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Andrew B Singleton

Showing results (161-170 of 397) with videos related to

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Annals of Neurology|August 28, 2018
A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson diseaseLasse Pihlstrøm, Cornelis Blauwendraat, Chiara Cappelletti, et al.
Plos One|March 20, 2012
Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's diseaseJavier Simón-Sánchez, Laura L Kilarski, Michael A Nalls, et al.
The Lancet. Neurology|June 13, 2015
CHCHD2 and Parkinson's diseaseIris E Jansen, Jose M Bras, Suzanne Lesage, et al.
Aging Cell|December 23, 2025
Mitochondrial DNA Variation in the Aging Human Cerebral Cortex and CerebellumAudrey A Omidsalar, David R Tyrpak, J Andrew MacKay, et al.
Annals of Neurology|February 26, 2005
Clinical and positron emission tomography of Parkinson's disease caused by LRRK2Dena G Hernandez, Coro Paisán-Ruíz, Aideen McInerney-Leo, et al.
Annals of Neurology|December 17, 2005
Clinical heterogeneity of alpha-synuclein gene duplication in Parkinson's diseaseKenya Nishioka, Shin Hayashi, Matthew J Farrer, et al.
Neurobiology of Aging|February 23, 2013
Variation in tau isoform expression in different brain regions and disease statesElisa Majounie, William Cross, Victoria Newsway, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutationsCoro Paisán-Ruiz, Rocio Guevara, Monica Federoff, et al.
Neurology|June 8, 2012
Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseasesAnna Sailer, Sonja W Scholz, J Raphael Gibbs, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|July 20, 2024
Assessing the lack of diversity in genetics research across neurodegenerative diseases: A systematic review of the GWAS Catalog and literatureCaroline Jonson, Kristin S Levine, Julie Lake, et al.
Pageof 40

Showing results (161-170 of 397) with videos related to

Sort By:
Pageof 40
Annals of Neurology|August 28, 2018
A comprehensive analysis of SNCA-related genetic risk in sporadic parkinson diseaseLasse Pihlstrøm, Cornelis Blauwendraat, Chiara Cappelletti, et al.
Plos One|March 20, 2012
Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's diseaseJavier Simón-Sánchez, Laura L Kilarski, Michael A Nalls, et al.
The Lancet. Neurology|June 13, 2015
CHCHD2 and Parkinson's diseaseIris E Jansen, Jose M Bras, Suzanne Lesage, et al.
Aging Cell|December 23, 2025
Mitochondrial DNA Variation in the Aging Human Cerebral Cortex and CerebellumAudrey A Omidsalar, David R Tyrpak, J Andrew MacKay, et al.
Annals of Neurology|February 26, 2005
Clinical and positron emission tomography of Parkinson's disease caused by LRRK2Dena G Hernandez, Coro Paisán-Ruíz, Aideen McInerney-Leo, et al.
Annals of Neurology|December 17, 2005
Clinical heterogeneity of alpha-synuclein gene duplication in Parkinson's diseaseKenya Nishioka, Shin Hayashi, Matthew J Farrer, et al.
Neurobiology of Aging|February 23, 2013
Variation in tau isoform expression in different brain regions and disease statesElisa Majounie, William Cross, Victoria Newsway, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2010
Early-onset L-dopa-responsive parkinsonism with pyramidal signs due to ATP13A2, PLA2G6, FBXO7 and spatacsin mutationsCoro Paisán-Ruiz, Rocio Guevara, Monica Federoff, et al.
Neurology|June 8, 2012
Exome sequencing in an SCA14 family demonstrates its utility in diagnosing heterogeneous diseasesAnna Sailer, Sonja W Scholz, J Raphael Gibbs, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|July 20, 2024
Assessing the lack of diversity in genetics research across neurodegenerative diseases: A systematic review of the GWAS Catalog and literatureCaroline Jonson, Kristin S Levine, Julie Lake, et al.
Pageof 40