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Peter Heutink

Showing results (191-200 of 240) with videos related to

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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.
Plos Computational Biology|March 2, 2018
Shared activity patterns arising at genetic susceptibility loci reveal underlying genomic and cellular architecture of human diseaseJ Kenneth Baillie, Andrew Bretherick, Christopher S Haley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2024
Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global ScaleJohanna Junker, Lara M Lange, Eva-Juliane Vollstedt, et al.
Brain : a Journal of Neurology|November 7, 2022
Mitochondrial haplogroups and cognitive progression in Parkinson's diseaseGanqiang Liu, Chunming Ni, Jiamin Zhan, 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.
American Journal of Human Genetics|March 5, 2016
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent MitophagySuzanne Lesage, Valérie Drouet, Elisa Majounie, et al.
Nature|February 28, 2017
An atlas of human long non-coding RNAs with accurate 5' endsChung-Chau Hon, Jordan A Ramilowski, Jayson Harshbarger, et al.
Nature Genetics|May 7, 2021
Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's diseaseGanqiang Liu, Jiajie Peng, Zhixiang Liao, et al.
Neurobiology of Aging|June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseasesCornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, et al.
Annals of Neurology|June 17, 2014
C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysisFrank P Diekstra, Vivianna M Van Deerlin, John C van Swieten, et al.
Pageof 24

Showing results (191-200 of 240) with videos related to

Sort By:
Pageof 24
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.
Plos Computational Biology|March 2, 2018
Shared activity patterns arising at genetic susceptibility loci reveal underlying genomic and cellular architecture of human diseaseJ Kenneth Baillie, Andrew Bretherick, Christopher S Haley, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|July 30, 2024
Team Science Approaches to Unravel Monogenic Parkinson's Disease on a Global ScaleJohanna Junker, Lara M Lange, Eva-Juliane Vollstedt, et al.
Brain : a Journal of Neurology|November 7, 2022
Mitochondrial haplogroups and cognitive progression in Parkinson's diseaseGanqiang Liu, Chunming Ni, Jiamin Zhan, 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.
American Journal of Human Genetics|March 5, 2016
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent MitophagySuzanne Lesage, Valérie Drouet, Elisa Majounie, et al.
Nature|February 28, 2017
An atlas of human long non-coding RNAs with accurate 5' endsChung-Chau Hon, Jordan A Ramilowski, Jayson Harshbarger, et al.
Nature Genetics|May 7, 2021
Genome-wide survival study identifies a novel synaptic locus and polygenic score for cognitive progression in Parkinson's diseaseGanqiang Liu, Jiajie Peng, Zhixiang Liao, et al.
Neurobiology of Aging|June 13, 2017
NeuroChip, an updated version of the NeuroX genotyping platform to rapidly screen for variants associated with neurological diseasesCornelis Blauwendraat, Faraz Faghri, Lasse Pihlstrom, et al.
Annals of Neurology|June 17, 2014
C9orf72 and UNC13A are shared risk loci for amyotrophic lateral sclerosis and frontotemporal dementia: a genome-wide meta-analysisFrank P Diekstra, Vivianna M Van Deerlin, John C van Swieten, et al.
Pageof 24