Showing results (751-760 of 909) with videos related to
Sort By:
Pageof 91
Lancet (London, England)|October 23, 2015
Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association studyIsabelle Cleynen, Gabrielle Boucher, Luke Jostins, et al.Nature Medicine|June 1, 2023
Genomic profiling informs diagnoses and treatment in vascular anomaliesDong Li, Sarah E Sheppard, Michael E March, et al.Nature Genetics|June 21, 2011
Identification of common variants influencing risk of the tauopathy progressive supranuclear palsyGünter U Höglinger, Nadine M Melhem, Dennis W Dickson, et al.Medrxiv : the Preprint Server for Health Sciences|April 16, 2025
Current Limitations of Electronic Health Record Systems in Supporting Pragmatic Clinical Trials: Insights from the eMERGE ConsortiumKavishwar B Wagholikar, Jennifer Allen Pacheco, Adam S Gordon, et al.Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 4, 2023
De novo variants in RNF213 are associated with a clinical spectrum ranging from Leigh syndrome to early-onset strokeTheresa Brunet, Benedikt Zott, Victoria Lieftüchter, et al.Scientific Reports|March 8, 2016
An integrative approach to investigate the respective roles of single-nucleotide variants and copy-number variants in Attention-Deficit/Hyperactivity DisorderLeandro de Araújo Lima, Ana Cecília Feio-dos-Santos, Sintia Iole Belangero, et al.Cell|August 2, 2022
A cross-disorder dosage sensitivity map of the human genomeRyan L Collins, Joseph T Glessner, Eleonora Porcu, et al.Plos Genetics|March 14, 2012
A genome-wide scan of Ashkenazi Jewish Crohn's disease suggests novel susceptibility lociEimear E Kenny, Itsik Pe'er, Amir Karban, et al.The American Journal of Psychiatry|March 16, 2012
Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3Nigel M Williams, Barbara Franke, Eric Mick, et al.The New England Journal of Medicine|December 25, 2009
Variants of DENND1B associated with asthma in childrenPatrick M A Sleiman, James Flory, Marcin Imielinski, et al.Pageof 91