Simon A Gayther

发表

Multiple loci with different cancer specificities within the 8q24 gene desert.

John L Hopper, Honglin Song, Thibaud Koessler, 2008, Journal of the National Cancer Institute.

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

Peter Kraft, Todd L Edwards, Nazneen Rahman, 2016, Cancer discovery.

Single nucleotide polymorphisms in the TP53 region and susceptibility to invasive epithelial ovarian cancer.

Mark Sherman, Honglin Song, Rebecca Sutphen, 2009, Cancer research.

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

Dong Liang, Thilo Dörk, Natalia Bogdanova, 2014, Molecular nutrition & food research.

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

Mads Thomassen, Nina Ditsch, Vijai Joseph, 2012, Breast Cancer Research.

Recruitment of newly diagnosed ovarian cancer patients proved challenging in a multicentre biobanking study.

Matthew Burnell, Martin Widschwendter, Andy Ryan, 2011, Journal of clinical epidemiology.

Biomarker-Based Ovarian Carcinoma Typing: A Histologic Investigation in the Ovarian Tumor Tissue Analysis Consortium

Francesmary Modugno, Christine Chow, Ellen L Goode, 2013, Cancer Epidemiology, Biomarkers & Prevention.

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

Harvey Risch, Yian A Chen, Mads Thomassen, 2018, Cancer research.

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

Wei Lu, Wei Zheng, Mads Thomassen, 2013, Nature Genetics.

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

Francesmary Modugno, James Paul, Honglin Song, 2015 .

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

Christiana Kartsonaki, Mads Thomassen, Julian Peto, 2010, Nature Genetics.

Variation in NF-κB Signaling Pathways and Survival in Invasive Epithelial Ovarian Cancer

Hannah Yang, James Paul, Honglin Song, 2014, Cancer Epidemiology, Biomarkers & Prevention.

Kernel canonical correlation analysis for assessing gene–gene interactions and application to ovarian cancer

Nicholas B Larson, Rebecca Sutphen, Ellen L Goode, 2013, European Journal of Human Genetics.

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

Francesmary Modugno, Honglin Song, Danielle Shadforth, 2007, Cancer research.

Polymorphism in the GALNT1 Gene and Epithelial Ovarian Cancer in Non-Hispanic White Women: The Ovarian Cancer Association Consortium

Hannah Yang, Shan Wang-Gohrke, Honglin Song, 2010, Cancer Epidemiology, Biomarkers & Prevention.

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

Mads Thomassen, Nina Ditsch, Muhammad Usman Rashid, 2015, JAMA.

Association Between BRCA1 and BRCA2 Mutations and Survival in Women With Invasive Epithelial Ovarian Cancer

Gord Glendon, Lesley McGuffog, Daniel Barrowdale, 2012 .

Age-dependent DNA methylation of genes that are suppressed in stem cells is a hallmark of cancer.

Wolfgang Wagner, Martin Widschwendter, Allison Jones, 2010, Genome research.

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

Shan Wang-Gohrke, Honglin Song, Georgia Chenevix-Trench, 2009, Human molecular genetics.

ESR1/SYNE1 Polymorphism and Invasive Epithelial Ovarian Cancer Risk: An Ovarian Cancer Association Consortium Study

Shan Wang-Gohrke, Honglin Song, Malcolm C Pike, 2010, Cancer Epidemiology, Biomarkers & Prevention.

A transcriptome-wide association study of high grade serous epithelial ovarian cancer identifies novel susceptibility genes and splice variants

Alexander Gusev, Bogdan Pasaniuc, Paul D P Pharoah, 2019, Nature Genetics.

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

Douglas F Easton, B. Ponder, D. Easton, 2001, Breast Cancer Research.

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

Dong Liang, Jane E. Carpenter, Peter Kraft, 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

Michael Khazen, Iqbal Warsi, Martin O Leach, 2009, Breast Cancer Research.

Combined and interactive effects of environmental and GWAS-identified risk factors in ovarian cancer.

Harvey Risch, Malcolm C Pike, Georgia Chenevix-Trench, 2013, Cancer epidemiology, biomarkers & prevention : a publication of the American Association for Cancer Research, cosponsored by the American Society of Preventive Oncology.

Robust Tests for Additive Gene-Environment Interaction in Case-Control Studies Using Gene-Environment Independence

Harvey Risch, Bhramar Mukherjee, Seunggeun Lee, 2018, American journal of epidemiology.

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

David V Conti, Honglin Song, Malcolm C Pike, 2011, Human molecular genetics.