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Briefings in Bioinformatics|July 22, 2024
Discovering predisposing genes for hereditary breast cancer using deep learningGal Passi, Sari Lieberman, Fouad Zahdeh, et al.Journal of Medical Genetics|May 22, 2016
Identification of genomic deletions causing inherited retinal degenerations by coverage analysis of whole exome sequencing dataSamer Khateb, Mor Hanany, Ayat Khalaileh, et al.Harefuah|July 2, 2023
[GENOTYPE-PHENOTYPE CORRELATIONS BY SPECIFIC FOUNDER VARIANTS IN BRCA IN ISRAELI WOMEN]Rachel Michaelson-Cohen, Yael Laitman, Inbal Kedar, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 9, 2016
Population screening for BRCA1/BRCA2 founder mutations in Ashkenazi Jews: proactive recruitment compared with self-referralSari Lieberman, Ariela Tomer, Avi Ben-Chetrit, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|December 20, 2019
Correction: Population screening for BRCA1/BRCA2 founder mutations in Ashkenazi Jews: proactive recruitment compared with self-referralSari Lieberman, Ariela Tomer, Avi Ben-Chetrit, et al.Gastroenterology|March 1, 2017
Features of Patients With Hereditary Mixed Polyposis Syndrome Caused by Duplication of GREM1 and Implications for Screening and SurveillanceSari Lieberman, Tom Walsh, Menachem Schechter, et al.Journal of the National Cancer Institute|December 14, 2024
TP53 missense allele predisposing to high risk of breast cancer but not pediatric cancersSuhair Lolas-Hamameh, Sari Lieberman, Alaa Sarahneh, et al.Clinical and Translational Gastroenterology|July 2, 2019
Variable Features of Juvenile Polyposis Syndrome With Gastric Involvement Among Patients With a Large Genomic Deletion of BMPR1ASari Lieberman, Rachel Beeri, Tom Walsh, et al.Genome Biology|September 16, 2011
Targeted genomic capture and massively parallel sequencing to identify genes for hereditary hearing loss in Middle Eastern familiesZippora Brownstein, Lilach M Friedman, Hashem Shahin, et al.Cancer|October 20, 2023
The benefit of pancreatic cancer surveillance in carriers of germline BRCA1/2 pathogenic variantsIdo Laish, Menachem Schechter, Alain Dancour, et al.Pageof 3