancy as a Risk Marker of Pregnancy Induced Hypertension.

artículo científico publicado en 2019

Serum concentration of iron as predictor of cancer risk among BRCA1 mutation carriers.

artículo científico publicado en 2012

Serum concentration of selected macro- and microelements and their correlation with the risk of breast and ovarian cancer among BRCA1 mutation carriers

Serum concentrations of Cu, Se, Fe and Zn in patients diagnosed with pancreatic cancer.

artículo científico publicado en 2015

Serum folate concentration and the incidence of lung cancer

artículo científico publicado en 2017

Serum selenium level and cancer risk: a nested case-control study

scientific article published on 23 December 2019

Serum selenium levels and the risk of progression of laryngeal cancer

artículo científico publicado en 2018

Serum selenium levels are associated with age-related cataract

artículo científico publicado en 2018

Serum selenium levels predict survival after breast cancer

artículo científico publicado en 2017

Seven prostate cancer susceptibility loci identified by a multi-stage genome-wide association study

artículo científico publicado en 2011

Sex specific associations in genome wide association analysis of renal cell carcinoma

scientific article published on 23 June 2019

Shared genetics underlying epidemiological association between endometriosis and ovarian cancer

artículo científico publicado en 2015

Shared heritability and functional enrichment across six solid cancers

artículo científico publicado en 2019

Shared heritability and functional enrichment across six solid cancers

Short report. The AIDIT and IMPACT conference 2006: Outcomes and future directions

artículo científico publicado en 2007

Should all BRCA1 mutation carriers with stage I breast cancer receive chemotherapy?

artículo científico publicado en 2013

Smoking and the risk of breast cancer among carriers of BRCA mutations

article

Smoking and the risk of breast cancer in BRCA1 and BRCA2 carriers: an update

artículo científico publicado en 2008

Smoking related cancers and loci at chromosomes 15q25, 5p15, 6p22.1 and 6p21.33 in the Polish population

artículo científico publicado en 2011

Sonographic imaging of Spigelian hernias

artículo científico publicado en 2012

Spontaneous and therapeutic abortions and the risk of breast cancer among BRCA mutation carriers

artículo científico publicado en 2006

Sulforaphane-mediated induction of a phase 2 detoxifying enzyme NAD(P)H:quinone reductase and apoptosis in human lymphoblastoid cells.

artículo científico publicado en 2004

Supernormal electro-oculograms in patients with neurofibromatosis type 1.

artículo científico publicado en 2004

Survival from breast cancer in patients with CHEK2 mutations.

artículo científico publicado en 2014

Survival in patients with rare subtypes of renal cell carcinoma

artículo científico publicado en 2002

Suspected HNPCC and Amsterdam criteria II: evaluation of mutation detection rate, an international collaborative study.

artículo científico publicado en 2002

Synergistic interaction of variants in CHEK2 and BRCA2 on breast cancer risk

artículo científico publicado en 2008

Tamoxifen and contralateral breast cancer in BRCA1 and BRCA2 carriers: an update

artículo científico publicado en 2006

Tamoxifen and the risk of ovarian cancer in BRCA1 mutation carriers

artículo científico publicado en 2009

Targeted prostate cancer screening in BRCA1 and BRCA2 mutation carriers: results from the initial screening round of the IMPACT study

artículo científico publicado en 2014

Targeted prostate cancer screening in men with mutations in BRCA1 and BRCA2 detects aggressive prostate cancer: preliminary analysis of the results of the IMPACT study

artículo científico publicado en 2010

Ten-year survival in patients with BRCA1-negative and BRCA1-positive breast cancer

artículo científico publicado en 2013

Thank you to all our manuscript reviewers in 2014.

artículo científico publicado en 2015

Thank you to all our manuscript reviewers in 2015.

artículo científico publicado en 2016

The 12p13.33/RAD52 locus and genetic susceptibility to squamous cell cancers of upper aerodigestive tract

artículo científico publicado en 2015

The 3' untranslated region C > T polymorphism of prohibitin is a breast cancer risk modifier in Polish women carrying a BRCA1 mutation

artículo científico publicado en 2006

The 30 kb deletion in the APOBEC3 cluster decreases APOBEC3A and APOBEC3B expression and creates a transcriptionally active hybrid gene but does not associate with breast cancer in the European population

artículo científico publicado en 2017

The 3020insC Allele of NOD2 Predisposes to Cancers of Multiple Organs

artículo científico publicado en 2005

The 3020insC NOD2 gene mutation in patients with ovarian cancer.

