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Genetics|October 14, 2017
RL-SKAT: An Exact and Efficient Score Test for Heritability and Set TestsRegev Schweiger, Omer Weissbrod, Elior Rahmani, et al.Nature Communications|August 2, 2019
Cell-type-specific resolution epigenetics without the need for cell sorting or single-cell biologyElior Rahmani, Regev Schweiger, Brooke Rhead, et al.Studies in Health Technology and Informatics|September 7, 2011
A standard based approach for biomedical knowledge representationAriel Farkash, Hani Neuvirth, Yaara Goldschmidt, et al.Nature Communications|November 23, 2018
Detecting heritable phenotypes without a model using fast permutation testing for heritability and set-testsRegev Schweiger, Eyal Fisher, Omer Weissbrod, et al.Big Data|August 20, 2016
Identifying and Investigating Unexpected Response to Treatment: A Diabetes Case StudyMichal Ozery-Flato, Liat Ein-Dor, Naama Parush-Shear-Yashuv, et al.American Journal of Human Genetics|April 10, 2012
A "Copernican" reassessment of the human mitochondrial DNA tree from its rootDoron M Behar, Mannis van Oven, Saharon Rosset, et al.Parkinsonism & Related Disorders|June 19, 2012
Dyskinesias in patients with Parkinson's disease: effect of the leucine-rich repeat kinase 2 (LRRK2) G2019S mutationGilad Yahalom, Natalie Kaplan, Aya Vituri, et al.Human Genetics|August 12, 2009
Extended Y chromosome haplotypes resolve multiple and unique lineages of the Jewish priesthoodMichael F Hammer, Doron M Behar, Tatiana M Karafet, et al.Human Genetics|July 17, 2010
Missense mutations in the APOL1 gene are highly associated with end stage kidney disease risk previously attributed to the MYH9 geneShay Tzur, Saharon Rosset, Revital Shemer, et al.Plos Genetics|July 3, 2007
The Genographic Project public participation mitochondrial DNA databaseDoron M Behar, Saharon Rosset, Jason Blue-Smith, et al.Pageof 8