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JAMA Pediatrics|September 2, 2025
Opioid Timeliness in the Emergency Department and Hospitalizations for Acute Sickle Cell PainIbrahim Gwarzo, Keli D Coleman, Kenneth McKinley, et al.Biorxiv : the Preprint Server for Biology|May 3, 2023
Loss-of-function mutation in Omicron variants reduces spike protein expression and attenuates SARS-CoV-2 infectionMichelle N Vu, R Elias Alvarado, Dorothea R Morris, et al.Nature Genetics|February 7, 2012
Germline mutations in DIS3L2 cause the Perlman syndrome of overgrowth and Wilms tumor susceptibilityDewi Astuti, Mark R Morris, Wendy N Cooper, et al.Journal of Neurology|September 12, 2014
SGCE and myoclonus dystonia: motor characteristics, diagnostic criteria and clinical predictors of genotypeKathryn J Peall, Manju A Kurian, Mark Wardle, et al.BMC Infectious Diseases|December 23, 2020
Effects of Tocilizumab in COVID-19 patients: a cohort studyChristine A Vu, Kailynn J DeRonde, Ana D Vega, et al.International Journal of Molecular Sciences|December 11, 2022
Potential of Non-Coding RNA as Biomarkers for Progressive Supranuclear PalsyFabio A Simoes, Greig Joilin, Oliver Peters, et al.Medrxiv : the Preprint Server for Health Sciences|February 4, 2022
COVID-19 vaccination recruits and matures cross-reactive antibodies to conserved epitopes in endemic coronavirus Spike proteinsEvan A Elko, Georgia A Nelson, Heather L Mead, et al.The Lancet. Neurology|October 24, 2024
Uncovering the genetic basis of Parkinson's disease globally: from discoveries to the clinicShen-Yang Lim, Ai Huey Tan, Azlina Ahmad-Annuar, et al.Medrxiv : the Preprint Server for Health Sciences|April 29, 2026
Bridging Genetics and Precision Medicine in Parkinson's Disease through GP2Kajsa Atterling Brolin, Lara M Lange, Emily Navarro-Jones, et al.Brain : a Journal of Neurology|July 21, 2019
Genetic analysis of Mendelian mutations in a large UK population-based Parkinson's disease studyManuela M X Tan, Naveed Malek, Michael A Lawton, et al.Pageof 247