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European Journal of Human Genetics : EJHG|November 21, 2013
Making the genomic leap in HCT: application of second-generation sequencing to clinical advances in hematopoietic cell transplantationYun R Li, John E Levine, Hakon Hakonarson, et al.American Journal of Human Genetics|August 14, 2012
Phasing of many thousands of genotyped samplesAmy L Williams, Nick Patterson, Joseph Glessner, et al.International Heart Journal|January 18, 2021
FLNC and MYLK2 Gene Mutations in a Chinese Family with Different Phenotypes of CardiomyopathyXianyu Qin, Ping Li, Hui-Qi Qu, et al.Brain, Behavior, and Immunity|April 27, 2024
Shared molecular mechanisms and transdiagnostic potential of neurodevelopmental disorders and immune disordersZhanjie Xiu, Ling Sun, Kunlun Liu, et al.American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|July 8, 2010
Analysis of GWAS top hits in ADHD suggests association to two polymorphisms located in genes expressed in the cerebellumFrancesca Lantieri, Joseph T Glessner, Hakon Hakonarson, et al.Plos One|March 26, 2013
Human coding synonymous single nucleotide polymorphisms at ramp regions of mRNA translationQuan Li, Hui-Qi QuBMC Medical Genetics|August 9, 2007
The TCF7L2 locus and type 1 diabetesHui-Qi Qu, Constantin PolychronakosPlos Genetics|October 10, 2009
From disease association to risk assessment: an optimistic view from genome-wide association studies on type 1 diabetesZhi Wei, Kai Wang, Hui-Qi Qu, et al.Plos Biology|February 4, 2010
Rare variants create synthetic genome-wide associationsSamuel P Dickson, Kai Wang, Ian Krantz, et al.Scientific Reports|April 2, 2021
JAK/STAT inhibitor therapy partially rescues the lipodystrophic autoimmune phenotype in Clec16a KO miceRahul Pandey, Marina Bakay, Bryan P Strenkowski, et al.Pageof 93