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List of works by Douglas F. Easton

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

scientific article

19p13.1 is a triple-negative-specific breast cancer susceptibility locus

scientific article published on 13 February 2012

2q36.3 is associated with prognosis for oestrogen receptor-negative breast cancer patients treated with chemotherapy

scientific article

4-Hydroxyandrostenedione in the prophylaxis of N-methyl-N-nitrosourea induced mammary tumourigenesis

scientific article

7q21-rs6964587 and breast cancer risk: an extended case-control study by the Breast Cancer Association Consortium

scientific article

9q31.2-rs865686 as a susceptibility locus for estrogen receptor-positive breast cancer: evidence from the Breast Cancer Association Consortium

scientific article published on 02 August 2012

A 45-year follow-up of kindred 107 and the search for BRCA2

scientific article published on 01 January 1995

A Common Variant at the 14q32 Endometrial Cancer Risk Locus Activates AKT1 through YY1 Binding

scientific article published on June 2016

A Cross-Cancer Genetic Association Analysis of the DNA Repair and DNA Damage Signaling Pathways for Lung, Ovary, Prostate, Breast, and Colorectal Cancer

scientific article

A Large-Scale Analysis of Genetic Variants within Putative miRNA Binding Sites in Prostate Cancer

scientific article

A Mendelian randomization analysis of circulating lipid traits and breast cancer risk

scientific article published on 23 December 2019

A Transcriptome-Wide Association Study Among 97,898 Women to Identify Candidate Susceptibility Genes for Epithelial Ovarian Cancer Risk

article

A combined analysis of genome-wide association studies in breast cancer

scientific article published on 26 September 2010

A combined genomewide linkage scan of 1,233 families for prostate cancer-susceptibility genes conducted by the international consortium for prostate cancer genetics

scientific article

A common coding variant in CASP8 is associated with breast cancer risk

article

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

scientific article published on 30 October 2011

A common variant in BRCA2 is associated with both breast cancer risk and prenatal viability

scientific article published in November 2000

A comprehensive evaluation of interaction between genetic variants and use of menopausal hormone therapy on mammographic density

scientific article

A comprehensive examination of breast cancer risk loci in African American women

scientific article

A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes

scientific article

A double blind randomised clinical trial of adjuvant aminoglutethimide versus placebo given to post menopausal patients with histologically confirmed stage II breast cancer

scientific article published in January 1986

A full-likelihood method for the evaluation of causality of sequence variants from family data

scientific article

A genetic risk score to guide age-specific, personalized prostate cancer screening

A genetic risk score to personalize prostate cancer screening, applied to population data

scientific article published on 24 June 2020

A genetic study and meta-analysis of the genetic predisposition of prostate cancer in a Chinese population

scientific article published on 08 February 2016

A genome wide linkage search for breast cancer susceptibility genes

scientific article published on July 2006

A genome-wide association scan (GWAS) for mean telomere length within the COGS project: identified loci show little association with hormone-related cancer risk

scientific article published on 29 July 2013

A genome-wide association scan on estrogen receptor-negative breast cancer

scientific article

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

scientific article

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

scientific article published on 18 October 2011

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

scientific article published on 19 September 2010

A genome-wide association study of early-onset breast cancer identifies PFKM as a novel breast cancer gene and supports a common genetic spectrum for breast cancer at any age.

scientific article

A genome-wide association study of prognosis in breast cancer

scientific article

A genome-wide association study of testicular germ cell tumor

scientific article

A genome-wide association study to identify genetic markers associated with endometrial cancer grade

scientific article published on 12 April 2012

A genome-wide association study to identify genetic susceptibility loci that modify ductal and lobular postmenopausal breast cancer risk associated with menopausal hormone therapy use: a two-stage design with replication

scientific article published on 20 February 2013

A genomic approach to therapeutic target validation identifies a glucose-lowering GLP1R variant protective for coronary heart disease

scientific article published on June 2016

A germline mutation in the androgen receptor gene in two brothers with breast cancer and Reifenstein syndrome

scientific article (publication date: October 1992)

A hypermutation phenotype and somatic MSH6 mutations in recurrent human malignant gliomas after alkylator chemotherapy

scientific 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

scientific article

A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10

scientific article published in Nature

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

scientific article

A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer

scientific article published on 14 September 2014

A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11.

scientific article

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

scientific article

A multicenter study of cancer incidence in CHEK2 1100delC mutation carriers

scientific article published on December 2006

A multilayered post-GWAS assessment on genetic susceptibility to pancreatic cancer

scientific article published on 01 February 2021

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

scientific article published on 16 January 2020

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

scientific article

A novel recurrent mutation in MITF predisposes to familial and sporadic melanoma

scientific article published on 13 November 2011

A novel tumour-based test to identify breast cancer due to BRCA1 and BRCA2 mutations.

scientific article published on 18 May 2010

A physical analysis of the Y chromosome shows no additional deletions, other than Gr/Gr, associated with testicular germ cell tumour

scientific article published on 9 January 2007

A pilot study of compositional analysis of the breast and estimation of breast mammographic density using three-dimensional T1-weighted magnetic resonance imaging

scientific article

A polymorphism in the base excision repair gene PARP2 is associated with differential prognosis by chemotherapy among postmenopausal breast cancer patients

scientific article published on 16 December 2015

A population study of mutations and LOH at breast cancer gene loci in tumours from sister pairs: two recurrent mutations seem to account for all BRCA1/BRCA2 linked breast cancer in Iceland

scientific article

A population-based audit of ethnicity and breast cancer risk in one general practice catchment area in North London, UK: implications for practice

scientific article published on 15 September 2007

A preliminary analysis of consortium data for markers tightly linked to multiple endocrine neoplasia type 2A.

scientific article

A prospective study of neurofibromatosis type 1 cancer incidence in the UK.

scientific article published on 20 June 2006

A recurrent truncating germline mutation in the BRIP1/FANCJ gene and susceptibility to prostate cancer

scientific article published on 06 January 2009

A response to "Personalised medicine and population health: breast and ovarian cancer"

scientific article published on 27 February 2019

A risk prediction algorithm based on family history and common genetic variants: application to prostate cancer with potential clinical impact

scientific article published on 18 July 2011

A risk prediction algorithm for ovarian cancer incorporating BRCA1, BRCA2, common alleles and other familial effects

scientific article published on 29 May 2015

A role for XRCC2 gene polymorphisms in breast cancer risk and survival

scientific article published on 31 May 2011

A screen of the complete protein kinase gene family identifies diverse patterns of somatic mutations in human breast cancer

scientific article published on 22 May 2005

A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers

scientific article published on 23 January 2017

A survey of homozygous deletions in human cancer genomes

scientific article

A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes

scientific article

A systematic review and meta‐analysis of family history and risk of ovarian cancer ⬇️

scientific article published on 01 May 1998

A systematic review of genetic polymorphisms and breast cancer risk.

scientific article

A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation

scientific article

A test of performance of breast MRI interpretation in a multicentre screening study

scientific article

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

scientific article published on 18 June 2018

A transforming growth factorbeta1 signal peptide variant increases secretion in vitro and is associated with increased incidence of invasive breast cancer.

