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Science Immunology|April 7, 2023
Human T follicular helper clones seed the germinal center-resident regulatory poolCarole Le Coz, Derek A Oldridge, Ramin S Herati, et al.Molecular Autism|January 29, 2014
Identification of rare DNA sequence variants in high-risk autism families and their prevalence in a large case/control populationNori Matsunami, Charles H Hensel, Lisa Baird, et al.Nature Communications|November 20, 2024
A framework for conducting GWAS using repeated measures data with an application to childhood BMIKimberley Burrows, Anni Heiskala, Jonathan P Bradfield, et al.Journal of Medical Genetics|June 30, 2026
Longest surviving patient with a homozygous splice-altering EGFR pathogenic variant presenting with skin autoinflammation and a Bartter-like salt-losing tubulopathyLeila Youssefian, Sajjad Biglari, Fatemeh Vahidnezhad, et al.Obesity (Silver Spring, Md.)|March 7, 2009
Investigation of the locus near MC4R with childhood obesity in Americans of European and African ancestryStruan F A Grant, Jonathan P Bradfield, Haitao Zhang, et al.Annals of the Rheumatic Diseases|January 7, 2021
Association of novel rare coding variants with juvenile idiopathic arthritisXinyi Meng, Xiaoyuan Hou, Ping Wang, et al.Proceedings of the National Academy of Sciences of the United States of America|June 10, 2014
Impact of puberty on the evolution of cerebral perfusion during adolescenceTheodore D Satterthwaite, Russell T Shinohara, Daniel H Wolf, et al.Medrxiv : the Preprint Server for Health Sciences|April 1, 2024
A framework for conducting time-varying genome-wide association studies: An application to body mass index across childhood in six multiethnic cohortsKimberley Burrows, Anni Heiskala, Jonathan P Bradfield, et al.American Journal of Medical Genetics. Part A|July 31, 2013
PECONPI: a novel software for uncovering pathogenic copy number variations in non-syndromic sensorineural hearing loss and other genetically heterogeneous disordersEllen A Tsai, Micah A Berman, Laura K Conlin, et al.American Journal of Medical Genetics. Part A|September 14, 2023
Microcystic lymphatic malformations in Turner syndrome are due to somatic mosaicism of PIK3CABede N Nriagu, Lydia S Williams, Niambi Brewer, et al.Pageof 91