artículo científico publicado en 2008

The 3020insC allele of NOD2 predisposes to early-onset breast cancer

artículo científico publicado en 2005

The 4154delA mutation carriers in the BRCA1 gene share a common ancestry.

artículo científico publicado en 2008

The APOBEC3B c.783delG Truncating Mutation Is Not Associated with an Increased Risk of Breast Cancer in the Polish Population

artículo científico publicado en 2023

The Association Between the Interleukin-1 Polymorphisms and Gastric Cancer Risk Depends on the Family History of Gastric Carcinoma in the Study Population

artículo científico publicado en 2006

The Association of the COMT V158M Polymorphism with Endometrial/Ovarian Cancer in HNPCC Families Adhering to the Amsterdam Criteria

artículo científico publicado en 2006

The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions

artículo científico publicado en 2008

The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions.

artículo científico publicado en 2008

The BRCA2 c.68-7T > A variant is not pathogenic: A model for clinical calibration of spliceogenicity

artículo científico publicado en 2018

The CHEK 2 GENE mutations and the risk of Gastric cancer

artículo científico publicado en 2012

The CYP17A1 -34T > C polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2010

The DIRC1 gene at chromosome 2q33 spans a familial RCC-associated t(2;3)(q33;q21) chromosome translocation

artículo científico publicado en 2001

The FANCM:p.Arg658* truncating variant is associated with risk of triple-negative breast cancer

scientific article published on 01 November 2019

The G84E mutation in the HOXB13 gene is associated with an increased risk of prostate cancer in Poland

artículo científico publicado en 2013

The HOXB13 p.Gly84Glu mutation is not associated with the risk of breast cancer

artículo científico publicado en 2012

The Influence of Maternal BMI on Adverse Pregnancy Outcomes in Older Women

scientific article published on 16 September 2020

The Leu33Pro polymorphism in the ITGB3 gene does not modify BRCA1/2-associated breast or ovarian cancer risks: results from a multicenter study among 15,542 BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2009

The NOD2 3020insC Mutation and The Risk of Familial Pancreatic Cancer?

artículo científico publicado en 2004

The NOD2 3020insC mutation and the risk of colorectal cancer

artículo científico publicado en 2004

The Prevalence of Founder Mutations among Individuals from Families with Familial Pancreatic Cancer Syndrome

artículo científico publicado en 2016

The RAD51 135 G>C polymorphism modifies breast cancer and ovarian cancer risk in Polish BRCA1 mutation carriers

artículo científico publicado en 2007

The Risk of Breast Cancer in BRCA1 and BRCA2 Mutation Carriers without a First-Degree Relative with Breast Cancer

artículo científico publicado en 2017

The Role of Early Pregnancy Maternal Selenium Levels on the Risk for Small-for-Gestational Age Newborns

artículo científico publicado en 2019

The VEGF_936_C>T 3'UTR polymorphism reduces BRCA1-associated breast cancer risk in Polish women

artículo científico publicado en 2008

The association between smoking and cancer incidence in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2018

The contribution of founder mutations in BRCA1 to breast and ovarian cancer in Lithuania

artículo científico publicado en 2010

The contribution of founder mutations in BRCA1 to breast cancer in Belarus.

artículo científico publicado en 2010

The effect on melanoma risk of genes previously associated with telomere length

artículo científico publicado en 2014

The impact of an expanded genetic testing program and selective oophorectomy on the incidence of ovarian cancer in West Pomerania

artículo científico publicado en 2016

The impact of oophorectomy on survival after breast cancer in BRCA1-positive breast cancer patients

artículo científico publicado en 2016

The impact of oophorectomy on survival from breast cancer in patients with CHEK2 mutations

artículo científico publicado en 2022

The impact of pregnancy on breast cancer survival in women who carry a BRCA1 or BRCA2 mutation

artículo científico publicado en 2013

The incidence of endometrial cancer in women with BRCA1 and BRCA2 mutations: an international prospective cohort study.

artículo científico publicado en 2013

The incidence of leukaemia in women with BRCA1 and BRCA2 mutations: an International Prospective Cohort Study

artículo científico publicado en 2016

The incidence of pancreatic cancer in BRCA1 and BRCA2 mutation carriers

artículo científico publicado en 2012

The influence of obesity-related factors in the etiology of renal cell carcinoma-A mendelian randomization study ⬇️

scientific article published on 03 January 2019

The influence of selenium concentration and variations in selenoprotein genes on the CHEK2-dependent cancers.

