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Brain : a Journal of Neurology
|
December 2, 2025
Long-read sequencing identifies FGF14 repeat expansions in Parkinson's disease
Fulya Akçimen, Kensuke Daida, Lara M Lange, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 7, 2024
LRRK2-Associated Parkinsonism With and Without <i>In Vivo</i> Evidence of Alpha-Synuclein Aggregates
Lana M Chahine, David-Erick Lafontant, Seung Ho Choi, et al.
NPJ Parkinson'S Disease
|
October 17, 2024
Parkinson's families project: a UK-wide study of early onset and familial Parkinson's disease
Clodagh Towns, Zih-Hua Fang, Manuela M X Tan, et al.
NPJ Dementia
|
June 22, 2026
Haplotype-resolved DNA methylation at the <i>APOE</i> locus identifies allele-specific epigenetic signatures relevant to Alzheimer's disease risk
Rylee M Genner, Melissa Meredith, Kensuke Daida, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 1, 2020
The Parkinson's Disease Genome-Wide Association Study Locus Browser
Francis P Grenn, Jonggeol J Kim, Mary B Makarious, et al.
Brain : a Journal of Neurology
|
November 8, 2005
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data
Naheed L Khan, Shushant Jain, John M Lynch, et al.
Nature
|
February 22, 2008
Genotype, haplotype and copy-number variation in worldwide human populations
Mattias Jakobsson, Sonja W Scholz, Paul Scheet, et al.
Brain : a Journal of Neurology
|
May 25, 2016
Genetic and phenotypic characterization of complex hereditary spastic paraplegia
Eleanna Kara, Arianna Tucci, Claudia Manzoni, et al.
Human Molecular Genetics
|
November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance
Steven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.
Molecular Neurobiology
|
November 24, 2016
Genome-Wide Association Analysis of the Sense of Smell in U.S. Older Adults: Identification of Novel Risk Loci in African-Americans and European-Americans
Jing Dong, Annah Wyss, Jingyun Yang, et al.
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of 40
Search research articles
Search
Showing results (261-270 of 397) with videos related to
Sort By:
Page
of 40
Brain : a Journal of Neurology
|
December 2, 2025
Long-read sequencing identifies FGF14 repeat expansions in Parkinson's disease
Fulya Akçimen, Kensuke Daida, Lara M Lange, et al.
Medrxiv : the Preprint Server for Health Sciences
|
August 7, 2024
LRRK2-Associated Parkinsonism With and Without <i>In Vivo</i> Evidence of Alpha-Synuclein Aggregates
Lana M Chahine, David-Erick Lafontant, Seung Ho Choi, et al.
NPJ Parkinson'S Disease
|
October 17, 2024
Parkinson's families project: a UK-wide study of early onset and familial Parkinson's disease
Clodagh Towns, Zih-Hua Fang, Manuela M X Tan, et al.
NPJ Dementia
|
June 22, 2026
Haplotype-resolved DNA methylation at the <i>APOE</i> locus identifies allele-specific epigenetic signatures relevant to Alzheimer's disease risk
Rylee M Genner, Melissa Meredith, Kensuke Daida, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
September 1, 2020
The Parkinson's Disease Genome-Wide Association Study Locus Browser
Francis P Grenn, Jonggeol J Kim, Mary B Makarious, et al.
Brain : a Journal of Neurology
|
November 8, 2005
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data
Naheed L Khan, Shushant Jain, John M Lynch, et al.
Nature
|
February 22, 2008
Genotype, haplotype and copy-number variation in worldwide human populations
Mattias Jakobsson, Sonja W Scholz, Paul Scheet, et al.
Brain : a Journal of Neurology
|
May 25, 2016
Genetic and phenotypic characterization of complex hereditary spastic paraplegia
Eleanna Kara, Arianna Tucci, Claudia Manzoni, et al.
Human Molecular Genetics
|
November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritance
Steven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.
Molecular Neurobiology
|
November 24, 2016
Genome-Wide Association Analysis of the Sense of Smell in U.S. Older Adults: Identification of Novel Risk Loci in African-Americans and European-Americans
Jing Dong, Annah Wyss, Jingyun Yang, et al.
Page
of 40