Publications
25
Citations
1,289
Est. group size
—
Recurring co-author estimate
Active years
13
Publishing since 2013
Claire Wegel conducts research in the medical genetics of Parkinson's disease, a progressive neurological disorder affecting movement. The work focuses on identifying genetic variants that cause or influence the disease, understanding differences in how it presents across patients, and addressing global and ethical aspects of genetic research such as returning results to participants.
Publication activity has been steady over recent years, averaging around two to three papers annually since 2019.
Generated by claude-opus-4-8 from public bibliographic data · Jul 11, 2026
- Global Perspectives on Returning Genetic Research Results in Parkinson Disease
Neurology Genetics · 2024
- Global Perspectives on Returning Genetic Research Results in Parkinson’s Disease
medRxiv · 2024
- Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
npj Parkinson s Disease · 2023
- Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)
npj Parkinson s Disease · 2023
- Author Correction: Elucidating causative gene variants in hereditary Parkinson’s disease in the Global Parkinson’s Genetics Program (GP2)
npj Parkinson s Disease · 2023
- Defining the causes of sporadic Parkinson’s disease in the global Parkinson’s genetics program (GP2)
medRxiv · 2022
- Global Parkinson’s Genetics Program (GP2) Monogenic Network Protocol: Elucidating causative gene variants in hereditary Parkinson’s disease
medRxiv · 2022
- Efficacy of Nilotinib in Patients With Moderately Advanced Parkinson Disease
JAMA Neurology · 2020
- Differences in the Presentation and Progression of Parkinson's Disease by Sex
Movement Disorders · 2020
- Differences in the presentation and progression of Parkinson’s disease by sex
medRxiv · 2020
- Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts
Movement Disorders · 2019
- Genetic risk of Parkinson disease and progression:
Neurology Genetics · 2019
- Genome-wide association study of Parkinson’s disease progression biomarkers in 12 longitudinal patients’ cohorts
bioRxiv (Cold Spring Harbor Laboratory) · 2019
- medRxiv×5
- npj Parkinson s Disease×3
- Movement Disorders×2
- Neurology Genetics×2
- JAMA Neurology×1
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 11, 2026.
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