Showing results (1431-1440 of 1,624) with videos related to
Sort By:
Pageof 163
Nature Communications|September 26, 2019
Genetic architecture of human plasma lipidome and its link to cardiovascular diseaseRubina Tabassum, Joel T Rämö, Pietari Ripatti, et al.Proceedings of the National Academy of Sciences of the United States of America|May 14, 2014
Atg16L1 T300A variant decreases selective autophagy resulting in altered cytokine signaling and decreased antibacterial defenseKara G Lassen, Petric Kuballa, Kara L Conway, et al.JAMA Ophthalmology|April 20, 2023
Overlap of Genetic Loci for Central Serous Chorioretinopathy With Age-Related Macular DegenerationJoel T Rämö, Erik Abner, Elon H C van Dijk, et al.Nature Genetics|June 27, 2018
De novo variants in neurodevelopmental disorders with epilepsyHenrike O Heyne, Tarjinder Singh, Hannah Stamberger, et al.Clinical Pharmacology and Therapeutics|May 9, 2019
Shared Genetic Risk Factors Across Carbamazepine-Induced Hypersensitivity ReactionsPaola Nicoletti, Sarah Barrett, Laurence McEvoy, et al.Cell Genomics|February 13, 2023
Leveraging global multi-ancestry meta-analysis in the study of idiopathic pulmonary fibrosis geneticsJuulia J Partanen, Paavo Häppölä, Wei Zhou, et al.Plos Genetics|February 7, 2009
Genome-wide association studies in an isolated founder population from the Pacific Island of KosraeJennifer K Lowe, Julian B Maller, Itsik Pe'er, et al.Nature Genetics|August 4, 2014
A framework for the interpretation of de novo mutation in human diseaseKaitlin E Samocha, Elise B Robinson, Stephan J Sanders, et al.Cancer Discovery|September 23, 2016
A Recurrent ERCC3 Truncating Mutation Confers Moderate Risk for Breast CancerJoseph Vijai, Sabine Topka, Danylo Villano, et al.American Journal of Human Genetics|February 18, 2010
Genome-wide association study in a high-risk isolate for multiple sclerosis reveals associated variants in STAT3 geneEveliina Jakkula, Virpi Leppä, Anna-Maija Sulonen, et al.Pageof 163