scientific article published in May 2003

A weighted cohort approach for analysing factors modifying disease risks in carriers of high-risk susceptibility genes

scientific article published on 01 July 2005

AA9int: SNP interaction pattern search using non-hierarchical additive model set

ATM Mutations and Phenotypes in Ataxia-Telangiectasia Families in the British Isles: Expression of Mutant ATM and the Risk of Leukemia, Lymphoma, and Breast Cancer ⬇️

scientific article published on February 1, 1998

ATM mutations that cause ataxia-telangiectasia are breast cancer susceptibility alleles

scientific article

ATM polymorphisms as risk factors for prostate cancer development

scientific article published on August 2004

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

scientific article published on July 2007

Absence of evidence for a familial breast cancer susceptibility gene at chromosome 8p12-p22

article

Absence of linkage to the ataxia telangiectasia locus in familial breast cancer

scientific article published in August 1993

Abstract 2030: The role of genetic variation in calcium-activated potassium channels in breast cancer patients treated with tamoxifen

scientific article published on 15 July 2016

Abstract 4836: Gene and environment interactions of height and selected candidate SNPs in prostate cancer: results from the PRACTICAL consortium

scientific article published on 15 April 2013

Abstract 5314: DNA methylation quantitative trait loci and breast cancer risk: Data from nearly 230,000 women of European descent

scientific article published in 2018

Abstract LB-448: Genome-wide association study identifies new prostate cancer susceptibility loci

scientific article published on 15 April 2011

Acute chemotherapy-related toxicity is not increased in BRCA1 and BRCA2 mutation carriers treated for breast cancer in the United Kingdom

scientific article published in December 2006

Adjuvant aminoglutethimide for postmenopausal patients with primary breast cancer: analysis at 8 years ⬇️

scientific article published on 01 October 1992

Adjuvant aminoglutethimide therapy for postmenopausal patients with primary breast cancer

scientific article published on 01 May 1987

After BRCA1 and BRCA2-what next? Multifactorial segregation analyses of three-generation, population-based Australian families affected by female breast cancer

scientific article

Age at menarche and menopause and breast cancer risk in the International BRCA1/2 Carrier Cohort Study

scientific article published in April 2007

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

scientific article

Alcohol Consumption, Cigarette Smoking, and Risk of Breast Cancer for BRCA1 and BRCA2 Mutation Carriers: Results from The BRCA1 and BRCA2 Cohort Consortium

scientific article published on 02 December 2019

Alcohol consumption and prostate cancer incidence and progression: A Mendelian randomisation study

scientific article published on 19 September 2016

Alcohol consumption and survival after a breast cancer diagnosis: a literature-based meta-analysis and collaborative analysis of data for 29,239 cases

scientific article

Allele losses in the region 17q12-21 in familial breast and ovarian cancer involve the wild-type chromosome

article by S.A. Smith et al published October 1992 in Nature Genetics

Allelic association of the human homologue of the mouse modifier Ptprj with breast cancer

scientific article published on 6 July 2005

Allelotype of uterine leiomyomas

scientific article published on 01 October 1999

Alzheimer disease is not associated with polymorphisms in the angiotensinogen and renin genes

scientific article published in December 2001

An analysis of prognostic factors in early stage Hodgkin's disease

scientific article published on 01 October 1986

An analysis of variation in expression of neurofibromatosis (NF) type 1 (NF1): evidence for modifying genes.

scientific article

An autosome-wide scan for linkage disequilibrium-based association in sporadic breast cancer cases in eastern Finland: three candidate regions found

scientific article published on 01 January 2005

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

scientific article

An international initiative to identify genetic modifiers of cancer risk in BRCA1 and BRCA2 mutation carriers: the Consortium of Investigators of Modifiers of BRCA1 and BRCA2 (CIMBA)

scientific article

An investigation of ACE as a risk factor for dementia and cognitive decline in the general population.

scientific article published in June 2002

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

scientific article published on 25 April 2015

Analysis and meta-analysis of two serotonin transporter gene polymorphisms in bipolar and unipolar affective disorders ⬇️

scientific article published on 01 February 1998

Analysis of Xq27-28 linkage in the international consortium for prostate cancer genetics (ICPCG) families ⬇️

scientific article published on June 19, 2012

Analysis of alpha-1 antichymotrypsin, presenilin-1, angiotensin-converting enzyme, and methylenetetrahydrofolate reductase loci as candidates for dementia

scientific article published on 01 April 1997

Analysis of single-nucleotide polymorphisms in the interleukin-4 receptor gene for association with inflammatory bowel disease

article

Analysis of the DND1 gene in men with sporadic and familial testicular germ cell tumors

scientific article

Analysis of the apo E/apo C-I, angiotensin converting enzyme and methylenetetrahydrofolate reductase genes as candidates affecting human longevity.

scientific article published in March 1997

Analysis of the contribution of HLA genes to genetic predisposition in inflammatory bowel disease

scientific article published in July 1996

Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue

scientific article

Androgen receptor polymorphisms: Association with prostate cancer risk, relapse and overall survival

scientific article published on 22 October 1999

Annexin A1 expression in a pooled breast cancer series: association with tumor subtypes and prognosis

scientific article published on 2 July 2015

Apo E and Apo CI loci are associated with dementia in younger but not older late-onset cases

scientific article published in July 1998

Apo E genotypes and risk of dementia in Down syndrome

scientific article published in August 1999

Apolipoprotein E genetic variation and Alzheimer's disease. a meta-analysis

scientific article published in May 1999

Apolipoprotein E4 is only a weak predictor of dementia and cognitive decline in the general population

scientific article

Apoptosis, ageing and cancer susceptibility.

scientific article published on February 2003

Apparent human BRCA1 knockout caused by mispriming during polymerase chain reaction: implications for genetic testing

scientific article published on 01 May 2001

Application of linked DNA markers to screening families with multiple endocrine neoplasia type 2A

scientific article published on 01 April 1990

Application of minisatellite DNA probes to linkage in MEN-2

scientific article published on 01 January 1987

Area and volumetric density estimation in processed full-field digital mammograms for risk assessment of breast cancer

scientific article

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

scientific article

Assessing interactions between the associations of common genetic susceptibility variants, reproductive history and body mass index with breast cancer risk in the breast cancer association consortium: a combined case-control study

scientific article

Assessing the role of insulin-like growth factors and binding proteins in prostate cancer using Mendelian randomization: Genetic variants as instruments for circulating levels

scientific article published on 26 May 2016

Assessing the usefulness of a novel MRI-based breast density estimation algorithm in a cohort of women at high genetic risk of breast cancer: the UK MARIBS study

scientific article

Assessment of interactions between 205 breast cancer susceptibility loci and 13 established risk factors in relation to breast cancer risk, in the Breast Cancer Association Consortium

scientific article published on 01 February 2020

Assessment of polygenic architecture and risk prediction based on common variants across fourteen cancers

scientific article published on 03 July 2020

Assessment of variation in immunosuppressive pathway genes reveals TGFBR2 to be associated with prognosis of estrogen receptor-negative breast cancer after chemotherapy

scientific article

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

scientific article published on 21 June 2016

Association analyses identify 31 new risk loci for colorectal cancer susceptibility

scientific article published on 14 May 2019

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

scientific article published on 11 June 2018

Association analysis identifies 65 new breast cancer risk loci.

