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BMJ (Clinical Research Ed.)|October 18, 2008
The prevention of progression of arterial disease and diabetes (POPADAD) trial: factorial randomised placebo controlled trial of aspirin and antioxidants in patients with diabetes and asymptomatic peripheral arterial diseaseJill Belch, Angus MacCuish, Iain Campbell, et al.BMC Medical Genetics|January 22, 2008
Genetic loci linked to type 1 diabetes and multiple sclerosis families in SardiniaMaristella Pitzalis, Patrizia Zavattari, Raffaele Murru, et al.The Journal of Molecular Diagnostics : JMD|January 22, 2022
Molecular Diagnostic Outcomes from 700 Cases: What Can We Learn from a Retrospective Analysis of Clinical Exome Sequencing?Jill R Murrell, Addie May I Nesbitt, Samuel W Baker, et al.Nature Communications|January 16, 2020
Rare copy number variants in over 100,000 European ancestry subjects reveal multiple disease associationsYun Rose Li, Joseph T Glessner, Bradley P Coe, et al.American Journal of Human Genetics|May 16, 2007
IRAK-M is involved in the pathogenesis of early-onset persistent asthmaLenuta Balaci, Maria Cristina Spada, Nazario Olla, et al.The New England Journal of Medicine|December 25, 2009
Variants of DENND1B associated with asthma in childrenPatrick M A Sleiman, James Flory, Marcin Imielinski, et al.Journal of Crohn'S & Colitis|April 23, 2021
Variants in STXBP3 are Associated with Very Early Onset Inflammatory Bowel Disease, Bilateral Sensorineural Hearing Loss and Immune DysregulationJodie Ouahed, Judith R Kelsen, Waldo A Spessott, et al.Journal of Medical Genetics|April 12, 2014
A meta-analysis identifies adolescent idiopathic scoliosis association with LBX1 locus in multiple ethnic groupsDouglas Londono, Ikuyo Kou, Todd A Johnson, et al.Nature Genetics|May 14, 2013
Genetic variants in GPR126 are associated with adolescent idiopathic scoliosisIkuyo Kou, Yohei Takahashi, Todd A Johnson, et al.Nature Genetics|December 6, 2011
Genome-wide copy number variation study associates metabotropic glutamate receptor gene networks with attention deficit hyperactivity disorderJosephine Elia, Joseph T Glessner, Kai Wang, et al.Pageof 21