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A Germline Mutation in the POT1 Gene Is a Candidate for Familial Non-Medullary Thyroid Cancer

scientific article published on 01 June 2020

A candidate CpG SNP approach identifies a breast cancer associated ESR1‐SNP ⬇️

artículo científico publicado el 11 de marzo de 2011

A coding IRAK2 protein variant compromises Toll-like receptor (TLR) signaling and is associated with colorectal cancer survival

artículo científico publicado en 2014

A common variant at the TERT-CLPTM1L locus is associated with estrogen receptor-negative breast cancer

artículo científico publicado en 2011

A comprehensive investigation on common polymorphisms in the MDR1/ABCB1 transporter gene and susceptibility to colorectal cancer

artículo científico publicado en 2012

A functional promoter polymorphism in the TERT gene does not affect inherited susceptibility to breast cancer

artículo científico publicado en 2009

A genome-wide association study identifies colorectal cancer susceptibility loci on chromosomes 10p14 and 8q23.3

article

A genome-wide association study of Hodgkin's lymphoma identifies new susceptibility loci at 2p16.1 (REL), 8q24.21 and 10p14 (GATA3)

scientific journal article

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

Allelotyping of pooled DNA with 250 K SNP microarrays

artículo científico publicado en 2007

Analysis of functional germline variants in APOBEC3 and driver genes on breast cancer risk in Moroccan study population

artículo científico publicado en 2016

Ancestry-shift refinement mapping of the C6orf97-ESR1 breast cancer susceptibility locus

artículo científico publicado en 2010

Association Between Telomere Length and Risk of Cancer and Non-Neoplastic Diseases: A Mendelian Randomization Study ⬇️

artículo científico publicado en 2017

Association between TAS2R38 gene polymorphisms and colorectal cancer risk: a case-control study in two independent populations of Caucasian origin

artículo científico publicado en 2011

Association of () polymorphisms with breast cancer risk

Association of HLA-DRB1, interleukin-6 and cyclin D1 polymorphisms with cervical cancer in the Swedish population--a candidate gene approach

artículo científico publicado en 2009

Association of NCOA3 polymorphisms with breast cancer risk

artículo científico publicado en 2005

Association of prolactin and its receptor gene regions with familial breast cancer.

artículo científico publicado en 2006

Association study identifying polymorphisms in CD47 and other extracellular matrix pathway genes as putative prognostic markers for colorectal cancer.

artículo científico publicado en 2012

Author Correction: Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility

artículo científico publicado en 2019

Author Correction: Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma

artículo científico publicado en 2019

B-RAFmutations in tumors from melanoma-breast cancer families

Basal cell carcinoma and variants in genes coding for immune response, DNA repair, folate and iron metabolism

artículo científico publicado en 2005

Bortezomib-induced peripheral neuropathy: A genome-wide association study on multiple myeloma patients

artículo científico publicado en 2017

Cancer Predisposition Genes in Cancer-Free Families

artículo científico publicado en 2020

Cancer in immigrants as a pointer to the causes of cancer

artículo científico publicado en 2014

Cancer of unknown primary is associated with diabetes

artículo científico publicado en 2015

Cancer risk in patients with type 2 diabetes mellitus and their relatives.

artículo científico publicado en 2015

Chemotherapy-induced peripheral neuropathy: evidence from genome-wide association studies and replication within multiple myeloma patients

Chromosome 7p11.2 (EGFR) variation influences glioma risk

scientific journal article

Coding variants in NOD-like receptors: An association study on risk and survival of colorectal cancer.

artículo científico publicado en 2018

Colorectal cancer risk and patients' survival: influence of polymorphisms in genes somatically mutated in colorectal tumors

artículo científico publicado en 2014

Common breast cancer susceptibility loci are associated with triple-negative breast cancer

artículo científico publicado en 2011

Common variation at 3p22.1 and 7p15.3 influences multiple myeloma risk

scientific journal article

Common variation at 3q26.2, 6p21.33, 17p11.2 and 22q13.1 influences multiple myeloma risk

scientific journal article

Concordance of survival in family members with prostate cancer

artículo científico publicado en 2008

Consensus pathways implicated in prognosis of colorectal cancer identified through systematic enrichment analysis of gene expression profiling studies

