Lista de obras -

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

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

artículo científico publicado en 2006

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 low selenium level is associated with lung and laryngeal cancers

artículo científico publicado en 2013

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

artículo científico publicado en 2013

ARLTS1 Trp149Stop Mutation and the Risk of Ovarian Cancer

scientific article published on 01 May 2007

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

scientific article published on 05 January 2019

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

scientific article published on 13 August 2019

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

Association of ADH4 genetic variants with alcohol dependence risk and related phenotypes: results from a larger multicenter association study

artículo científico publicado en 2011

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

artículo científico publicado en 2011

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

artículo científico publicado en 2018

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 compared to ovarian cancer in Belarus

artículo científico publicado en 2014

BRCA1 mutations and colorectal cancer in Poland.

artículo científico publicado en 2010

BRCA1 mutations and prostate cancer in Poland

artículo científico publicado en 2008

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

artículo científico publicado en 2018

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

Breast cancer predisposing alleles in Poland

artículo científico publicado en 2005

Breast cancer susceptibility genes

article

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 as markers for high risk of breast cancer

artículo científico publicado en 2012

CHEK2-positive breast cancers in young Polish women

scientific article published on 01 August 2006

CYP1B1 and predisposition to breast cancer in Poland

article

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

artículo científico publicado en 2006

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

artículo científico publicado en 2009

Clinical genetics of melanoma

article

Clinical genetics of melanoma.

artículo científico publicado en 2012

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

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

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

artículo científico publicado en 2008

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

scientific article published on 24 September 2020

Copper as diagnostic marker of cancers.

artículo científico publicado en 2015

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

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 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

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

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

artículo científico publicado en 2006

Dupuytren's disease and the risk of malignant neoplasms

artículo científico publicado en 2014

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

Epistatic relationship between the cancer susceptibility genes CHEK2 and p27

scientific article published on 01 March 2007

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

artículo científico publicado en 2007

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

artículo científico publicado en 2008

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

artículo científico publicado en 2010

Familial malignant melanoma - overview

artículo científico publicado en 2004

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 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

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

artículo científico publicado en 2014

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

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 polymorphisms may influence the vertical growth rate of melanoma

article published in 2018

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

artículo científico publicado en 2009

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

artículo científico publicado en 2010

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 new melanoma susceptibility loci

artículo científico publicado en 2012

Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3

scientific journal article

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

artículo científico publicado en 2015

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 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 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

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

artículo científico publicado en 2004

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

artículo científico publicado en 2003

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

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 in XRCC2 and the risk of breast cancer

scientific article published on 28 August 2019

Iron and breast cancer risk

artículo científico publicado en 2012

Iron as diagnostic marker of cancer.

artículo científico publicado en 2015

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

artículo científico publicado en 2013

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

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

MC1R variants increased the risk of sporadic cutaneous melanoma in darker-pigmented Caucasians: a pooled-analysis from the M-SKIP project

artículo científico publicado en 2014

Magnesium as a diagnostic marker of cancer.

artículo científico publicado en 2015

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

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

Melanocortin-1 receptor, skin cancer and phenotypic characteristics (M-SKIP) project: study design and methods for pooling results of genetic epidemiological studies ⬇️

artículo científico publicado el 3 de agosto de 2012

Melanoma risk factors, perceived threat and intentional tanning: an international online survey

artículo científico publicado en 2010

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

artículo científico publicado en 2012

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

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

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 therapy with cisplatin in BRCA1-positive breast cancer patients

Nuclear Pedigree Criteria of Suspected HNPCC.

artículo científico publicado en 2003

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

artículo científico publicado en 2001

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

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

scientific article published on 11 May 2012

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

artículo científico publicado en 2014

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

artículo científico publicado en 2006

Predictors of sun protection behaviors and severe sunburn in an international online study

artículo científico publicado en 2010

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

artículo científico publicado en 2014

Principles of genetic predisposition to malignancies

artículo científico publicado en 2008

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

artículo científico publicado en 2012

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

artículo científico publicado en 2013

Rapid test for detection of high risk of breast cancer

artículo científico publicado en 2012

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

artículo científico publicado en 2004

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

Selection criteria for genetic assessment of patients with familial melanoma

artículo científico publicado en 2009

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 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

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

artículo científico publicado en 2017

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

scientific article published on 23 December 2019

Serum selenium levels predict survival after breast cancer

artículo científico publicado en 2017

Skin examination behavior: the role of melanoma history, skin type, psychosocial factors, and region of residence in determining clinical and self-conducted skin examination

artículo científico publicado en 2012

Some molecular and clinical aspects of genetic predisposition to malignant melanoma and tumours of various site of origin

artículo científico publicado en 2007

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

artículo científico publicado en 2008

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

artículo científico publicado en 2005

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

artículo científico publicado en 2013

The NOD2 3020insC mutation and the risk of colorectal cancer

artículo científico publicado en 2004

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

artículo científico publicado en 2013

The risk of breast cancer in women with a CHEK2 mutation

artículo científico publicado en 2012

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 usefulness of Doppler angiography in differential diagnosis of benign and malignant breast lesions

artículo científico publicado en 2004

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

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

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

Vitamins A, E and D and cancer risk in BRCA1 carriers

artículo científico publicado en 2012

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 as diagnostic marker of cancers.

artículo científico publicado en 2015

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

scientific article published on 01 July 1993

Lista de obras de

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

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

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 low selenium level is associated with lung and laryngeal cancers

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

ARLTS1 Trp149Stop Mutation and the Risk of Ovarian Cancer

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

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

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

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

Association of ADH4 genetic variants with alcohol dependence risk and related phenotypes: results from a larger multicenter association study

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

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

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

BARD1 and breast cancer in Poland.

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

BRCA1 founder mutations compared to ovarian cancer in Belarus

BRCA1 mutations and colorectal cancer in Poland.

BRCA1 mutations and prostate cancer in Poland

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

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

Blood cadmium levels as a marker for early lung cancer detection

Breast cancer predisposing alleles in Poland

Breast cancer susceptibility genes

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

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

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

CDKN2A-positive breast cancers in young women from Poland.

CHAPTER 22. Selenium and Cancer

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

CHEK2 is a multiorgan cancer susceptibility gene

CHEK2 mutations and HNPCC-related colorectal cancer.

CHEK2 mutations as markers for high risk of breast cancer

CHEK2-positive breast cancers in young Polish women

CYP1B1 and predisposition to breast cancer in Poland

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

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

Clinical genetics of melanoma

Clinical genetics of melanoma.

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

Common variants of DNA repair genes and malignant melanoma

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

Common variants of xeroderma pigmentosum genes and prostate cancer risk

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

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

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

Copper as diagnostic marker of cancers.

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

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

Corrigendum: Germline RECQL mutations are associated with breast cancer susceptibility

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

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

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

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

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

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

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

Dupuytren's disease and the risk of malignant neoplasms

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

Epistatic relationship between the cancer susceptibility genes CHEK2 and p27

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

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

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

Familial malignant melanoma - overview

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).

Fhit protein expression in hereditary and sporadic colorectal cancers

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

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

Folic acid and cancer risk in BRCA1 carriers.

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.