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Frontiers in Genetics|September 26, 2019
Association of Rare Recurrent Copy Number Variants With Congenital Heart Defects Based on Next-Generation Sequencing Data From Family TriosYichuan Liu, Xiao Chang, Joseph Glessner, et al.Plos One|May 3, 2014
Transcriptome profiling of human ulcerative colitis mucosa reveals altered expression of pathways enriched in genetic susceptibility lociChristopher J Cardinale, Zhi Wei, Jin Li, et al.Experimental Biology and Medicine (Maywood, N.J.)|July 8, 2021
Deep learning prediction of attention-deficit hyperactivity disorder in African Americans by copy number variationYichuan Liu, Hui-Qi Qu, Xiao Chang, et al.Human Molecular Genetics|November 28, 2009
An integrated expression phenotype mapping approach defines common variants in LEP, ALOX15 and CAPNS1 associated with induction of IL-6Benjamin P Fairfax, Fredrik O Vannberg, Jayachandran Radhakrishnan, et al.JAMA Psychiatry|August 24, 2017
Association Between Mitochondrial DNA Haplogroup Variation and Autism Spectrum DisordersDimitra Chalkia, Larry N Singh, Jeremy Leipzig, et al.Human Molecular Genetics|April 10, 2010
In silico replication of the genome-wide association results of the Type 1 Diabetes Genetics ConsortiumHui-Qi Qu, Jonathan P Bradfield, Quan Li, et al.American Journal of Medical Genetics. Part A|October 12, 2021
Rare neurological manifestations in a Saudi Arabian patient with Ehlers-Danlos syndrome and a novel homozygous variant in the TNXB geneTalal M Al-Harbi, Haya Al-Rammah, Naif Al-Zahrani, et al.Genes|March 6, 2021
Rare Recurrent Variants in Noncoding Regions Impact Attention-Deficit Hyperactivity Disorder (ADHD) Gene Networks in Children of both African American and European American AncestryYichuan Liu, Xiao Chang, Hui-Qi Qu, et al.Molecular Cytogenetics|August 5, 2022
Interstitial deletion 4p15.32p16.1 and complex chromoplexy in a female proband with severe neurodevelopmental delay, growth failure and dysmorphismDong Li, Alanna Strong, Cuiping Hou, et al.Plos One|March 25, 2016
Methylation Microarray Studies Highlight PDGFA Expression as a Factor in Biliary AtresiaZenobia C Cofer, Shuang Cui, Steven F EauClaire, et al.Pageof 91