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Andrew B Singleton

Showing results (91-100 of 397) with videos related to

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Patterns (New York, N.Y.)|March 15, 2024
Federated learning for multi-omics: A performance evaluation in Parkinson's diseaseBenjamin P Danek, Mary B Makarious, Anant Dadu, et al.
European Journal of Human Genetics : EJHG|January 11, 2020
High-resolution inference of genetic relationships among Jewish populationsNaama M Kopelman, Lewi Stone, Dena G Hernandez, et al.
JAMA Neurology|July 16, 2014
Genome-wide analysis of the heritability of amyotrophic lateral sclerosisMargaux F Keller, Luigi Ferrucci, Andrew B Singleton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2006
Assessing the role of DRD5 and DYT1 in two different case-control series with primary blepharospasmJordi Clarimon, Francesco Brancati, Elizabeth Peckham, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2002
Case-control study of dopamine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's diseaseJohn L Goudreau, Demetrius M Maraganore, Matthew J Farrer, et al.
Neurobiology of Disease|August 9, 2005
Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosisMichael L Garcia, Andrew B Singleton, Dena Hernandez, et al.
Journal of Alzheimer'S Disease : JAD|June 4, 2016
A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern ItalyCeleste Sassi, Rosa Capozzo, Raphael Gibbs, et al.
Nature Reviews. Drug Discovery|January 29, 2024
Open science in precision medicine for neurodegenerative diseasesHampton L Leonard, Mike A Nalls, Aaron Day-Williams, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 20, 2021
Coding and Noncoding Variation in LRRK2 and Parkinson's Disease RiskJulie Lake, Xylena Reed, Rebekah G Langston, et al.
Medrxiv : the Preprint Server for Health Sciences|July 29, 2024
Association of CSF α-Synuclein Seed Amplification Assay Positivity with Disease Progression and Cognitive Decline: A Longitudinal Alzheimer's Disease Neuroimaging Initiative StudyDuygu Tosun, Zachary Hausle, Pamela Thropp, et al.
Pageof 40

Showing results (91-100 of 397) with videos related to

Sort By:
Pageof 40
Patterns (New York, N.Y.)|March 15, 2024
Federated learning for multi-omics: A performance evaluation in Parkinson's diseaseBenjamin P Danek, Mary B Makarious, Anant Dadu, et al.
European Journal of Human Genetics : EJHG|January 11, 2020
High-resolution inference of genetic relationships among Jewish populationsNaama M Kopelman, Lewi Stone, Dena G Hernandez, et al.
JAMA Neurology|July 16, 2014
Genome-wide analysis of the heritability of amyotrophic lateral sclerosisMargaux F Keller, Luigi Ferrucci, Andrew B Singleton, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|November 30, 2006
Assessing the role of DRD5 and DYT1 in two different case-control series with primary blepharospasmJordi Clarimon, Francesco Brancati, Elizabeth Peckham, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|December 5, 2002
Case-control study of dopamine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's diseaseJohn L Goudreau, Demetrius M Maraganore, Matthew J Farrer, et al.
Neurobiology of Disease|August 9, 2005
Mutations in neurofilament genes are not a significant primary cause of non-SOD1-mediated amyotrophic lateral sclerosisMichael L Garcia, Andrew B Singleton, Dena Hernandez, et al.
Journal of Alzheimer'S Disease : JAD|June 4, 2016
A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern ItalyCeleste Sassi, Rosa Capozzo, Raphael Gibbs, et al.
Nature Reviews. Drug Discovery|January 29, 2024
Open science in precision medicine for neurodegenerative diseasesHampton L Leonard, Mike A Nalls, Aaron Day-Williams, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|September 20, 2021
Coding and Noncoding Variation in LRRK2 and Parkinson's Disease RiskJulie Lake, Xylena Reed, Rebekah G Langston, et al.
Medrxiv : the Preprint Server for Health Sciences|July 29, 2024
Association of CSF α-Synuclein Seed Amplification Assay Positivity with Disease Progression and Cognitive Decline: A Longitudinal Alzheimer's Disease Neuroimaging Initiative StudyDuygu Tosun, Zachary Hausle, Pamela Thropp, et al.
Pageof 40