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Cell|April 19, 2016
Pooled ChIP-Seq Links Variation in Transcription Factor Binding to Complex Disease RiskAshley K Tehranchi, Marsha Myrthil, Trevor Martin, et al.
American Journal of Human Genetics|November 7, 2017
Inferring Relevant Cell Types for Complex Traits by Using Single-Cell Gene ExpressionDiego Calderon, Anand Bhaskar, David A Knowles, et al.
Nature|June 10, 2010
The genome-wide structure of the Jewish peopleDoron M Behar, Bayazit Yunusbayev, Mait Metspalu, et al.
Nature Communications|December 19, 2013
Phylogenetic applications of whole Y-chromosome sequences and the Near Eastern origin of Ashkenazi LevitesSiiri Rootsi, Doron M Behar, Mari Järve, et al.
Bioinformatics (Oxford, England)|February 22, 2015
Deep sequencing analysis of viral infection and evolution allows rapid and detailed characterization of viral mutant spectrumOfer Isakov, Antonio V Bordería, David Golan, et al.
Genome Research|February 22, 2019
Bayesian-based noninvasive prenatal diagnosis of single-gene disordersTom Rabinowitz, Avital Polsky, David Golan, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|March 25, 2017
A null variant in the apolipoprotein L3 gene is associated with non-diabetic nephropathyKarl L Skorecki, Jessica H Lee, Carl D Langefeld, et al.
Science (New York, N.Y.)|April 30, 2016
RNA splicing is a primary link between genetic variation and diseaseYang I Li, Bryce van de Geijn, Anil Raj, et al.
Breast Cancer Research and Treatment|April 4, 2013
Involvement of IGF-1R regulation by miR-515-5p modifies breast cancer risk among BRCA1 carriersAvital Gilam, Liat Edry, Efrat Mamluk-Morag, et al.
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