scientific article published on 23 October 2017

Association analysis of 9,560 prostate cancer cases from the International Consortium of Prostate Cancer Genetics confirms the role of reported prostate cancer associated SNPs for familial disease

scientific article published on 26 October 2013

Association between Adult Height and Risk of Colorectal, Lung, and Prostate Cancer: Results from Meta-analyses of Prospective Studies and Mendelian Randomization Analyses

scientific article

Association between BRCA1 and BRCA2 mutations and survival in women with invasive epithelial ovarian cancer

scientific article

Association between Prostinogen (KLK15) genetic variants and prostate cancer risk and aggressiveness in Australia and a meta-analysis of GWAS data

scientific article

Association between a germline OCA2 polymorphism at chromosome 15q13.1 and estrogen receptor-negative breast cancer survival

scientific article

Association between common germline genetic variation in 94 candidate genes or regions and risks of invasive epithelial ovarian cancer

scientific article

Association between common variation in 120 candidate genes and breast cancer risk

scientific article published on 2 February 2007

Association between invasive ovarian cancer susceptibility and 11 best candidate SNPs from breast cancer genome-wide association study

scientific article published on 20 March 2009

Association between leptin receptor gene polymorphisms and early-onset prostate cancer

article

Association between the GCG polymorphism of the selenium dependent GPX1 gene and the risk of young onset prostate cancer

scientific article

Association of ESR1 gene tagging SNPs with breast cancer risk

scientific article published on 06 January 2009

Association of Genomic Domains in BRCA1 and BRCA2 with Prostate Cancer Risk and Aggressiveness

scientific article published on 13 November 2019

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

scientific article

Association of a common AKAP9 variant with breast cancer risk: a collaborative analysis

scientific article published on 11 March 2008

Association of breast cancer risk in BRCA1 and BRCA2 mutation carriers with genetic variants showing differential allelic expression: identification of a modifier of breast cancer risk at locus 11q22.3.

scientific article

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 folate-pathway gene polymorphisms with the risk of prostate cancer: a population-based nested case-control study, systematic review, and meta-analysis

scientific article published on 25 August 2009

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

scientific article published on 06 April 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

scientific article published on 18 August 2021

Association of germline variation with the survival of women with BRCA1/2 pathogenic variants and breast cancer

scientific article published on 10 September 2020

Association of single-nucleotide polymorphisms in the cell cycle genes with breast cancer in the British population

scientific article published on 3 January 2008

Association of tamoxifen use and reduced risk of contralateral breast cancer for BRCA1 and BRCA2 mutation carriers

scientific article published on 12 April 2012

Association of the Progesterone Receptor Gene with Breast Cancer Risk: A Single-Nucleotide Polymorphism Tagging Approach

article

Association of the variants CASP8 D302H and CASP10 V410I with breast and ovarian cancer risk in BRCA1 and BRCA2 mutation carriers

scientific article

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

scientific article

Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants

scientific article

Association studies for finding cancer-susceptibility genetic variants

scientific article

Association study of prostate cancer susceptibility variants with risks of invasive ovarian, breast, and colorectal cancer

scientific article

Associations among Mammographic Density, Circulating Sex Hormones, and Polymorphisms in Sex Hormone Metabolism Genes in Postmenopausal Women

article

Associations of a Breast Cancer Polygenic Risk Score With Tumor Characteristics and Survival

scholarly article

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

scientific article

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

scientific article published on 31 December 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

scientific article published on 18 August 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

Atlas of prostate cancer heritability in European and African-American men pinpoints tissue-specific regulation

scientific article published on 7 April 2016

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

Author Correction: Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia

scientific article published in Nature Communications

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

scientific article published in Nature Communications

Author Correction: Germline variation at 8q24 and prostate cancer risk in men of European ancestry

scientific article published in Nature Communications

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

scientific article published in Nature Communications

Author Correction: The evolutionary history of lethal metastatic prostate cancer

scientific article published on 29 July 2020

Authors' response: Associations of obesity and circulating insulin and glucose with breast cancer risk

scientific article published on 01 June 2019

Average age-specific cumulative risk of breast cancer according to type and site of germline mutations in BRCA1 and BRCA2 estimated from multiple-case breast cancer families attending Australian family cancer clinics

scientific article

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

scientific article

BOADICEA breast cancer risk prediction model: updates to cancer incidences, tumour pathology and web interface

scientific article published on 17 December 2013

BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors

scientific article published on 15 January 2019

BRCA Challenge: BRCA Exchange as a global resource for variants in BRCA1 and BRCA2

scientific article published on 26 December 2018

BRCA1 and BRCA2 Cancer Risks

BRCA1 and BRCA2 Pathogenic Sequence Variants in Women of African Origin or Ancestry

scientific article published on 03 July 2019

BRCA1 and BRCA2 mutation predictions using the BOADICEA and BRCAPRO models and penetrance estimation in high-risk French-Canadian families

scientific article

BRCA1 and BRCA2 mutations in a population-based study of male breast cancer

scientific article

BRCA1, BRCA2 and pedigree genetic analysis to determine genetic risk in the UK Royal Marsden Hospital tamoxifen prevention trial.

scientific article published on 12 March 2000

BRCA1/BRCA2 mutation status and analysis of cancer family history in participants of the Royal Marsden Hospital tamoxifen chemoprevention trial

article

BRCA2 Hypomorphic Missense Variants Confer Moderate Risks of Breast Cancer

scientific article published on 10 March 2017

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

scientific article

BRCA2 arg372hispolymorphism and epithelial ovarian cancer risk

article

BRCA2 is a moderate penetrance gene contributing to young-onset prostate cancer: implications for genetic testing in prostate cancer patients

scientific article published on 27 September 2011

Basal-like grade III invasive ductal carcinoma of the breast: patterns of metastasis and long-term survival ⬇️

scientific article published on January 2007

Blood lipids and prostate cancer: a Mendelian randomization analysis

scientific article published on 19 March 2016

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

scientific article published in December 2017

Bone marrow micrometastases in primary breast cancer: Prognostic significance after 6 years' follow-up ⬇️

scientific article published on 01 January 1991

Breast Cancer Polygenic Risk Score and Contralateral Breast Cancer Risk

scientific article published on 28 September 2020

Breast and Prostate Cancer Risks for Male BRCA1 and BRCA2 Pathogenic Variant Carriers Using Polygenic Risk Scores

scientific article published on 11 January 2022

Breast and ovarian cancer incidence in BRCA1-mutation carriers. Breast Cancer Linkage Consortium.