artículo científico publicado en 2011

Copy number variations of GSTT1 and GSTM1, colorectal cancer risk and possible effect modification of cigarette smoking and menopausal hormone therapy

artículo científico publicado en 2012

Correction: Familial risks of ovarian cancer by age at diagnosis, proband type and histology

artículo científico publicado en 2018

Correction: Inherited variants in genes somatically mutated in thyroid cancer

artículo científico publicado en 2018

Correspondence: SEMA4A variation and risk of colorectal cancer

artículo científico publicado en 2016

Could polymorphisms in ATP-binding cassette C3/multidrug resistance associated protein 3 (ABCC3/MRP3) modify colorectal cancer risk?

Cytogenetic aberrations in multiple myeloma are associated with shifts in serum immunoglobulin isotypes distribution and levels

artículo científico publicado en 2018

Deciphering the 8q24.21 association for glioma

artículo científico publicado en 2013

Dectin-1 and DC-SIGN polymorphisms associated with invasive pulmonary Aspergillosis infection

artículo científico publicado en 2012

Determination of allele frequency in pooled DNA: comparison of three PCR-based methods

artículo científico publicado en 2005

Do reproductive factors influence T, N, and M classes of ductal and lobular breast cancers? A nation-wide follow-up study

artículo científico publicado en 2013

Effect of autoimmune diseases on incidence and survival in subsequent multiple myeloma

artículo científico publicado en 2012

Effect of autoimmune diseases on risk and survival in female cancers

artículo científico publicado en 2012

Effect of type 2 diabetes predisposing genetic variants on colorectal cancer risk

artículo científico publicado en 2012

Eight novel loci implicate shared genetic etiology in multiple myeloma, AL amyloidosis, and monoclonal gammopathy of unknown significance

artículo científico publicado en 2019

Ethnic differences in breast cancer risk and survival: a study on immigrants in Sweden

artículo científico publicado en 2013

Etiologic impact of known cancer susceptibility genes

artículo científico publicado en 2007

Evidence of Inbreeding in Hodgkin Lymphoma

artículo científico publicado en 2016

Familial Cancer Variant Prioritization Pipeline version 2 (FCVPPv2) applied to a papillary thyroid cancer family

artículo científico publicado en 2018

Familial Ovarian Cancer Clusters with Other Cancers

artículo científico publicado en 2018

Familial Risks Between Urolithiasis and Cancer

artículo científico publicado en 2018

Familial associations of female breast cancer with other cancers

artículo científico publicado en 2017

Familial associations of male breast cancer with other cancers

artículo científico publicado en 2017

Familial risks for gallstones in the population of Sweden

artículo científico publicado en 2017

Familial risks in and between stone diseases: sialolithiasis, urolithiasis and cholelithiasis in the population of Sweden.

artículo científico publicado en 2018

Familial risks in urolithiasis in the population of sweden

artículo científico publicado en 2017

Familial risks of second primary cancers and mortality in ovarian cancer patients

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

artículo científico publicado en 2013

Functional TLR5 genetic variants affect human colorectal cancer survival

artículo científico publicado en 2013

Functional germline variants in driver genes of breast cancer

artículo científico publicado en 2017

GWAS-identified common variants for obesity are not associated with the risk of developing colorectal cancer

artículo científico publicado en 2014

Genetic Predisposition to Multiple Myeloma at 5q15 Is Mediated by an ELL2 Enhancer Polymorphism

artículo científico publicado en 2017

Genetic Susceptibility to Bortezomib-Induced Peripheral Neuroropathy: Replication of the Reported Candidate Susceptibility Loci

artículo científico publicado en 2016

Genetic correlation between multiple myeloma and chronic lymphocytic leukaemia provides evidence for shared aetiology ⬇️

scholarly article by Molly Went et al published 21 December 2018 in Blood Cancer Journal

Genetic polymorphisms in host innate immune sensor genes and the risk of nasopharyngeal carcinoma in North Africa

artículo científico publicado en 2013

Genetic variants in C-type lectin genes are associated with colorectal cancer susceptibility and clinical outcome

artículo científico publicado en 2013

Genetic variants in hormone-related genes and risk of breast cancer

artículo científico publicado en 2013

Genetic variation associated with chromosomal aberration frequency: A genome-wide association study

artículo científico publicado en 2018

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 ALCAM and other chromosomal instability genes in breast cancer survival.

