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Biorxiv : the Preprint Server for Biology|November 19, 2025
Random forest model improves annotation and discovery of variants of uncertain significance in Alzheimer's and other neurological disordersCaroline Jonson, Mary B Makarious, Mathew J Koretsky, et al.
G3 (Bethesda, Md.)|November 20, 2024
GenoTools: an open-source Python package for efficient genotype data quality control and analysisDan Vitale, Mathew J Koretsky, Nicole Kuznetsov, et al.
Human Molecular Genetics|July 30, 2011
Allelic heterogeneity and more detailed analyses of known loci explain additional phenotypic variation and reveal complex patterns of associationAndrew R Wood, Dena G Hernandez, Michael A Nalls, et al.
Cell Reports Methods|September 20, 2023
A fully automated FAIMS-DIA mass spectrometry-based proteomic pipelineLuke Reilly, Erika Lara, Daniel Ramos, et al.
Patterns (New York, N.Y.)|July 6, 2023
Application of Aligned-UMAP to longitudinal biomedical studiesAnant Dadu, Vipul K Satone, Rachneet Kaur, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|April 20, 2026
The Global Parkinson's Disease Genetics (GP2) Genome BrowserZih-Hua Fang, Riley H Grant, Dan Vitale, et al.
AIDS Research and Therapy|September 30, 2025
The association of antiretroviral therapy type and duration of use with stroke in people living with HIV in ZambiaStanley Zimba, Owen Ngalamika, Emmanuel Mukambo, et al.
Research Square|July 9, 2025
Antiretroviral Therapy and Risk of Stroke in People with HIV in ZambiaStanley Zimba, Owen Ngalamika, Emmanuel Mukambo, et al.
Experimental Gerontology|April 3, 2003
mt4216C variant in linkage with the mtDNA TJ cluster may confer a susceptibility to mitochondrial dysfunction resulting in an increased risk of Parkinson's disease in the IrishOwen A Ross, Rose McCormack, Lynn D Maxwell, et al.
Parkinsonism & Related Disorders|April 8, 2014
EIF4G1 gene mutations are not a common cause of Parkinson's disease in the Japanese populationKenya Nishioka, Manabu Funayama, Carles Vilariño-Güell, et al.
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