scientific article published on January 1995

Breast and ovarian cancer risks in a large series of clinically ascertained families with a high proportion of BRCA1 and BRCA2 Dutch founder mutations

scientific article published on 27 November 2013

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

scientific article published in July 2005

Breast cancer risk and 6q22.33: combined results from Breast Cancer Association Consortium and Consortium of Investigators on Modifiers of BRCA1/2

scientific article

Breast cancer risk factors and their effects on survival: a Mendelian randomisation study

scientific article published on 17 November 2020

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

scientific article

Breast cancer risks for BRCA1/2 carriers

scientific article

Breast cancer screening: time to target women at risk ⬇️

scientific article published on June 6, 2013

Breast cancer susceptibility polymorphisms and endometrial cancer risk: a Collaborative Endometrial Cancer Study

scientific article published on 30 September 2011

Breast cancer susceptibility risk associations and heterogeneity by E-cadherin tumor tissue expression

scientific article

Breast-Cancer Risk in Families With Mutations in PALB2

Breast-cancer risk in families with mutations in PALB2

scientific article

CAG and GGC repeat polymorphisms in the androgen receptor gene and breast cancer susceptibility in BRCA1/2 carriers and non-carriers

scientific article published on July 2001

CHEK2 variant I157T may be associated with increased breast cancer risk

scientific article published in September 2004

CHEK2*1100delC heterozygosity in women with breast cancer associated with early death, breast cancer-specific death, and increased risk of a second breast cancer

scientific article

CHEK2, MGMT, SULT1E1 and SULT1A1 polymorphisms and endometrial cancer risk

scientific article

COMPLEXO: identifying the missing heritability of breast cancer via next generation collaboration

scientific article published on 21 June 2013

CYP17 promoter polymorphism and breast cancer in Australian women under age forty years

scientific article published on 01 October 2000

CYP19A1 fine-mapping and Mendelian randomization: estradiol is causal for endometrial cancer

scientific article

CanRisk Tool - A web interface for the prediction of breast and ovarian cancer risk and the likelihood of carrying genetic pathogenic variants

scientific article published on 17 December 2020

Cancer Incidence in BRCA1 mutation carriers

scientific article

Cancer Risks Associated With Germline PALB2 Pathogenic Variants: An International Study of 524 Families

scientific article published on 16 December 2019

Cancer Risks Associated With and Pathogenic Variants

scientific article published on 10 May 2022

Cancer Risks in Two Large Breast Cancer Families Linked to BRCA2 on Chromosome 13q12‐13 ⬇️

scientific article published on July 1, 1997

Cancer incidence in relatives of British Fanconi Anaemia patients

scientific article

Cancer mortality in relatives of women with breast cancer: the OPCS Study. Office of Population Censuses and Surveys

scientific article published in January 1996

Cancer mortality in relatives of women with ovarian cancer: the OPCS Study. Office of Population Censuses and Surveys

scientific article published in January 1996

Cancer mortality in the first degree relatives of young breast cancer patients

scientific article

Cancer risks and mortality in heterozygous ATM mutation carriers

scientific article

Cancer risks for BRCA1 and BRCA2 mutation carriers: results from prospective analysis of EMBRACE.

scientific article

Cancer risks in A-T heterozygotes

scientific article published on December 1994

Cancer treatment trials--past failures, current progress and future prospects.

scientific article published on January 1989

Cancers of the respiratory tract in mustard gas workers

scientific article

Candidate Causal Variants at the 8p12 Breast Cancer Risk Locus Regulate DUSP4

scientific article published on 10 January 2020

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

scientific article

Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk

scientific article published in February 2015

Changing distribution of adenocarcinoma of the stomach

scientific article published on 01 June 1987

Characterisation of PALB2 tumours through whole-exome and whole-transcriptomic analyses

scientific article published on 23 April 2021

Characterization of the Cancer Spectrum in Men With Germline BRCA1 and BRCA2 Pathogenic Variants: Results From the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

scientific article published on 02 July 2020

Chromatin interactome mapping at 139 independent breast cancer risk signals

scientific article published on 07 January 2020

Chromosomes 4 and 8 implicated in a genome wide SNP linkage scan of 762 prostate cancer families collected by the ICPCG

scientific article published on 11 July 2011

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

scientific article published on 22 September 2015

ClinGen and Genetic Testing

scientific article published on 01 October 2015

Clinical implications of family history of prostate cancer and genetic risk single nucleotide polymorphism (SNP) profiles in an active surveillance cohort

scientific article published on 15 January 2013

Clinical presentation as a predictor of laparotomy findings in supradiaphragmatic stage I and II Hodgkin's disease

scientific article published in January 1986

Clinical software development for the Web: lessons learned from the BOADICEA project ⬇️

scientific article published on April 10, 2012

Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey

scientific article published on 5 March 2018

Combined associations of a polygenic risk score and classical risk factors with breast cancer risk

scientific article published on 02 May 2020

Combined effects of single nucleotide polymorphisms TP53 R72P and MDM2 SNP309, and p53 expression on survival of breast cancer patients

scientific article

Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms

scientific article published on 23 March 2016

Combined quantitative measures of ER, PR, HER2, and KI67 provide more prognostic information than categorical combinations in luminal breast cancer.

scientific article

Common BRCA1 variants and susceptibility to breast and ovarian cancer in the general population

scientific article published on 01 February 1997

Common ERBB2 polymorphisms and risk of breast cancer in a white British population: a case-control study

scientific article

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

scientific article published on 19 June 2015

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

scientific article

Common Polymorphisms in ERCC2 (Xeroderma pigmentosum D) are not Associated with Breast Cancer Risk

scientific article published on 01 July 2005

Common Variants in RB1 Gene and Risk of Invasive Ovarian Cancer

article

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

scientific article published on 18 May 2011

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

scientific article

Common breast cancer susceptibility alleles are associated with tumour subtypes in BRCA1 and BRCA2 mutation carriers: results from the Consortium of Investigators of Modifiers of BRCA1/2.

scientific article published on 2 November 2011

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

scientific article published on 15 August 2011

Common breast cancer susceptibility variants in LSP1 and RAD51L1 are associated with mammographic density measures that predict breast cancer risk

scientific article published on 27 March 2012

Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

scientific article

Common genetic determinants of breast-cancer risk in East Asian women: a collaborative study of 23 637 breast cancer cases and 25 579 controls

scientific article published on 27 March 2013

Common genetic variants and modification of penetrance of BRCA2-associated breast cancer

scientific article

Common genetic variants associated with disease from genome-wide association studies are mutually exclusive in prostate cancer and rheumatoid arthritis

scientific article published on 18 September 2012

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

scientific article

Common genetic variation in candidate genes and susceptibility to subtypes of breast cancer

scientific article

Common germline genetic variation in antioxidant defense genes and survival after diagnosis of breast cancer

scientific article

Common germline polymorphisms associated with breast cancer-specific survival

scientific article published on 22 April 2015

Common germline polymorphisms in COMT, CYP19A1, ESR1, PGR, SULT1E1 and STS and survival after a diagnosis of breast cancer

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Common germline variation in mismatch repair genes and survival after a diagnosis of colorectal cancer

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

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Common polymorphisms in checkpoint kinase 2 are not associated with breast cancer risk

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Common polymorphisms in the prostaglandin pathway genes and their association with breast cancer susceptibility and survival

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Common single-nucleotide polymorphisms in DNA double-strand break repair genes and breast cancer risk

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Common susceptibility loci for male breast cancer

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Common variants associated with breast cancer in genome-wide association studies are modifiers of breast cancer risk in BRCA1 and BRCA2 mutation carriers

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

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

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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

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

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Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers

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Common variants in ZNF365 are associated with both mammographic density and breast cancer risk

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Common variants in breast cancer risk loci predispose to distinct tumor subtypes

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Common variants in mismatch repair genes and risk of colorectal cancer

