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Medrxiv : the Preprint Server for Health Sciences
|
January 23, 2024
Assessing the lack of diversity in genetics research across neurodegenerative diseases: a systematic review of the GWAS Catalog and literature
Caroline Jonson, Kristin S Levine, Julie Lake, et al.
Brain : a Journal of Neurology
|
June 29, 2012
Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease
Janel O Johnson, J Raphael Gibbs, Andre Megarbane, et al.
The Lancet. Neurology
|
February 5, 2008
DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA
Sarah Camargos, Sonja Scholz, Javier Simón-Sánchez, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
May 21, 2024
A cross-sectional study of α-synuclein seed amplification assay in Alzheimer's disease neuroimaging initiative: Prevalence and associations with Alzheimer's disease biomarkers and cognitive function
Duygu Tosun, Zachary Hausle, Hirotaka Iwaki, et al.
Nucleic Acids Research
|
February 26, 2013
Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies
Adaikalavan Ramasamy, Daniah Trabzuni, J Raphael Gibbs, et al.
Nature Genetics
|
September 12, 2017
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
Diana Chang, Mike A Nalls, Ingileif B Hallgrímsdóttir, et al.
Biorxiv : the Preprint Server for Biology
|
April 8, 2024
GenoTools: An Open-Source Python Package for Efficient Genotype Data Quality Control and Analysis
Dan Vitale, Mathew Koretsky, Nicole Kuznetsov, et al.
International Journal of Geriatric Psychiatry
|
February 2, 2019
A candidate gene study of risk for dementia in older, postmenopausal women: Results from the Women's Health Initiative Memory Study
Ira Driscoll, Beverly M Snively, Mark A Espeland, et al.
Human Molecular Genetics
|
September 20, 2008
A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20
Melanie A Knight, Dena Hernandez, Scott J Diede, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 8, 2026
The Global Parkinson's Disease Genetics (GP2) Genome Browser
Zih-Hua Fang, Riley H Grant, Dan Vitale, et al.
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of 40
Search research articles
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Showing results (171-180 of 397) with videos related to
Sort By:
Page
of 40
Medrxiv : the Preprint Server for Health Sciences
|
January 23, 2024
Assessing the lack of diversity in genetics research across neurodegenerative diseases: a systematic review of the GWAS Catalog and literature
Caroline Jonson, Kristin S Levine, Julie Lake, et al.
Brain : a Journal of Neurology
|
June 29, 2012
Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease
Janel O Johnson, J Raphael Gibbs, Andre Megarbane, et al.
The Lancet. Neurology
|
February 5, 2008
DYT16, a novel young-onset dystonia-parkinsonism disorder: identification of a segregating mutation in the stress-response protein PRKRA
Sarah Camargos, Sonja Scholz, Javier Simón-Sánchez, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association
|
May 21, 2024
A cross-sectional study of α-synuclein seed amplification assay in Alzheimer's disease neuroimaging initiative: Prevalence and associations with Alzheimer's disease biomarkers and cognitive function
Duygu Tosun, Zachary Hausle, Hirotaka Iwaki, et al.
Nucleic Acids Research
|
February 26, 2013
Resolving the polymorphism-in-probe problem is critical for correct interpretation of expression QTL studies
Adaikalavan Ramasamy, Daniah Trabzuni, J Raphael Gibbs, et al.
Nature Genetics
|
September 12, 2017
A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci
Diana Chang, Mike A Nalls, Ingileif B Hallgrímsdóttir, et al.
Biorxiv : the Preprint Server for Biology
|
April 8, 2024
GenoTools: An Open-Source Python Package for Efficient Genotype Data Quality Control and Analysis
Dan Vitale, Mathew Koretsky, Nicole Kuznetsov, et al.
International Journal of Geriatric Psychiatry
|
February 2, 2019
A candidate gene study of risk for dementia in older, postmenopausal women: Results from the Women's Health Initiative Memory Study
Ira Driscoll, Beverly M Snively, Mark A Espeland, et al.
Human Molecular Genetics
|
September 20, 2008
A duplication at chromosome 11q12.2-11q12.3 is associated with spinocerebellar ataxia type 20
Melanie A Knight, Dena Hernandez, Scott J Diede, et al.
Medrxiv : the Preprint Server for Health Sciences
|
January 8, 2026
The Global Parkinson's Disease Genetics (GP2) Genome Browser
Zih-Hua Fang, Riley H Grant, Dan Vitale, et al.
Page
of 40