artículo científico publicado en 2015

The intron 3 16 bp duplication polymorphism of p53 (rs17878362) is not associated with increased risk of developing triple-negative breast cancer

scientific article published on 14 November 2018

The potential role of miRNAs in therapy of breast and ovarian cancers associated with BRCA1 mutation

artículo científico publicado en 2017

The presence of prostate cancer at biopsy is predicted by a number of genetic variants

artículo científico publicado en 2013

The reliability of immunohistochemistry as a prescreening method for the diagnosis of hereditary nonpolyposis colorectal cancer (HNPCC)--results of an international collaborative study

artículo científico publicado el 1 de enero de 2001

The risk of breast cancer in women with a BRCA1 mutation from North America and Poland

artículo científico publicado en 2011

The risk of breast cancer in women with a CHEK2 mutation

artículo científico publicado en 2012

The risk of endometrial cancer in women with BRCA1 and BRCA2 mutations. A prospective study.

artículo científico publicado en 2006

The risk of gastric cancer in carriers of CHEK2 mutations

artículo científico publicado en 2013

The rs1447295 and DG8S737 markers on chromosome 8q24 and cancer risk in the Polish population.

artículo científico publicado en 2010

The spectrum of mutations predisposing to familial breast cancer in Poland

scientific article published on 26 June 2019

The variant allele of the rs188140481 polymorphism confers a moderate increase in the risk of prostate cancer in Polish men

artículo científico publicado en 2015

The −149C>T SNP within the ΔDNMT3B gene, is not associated with early disease onset in hereditary non-polyposis colorectal cancer

artículo científico publicado en 2008

Timing of oral contraceptive use and the risk of breast cancer in BRCA1 mutation carriers

artículo científico publicado en 2014

Trans-ancestry genome-wide association meta-analysis of prostate cancer identifies new susceptibility loci and informs genetic risk prediction

artículo científico publicado en 2021

Transcriptome-wide association study of breast cancer risk by estrogen-receptor status

artículo científico publicado en 2020

Translocation (X;1)(p11.2;q21) in a papillary renal cell carcinoma in a 14-year-old girl.

artículo científico publicado en 1998

Transmission electron microscopy in the diagnosis of metastases of malignant melanoma using specimens obtained by fine-needle puncture biopsy

artículo científico publicado el 1 de enero de 1988

Transmission electron microscopy in the differential diagnosis of thyroid tumors using specimens obtained by fine-needle puncture biopsy

artículo científico publicado el 1 de enero de 1988

Transmission of mutant alleles to female offspring of BRCA1 carriers in Poland

artículo científico publicado en 2005

Treatment of infertility does not increase the risk of ovarian cancer among women with a BRCA1 or BRCA2 mutation

artículo científico publicado en 2015

Two truncating variants in FANCC and breast cancer risk

artículo científico publicado en 2019

Unraveling genetic predisposition to familial or early onset gastric cancer using germline whole-exome sequencing

artículo científico publicado en 2017

Usefulness of polymorphic markers in exclusion of BRCA1/BRCA2 mutations in families with aggregation of breast/ovarian cancers.

artículo científico publicado en 2003

Value of pedigree/clinical data, immunohistochemistry and microsatellite instability analyses in reducing the cost of determining hMLH1 and hMSH2 gene mutations in patients with colorectal cancer

artículo científico publicado en 2000

Variant alleles of the CYP1B1 gene are associated with colorectal cancer susceptibility

artículo científico publicado en 2010

Variants in genes encoding small GTPases and association with epithelial ovarian cancer susceptibility

artículo científico publicado en 2018

Variation in NF-κB signaling pathways and survival in invasive epithelial ovarian cancer

artículo científico publicado en 2014

Vitamin D receptor variants and breast cancer risk in the Polish population

artículo científico publicado en 2008

Vitamin D receptor variants and the malignant melanoma risk: a population-based study

artículo científico publicado en 2009

Weight gain after oophorectomy among women with a BRCA1 or BRCA2 mutation

artículo científico publicado en 2015

Why choose the treatment with cisplatin for BRCA1 breast cancers patients?

artículo científico publicado en 2012

XPD common variants and their association with melanoma and breast cancer risk.

artículo científico publicado en 2006

Xeroderma pigmentosum genes and melanoma risk

artículo científico publicado en 2013

Zinc and breast cancer risk

artículo científico publicado en 2012

Zinc as diagnostic marker of cancers.

