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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.
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.
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