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Common variants in mismatch repair genes and risk of invasive ovarian cancer

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Common variants in the ATM, BRCA1, BRCA2, CHEK2 and TP53 cancer susceptibility genes are unlikely to increase breast cancer risk

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Common variants of the BRCA1 wild-type allele modify the risk of breast cancer in BRCA1 mutation carriers

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Common variation in EMSY and risk of breast and ovarian cancer: a case-control study using HapMap tagging SNPs

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Common variation in Kallikrein genes KLK5, KLK6, KLK12, and KLK13 and risk of prostate cancer and tumor aggressiveness

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Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk

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Comparison of 6q25 breast cancer hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

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Comparison of conservative surgery and radiotherapy with mastectomy in the treatment of early breast cancer

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Compelling evidence for a prostate cancer gene at 22q12.3 by the International Consortium for Prostate Cancer Genetics

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Comprehensive Functional Characterization and Clinical Interpretation of 20 Splice-Site Variants of the <i>RAD51C</i> Gene

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Comprehensive functional annotation of 77 prostate cancer risk loci

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Comprehensive genetic assessment of the ESR1 locus identifies a risk region for endometrial cancer

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

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Consistent loss of the wild type allele in breast cancers from a family linked to the BRCA2 gene on chromosome 13q12-13.

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Consortium analysis of 7 candidate SNPs for ovarian cancer

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Constitutional mutation in exon 8 of the p53 gene in a patient with multiple primary tumours: molecular and immunohistochemical findings

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Contribution of BRCA1 and BRCA2 germ-line mutations to the incidence of breast cancer in young women: results from a prospective population-based study in France

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Contribution of BRCA1 mutations to ovarian cancer

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Contribution of germline mutations in BRCA2, P16(INK4A), P14(ARF) and P15 to uveal melanoma

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Correction to: Clinicians' use of breast cancer risk assessment tools according to their perceived importance of breast cancer risk factors: an international survey

scientific article published on 01 October 2019

Correction to: Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer

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Correction to: Risk-reducing salpingo-oophorectomy, natural menopause, and breast cancer risk: an international prospective cohort of BRCA1 and BRCA2 mutation carriers

scientific article published on 26 February 2020

Correction: BOADICEA: a comprehensive breast cancer risk prediction model incorporating genetic and nongenetic risk factors

scientific article published on 01 June 2019

Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer

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Correction: Common Genetic Variants and Modification of Penetrance of BRCA2-Associated Breast Cancer.

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Correction: Comparison of 6q25 Breast Cancer Hits from Asian and European Genome Wide Association Studies in the Breast Cancer Association Consortium (BCAC)

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Correction: Evaluating Genome-Wide Association Study-Identified Breast Cancer Risk Variants in African-American Women.

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Corrections to: Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries. ⬇️

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

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Corrigendum: A somatic-mutational process recurrently duplicates germline susceptibility loci and tissue-specific super-enhancers in breast cancers

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Corrigendum: Rare coding variants and X-linked loci associated with age at menarche

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Cost-effectiveness of screening with contrast enhanced magnetic resonance imaging vs X-ray mammography of women at a high familial risk of breast cancer

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Critical assessment of new risk factors for breast cancer: considerations for development of an improved risk prediction model

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Critical research gaps and translational priorities for the successful prevention and treatment of breast cancer

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Cross Cancer Genomic Investigation of Inflammation Pathway for Five Common Cancers: Lung, Ovary, Prostate, Breast, and Colorectal Cancer

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Cross-Cancer Genome-Wide Analysis of Lung, Ovary, Breast, Prostate, and Colorectal Cancer Reveals Novel Pleiotropic Associations

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Crowdsourcing the General Public for Large Scale Molecular Pathology Studies in Cancer

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Cumulative Burden of Colorectal Cancer-Associated Genetic Variants Is More Strongly Associated With Early-Onset vs Late-Onset Cancer

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

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DNA mismatch repair gene MSH6 implicated in determining age at natural menopause

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Decreased breast cancer risk in systemic lupus erythematosus: the search for a genetic basis continues

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Detecting rare copy number variants from Illumina genotyping arrays with the CamCNV pipeline: Segmentation of z-scores improves detection and reliability

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Diagnostic radiation procedures and risk of prostate cancer

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Dietary fat and early-onset prostate cancer risk

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Differential Burden of Rare and Common Variants on Tumor Characteristics, Survival, and Mode of Detection in Breast Cancer

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Discovery of common and rare genetic risk variants for colorectal cancer

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Do MDM2 SNP309 and TP53 R72P interact in breast cancer susceptibility? A large pooled series from the breast cancer association consortium

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E-cadherin breast tumor expression, risk factors and survival: Pooled analysis of 5,933 cases from 12 studies in the Breast Cancer Association Consortium.

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Educational attainment and mean leukocyte telomere length in women in the European Prospective Investigation into Cancer (EPIC)-Norfolk population study

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Effect of BRCA Mutations on Metastatic Relapse and Cause-specific Survival After Radical Treatment for Localised Prostate Cancer

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Effect of chest X-rays on the risk of breast cancer among BRCA1/2 mutation carriers in the international BRCA1/2 carrier cohort study: a report from the EMBRACE, GENEPSO, GEO-HEBON, and IBCCS Collaborators' Group

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Effect of germ-line genetic variation on breast cancer survival in a population-based study

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Effects of BRCA2 cis-regulation in normal breast and cancer risk amongst BRCA2 mutation carriers

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Effects of common germ-line genetic variation in cell cycle genes on ovarian cancer survival

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Effects of common germline genetic variation in cell cycle control genes on breast cancer survival: results from a population-based cohort

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Elevated expression of Ki-67 identifies aggressive prostate cancers but does not distinguish BRCA1 or BRCA2 mutation carriers

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Eligibility for magnetic resonance imaging screening in the United Kingdom: effect of strict selection criteria and anonymous DNA testing on breast cancer incidence in the MARIBS Study

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Endometrial cancer and genetic variation in PTEN, PIK3CA, AKT1, MLH1, and MSH2 within a population-based case-control study

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Epidemiological and ES cell-based Functional Evaluation of BRCA2 Variants Identified in Families with Breast Cancer

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

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

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Erratum: Corrigendum: A common coding variant in CASP8 is associated with breast cancer risk

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Erratum: Corrigendum: Analysis of the genetic phylogeny of multifocal prostate cancer identifies multiple independent clonal expansions in neoplastic and morphologically normal prostate tissue

scholarly article by Colin S Cooper et al published June 2015 in Nature Genetics

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

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Erratum: Corrigendum: Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk

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Erratum: Identification of the breast cancer susceptibility gene BRCA2

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Estimates of the gene frequency of BRCA1 and its contribution to breast and ovarian cancer incidence

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Etiology of hormone receptor positive breast cancer differs by levels of histologic grade and proliferation

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European polygenic risk score for prediction of breast cancer shows similar performance in Asian women

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Evaluating clinician acceptability of the prototype CanRisk tool for predicting risk of breast and ovarian cancer: A multi-methods study

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Evaluating genetic risk for prostate cancer among Japanese and Latinos

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Evaluating genetic variants associated with breast cancer risk in high and moderate-penetrance genes in Asians

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Evaluating genome-wide association study-identified breast cancer risk variants in African-American women

