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Journal of Neurodevelopmental Disorders|April 29, 2023
Rare recurrent copy number variations in metabotropic glutamate receptor interacting genes in children with neurodevelopmental disordersJoseph T Glessner, Munir E Khan, Xiao Chang, et al.
Brain : a Journal of Neurology|May 7, 2026
Targeting glutamatergic pathways: genetic insights into comorbid neurodevelopmental disordersJoseph T Glessner, Munir E Khan, Xiao Chang, 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.
World Psychiatry : Official Journal of the World Psychiatric Association (WPA)|October 3, 2014
The psychosis spectrum in a young U.S. community sample: findings from the Philadelphia Neurodevelopmental CohortMonica E Calkins, Tyler M Moore, Kathleen R Merikangas, et al.
JAMA Network Open|June 7, 2021
A Mendelian Randomization Approach Using 3-HMG-Coenzyme-A Reductase Gene Variation to Evaluate the Association of Statin-Induced Low-Density Lipoprotein Cholesterol Lowering With Noncardiovascular Disease PhenotypesGe Liu, Mingjian Shi, Jonathan D Mosley, et al.
Clinical and Translational Medicine|June 20, 2023
Trans-ethnic polygenic risk scores for body mass index: An international hundred K+ cohorts consortium studyHui-Qi Qu, John J Connolly, Peter Kraft, et al.
Medrxiv : the Preprint Server for Health Sciences|January 30, 2023
Trans-ethnic Polygenic Risk Scores for Body Mass Index: An International Hundred K+ Cohorts Consortium StudyHuiqi Qu, John J Connolly, Peter Kraft, et al.
Pharmacogenetics and Genomics|August 12, 2021
Genetic association of primary nonresponse to anti-TNFα therapy in patients with inflammatory bowel diseaseTanima De, Honghong Zhang, Cristina Alarcon, et al.
JAMA Internal Medicine|June 28, 2021
Association Between a Common, Benign Genotype and Unnecessary Bone Marrow Biopsies Among African American PatientsSara L Van Driest, Noura S Abul-Husn, Joseph T Glessner, et al.
Genetics in Medicine Open|March 5, 2026
Single vs dual genetic disease in children with congenital anomalies and solid tumorsDeborah J Watson, Amir Hossein Saeidian, Xiang Wang, et al.
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