Publications
178
Citations
9,422
Est. group size
—
Recurring co-author estimate
Active years
20
Publishing since 2007
Typically publishes in teams of ~13 · 14% small-team papers (≤3 authors) · across 37 venues
- Pathogenic variants in BORCS5 cause a spectrum of neurodevelopmental and neurodegenerative disorders with lysosomal dysfunction
Journal of Clinical Investigation · 2026
- Parkinson's disease genetics across diverse ancestries: an observational genetic study of causal and risk variants with translational implications
The Lancet Neurology · 2026
- Genome‐Wide Assessment Reveals Ancestral Differences in Homozygosity Patterns Potentially Linked to Parkinson's Disease Etiology
Movement Disorders · 2026
- Genome-Wide Assessment Reveals Ancestral Differences in Homozygosity Patterns Potentially Linked to Parkinson's Disease Etiology
Digital Repository at the University of Maryland (University of Maryland College Park) · 2026
- Author Correction: TMEM175, SCARB2 and CTSB associations with Parkinson’s disease risk across populations
npj Parkinson s Disease · 2026
- Genome-wide association and population-tailored polygenic risk for Parkinson’s disease in Taiwan
npj Parkinson s Disease · 2026
- PD GENEration: An International Parkinson’s Disease Genetic Research Study
medRxiv · 2026
- Is <i>SORL1</i> a common genetic target across neurodegenerative diseases? A multi-ancestry biobank study
Brain · 2026
- <i>GCH1</i> p.Ser80Asn Confers Risk for Parkinson’s Disease in East Asian Populations
medRxiv · 2026
- Repeat expansions in Parkinson’s disease and parkinsonism across ancestries: insights from a global genetic cohort
medRxiv · 2026
- Novel In‐Frame <scp><i>FGF14</i></scp> Deletion Causes Spinocerebellar Ataxia Type <scp>27A</scp>: Clinical Response to Deep Brain Stimulation and 4‐Aminopyridine
Movement Disorders · 2025
- Commander complex regulates lysosomal function and is implicated in Parkinson’s disease risk
Science · 2025
- The Spectrum of Neurologic Phenotypes Associated With <scp><i>NUS1</i></scp> Pathogenic Variants: A Comprehensive Case Series
Annals of Neurology · 2025
- Rare but Relevant? Assessing Variants in Dystonia‐Linked Genes in Parkinson's Disease
Movement Disorders · 2025
- Mutations in the Key Autophagy Tethering Factor <scp>EPG5</scp> Link Neurodevelopmental and Neurodegenerative Disorders Including Early‐Onset Parkinsonism
Annals of Neurology · 2025
- Movement Disorders×24
- Neurology×12
- npj Parkinson s Disease×10
- medRxiv×10
- Parkinsonism & Related Disorders×9
- Roger L. Albin
Medicine · University of Michigan
- Kelvin L. Chou
Medicine · University of Michigan
- Jaimie Barr
Medicine · University of Michigan
- Sang-Jin Lee
Medicine · University of Michigan
- C. Chauncey Spears
Medicine · University of Michigan
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 25, 2026.
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