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Evaluating the effectiveness of using standard mammogram form to predict breast cancer risk: case-control study

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Evaluating the power to discriminate between highly correlated SNPs in genetic association studies

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Evaluating the role of alcohol consumption in breast and ovarian cancer susceptibility using population-based cohort studies and two-sample Mendelian randomization analyses

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Evaluation of BRCA1 and BRCA2 mutation prevalence, risk prediction models and a multistep testing approach in French-Canadian families with high risk of breast and ovarian cancer

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Evaluation of Fanconi Anemia genes in familial breast cancer predisposition

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

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Evaluation of a prospective scoring system designed for a multicenter breast MR imaging screening study

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Evaluation of an algorithm of tagging SNPs selection by linkage disequilibrium

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Evaluation of association methods for analysing modifiers of disease risk in carriers of high-risk mutations

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Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies

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Evaluation of associations between genetically predicted circulating protein biomarkers and breast cancer risk

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Evaluation of chromosome 6p22 as a breast cancer risk modifier locus in a follow-up study of BRCA2 mutation carriers

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Evaluation of linkage of breast cancer to the putative BRCA3 locus on chromosome 13q21 in 128 multiple case families from the Breast Cancer Linkage Consortium

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Evaluation of the XRCC1 gene as a phenotypic modifier in BRCA1/2 mutation carriers. Results from the consortium of investigators of modifiers of BRCA1/BRCA2.

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Evaluation of variation in the phosphoinositide-3-kinase catalytic subunit alpha oncogene and breast cancer risk

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Evidence for SMAD3 as a modifier of breast cancer risk in BRCA2 mutation carriers

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Evidence for further breast cancer susceptibility genes in addition to BRCA1 and BRCA2 in a population-based study

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Evidence of a Causal Association Between Insulinemia and Endometrial Cancer: A Mendelian Randomization Analysis

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Evidence of gene-environment interactions between common breast cancer susceptibility loci and established environmental risk factors

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Evidence of linkage of the inflammatory bowel disease susceptibility locus on chromosome 16 (IBD1) to ulcerative colitis

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

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

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Exclusion of linkage of loci on chromosome 19 with multiple endocrine neoplasia, type 2

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Exome array analysis identifies ETFB as a novel susceptibility gene for anthracycline-induced cardiotoxicity in cancer patients

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Exome array analysis identifies GPR35 as a novel susceptibility gene for anthracycline-induced cardiotoxicity in childhood cancer

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Exploring the link between MORF4L1 and risk of breast cancer

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Exposure to diagnostic radiation and risk of breast cancer among carriers of BRCA1/2 mutations: retrospective cohort study (GENE-RAD-RISK).

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

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FGFR2 variants and breast cancer risk: fine-scale mapping using African American studies and analysis of chromatin conformation

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Familial cylindromatosis (turban tumour syndrome) gene localised to chromosome 16q12-q13: evidence for its role as a tumour suppressor gene

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Familial prostate cancer: the evidence and the Cancer Research Campaign/British Prostate Group (CRC/BPG) UK Familial Prostate Cancer Study

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Familial relative risks for breast cancer by pathological subtype: a population-based cohort study

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Familial risks of breast cancer

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Familial site-specific ovarian cancer is linked to BRCA1 on 17q12-21.

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Family history and the risk of breast cancer: a systematic review and meta-analysis

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Family history of breast cancer: referral guidelines changed after acceptance of 10 minute consultation

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FastPop: a rapid principal component derived method to infer intercontinental ancestry using genetic data

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

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Fine scale mapping of the breast cancer 16q12 locus

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

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

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

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

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

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

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

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

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Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk

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Fine-mapping the HOXB region detects common variants tagging a rare coding allele: evidence for synthetic association in prostate cancer

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

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

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

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

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Five endometrial cancer risk loci identified through genome-wide association analysis

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Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium

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Floating absolute risk: an alternative to relative risk in survival and case-control analysis avoiding an arbitrary reference group

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Frequency of familial melanoma and MLM2 gene.

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From association to cause: fine mapping of the TNRC9 gene region, a novel susceptibility locus identified in the first genome-wide association study for breast cancer.

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

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Functional complementation studies identify candidate genes and common genetic variants associated with ovarian cancer survival

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Functional complementation studies identify candidate genes and common genetic variants associated with ovarian cancer survival

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

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Functional polymorphisms in the TERT promoter are associated with risk of serous epithelial ovarian and breast cancers

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

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

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GWAS meta-analysis of 16 852 women identifies new susceptibility locus for endometrial cancer

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Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array

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Gene and pathway level analyses of germline DNA-repair gene variants and prostate cancer susceptibility using the iCOGS-genotyping array

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Gene-environment interactions involving functional variants: Results from the Breast Cancer Association Consortium

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Gene-gene interactions in breast cancer susceptibility

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Gene-panel sequencing and the prediction of breast-cancer risk

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Generalizability of established prostate cancer risk variants in men of African ancestry

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Genetic Risk Score Mendelian Randomization Shows that Obesity Measured as Body Mass Index, but not Waist:Hip Ratio, Is Causal for Endometrial Cancer

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

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Genetic analyses of gynecological disease identify genetic relationships between uterine fibroids and endometrial cancer, and a novel endometrial cancer genetic risk region at the WNT4 1p36.12 locus

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Genetic and Histopathologic Evaluation ofBRCA1andBRCA2DNA Sequence Variants of Unknown Clinical Significance

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Genetic association of an LBP-1c/CP2/LSF gene polymorphism with late onset Alzheimer's disease

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Genetic evidence and integration of various data sources for classifying uncertain variants into a single model

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Genetic heterogeneity and localization of a familial breast-ovarian cancer gene on chromosome 17q12-q21

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Genetic heterogeneity and penetrance analysis of the BRCA1 and BRCA2 genes in breast cancer families. The Breast Cancer Linkage Consortium

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Genetic heterogeneity of breast-ovarian cancer revisited. Breast Cancer Linkage Consortium

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Genetic insights into biological mechanisms governing human ovarian ageing

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Genetic linkage analysis in familial breast and ovarian cancer: results from 214 families. The Breast Cancer Linkage Consortium

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Genetic linkage studies map the multiple endocrine neoplasia type 2 loci to a small interval on chromosome 10q11.2

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Genetic models for the familial aggregation of mammographic breast density

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Genetic modifiers of CHEK2*1100delC-associated breast cancer risk

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Genetic modifiers of menopausal hormone replacement therapy and breast cancer risk: a genome-wide interaction study

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Genetic overlap between endometriosis and endometrial cancer: evidence from cross-disease genetic correlation and GWAS meta-analyses

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Genetic predisposition to ductal carcinoma in situ of the breast

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

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Genetic predisposition to mosaic Y chromosome loss in blood

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Genetic predisposition to mosaic Y chromosome loss in blood is associated with genomic instability in other tissues and susceptibility to non-haematological cancers

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Genetic susceptibility to naevi – a twin study ⬇️

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Genetic susceptibility to radiation-induced breast cancer after Hodgkin lymphoma

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Genetic variant predictors of gene expression provide new insight into risk of colorectal cancer

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Genetic variants in ER cofactor genes and endometrial cancer risk

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Genetic variants in epigenetic genes and breast cancer risk.