artículo científico publicado en 2011

Genetic variation in adipokine genes and risk of colorectal cancer.

artículo científico publicado en 2009

Genetic variation in genes encoding for polymerase ζ subunits associates with breast cancer risk, tumour characteristics and survival

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 major mitotic checkpoint genes does not affect familial breast cancer risk

artículo científico publicado en 2007

Genetics of gallbladder cancer

artículo científico publicado en 2017

Genome-wide analysis associates familial colorectal cancer with increases in copy number variations and a rare structural variation at 12p12.3.

artículo científico publicado en 2013

Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibility.

artículo científico publicado en 2010

Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer

artículo científico publicado en 2013

Genome-wide association study identifies multiple susceptibility loci for multiple myeloma ⬇️

artículo científico publicado en 2016

Genome-wide association study identifies variation at 6q25.1 associated with survival in multiple myeloma ⬇️

artículo científico publicado en 2016

Genome-wide association study implicates immune dysfunction in the development of Hodgkin lymphoma

artículo científico publicado en 2018

Genome-wide association study of classical Hodgkin lymphoma identifies key regulators of disease susceptibility

artículo científico publicado en 2017

Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts.

artículo científico publicado en 2017

Genome-wide association study on differentiated thyroid cancer

scientific journal article

Genome-wide investigation of gene-environment interactions in colorectal cancer

artículo científico publicado en 2012

Genomewide association study on monoclonal gammopathy of unknown significance (MGUS).

artículo científico publicado en 2017

Germline genetics of cancer of unknown primary (CUP) and its specific subtypes

artículo científico publicado en 2016

Heritability estimates on Hodgkin's lymphoma: a genomic- versus population-based approach

artículo científico publicado en 2014

High-throughput genotyping of a common deletion polymorphism disrupting the TRY6 gene and its association with breast cancer risk

artículo científico publicado en 2007

Human estrogen receptor beta 548 is not a common variant in three distinct populations

artículo científico publicado en 2003

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

artículo científico publicado en 2016

Identification of multiple risk loci and regulatory mechanisms influencing susceptibility to multiple myeloma

scientific article published in Nature Communications

Impact of functional germline variants and a deletion polymorphism in APOBEC3A and APOBEC3B on breast cancer risk and survival in a Swedish study population

artículo científico publicado en 2015

Inbreeding and homozygosity in breast cancer survival

artículo científico publicado en 2015

Incidence Differences Between First Primary Cancers and Second Primary Cancers Following Skin Squamous Cell Carcinoma as Etiological Clues

artículo científico publicado en 2020

Incidence and familial risks in pituitary adenoma and associated tumors

artículo científico publicado en 2007

Incidence and survival in non-hereditary amyloidosis in Sweden

artículo científico publicado en 2012

Incidence of hereditary amyloidosis and autoinflammatory diseases in Sweden: endemic and imported diseases

artículo científico publicado en 2013

Increased risk of hepatobiliary cancers after hospitalization for autoimmune disease

artículo científico publicado en 2013

Inherited genetic susceptibility to monoclonal gammopathy of unknown significance

artículo científico publicado en 2014

Inherited variants in genes somatically mutated in thyroid cancer

artículo científico publicado en 2017

Investigation of single and synergic effects of NLRC5 and PD-L1 variants on the risk of colorectal cancer

artículo científico publicado en 2018

Levels of DNA damage (Micronuclei) in patients suffering from chronic kidney disease. Role of GST polymorphisms

artículo científico publicado en 2018

Low-risk variants FGFR2, TNRC9 and LSP1 in German familial breast cancer patients

artículo científico publicado en 2010

Metabolic gene variants associated with chromosomal aberrations in healthy humans

artículo científico publicado en 2015

Micronuclei in cord blood lymphocytes and associations with biomarkers of exposure to carcinogens and hormonally active factors, gene polymorphisms, and gene expression: the NewGeneris cohort ⬇️

artículo científico publicado en 2013

Multiple myeloma: family history and mortality in second primary cancers

scholarly article by Subhayan Chattopadhyay et al published 7 August 2018 in Blood Cancer Journal

