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Cancer|November 30, 2018
Uterine cancer in Jewish Israeli BRCA1/2 mutation carriersYael Laitman, Rachel Michaelson-Cohen, Einat Levi, et al.
Neurobiology of Aging|July 17, 2021
A recessive S174X mutation in Optineurin causes amyotrophic lateral sclerosis through a loss of function via allele-specific nonsense-mediated decayMarc Gotkine, Martina de Majo, Chun Hao Wong, et al.
Breast Cancer Research and Treatment|December 22, 2015
Screening for germline mutations in breast/ovarian cancer susceptibility genes in high-risk families in IsraelTamar Yablonski-Peretz, Shani Paluch-Shimon, Lior Soussan Gutman, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|July 4, 2020
Teaching clinicians practical genomic medicine: 7 years' experience in a tertiary care centerRachel Michaelson-Cohen, Liat Salzer-Sheelo, Rivka Sukenik-Halevy, et al.
BJOG : an International Journal of Obstetrics and Gynaecology|May 3, 2023
Care after premenopausal risk-reducing salpingo-oophorectomy in high-risk women: Scoping review and international consensus recommendationsDenise R Nebgen, Susan M Domchek, Joanne Kotsopoulos, et al.
American Journal of Human Genetics|February 29, 2024
Bi-allelic variants in SNF8 cause a disease spectrum ranging from severe developmental and epileptic encephalopathy to syndromic optic atrophyMelanie Brugger, Antonella Lauri, Yan Zhen, et al.
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