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Plos Pathogens|September 25, 2020
CX3CL1 and IL-15 Promote CD8 T cell chemoattraction in HIV and in atherosclerosisSoumya Panigrahi, Bonnie Chen, Mike Fang, et al.
NPJ Parkinson'S Disease|March 26, 2025
The LRRK2 p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
Brain : a Journal of Neurology|February 1, 2013
SGCE mutations cause psychiatric disorders: clinical and genetic characterizationKathryn J Peall, Daniel J Smith, Manju A Kurian, et al.
Blood|April 30, 2011
Hospitalization for pain in patients with sickle cell disease treated with sildenafil for elevated TRV and low exercise capacityRoberto F Machado, Robyn J Barst, Nancy A Yovetich, et al.
Journal of Cancer Education : the Official Journal of the American Association for Cancer Education|June 22, 2014
The feasibility and educational value of Hear My Voice, a chaplain-led spiritual life review process for patients with brain cancers and progressive neurologic conditionsKatherine M Piderman, Carmen Radecki Breitkopf, Sarah M Jenkins, et al.
NPJ Parkinson'S Disease|October 17, 2024
Parkinson's families project: a UK-wide study of early onset and familial Parkinson's diseaseClodagh Towns, Zih-Hua Fang, Manuela M X Tan, et al.
American Journal of Hematology|January 6, 2023
Intranasal fentanyl and discharge from the emergency department among children with sickle cell disease and vaso-occlusive pain: A multicenter pediatric emergency medicine perspectiveChris A Rees, David C Brousseau, Fahd A Ahmad, et al.
Annals of Neurology|July 29, 2025
Exenatide Once Weekly in the Treatment of Patients with Multiple System AtrophyNirosen Vijiaratnam, Christine Girges, Martin Wiegand, et al.
Biorxiv : the Preprint Server for Biology|September 11, 2023
SARS-CoV-2 hijacks fragile X mental retardation proteins for efficient infectionDimitriya H Garvanska, Rojelio E Alvarado, Filip Oskar Mundt, et al.
Human Molecular Genetics|November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritanceSteven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.
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