New cancer susceptibility loci: population and familial risks

artículo científico publicado en 2008

Novel genetic variants in differentiated thyroid cancer and assessment of the cumulative risk

artículo científico publicado en 2015

Novel genome-wide association study-based candidate loci for differentiated thyroid cancer risk

artículo científico publicado en 2014

Origin of B-Cell Neoplasms in Autoimmune Disease

artículo científico publicado en 2016

Pedigree based DNA sequencing pipeline for germline genomes of cancer families

artículo científico publicado en 2016

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

artículo científico publicado en 2019

Polymorphisms and haplotype structures in genes for transforming growth factor beta1 and its receptors in familial and unselected breast cancers

artículo científico publicado en 2004

Polymorphisms in CTNNBL1 in relation to colorectal cancer with evolutionary implications

artículo científico publicado en 2010

Polymorphisms in genes involved in GH1 release and their association with breast cancer risk

artículo científico publicado en 2006

Polymorphisms in predicted microRNA-binding sites in integrin genes and breast cancer: ITGB4 as prognostic marker

artículo científico publicado en 2008

Polymorphisms in telomere-associated genes, breast cancer susceptibility and prognosis

artículo científico publicado en 2009

Polymorphisms in the IGF-1 and IGFBP 3 promoter and the risk of breast cancer.

artículo científico publicado en 2005

Polymorphisms in the KDR and POSTN genes: association with breast cancer susceptibility and prognosis

artículo científico publicado en 2006

Polymorphisms in the estrogen receptor beta gene and risk of breast cancer: no association

artículo científico publicado en 2003

Polymorphisms in the growth hormone receptor: a case-control study in breast cancer

artículo científico publicado en 2006

Polymorphisms in the insulin like growth factor 1 and IGF binding protein 3 genes and risk of colorectal cancer.

artículo científico publicado en 2007

Polymorphisms in the mitochondrial oxidative phosphorylation chain genes as prognostic markers for colorectal cancer

artículo científico publicado en 2012

Polymorphisms in the transforming growth factor beta 1 pathway in relation to colorectal cancer progression.

artículo científico publicado en 2010

Polymorphisms of genes coding for ghrelin and its receptor in relation to colorectal cancer risk: a two-step gene-wide case-control study

artículo científico publicado en 2010

Polymorphisms within micro-RNA-binding sites and risk of sporadic colorectal cancer

artículo científico

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

artículo científico publicado en 2015

Preventable breast cancer is postmenopausal

Promoter polymorphisms in matrix metalloproteinases and their inhibitors: few associations with breast cancer susceptibility and progression

artículo científico publicado en 2006

Proper controls for SNP studies?

artículo científico publicado en 2002

Re: "underlying genetic models of inheritance in established type 2 diabetes associations".

artículo científico publicado en 2010

Re: Integrin beta3 Leu33Pro homozygosity and risk of cancer

artículo científico publicado en 2004

Re: Role of the oxidative DNA damage repair gene OGG1 in colorectal tumorigenesis

artículo científico publicado en 2014

Recurrent Coding Sequence Variation Explains Only A Small Fraction of the Genetic Architecture of Colorectal Cancer ⬇️

artículo científico publicado en 2015

Recurrent Germline Variant in <i>RAD21</i> Predisposes Children to Lymphoblastic Leukemia or Lymphoma

artículo científico publicado en 2022

Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer

article

Repeat polymorphisms in ESR2 and AR and colorectal cancer risk and prognosis: results from a German population-based case-control study

artículo científico publicado en 2014

Risk of Next Melanoma in Patients With Familial and Sporadic Melanoma by Number of Previous Melanomas

artículo científico publicado en 2015

Risk of cancer in patients with medically diagnosed hay fever or allergic rhinitis

artículo científico publicado en 2014

Runs of homozygosity and inbreeding in thyroid cancer

artículo científico publicado en 2016

SNPs related to vitamin D and breast cancer risk: a case-control study

artículo científico publicado en 2018

Searching for the missing heritability of complex diseases

Second Primary Cancers in Melanoma Patients Critically Shorten Survival

scientific article published on 23 January 2020

Selected polymorphisms in sex hormone-related genes, circulating sex hormones and risk of endometrial cancer.

