Showing results (781-790 of 909) with videos related to

Sort By:
Pageof 91
Diabetes Care|September 27, 2018
First Genome-Wide Association Study of Latent Autoimmune Diabetes in Adults Reveals Novel Insights Linking Immune and Metabolic DiabetesDiana L Cousminer, Emma Ahlqvist, Rajashree Mishra, et al.
American Journal of Respiratory and Critical Care Medicine|March 7, 2018
Whole-Genome Sequencing of Pharmacogenetic Drug Response in Racially Diverse Children with AsthmaAngel C Y Mak, Marquitta J White, Walter L Eckalbar, et al.
The Journal of Clinical Investigation|June 11, 2026
Biallelic inactivating variants in the chromatin remodeler DMAP1 cause a syndromic neurodevelopmental disorderQin Wang, Andrew K Sobering, Christian Tirrito, et al.
Nature|May 1, 2009
Common genetic variants on 5p14.1 associate with autism spectrum disordersKai Wang, Haitao Zhang, Deqiong Ma, et al.
Nature Communications|July 11, 2023
Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disordersCarolina Gracia-Diaz, Yijing Zhou, Qian Yang, et al.
Gastroenterology|July 6, 2016
A Frameshift in CSF2RB Predominant Among Ashkenazi Jews Increases Risk for Crohn's Disease and Reduces Monocyte Signaling via GM-CSFLing-Shiang Chuang, Nicole Villaverde, Ken Y Hui, et al.
Nature|May 1, 2009
Autism genome-wide copy number variation reveals ubiquitin and neuronal genesJoseph T Glessner, Kai Wang, Guiqing Cai, et al.
The Journal of Allergy and Clinical Immunology|December 10, 2013
Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variantsRalf Jp van der Valk, Liesbeth Duijts, Nicolas J Timpson, et al.
Nature Communications|October 10, 2015
Genetic sharing and heritability of paediatric age of onset autoimmune diseasesYun R Li, Sihai D Zhao, Jin Li, et al.
Human Mutation|February 7, 2015
De novo heterozygous mutations in SMC3 cause a range of Cornelia de Lange syndrome-overlapping phenotypesMaría Concepción Gil-Rodríguez, Matthew A Deardorff, Morad Ansari, et al.
Pageof 91