Susan L. Neuhausen

发表

Amanda B. Spurdle, Marcelo A. Carvalho, Fergus J. Couch, 2015 .

Amanda B. Spurdle, Marcelo A. Carvalho, Fergus J. Couch, 2015 .

Collaborative science in the next-generation sequencing era: a viewpoint on how to combine exome sequencing data across sites to identify novel disease susceptibility genes

Steven N. Hart, Robert J. Klein, Vignesh Ravichandran, 2016, Briefings Bioinform..

The contribution of pathogenic variants in breast cancer susceptibility genes to familial breast cancer risk

Steven N. Hart, Chunling Hu, Mark E. Robson, 2017, npj Breast Cancer.

RAD51C Germline Mutations in Breast and Ovarian Cancer Cases from High-Risk Families

Susan L. Neuhausen, Aaron Adamson, Jeffrey N. Weitzel, 2011, PloS one.

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

Matthias W. Beckmann, Peter A. Fasching, Simon S. Cross, 2016, American journal of human genetics.

A Role for XRCC4 in Age at Diagnosis and Breast Cancer Risk

Nicola J. Camp, Kristina Allen-Brady, Lisa A. Cannon-Albright, 2006, Cancer Epidemiology Biomarkers & Prevention.

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

Gary D. Bader, Christine L. Clarke, Gary D Bader, 2020, Nature Communications.

Identification of a BRCA2-Specific Modifier Locus at 6p24 Related to Breast Cancer Risk

Mads Thomassen, Julian Peto, Peter A. Fasching, 2013, PLoS genetics.

Association Analysis of the Extended MHC Region in Celiac Disease Implicates Multiple Independent Susceptibility Loci

Peter H. R. Green, Chad Garner, Susan L. Neuhausen, 2012, PloS one.

Breast cancer risk variants at 6 q 25 display different phenotype associations and regulate ESR 1 , RMND 1 and CCDC 170

Wei Zheng, Mads Thomassen, Nicholas A. Sinnott-Armstrong, 2016 .

DNA Glycosylases Involved in Base Excision Repair May Be Associated with Cancer Risk in BRCA1 and BRCA2 Mutation Carriers

Olufunmilayo I. Olopade, Mads Thomassen, Torben A. Kruse, 2014, PLoS genetics.

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

Joshua M. Korn, Christiana Kartsonaki, Amanda B. Spurdle, 2010, PLoS Genetics.

Oral Contraceptives and the Risk of Hereditary Ovarian Cancer

Bruce A.J. Ponder, Paolo Radice, Susan L. Neuhausen, 1998 .

A polygenic risk score for breast cancer in U.S. Latinas and Latin-American women

Christopher A. Haiman, Luis G. Carvajal-Carmona, Lawrence H. Kushi, 2019, bioRxiv.

Pathology of Breast and Ovarian Cancers among BRCA1 and BRCA2 Mutation Carriers: Results from the Consortium of Investigators of Modifiers of BRCA1/2 (CIMBA)

Päivi Heikkilä, Mads Thomassen, Stephen Fox, 2011, Cancer Epidemiology, Biomarkers & Prevention.

Inheritance of deleterious mutations at both BRCA1 and BRCA2 in an international sample of 32,295 women

Olufunmilayo I. Olopade, Mads Thomassen, Dieter Niederacher, 2016, Breast Cancer Research.

Genome-Wide Association Study of Celiac Disease in North America Confirms FRMD4B as New Celiac Locus

Linda Steele, Chad Garner, Susan L. Neuhausen, 2014, PloS one.