Showing results (461-470 of 908) with videos related to
Sort By:
Pageof 91
Neurology. Genetics|January 26, 2023
Expanding the Allelic Heterogeneity of ANO10-Associated Autosomal Recessive Cerebellar AtaxiaSean Massey, Yiran Guo, Lisa G Riley, et al.Medrxiv : the Preprint Server for Health Sciences|May 2, 2025
The gSOS Polygenic Score is Associated with Bone Density and Fracture Risk in ChildhoodJonathan A Mitchell, Jonathan Bradfield, Shana E McCormack, et al.Plos One|January 24, 2013
Identification of rare recurrent copy number variants in high-risk autism families and their prevalence in a large ASD populationNori Matsunami, Dexter Hadley, Charles H Hensel, et al.JCI Insight|May 8, 2020
Type I IFN response associated with mTOR activation in the TAFRO subtype of idiopathic multicentric Castleman diseaseRuth-Anne Langan Pai, Alberto Sada Japp, Michael Gonzalez, et al.Human Mutation|December 6, 2008
SNP array mapping of chromosome 20p deletions: genotypes, phenotypes, and copy number variationBinita M Kamath, Brian D Thiel, Xiaowu Gai, et al.Nature Communications|March 16, 2026
Multitrait GWAS and functional validation reveal genetic loci for gastric cancerHuanxin Ding, Chuxuan Liu, Qing Sun, et al.The American Journal of Gastroenterology|October 21, 2010
NOD2 gene polymorphism rs2066844 associates with need for combined liver-intestine transplantation in children with short-gut syndromeMylarappa Ningappa, Brandon W Higgs, Daniel E Weeks, et al.Journal of Immunology (Baltimore, Md. : 1950)|July 19, 2015
Copy Number Variations in CTNNA3 and RBFOX1 Associate with Pediatric Food AllergyJin Li, Irene Fung, Joseph T Glessner, et al.Genes|September 28, 2021
Genetic Variation in PADI6-PADI4 on 1p36.13 Is Associated with Common Forms of Human Generalized EpilepsyRussell J Buono, Jonathan P Bradfield, Zhi Wei, et al.Frontiers in Immunology|June 15, 2026
Identification of IL7R as a key genetic risk locus in childhood steroid-sensitive nephrotic syndrome and IgA nephropathyCong Wang, Yue Jiang, Yingchao Song, et al.Pageof 91