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Proceedings of the National Academy of Sciences of the United States of America|December 14, 2021
High-impact rare genetic variants in severe schizophreniaAnthony W Zoghbi, Ryan S Dhindsa, Terry E Goldberg, et al.
Pharmacogenetics and Genomics|December 14, 2007
Promoter polymorphisms and allelic imbalance in ABCB1 expressionCorinne Loeuillet, Michael Weale, Samuel Deutsch, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|January 15, 2016
Privacy-preserving genomic testing in the clinic: a model using HIV treatmentPaul J McLaren, Jean Louis Raisaro, Manel Aouri, et al.
Proceedings of the National Academy of Sciences of the United States of America|July 19, 2017
Severe viral respiratory infections in children with <i>IFIH1</i> loss-of-function mutationsSamira Asgari, Luregn J Schlapbach, Stéphanie Anchisi, et al.
JAMA Network Open|October 28, 2022
Risk Variants in the Exomes of Children With Critical IllnessJoshua E Motelow, Natalie C Lippa, Joseph Hostyk, et al.
Medrxiv : the Preprint Server for Health Sciences|October 24, 2023
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies <i>ANTXR2</i> as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.
JAMA Cardiology|December 16, 2020
Assessing the Role of Rare Genetic Variation in Patients With Heart FailureGundula Povysil, Olympe Chazara, Keren J Carss, et al.
Plos Biology|February 19, 2009
Tissue-specific genetic control of splicing: implications for the study of complex traitsErin L Heinzen, Dongliang Ge, Kenneth D Cronin, et al.
Research Square|January 10, 2024
Rare variant analyses validate known ALS genes in a multi-ethnic population and identifies <i>ANTXR2</i> as a candidate in PLSTess D Pottinger, Joshua E Motelow, Gundula Povysil, et al.
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