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Brain : a Journal of Neurology|April 12, 2017
Glycation potentiates α-synuclein-associated neurodegeneration in synucleinopathiesHugo Vicente Miranda, Éva M Szego, Luís M A Oliveira, et al.
Influenza and Other Respiratory Viruses|January 26, 2023
Influenza vaccine effectiveness against influenza A subtypes in Europe: Results from the 2021-2022 I-MOVE primary care multicentre studyEsther Kissling, Francisco Pozo, Iván Martínez-Baz, et al.
HGG Advances|June 30, 2024
Stratified analyses refine association between TLR7 rare variants and severe COVID-19Jannik Boos, Caspar I van der Made, Gayatri Ramakrishnan, et al.
American Journal of Human Genetics|December 5, 2017
Monoallelic BMP2 Variants Predicted to Result in Haploinsufficiency Cause Craniofacial, Skeletal, and Cardiac Features Overlapping Those of 20p12 DeletionsTiong Yang Tan, Claudia Gonzaga-Jauregui, Elizabeth J Bhoj, et al.
JACC. Cardiovascular Imaging|February 20, 2022
AI Evaluation of Stenosis on Coronary CTA, Comparison With Quantitative Coronary Angiography and Fractional Flow Reserve: A CREDENCE Trial SubstudyWilliam F Griffin, Andrew D Choi, Joanna S Riess, et al.
JAMA Oncology|October 12, 2023
Berzosertib Plus Topotecan vs Topotecan Alone in Patients With Relapsed Small Cell Lung Cancer: A Randomized Clinical TrialNobuyuki Takahashi, Zhonglin Hao, Liza C Villaruz, et al.
Neurobiology of Aging|December 29, 2009
A large-scale genetic association study to evaluate the contribution of Omi/HtrA2 (PARK13) to Parkinson's diseaseRejko Krüger, Manu Sharma, Olaf Riess, et al.
Frontiers in Neurology|July 14, 2020
Genetic Architecture of Parkinson's Disease in the Indian Population: Harnessing Genetic Diversity to Address Critical Gaps in Parkinson's Disease ResearchRoopa Rajan, K P Divya, Rukmini Mridula Kandadai, et al.
Annals of Neurology|November 14, 2023
Stage-Dependent Biomarker Changes in Spinocerebellar Ataxia Type 3Jennifer Faber, Moritz Berger, Carlo Wilke, et al.
Journal of Medical Genetics|November 6, 2021
Bi-allelic loss-of-function variants in <i>KIF21A</i> cause severe fetal akinesia with arthrogryposis multiplexRuth J Falb, Amelie J Müller, Wolfram Klein, et al.
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