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Genetics in Medicine : Official Journal of the American College of Medical Genetics|May 22, 2026
Development of polyphenotypic scores to prioritize detection of G6PD rs1050828 carriers in African and African American populationsTianyuan Lu, David Stein, Wenmin Zhang, et al.
Current Opinion in Allergy and Clinical Immunology|September 23, 2017
Whole exome sequencing in inborn errors of immunity: use the power but mind the limitsGiorgia Bucciol, Erika Van Nieuwenhove, Leen Moens, et al.
Scientific Reports|May 9, 2022
Novel brown adipose tissue candidate genes predicted by the human gene connectomeDiego F Salazar-Tortosa, David Enard, Yuval Itan, et al.
Briefings in Bioinformatics|May 22, 2022
VIPPID: a gene-specific single nucleotide variant pathogenicity prediction tool for primary immunodeficiency diseasesMingyan Fang, Zheng Su, Hassan Abolhassani, et al.
Genome Medicine|January 17, 2020
De novo variants in exomes of congenital heart disease patients identify risk genes and pathwaysCigdem Sevim Bayrak, Peng Zhang, Martin Tristani-Firouzi, et al.
The American Journal of Tropical Medicine and Hygiene|January 8, 2014
Defining risk groups to yellow fever vaccine-associated viscerotropic disease in the absence of denominator dataStephen J Seligman, Joel E Cohen, Yuval Itan, et al.
Research Square|March 31, 2025
Inherited burden for disease predisposition in diverse populationsBarış Kayaalp, Meltem Ece Kars, Yuval Itan, et al.
JACC. Case Reports|July 28, 2021
Sudden Cardiac Arrest in a Patient With Mitral Valve Prolapse and LMNA and SCN5A MutationsAsha M Mahajan, Yuval Itan, Marina Cerrone, et al.
NPJ Genomic Medicine|February 18, 2026
Inherited burden for disease predisposition in diverse populationsBarış Kayaalp, Meltem Ece Kars, Yuval Itan, et al.
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