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Frontiers in Genetics|January 24, 2024
ACCESS: an empirically-based framework developed by the International Nursing CASCADE Consortium to address genomic disparities through the nursing workforceMaria C Katapodi, Carla Pedrazzani, Sivia Barnoy, et al.
Familial Cancer|June 14, 2005
The Tyr978X BRCA1 mutation: occurrence in non-Jewish Iranians and haplotype in French-Canadian and non-Ashkenazi JewsLluís Quintana-Murci, Inbar Gal, Tangiz Bakhan, et al.
American Journal of Human Genetics|April 10, 2012
A nonsense mutation in the human homolog of Drosophila rogdi causes Kohlschutter-Tonz syndromeAdi Mory, Efrat Dagan, Barbara Illi, et al.
Breast Cancer Research and Treatment|October 21, 2010
Germline mutations in BRCA1 and BRCA2 genes in ethnically diverse high risk families in IsraelYael Laitman, Roni Tsipora Borsthein, Dominique Stoppa-Lyonnet, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 16, 2006
Familial clustering of site-specific cancer risks associated with BRCA1 and BRCA2 mutations in the Ashkenazi Jewish populationSharon Simchoni, Eitan Friedman, Bella Kaufman, et al.
Public Health Genomics|June 29, 2026
Optimizing reporting and outreach for surveillance and risk-reducing surgeries for cancer genetic predisposition: Findings of a workshop organized by the International Cascade ConsortiumBardha Citaku-Qerimi, Hanna Yttring, Sofia E Andersson, et al.
Brain : a Journal of Neurology|February 27, 2016
EPG5-related Vici syndrome: a paradigm of neurodevelopmental disorders with defective autophagySusan Byrne, Lara Jansen, Jean-Marie U-King-Im, et al.
Human Molecular Genetics|August 7, 2009
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriersAntonis C Antoniou, Olga M Sinilnikova, Lesley McGuffog, et al.
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