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

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

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Genetic variation in TYMS in the one-carbon transfer pathway is associated with ovarian carcinoma types in the Ovarian Cancer Association Consortium

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

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Genetic variation in prostate-specific antigen-detected prostate cancer and the effect of control selection on genetic association studies

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Genetic variation in stromal proteins decorin and lumican with breast cancer: investigations in two case-control studies

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Genetic variation in the chromosome 17q23 amplicon and breast cancer risk

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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

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

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Genetically Predicted Levels of DNA Methylation Biomarkers and Breast Cancer Risk: Data From 228 951 Women of European Descent

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

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

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

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

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

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

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Genome-wide association studies in common cancers--what have we learnt?

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Genome-wide association study for ovarian cancer susceptibility using pooled DNA.

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

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

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Genome-wide association study identifies a common variant associated with risk of endometrial cancer

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Genome-wide association study identifies a common variant in RAD51B associated with male breast cancer risk

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Genome-wide association study identifies a possible susceptibility locus for endometrial cancer

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Genome-wide association study identifies five new breast cancer susceptibility loci

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Genome-wide association study identifies multiple loci associated with both mammographic density and breast cancer risk

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

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Genome-wide association study identifies new prostate cancer susceptibility loci

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Genome-wide association study identifies novel breast cancer susceptibility loci

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Genome-wide association study identifies susceptibility loci for B-cell childhood acute lymphoblastic leukemia ⬇️

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Genome-wide association study identifies three new melanoma susceptibility loci

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

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

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Genome-wide association study of circulating estradiol, testosterone, and sex hormone-binding globulin in postmenopausal women

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

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Genome-wide association study of endometrial cancer in E2C2

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

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Genome-wide association study of prostate cancer-specific survival

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

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

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Genome-wide association study of susceptibility loci for breast cancer in Sardinian population

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Genome-wide linkage analysis of 1,233 prostate cancer pedigrees from the International Consortium for Prostate Cancer Genetics using novel sumLINK and sumLOD analyses

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Genome-wide linkage disequilibrium mapping of late-onset Alzheimer’s disease in Finland ⬇️

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Genome-wide linkage screen for testicular germ cell tumour susceptibility loci

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

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Genomic analyses for age at menarche identify 389 independent signals and indicate BMI-independent effects of puberty timing on cancer susceptibility

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Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk

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Genomic analysis of male puberty timing highlights shared genetic basis with hair colour and lifespan ⬇️

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Germline BRCA mutation and outcome in young-onset breast cancer (POSH): a prospective cohort study ⬇️

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Germline BRCA mutations are associated with higher risk of nodal involvement, distant metastasis, and poor survival outcomes in prostate cancer

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Germline BRCA1 mutations increase prostate cancer risk

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

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Germline determinants of the somatic mutation landscape in 2,642 cancer genomes

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Germline mutations in fumarate hydratase (FH) do not predispose to prostate cancer

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Germline mutations of the BRCA1 gene in breast and ovarian cancer families provide evidence for a genotype–phenotype correlation

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

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Germline variation at 8q24 and prostate cancer risk in men of European ancestry

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HLA and inflammatory bowel disease

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HOXB13 is a susceptibility gene for prostate cancer: results from the International Consortium for Prostate Cancer Genetics (ICPCG).

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HPC2/ELAC2 polymorphisms and prostate cancer risk: analysis by age of onset of disease

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Hand pattern indicates prostate cancer risk

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HapMap-based study of the 17q21 ERBB2 amplicon in susceptibility to breast cancer

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Haplotype and phenotype analysis of nine recurrent BRCA2 mutations in 111 families: results of an international study

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Haplotype and phenotype analysis of six recurrent BRCA1 mutations in 61 families: results of an international study

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Haplotype structure in Ashkenazi Jewish BRCA1 and BRCA2 mutation carriers

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

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

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Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium

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Height, selected genetic markers and prostate cancer risk: results from the PRACTICAL consortium

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Heterogeneity of breast cancer associations with five susceptibility loci by clinical and pathological characteristics

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High prevalence of the 999del5 mutation in icelandic breast and ovarian cancer patients

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High risk genes predisposing to prostate cancer development—do they exist?

High-throughput allelic expression imbalance analyses identify candidate breast cancer risk genes

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High-throughput automated scoring of Ki67 in breast cancer tissue microarrays from the Breast Cancer Association Consortium

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How many more breast cancer predisposition genes are there?

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Human familial and sporadic breast cancer: analysis of the coding regions of the 17 beta-hydroxysteroid dehydrogenase 2 gene (EDH17B2) using a single-strand conformation polymorphism assay

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Hyaluronan-mediated motility receptor gene single nucleotide polymorphisms and risk of breast cancer

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IGF1 and IGFBP3 tagging polymorphisms are associated with circulating levels of IGF1, IGFBP3 and risk of breast cancer

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

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

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Survival of patients with breast cancer attending Bristol Cancer Help Centre

scientific article published on 01 September 1990

Systematic Population-Based Assessment of Cancer Risk in First-Degree Relatives of Cancer Probands

scientific article published on 01 November 1994

TGF-β signaling pathway and breast cancer susceptibility

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TP53-based interaction analysis identifies cis-eQTL variants for TP53BP2, FBXO28, and FAM53A that associate with survival and treatment outcome in breast cancer

scientific article published on 5 February 2017

Tagging single nucleotide polymorphisms in cell cycle control genes and susceptibility to invasive epithelial ovarian cancer

scientific article published in April 2007

Tagging single nucleotide polymorphisms in the BRIP1 gene and susceptibility to breast and ovarian cancer

scientific article published on 7 March 2007

Tagging single-nucleotide polymorphisms in antioxidant defense enzymes and susceptibility to breast cancer

scientific article

Tagging single-nucleotide polymorphisms in candidate oncogenes and susceptibility to ovarian cancer

scientific article published on 24 February 2009

Tamoxifen and risk of contralateral breast cancer for BRCA1 and BRCA2 mutation carriers

scientific article published on 05 August 2013

Targeted Resequencing of the Coding Sequence of 38 Genes Near Breast Cancer GWAS Loci in a Large Case-Control Study

scientific article published on 14 January 2019

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

scientific article published on 14 September 2010

Teacher questionnaire compared with observational data on effects of sex and sibling status on preschool behaviour

scientific article published on April 1984

Telomere length in prospective and retrospective cancer case-control studies

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Telomere length shows no association with BRCA1 and BRCA2 mutation status

scientific article published on 29 January 2014

Telomere structure and maintenance gene variants and risk of five cancer types

scientific article published on 15 December 2016

Testicular microlithiasis as a familial risk factor for testicular germ cell tumour

scientific article published on 30 October 2007

The ACE gene and Alzheimer's disease susceptibility

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The AIB1 Polyglutamine Repeat Does Not Modify Breast Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

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The BACE gene: genomic structure and candidate gene study in late-onset Alzheimer's disease.

