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The Journal of Clinical Endocrinology and Metabolism|May 15, 2014
Autosomal dominant hypoparathyroidism caused by germline mutation in GNA11: phenotypic and molecular characterizationDong Li, Evan E Opas, Florin Tuluc, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines|April 8, 2026
Convergent genetic pathways linking neuropsychiatric and ocular disorders in childrenMeng Pan, Wentao Zhou, Hui-Qi Qu, et al.
Acta Neurologica Scandinavica|May 10, 2019
Drug-resistant epilepsy classified by a phenotyping algorithm associates with NTRK2Berta Almoguera, Emily McGinnis, Debra Abrams, et al.
Journal of Pediatric Orthopedics|October 1, 2015
Candidate Loci are Revealed by an Initial Genome-wide Association Study of Juvenile Osteochondritis DissecansJoseph L Yellin, Ashley Trocle, Struan F A Grant, et al.
Inflammatory Bowel Diseases|April 23, 2016
Pathway-based Genome-wide Association Studies Reveal the Association Between Growth Factor Activity and Inflammatory Bowel DiseaseJin Li, Zhi Wei, Xiao Chang, et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology|February 14, 2012
Replication of neuroblastoma SNP association at the BARD1 locus in African-AmericansValeria Latorre, Sharon J Diskin, Maura A Diamond, et al.
Frontiers in Immunology|February 23, 2023
Genome-wide association study of the age of onset of type 1 diabetes reveals HTATIP2 as a novel T cell regulatorChristopher J Cardinale, Xiao Chang, Zhi Wei, et al.
Medrxiv : the Preprint Server for Health Sciences|June 2, 2021
Circulating LIGHT (TNFSF14) and Interleukin-18 Levels in Sepsis-Induced Multi-Organ InjuriesHui-Qi Qu, James Snyder, John Connolly, et al.
European Journal of Human Genetics : EJHG|November 1, 2022
ParseCNV2: efficient sequencing tool for copy number variation genome-wide association studiesJoseph T Glessner, Jin Li, Yichuan Liu, et al.
Cancer Genetics|March 21, 2012
Clinical utilization of high-resolution single nucleotide polymorphism based oligonucleotide arrays in diagnostic studies of pediatric patients with solid tumorsMargaret J Dougherty, Laura S Tooke, Lisa M Sullivan, et al.
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