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The Journal of Allergy and Clinical Immunology|May 20, 2022
Multiancestral polygenic risk score for pediatric asthmaBahram Namjou, Michael Lape, Edyta Malolepsza, et al.Scientific Reports|April 17, 2019
Heritability and genome-wide association study of benign prostatic hyperplasia (BPH) in the eMERGE networkJacklyn N Hellwege, Sarah Stallings, Eric S Torstenson, et al.Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|July 14, 2023
Trans-ethnic genomic informed risk assessment for Alzheimer's disease: An International Hundred K+ Cohorts Consortium studyPatrick M Sleiman, Hui-Qi Qu, John J Connolly, et al.JAMA Cardiology|January 24, 2019
Association of Thyroid Function Genetic Predictors With Atrial Fibrillation: A Phenome-Wide Association Study and Inverse-Variance Weighted Average Meta-analysisJoe-Elie Salem, M Benjamin Shoemaker, Lisa Bastarache, et al.Neurobiology of Aging|August 4, 2019
Genetic risk for Alzheimer's disease and functional brain connectivity in children and adolescentsLuiza Kvitko Axelrud, João Ricardo Sato, Marcos Leite Santoro, et al.Plos One|July 30, 2016
Electronic Health Record Based Algorithm to Identify Patients with Autism Spectrum DisorderTodd Lingren, Pei Chen, Joseph Bochenek, et al.Journal of the American Medical Informatics Association : JAMIA|December 7, 2022
Characterizing variability of electronic health record-driven phenotype definitionsPascal S Brandt, Abel Kho, Yuan Luo, et al.Carcinogenesis|October 13, 2019
Neural crest-derived tumor neuroblastoma and melanoma share 1p13.2 as susceptibility locus that shows a long-range interaction with the SLC16A1 geneMarianna Avitabile, Mariangela Succoio, Alessandro Testori, et al.American Journal of Human Genetics|September 13, 2016
GRIN2D Recurrent De Novo Dominant Mutation Causes a Severe Epileptic Encephalopathy Treatable with NMDA Receptor Channel BlockersDong Li, Hongjie Yuan, Xilma R Ortiz-Gonzalez, et al.American Journal of Obstetrics and Gynecology|January 27, 2022
Cell-free DNA screening for trisomies 21, 18, and 13 in pregnancies at low and high risk for aneuploidy with genetic confirmationPe'er Dar, Bo Jacobsson, Cora MacPherson, et al.Pageof 91