artículo científico publicado en 2012

Shared ancestral susceptibility to colorectal cancer and other nutrition related diseases

artículo científico publicado en 2012

Single nucleotide polymorphisms (SNPs) are inherited from parents and they measure heritable events

artículo científico publicado en 2005

Single nucleotide polymorphisms in breast cancer

artículo científico publicado en 2004

Single nucleotide polymorphisms in chromosomal instability genes and risk and clinical outcome of breast cancer: a Swedish prospective case-control study

artículo científico publicado en 2008

Single nucleotide polymorphisms in the 20q13 amplicon genes in relation to breast cancer risk and clinical outcome

artículo científico publicado en 2011

Single nucleotide polymorphisms in theXPGgene: Determination of role in DNA repair and breast cancer risk

article by Rajiv Kumar et al published 25 November 2002 in International Journal of Cancer

Subsequent Type 2 Diabetes in Patients with Autoimmune Disease

artículo científico publicado en 2015

Subsequent brain tumors in patients with autoimmune disease

artículo científico publicado en 2013

Surveillance Bias in Cancer Risk After Unrelated Medical Conditions: Example Urolithiasis

artículo científico

Survival in bladder and renal cell cancers is familial

artículo científico publicado en 2008

Survival in breast cancer is familial

artículo científico publicado en 2007

Survival in familial and non-familial breast cancer by age and stage at diagnosis

artículo científico publicado en 2015

Survival in non-Hodgkin's lymphoma by histology and family history

artículo científico publicado en 2009

Survival in ovarian cancer patients by histology and family history

artículo científico publicado en 2008

Systematic enrichment analysis of gene expression profiling studies identifies consensus pathways implicated in colorectal cancer development

artículo científico publicado en 2011

Systematic pathway enrichment analysis of a genome-wide association study on breast cancer survival reveals an influence of genes involved in cell adhesion and calcium signaling on the patients' clinical outcome

artículo científico publicado en 2014

Ten recently identified associations between nsSNPs and colorectal cancer could not be replicated in German families

article

Thalassemia and sickle cell anemia in Swedish immigrants: Genetic diseases have become global

artículo científico publicado en 2015

The 'common disease-common variant' hypothesis and familial risks

artículo científico publicado en 2008

The 7p15.3 (rs4487645) association for multiple myeloma shows strong allele-specific regulation of the MYC-interacting gene CDCA7L in malignant plasma cells

artículo científico publicado en 2014

The CCND1 c.870G>A polymorphism is a risk factor for t(11;14)(q13;q32) multiple myeloma

artículo científico publicado en 2013

The GH1/IGF-1 axis polymorphisms and their impact on breast cancer development

artículo científico publicado en 2007

The Incidence of Senile Cataract and Glaucoma is Increased in Patients with Plasma Cell Dyscrasias: Etiologic Implications

artículo científico publicado en 2016

The balance between heritable and environmental aetiology of human disease

artículo científico publicado en 2006

The insulin-like growth factor-1 pathway mediator genes: SHC1 Met300Val shows a protective effect in breast cancer.

artículo científico publicado en 2004

The single nucleotide polymorphism IVS1+309 in mouse double minute 2 does not affect risk of familial breast cancer.

artículo científico publicado en 2006

Thyroid-associated genetic polymorphisms in relation to breast cancer risk in the Malmö Diet and Cancer Study

artículo científico publicado en 2017

Variation at 3p24.1 and 6q23.3 influences the risk of Hodgkin's lymphoma

scientific journal article

Vascular endothelial growth factor polymorphisms in relation to breast cancer development and prognosis

artículo científico publicado en 2005

Whole Genome Sequencing of Familial Non-Medullary Thyroid Cancer Identifies Germline Alterations in MAPK/ERK and PI3K/AKT Signaling Pathways

artículo científico publicado en 2019

c-MYC Asn11Ser is associated with increased risk for familial breast cancer

artículo científico publicado en 2005

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