artículo científico publicado en 2015

[A rapid method of preparing specimens obtained by fine-needle biopsy for transmission electron microscopy]

scientific article published on 01 April 1985

[Behavior of SCC antigen in girls with a high risk of developing cervical carcinoma]

scientific article published on 01 June 1993

[Detection of tumor virus infections with HPV 16, 18, and 33 from cytologic material in the uterine neck using the PCR method]

artículo científico publicado en 1993

[Diagnosis of Mycobacterium tuberculosis infections using PCR methods]

scientific article published on 01 January 1995

[Differential diagnosis of cancer by fine-needle aspirates using transmission electron microscopy. III. Undifferentiated cancer (anaplastic)]

scientific article published on 01 April 1987

[Differential diagnosis of cancer in fine needle aspirates using transmission electron microscopy. I. Adenocarcinoma]

artículo científico publicado en 1986

[Differential diagnosis of cancer in fine-needle biopsy aspirates using the transmission electron microscope. II. Squamous cell carcinoma]

artículo científico publicado en 1986

[HLA-G alleles and risk of early pregnancy loss]

artículo científico publicado en 2008

[HPV virus infections and other promotion factors of the carcinogenic process in girls]

scientific article published on 01 July 1993

[RFLP-PCR technique for exclusion of carrier status of the mutated Rb gene]

scientific article published on 01 June 1993

[Transmission electron microscopy in the differential diagnosis of malignant neoplasms using fine-needle aspirates]

artículo científico publicado en 1989

[Transmission electron microscopy in the differential diagnosis of malignant small round cell tumors of childhood using biopsy aspirates]

artículo científico publicado en 1988

[Transmission electron microscopy in the differential diagnosis of non-Hodgkin's lymphoma using fine-needle aspirates]

artículo científico publicado en 1988

[Transmission electron microscopy in the differential diagnosis of soft tissue and bone sarcomas and germinal tumors using fine needle aspirates]

artículo científico publicado en 1988

[VNTR-PCR in diagnosis of inherited Rb gene mutation]

artículo científico publicado en 1994

p53 and ovarian carcinoma survival: an Ovarian Tumor Tissue Analysis consortium study

artículo científico publicado en 2023

rs2735383, located at a microRNA binding site in the 3'UTR of NBS1, is not associated with breast cancer risk

artículo científico publicado en 2016

rs495139 in the TYMS-ENOSF1 Region and Risk of Ovarian Carcinoma of Mucinous Histology

artículo científico publicado en 2018

Lista de obras de Jan Lubiński

11q13 is a susceptibility locus for hormone receptor positive breast cancer

A Lowering of Breast and Ovarian Cancer Risk in Women with a BRCA1 Mutation by Selenium Supplementation of Diet

A Range of Cancers Is Associated with the rs6983267 Marker on Chromosome 8

A case of carotid body paraganglioma and haemangioblastoma of the spinal cord in a patient with the N131K missense mutation in the VHL gene

A combination of the immunohistochemical markers CK7 and SATB2 is highly sensitive and specific for distinguishing primary ovarian mucinous tumors from colorectal and appendiceal metastases

A common missense variant in BRCA2 predisposes to early onset breast cancer

A common nonsense mutation of the BLM gene and prostate cancer risk and survival

A common variant of CDKN2A (p16) predisposes to breast cancer

A comparison of ovarian cancer mortality in women with BRCA1 mutations undergoing annual ultrasound screening or preventive oophorectomy

A deletion in CHEK2 of 5,395 bp predisposes to breast cancer in Poland

A genome-wide analysis of populations from European Russia reveals a new pole of genetic diversity in northern Europe

A genome-wide association study for extremely high intelligence.

A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.

A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23

A genome-wide association study identifies susceptibility loci for ovarian cancer at 2q31 and 8q24.

A genome-wide association study of upper aerodigestive tract cancers conducted within the INHANCE consortium

A high frequency of BRCA2 gene mutations in Polish families with ovarian and stomach cancer

A high proportion of founder BRCA1 mutations in Polish breast cancer families

A large germline deletion in the Chek2 kinase gene is associated with an increased risk of prostate cancer

A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46,450 cases and 42,461 controls from the breast cancer association consortium

A locus on 19p13 modifies risk of breast cancer in BRCA1 mutation carriers and is associated with hormone receptor-negative breast cancer in the general population

A low selenium level is associated with lung and laryngeal cancers

A meta-analysis of genome-wide association studies to identify prostate cancer susceptibility loci associated with aggressive and non-aggressive disease

A network analysis to identify mediators of germline-driven differences in breast cancer prognosis

A nonsense mutation (E1978X) in the ATM gene is associated with breast cancer

A nonsynonymous polymorphism in IRS1 modifies risk of developing breast and ovarian cancers in BRCA1 and ovarian cancer in BRCA2 mutation carriers

A novel deleterious c.2656G>T MSH2 germline mutation in a Pakistani family with a phenotypic overlap of hereditary breast and ovarian cancer and Lynch syndrome

