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Andrew Singleton

Showing results (111-120 of 286) with videos related to

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Medrxiv : the Preprint Server for Health Sciences|June 12, 2026
A genome-wide association study of young onset Parkinson's disease in European ancestryIngeborg Haugesag Lie, Janna van Wetering, Miko Valori, et al.
Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Multi-ancestry population attributable risk assessment of common genetic variation in Alzheimer's and Parkinson's diseasesLietsel Jones, Catalina Cerquera-Cleves, Artur Fs Schuh, et al.
Lancet (London, England)|February 1, 2005
Genetic screening for a single common LRRK2 mutation in familial Parkinson's diseaseWilliam C Nichols, Nathan Pankratz, Dena Hernandez, et al.
Science (New York, N.Y.)|September 22, 2012
Genomic variation in seven Khoe-San groups reveals adaptation and complex African historyCarina M Schlebusch, Pontus Skoglund, Per Sjödin, et al.
Rejuvenation Research|May 22, 2012
Leukocyte CCR2 expression is associated with mini-mental state examination score in older adultsLorna W Harries, Rachel M Bradley-Smith, David J Llewellyn, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 8, 2013
No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's diseaseSilke Appenzeller, Claudia Schulte, Sandra Thier, et al.
JAMA Neurology|January 16, 2013
Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvementRita João Guerreiro, Ebba Lohmann, José Miguel Brás, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2002
Phenomenology of "Lubag" or X-linked dystonia-parkinsonismVirgilio Gerald H Evidente, Joel Advincula, Raymund Esteban, et al.
Neurobiology of Aging|July 19, 2017
Mutations in TYROBP are not a common cause of dementia in a Turkish cohortLee Darwent, Susana Carmona, Ebba Lohmann, et al.
Annals of Neurology|July 18, 2018
Mendelian randomization study shows no causal relationship between circulating urate levels and Parkinson's diseaseDemis A Kia, Alastair J Noyce, Jon White, et al.
Pageof 29

Showing results (111-120 of 286) with videos related to

Sort By:
Pageof 29
Medrxiv : the Preprint Server for Health Sciences|June 12, 2026
A genome-wide association study of young onset Parkinson's disease in European ancestryIngeborg Haugesag Lie, Janna van Wetering, Miko Valori, et al.
Medrxiv : the Preprint Server for Health Sciences|October 7, 2024
Multi-ancestry population attributable risk assessment of common genetic variation in Alzheimer's and Parkinson's diseasesLietsel Jones, Catalina Cerquera-Cleves, Artur Fs Schuh, et al.
Lancet (London, England)|February 1, 2005
Genetic screening for a single common LRRK2 mutation in familial Parkinson's diseaseWilliam C Nichols, Nathan Pankratz, Dena Hernandez, et al.
Science (New York, N.Y.)|September 22, 2012
Genomic variation in seven Khoe-San groups reveals adaptation and complex African historyCarina M Schlebusch, Pontus Skoglund, Per Sjödin, et al.
Rejuvenation Research|May 22, 2012
Leukocyte CCR2 expression is associated with mini-mental state examination score in older adultsLorna W Harries, Rachel M Bradley-Smith, David J Llewellyn, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 8, 2013
No association between polymorphisms in the glutamate transporter SLC1A2 and Parkinson's diseaseSilke Appenzeller, Claudia Schulte, Sandra Thier, et al.
JAMA Neurology|January 16, 2013
Using exome sequencing to reveal mutations in TREM2 presenting as a frontotemporal dementia-like syndrome without bone involvementRita João Guerreiro, Ebba Lohmann, José Miguel Brás, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2002
Phenomenology of "Lubag" or X-linked dystonia-parkinsonismVirgilio Gerald H Evidente, Joel Advincula, Raymund Esteban, et al.
Neurobiology of Aging|July 19, 2017
Mutations in TYROBP are not a common cause of dementia in a Turkish cohortLee Darwent, Susana Carmona, Ebba Lohmann, et al.
Annals of Neurology|July 18, 2018
Mendelian randomization study shows no causal relationship between circulating urate levels and Parkinson's diseaseDemis A Kia, Alastair J Noyce, Jon White, et al.
Pageof 29