Evaluation of Association Methods for Analysing Modifiers of Disease Risk in Carriers of High-Risk Mutations-Reference-Cited by-同舟云学术

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Evaluation of Association Methods for Analysing Modifiers of Disease Risk in Carriers of High-Risk Mutations

Published:2012-04 Issue:3 Volume:36 Page:274-291
ISSN:0741-0395
Container-title:Genetic Epidemiology
language:en
Short-container-title:Genet. Epidemiol.

Author:

Barnes Daniel R.¹,Lee Andrew¹,Investigators EMBRACE¹,Investigators kConFab²,Easton Douglas F.¹,Antoniou Antonis C.¹

Affiliation:

1. Department of Public Health and Primary Care; Centre for Cancer Genetic Epidemiology, University of Cambridge; Cambridge, United Kingdom

2. Kathleen Cuningham Consortium for Research into Familial Breast Cancer; Peter MacCallum Cancer Centre; Melbourne, Australia

Publisher

Wiley

Subject

Genetics (clinical),Epidemiology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1002/gepi.21620/fullpdf

Reference36 articles.

1. Common genetic variants and cancer risk in Mendelian cancer syndromes;Antoniou;Curr Opin Genet Dev,2010

2. Evidence for further breast cancer susceptibility genes in addition to BRCA1 and BRCA2 in a population-based study;Antoniou;Genet Epidemiol,2001

3. 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;Antoniou;Am J Hum Genet,2003

4. A weighted cohort approach for analysing factors modifying disease risks in carriers of high-risk susceptibility genes;Antoniou;Genet Epidemiol,2005

5. Genetic Modifiers of Cancer Risk in BRCA1/2 Mutation Carriers Study (GEMO), Timothy R. Rebbeck, Theresa Wagner, Henry T. Lynch, Susan M. Domchek, Katherine L. Nathanson, Judy E. Garber, Jeffrey Weitzel, Steven A. Narod, Gail Tomlinson, Olufunmilayo I. Olopade, Andrew Godwin, Claudine Isaacs, Anna Jakubowska, Jan Lubinski, Jacek Gronwald, Bohdan Górski, Tomasz Byrski, Tomasz Huzarski, Susan Peock, Margaret Cook, Caroline Baynes, Alexandra Murray, Mark Rogers, Peter A. Daly, Huw Dorkins, Epidemiological Study of BRCA1 and BRCA2 Mutation Carriers (EMBRACE), Rita K. Schmutzler, Beatrix Versmold, Christoph Engel, Alfons Meindl, Norbert Arnold, Dieter Niederacher, Helmut Deissler, German Consortium for Hereditary Breast and Ovarian Cancer (GCHBOC), Amanda B. Spurdle, Xiaoqing Chen, Nicola Waddell, Nicole Cloonan, Kathleen Cuningham Consortium for Research into Familial Breast Cancer (kConFab), Tomas Kirchhoff, Kenneth Offit, Eitan Friedman, Bella Kaufmann, Yael Laitman, Gilli Galore, Gad Rennert, Flavio Lejbkowicz, Leon Raskin, Irene L. Andrulis, Eduard Ilyushik, Hilmi Ozcelik, Peter Devilee, Maaike P.G. Vreeswijk, Mark H. Greene, Sheila A. Prindiville, Ana Osorio, Javier Benítez, Michal Zikan, Csilla I. Szabo, Outi Kilpivaara, Heli Nevanlinna, Ute Hamann, Francine Durocher, Adalgeir Arason, Fergus J. Couch, Douglas F. Easton, Georgia Chenevix-Trench, Consortiumof Investigators of Modifiers of BRCA1/2 (CIMBA);Antoniou;Am J Hum Genet,2007

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1. Large-scale genome-wide association study of 398,238 women unveils seven novel loci associated with high-grade serous epithelial ovarian cancer risk;2024-03-04

2. A new inverse probability of selection weighted Cox model to deal with outcome-dependent sampling in survival analysis;2023-02-07

3. Variable number tandem repeats (VNTRs) as modifiers of breast cancer risk in carriers of BRCA1 185delAG;European Journal of Human Genetics;2022-11-25

4. Copy number variants as modifiers of breast cancer risk for BRCA1/BRCA2 pathogenic variant carriers;Communications Biology;2022-10-06

5. Polygenic risk scores and breast and epithelial ovarian cancer risks for carriers of BRCA1 and BRCA2 pathogenic variants;Genetics in Medicine;2020-10

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