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Briefings in Bioinformatics|September 12, 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 genesSteven N Hart, Kara N Maxwell, Tinu Thomas, et al.
Frontiers in Oncology|September 18, 2015
Disseminated Medulloblastoma in a Child with Germline BRCA2 6174delT Mutation and without Fanconi AnemiaJingying Xu, Ashley Sloane Margol, Anju Shukla, et al.
BMJ Open|October 27, 2021
Molecular markers of risk of subsequent invasive breast cancer in women with ductal carcinoma in situ: protocol for a population-based cohort studyThomas E Rohan, Mindy Ginsberg, Yihong Wang, et al.
Gynecologic Oncology|June 2, 2026
Clinical relevance of transcriptome profiling for assessing prognosis, platinum insensitivity, and precision therapeutics in endometrial cancerJesus Gonzalez-Bosquet, Maryam Shahi, Siddhartha Yadav, et al.
Pancreatology : Official Journal of the International Association of Pancreatology (IAP) ... [Et Al.]|July 17, 2022
Tissue methylated DNA markers for sporadic pancreatic cancer are strongly associated with familial and genetically predisposed pancreatic cancerShounak Majumder, William R Taylor, Patrick H Foote, et al.
American Journal of Human Genetics|February 4, 2018
Assessment of the Clinical Relevance of BRCA2 Missense Variants by Functional and Computational ApproachesLucia Guidugli, Hermela Shimelis, David L Masica, et al.
Breast Cancer Research and Treatment|January 11, 2015
A polygenic risk score for breast cancer in women receiving tamoxifen or raloxifene on NSABP P-1 and P-2Celine M Vachon, Daniel J Schaid, James N Ingle, et al.
Nature Communications|November 22, 2017
Germline variation in ADAMTSL1 is associated with prognosis following breast cancer treatment in young womenLatha Kadalayil, Sofia Khan, Heli Nevanlinna, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|April 13, 2006
A two-gene expression ratio of homeobox 13 and interleukin-17B receptor for prediction of recurrence and survival in women receiving adjuvant tamoxifenMatthew P Goetz, Vera J Suman, James N Ingle, et al.
Human Mutation|March 12, 2011
Splicing and multifactorial analysis of intronic BRCA1 and BRCA2 sequence variants identifies clinically significant splicing aberrations up to 12 nucleotides from the intron/exon boundaryPhillip J Whiley, Lucia Guidugli, Logan C Walker, et al.
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