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Obesity (Silver Spring, Md.)|May 30, 2009
The role of obesity-associated loci identified in genome-wide association studies in the determination of pediatric BMIJianhua Zhao, Jonathan P Bradfield, Mingyao Li, et al.
Diabetes|November 26, 2009
Examination of all type 2 diabetes GWAS loci reveals HHEX-IDE as a locus influencing pediatric BMIJianhua Zhao, Jonathan P Bradfield, Haitao Zhang, et al.
Neurology|August 3, 2014
TUBB4A de novo mutations cause isolated hypomyelinationAmy Pizzino, Tyler Mark Pierson, Yiran Guo, et al.
Immunity|December 17, 2013
Thymic stromal lymphopoietin-mediated extramedullary hematopoiesis promotes allergic inflammationMark C Siracusa, Steven A Saenz, Elia D Tait Wojno, et al.
Nature Communications|September 20, 2017
Common variants in MMP20 at 11q22.2 predispose to 11q deletion and neuroblastoma riskXiao Chang, Yan Zhao, Cuiping Hou, et al.
HGG Advances|December 7, 2025
Healthcare professionals' experiences returning monogenic, polygenic, and integrated risk results in the eMERGE studySabrina A Suckiel, Laura Golfinopoulos, Courtney L Scherr, et al.
Human Reproduction (Oxford, England)|July 26, 2015
Pathway analysis supports association of nonsyndromic cryptorchidism with genetic loci linked to cytoskeleton-dependent functionsJulia Spencer Barthold, Yanping Wang, Thomas F Kolon, et al.
Molecular Vision|March 28, 2020
Exome sequencing identifies PEX6 mutations in three cases diagnosed with Retinitis Pigmentosa and hearing impairmentGema García-García, Iker Sanchez-Navarro, Elena Aller, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|November 27, 2020
De novo loss-of-function variants in X-linked MED12 are associated with Hardikar syndrome in femalesDong Li, Alanna Strong, Kaitlyn M Shen, et al.
Human Molecular Genetics|January 11, 2011
Genome-wide association studies of adolescent idiopathic scoliosis suggest candidate susceptibility genesSwarkar Sharma, Xiaochong Gao, Douglas Londono, et al.
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