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Andrew B Singleton

Showing results (301-310 of 397) with videos related to

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Nature Communications|June 17, 2022
Deficiency in endocannabinoid synthase DAGLB contributes to early onset Parkinsonism and murine nigral dopaminergic neuron dysfunctionZhenhua Liu, Nannan Yang, Jie Dong, et al.
Genome Biology|February 1, 2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencingIris E Jansen, Hui Ye, Sasja Heetveld, et al.
Neurobiology of Aging|September 3, 2020
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's diseaseEmmeline E Brown, Cornelis Blauwendraat, Joanne Trinh, et al.
Stroke|January 31, 2013
Common variants within oxidative phosphorylation genes influence risk of ischemic stroke and intracerebral hemorrhageChristopher D Anderson, Alessandro Biffi, Michael A Nalls, et al.
Brain : a Journal of Neurology|June 22, 2023
Large-scale rare variant burden testing in Parkinson's diseaseMary B Makarious, Julie Lake, Vanessa Pitz, et al.
Annals of Neurology|May 29, 2009
SNCA variants are associated with increased risk for multiple system atrophySonja W Scholz, Henry Houlden, Claudia Schulte, et al.
Science (New York, N.Y.)|March 29, 2008
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophreniaTom Walsh, Jon M McClellan, Shane E McCarthy, et al.
Annals of Neurology|April 26, 2021
Investigation of Autosomal Genetic Sex Differences in Parkinson's DiseaseCornelis Blauwendraat, Hirotaka Iwaki, Mary B Makarious, et al.
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in <i>GBA1</i>Pilar Álvarez Jerez, Peter A Wild Crea, Daniel M Ramos, et al.
Human Molecular Genetics|March 1, 2013
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT NetworkZhao Chen, Hua Tang, Rehan Qayyum, et al.
Pageof 40

Showing results (301-310 of 397) with videos related to

Sort By:
Pageof 40
Nature Communications|June 17, 2022
Deficiency in endocannabinoid synthase DAGLB contributes to early onset Parkinsonism and murine nigral dopaminergic neuron dysfunctionZhenhua Liu, Nannan Yang, Jie Dong, et al.
Genome Biology|February 1, 2017
Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencingIris E Jansen, Hui Ye, Sasja Heetveld, et al.
Neurobiology of Aging|September 3, 2020
Analysis of DNM3 and VAMP4 as genetic modifiers of LRRK2 Parkinson's diseaseEmmeline E Brown, Cornelis Blauwendraat, Joanne Trinh, et al.
Stroke|January 31, 2013
Common variants within oxidative phosphorylation genes influence risk of ischemic stroke and intracerebral hemorrhageChristopher D Anderson, Alessandro Biffi, Michael A Nalls, et al.
Brain : a Journal of Neurology|June 22, 2023
Large-scale rare variant burden testing in Parkinson's diseaseMary B Makarious, Julie Lake, Vanessa Pitz, et al.
Annals of Neurology|May 29, 2009
SNCA variants are associated with increased risk for multiple system atrophySonja W Scholz, Henry Houlden, Claudia Schulte, et al.
Science (New York, N.Y.)|March 29, 2008
Rare structural variants disrupt multiple genes in neurodevelopmental pathways in schizophreniaTom Walsh, Jon M McClellan, Shane E McCarthy, et al.
Annals of Neurology|April 26, 2021
Investigation of Autosomal Genetic Sex Differences in Parkinson's DiseaseCornelis Blauwendraat, Hirotaka Iwaki, Mary B Makarious, et al.
Medrxiv : the Preprint Server for Health Sciences|January 13, 2025
African ancestry neurodegeneration risk variant disrupts an intronic branchpoint in <i>GBA1</i>Pilar Álvarez Jerez, Peter A Wild Crea, Daniel M Ramos, et al.
Human Molecular Genetics|March 1, 2013
Genome-wide association analysis of red blood cell traits in African Americans: the COGENT NetworkZhao Chen, Hua Tang, Rehan Qayyum, et al.
Pageof 40