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American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 15, 2010
In their own words: reports of stigma and genetic discrimination by people at risk for Huntington disease in the International RESPOND-HD studyJanet K Williams, Cheryl Erwin, Andrew R Juhl, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|April 12, 2019
Variant classification changes over time in BRCA1 and BRCA2Chloe Mighton, George S Charames, Marina Wang, et al.
Breast Cancer Research and Treatment|March 12, 2010
Absence of genomic BRCA1 and BRCA2 rearrangements in Ashkenazi breast and ovarian cancer familiesZsofia K Stadler, Emmanuel Saloustros, Nichole A L Hansen, et al.
Nature Reviews. Clinical Oncology|June 15, 2016
Counselling framework for moderate-penetrance cancer-susceptibility mutationsNadine Tung, Susan M Domchek, Zsofia Stadler, et al.
Hematology/Oncology Clinics of North America|September 7, 2010
Genome-wide association studies of cancer predispositionZsofia K Stadler, Joseph Vijai, Peter Thom, et al.
Frontiers in Genetics|March 5, 2014
Genome-wide analysis of the role of copy-number variation in pancreatic cancer riskJason A Willis, Semanti Mukherjee, Irene Orlow, et al.
Annals of Surgery|April 7, 2007
Single-amplicon MSH2 A636P mutation testing in Ashkenazi Jewish patients with colorectal cancer: role in presurgical managementJose G Guillem, Emily Glogowski, Harvey G Moore, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|July 20, 2007
BRCA mutations in women with ductal carcinoma in situKaren Lisa Smith, Muriel Adank, Noah Kauff, et al.
CMAJ Open|November 25, 2020
Use of real-world evidence in cancer drug funding decisions in Canada: a qualitative study of stakeholders' perspectivesMarc Clausen, Chloe Mighton, Ruhi Kiflen, et al.
European Journal of Human Genetics : EJHG|November 11, 2011
Health-care providers' views on pursuing reproductive benefit through newborn screening: the case of sickle cell disordersYvonne Bombard, Fiona A Miller, Robin Z Hayeems, et al.
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