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The BOADICEA model of genetic susceptibility to breast and ovarian cancer

scientific article published on October 2004

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

scientific article published on 18 March 2008

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

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

scientific article published on 20 February 2018

The CASP8 -652 6N del promoter polymorphism and breast cancer risk: a multicenter study

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The CEPH consortium primary linkage map of human chromosome 10

scientific article published on 01 March 1990

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

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The Effects of Common Genetic Variants in Oncogenes on Ovarian Cancer Survival

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

scientific article published on 01 November 2019

The Influence of Number and Timing of Pregnancies on Breast Cancer Risk for Women With or Mutations

The International Testicular Cancer Linkage Consortium: a clinicopathologic descriptive analysis of 461 familial malignant testicular germ cell tumor kindred

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The KL-VS sequence variant of Klotho and cancer risk in BRCA1 and BRCA2 mutation carriers

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The OncoArray Consortium: A Network for Understanding the Genetic Architecture of Common Cancers

scientific article published on 03 October 2016

The Relationship Between Micrometastases in the Bone Marrow, Histopathologic Features of the Primary Tumor in Breast Cancer and Prognosis ⬇️

scientific article published on 01 July 1988

The Reliable Identification of Disease-Gene Associations

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The SNP rs6500843 in 16p13.3 is associated with survival specifically among chemotherapy-treated breast cancer patients

scientific article published on April 2015

The TP53 Arg72Pro and MDM2 309G>T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers

scientific article published on 25 August 2009

The UK national study of magnetic resonance imaging as a method of screening for breast cancer (MARIBS)

scientific article published on 01 September 2002

The Y deletion gr/gr and susceptibility to testicular germ cell tumor

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The admixture maximum likelihood test to test for association between rare variants and disease phenotypes ⬇️

scientific article published on June 6, 2013

The admixture maximum likelihood test: a novel experiment-wise test of association between disease and multiple SNPs

scientific article published on 01 November 2006

The androgen receptor CAG repeat polymorphism and modification of breast cancer risk in BRCA1 and BRCA2 mutation carriers

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The clinical and screening age-at-onset distribution for the MEN-2 syndrome

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The contribution of germline BRCA1 and BRCA2 mutations to familial ovarian cancer: no evidence for other ovarian cancer-susceptibility genes

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The contribution of inherited predisposition to cancer incidence

scientific article published on January 1990

The contribution of rare variation to prostate cancer heritability

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The contributions of breast density and common genetic variation to breast cancer risk

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The cost-utility of magnetic resonance imaging for breast cancer in BRCA1 mutation carriers aged 30–49

article published in 2007

The effect of sample size on polygenic hazard models for prostate cancer

scientific article published on 08 June 2020

The effects of height and BMI on prostate cancer incidence and mortality: a Mendelian randomization study in 20,848 cases and 20,214 controls from the PRACTICAL consortium

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The evolutionary history of lethal metastatic prostate cancer

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The extent of linkage disequilibrium in four populations with distinct demographic histories

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The frequency of germ-line mutations in the breast cancer predisposition genes BRCA1 and BRCA2 in familial prostate cancer. The Cancer Research Campaign/British Prostate Group United Kingdom Familial Prostate Cancer Study Collaborators

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The functional ALDH2 polymorphism is associated with breast cancer risk: A pooled analysis from the Breast Cancer Association Consortium.

scientific article published on 7 May 2019

The genetic epidemiology of BRCA1. Breast Cancer Linkage Consortium

scientific article published on 01 September 1994

The genetic epidemiology of breast cancer genes

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The genetic epidemiology of early-onset epithelial ovarian cancer: a population-based study

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The genetic epidemiology of prostate cancer and its clinical implications

scientific article published on 03 December 2013

The genetic interplay between body mass index, breast size and breast cancer risk: a Mendelian randomization analysis

scientific article published on 01 June 2019

The genetics of breast and ovarian cancer

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The genetics of familial breast cancer and their practical implications

scientific article published on January 1994

The heritability of mammographic breast density and circulating sex-hormone levels: two independent breast cancer risk factors

scientific article published on 16 October 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 inherited component of cancer

scientific article published on July 1994

The landscape of cancer genes and mutational processes in breast cancer

scientific article (publication date: 16 May 2012)

The management of advanced testicular teratoma

scientific article published on 01 July 1988

The pathology of familial breast cancer: predictive value of immunohistochemical markers estrogen receptor, progesterone receptor, HER-2, and p53 in patients with mutations in BRCA1 and BRCA2.

scientific article published in May 2002

The role of KRAS rs61764370 in invasive epithelial ovarian cancer: implications for clinical testing

scientific article published on 8 March 2011

The role of genetic breast cancer susceptibility variants as prognostic factors

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The rs10993994 risk allele for prostate cancer results in clinically relevant changes in microseminoprotein-beta expression in tissue and urine

scientific article published in 2010

The search for low-penetrance breast cancer genes.

scientific article

The study of nevi in British twins: Study design and description of the data set ⬇️

scientific article published on January 1, 1992

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

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

scientific article published in January 2021

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

scientific article published on 01 March 2020

Truncating mutations in the Fanconi anemia J gene BRIP1 are low-penetrance breast cancer susceptibility alleles

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Two ATM variants and breast cancer risk

scientific article published in June 2005

Two Novel Susceptibility Loci for Prostate Cancer in Men of African Ancestry.

scientific article published in August 2017

Two percent of men with early-onset prostate cancer harbor germline mutations in the BRCA2 gene

scientific article

Two truncating variants in FANCC and breast cancer risk

scientific article published on 29 August 2019

Uncovering the Contribution of Moderate-Penetrance Susceptibility Genes to Breast Cancer by Whole-Exome Sequencing and Targeted Enrichment Sequencing of Candidate Genes in Women of European Ancestry

scientific article published on 11 July 2022

Use of deep whole genome sequencing data to identify structure risk variants in breast cancer susceptibility genes.

scientific article published on 8 January 2018

Use of the BOADICEA Web Application in clinical practice: appraisals by clinicians from various countries

scientific article published on 16 June 2017

Using human genetics to understand the disease impacts of testosterone in men and women

scientific article published on 10 February 2020

VEXOR: an integrative environment for prioritization of functional variants in fine-mapping analysis

scientific article published on May 2017

Validation of loci at 2q14.2 and 15q21.3 as risk factors for testicular cancer

scientific article published on 7 December 2017

Validation of prostate cancer risk-related loci identified from genome-wide association studies using family-based association analysis: evidence from the International Consortium for Prostate Cancer Genetics (ICPCG)

scientific article published on 25 December 2011

Variants in CHEK2 other than 1100delC do not make a major contribution to breast cancer susceptibility

scientific article

Variants in DNA double-strand break repair genes and breast cancer susceptibility

scientific article

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

scientific article published in PLoS ONE

Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer

scientific article

Variation in BRCA1 cancer risks by mutation position

scientific article published on 01 April 2002

Variation in cancer risks, by mutation position, in BRCA2 mutation carriers

scientific article

Variation of risks of breast and ovarian cancer associated with different germline mutations of the BRCA2 gene

scientific article published on 01 January 1997

Where are the prostate cancer genes?—A summary of eight genome wide searches ⬇️

scientific article published on 01 December 2003

Younger age-at-diagnosis for familial malignant testicular germ cell tumor

scientific article

[The genetics of medullary cancer of the thyroid]

scientific article published on 01 January 1988

pedigreejs: a web-based graphical pedigree editor

scientific article published on 31 October 2017

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

scientific article

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