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Research Square|October 7, 2024
The LRRK2 p.L1795F variant causes Parkinson's disease in the European populationLara M Lange, Kristin Levine, Susan H Fox, et al.
Journal of Parkinson'S Disease|September 26, 2015
Precompetitive Data Sharing as a Catalyst to Address Unmet Needs in Parkinson's DiseaseDiane Stephenson, Michele T Hu, Klaus Romero, et al.
NPJ Parkinson'S Disease|September 12, 2023
Defining the causes of sporadic Parkinson's disease in the global Parkinson's genetics program (GP2)Clodagh Towns, Madeleine Richer, Simona Jasaityte, et al.
Journal of Immunology (Baltimore, Md. : 1950)|December 4, 2023
Cytomegalovirus Infection Facilitates the Costimulation of CD57+CD28- CD8 T Cells in HIV Infection and Atherosclerosis via the CD2-LFA-3 AxisNicole E Winchester, Soumya Panigrahi, Anokhi Haria, et al.
The British Journal of Surgery|March 13, 2020
Timing of procedural stroke and death in asymptomatic patients undergoing carotid endarterectomy: individual patient analysis from four RCTsM H F Poorthuis, R Bulbulia, D R Morris, et al.
Annals of Neurology|August 2, 2018
Variation at the TRIM11 locus modifies progressive supranuclear palsy phenotypeEdwin Jabbari, John Woodside, Manuela M X Tan, et al.
American Journal of Respiratory and Critical Care Medicine|March 18, 2014
An official American Thoracic Society clinical practice guideline: diagnosis, risk stratification, and management of pulmonary hypertension of sickle cell diseaseElizabeth S Klings, Roberto F Machado, Robyn J Barst, et al.
Journal of Movement Disorders|January 31, 2024
Loss-of-Function Variant in the SMPD1 Gene in Progressive Supranuclear Palsy-Richardson Syndrome Patients of Chinese AncestryShen-Yang Lim, Ai Huey Tan, Jia Nee Foo, et al.
Scientific Reports|March 11, 2025
Radiative impact of record-breaking wildfires from integrated ground-based dataEvgueni Kassianov, Connor J Flynn, James C Barnard, et al.
Medrxiv : the Preprint Server for Health Sciences|July 3, 2026
Large-scale functional annotation establishes a reference framework for human LRRK2 variantsAnthea Cheung, Neringa Pratuseviciute, Kirsten Black, et al.
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