A novel founder CHEK2 mutation is associated with increased prostate cancer risk

A personalised approach to prostate cancer screening based on genotyping of risk founder alleles

A prior diagnosis of breast cancer is a risk factor for breast cancer in BRCA1 and BRCA2 carriers

A protein truncating BRCA1 allele with a low penetrance of breast cancer

A rare truncating BRCA2 variant and genetic susceptibility to upper aerodigestive tract cancer

A sex-specific association between a 15q25 variant and upper aerodigestive tract cancers

A six-nucleotide deletion in the CASP8 promoter is not associated with a susceptibility to breast and prostate cancers in the Polish population

A survey of preventive measures among BRCA1 mutation carriers from Poland

A transcriptome-wide association study of 229,000 women identifies new candidate susceptibility genes for breast cancer

A variant in FTO shows association with melanoma risk not due to BMI

AIDIT and IMPACT: building research collaborations in targeted prostate cancer screening

ARLTS1 Trp149Stop Mutation and the Risk of Ovarian Cancer

AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a consortium of investigators of modifiers of BRCA1/2 study

Abdominal integument atrophy after operative procedures

Abnormalities of chromosome 5q correlate with morphologic features of better prognosis in clear cell renal carcinomas

Absence or reduction of Fhit expression in most clear cell renal carcinomas.

Abstract LB-159: Methylation of BRCA1 gene in blood is not inherited via maternal germ line and may predispose to triple-negative or medullary breast cancer

Activity of trabectedin in germline BRCA1/2-mutated metastatic breast cancer: results of an international first-in-class phase II study

Acute myeloid leukemia in a 38-year-old hemodialyzed patient with von Hippel-Lindau disease

Adult body mass index and risk of ovarian cancer by subtype: a Mendelian randomization study

Adult height is associated with increased risk of ovarian cancer: a Mendelian randomisation study.

Age at diagnosis of cancer as predictor of mutation occurrence in families suspected of HNPCC

Age at diagnosis to discriminate those patients for whom constitutional DNA sequencing is appropriate in sporadic unilateral retinoblastoma

Age at first birth and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers

Age at first full-term birth and breast cancer risk in BRCA1 and BRCA2 mutation carriers

Age at menarche and the risk of breast cancer in BRCA1 and BRCA2 mutation carriers

Age of diagnosis of colorectal cancer in HNPCC patients is more complex than that predicted by R72P polymorphism in TP53.

Age- and Tumor Subtype-Specific Breast Cancer Risk Estimates for CHEK2*1100delC Carriers

Age-specific ovarian cancer risks among women with a BRCA1 or BRCA2 mutation

Age-specific risks of incident, contralateral and ipsilateral breast cancer among 1776 Polish BRCA1 mutation carriers

Alcohol consumption and the risk of breast cancer among BRCA1 and BRCA2 mutation carriers

Allelic modification of breast cancer risk in women with an NBN mutation

An Assessment of Serum Selenium Concentration in Women with Endometrial Cancer

An Assessment of Serum Selenium Concentration in Women with Ovarian Cancer

An evaluation of the polymorphisms Ins16bp and Arg72Pro in p53 as breast cancer risk modifiers in BRCA1 and BRCA2 mutation carriers

An inherited NBN mutation is associated with poor prognosis prostate cancer

An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression

An international survey of surveillance schemes for unaffected BRCA1 and BRCA2 mutation carriers

An original phylogenetic approach identified mitochondrial haplogroup T1a1 as inversely associated with breast cancer risk in BRCA2 mutation carriers

Analysis of germline variants in CDH1, IGFBP3, MMP1, MMP3, STK15 and VEGF in familial and sporadic renal cell carcinoma

Analysis of over 10,000 Cases finds no association between previously reported candidate polymorphisms and ovarian cancer outcome

Anthropometric Measures and Risk of Ovarian Cancer Among BRCA1 and BRCA2 Mutation Carriers

Antigens HLA-G, sHLA- G and sHLA- class I in reproductive failure

Are two-centimeter breast cancers large or small?

Arsenic (As) and breast cancer risk.

Aryl hydrocarbon receptor interacting protein(AIP) gene mutation analysis in children and adolescents with sporadic pituitary adenomas

Assessing associations between the AURKA-HMMR-TPX2-TUBG1 functional module and breast cancer risk in BRCA1/2 mutation carriers

Assessing the genetic architecture of epithelial ovarian cancer histological subtypes

Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with risk of clear cell ovarian cancer

Association analyses of more than 140,000 men identify 63 new prostate cancer susceptibility loci

Association analysis identifies 65 new breast cancer risk loci.

Association between early-onset breast and laryngeal cancers.