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Andrew Singleton

Showing results (131-140 of 286) with videos related to

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Stroke|September 24, 2011
Siblings with ischemic stroke study: results of a genome-wide scan for stroke lociJames F Meschia, Michael Nalls, Mar Matarin, et al.
Plos One|September 30, 2011
Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysisJames F Meschia, Andrew Singleton, Michael A Nalls, et al.
Neurobiology of Aging|December 14, 2011
Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's diseaseRita João Guerreiro, Ebba Lohmann, Emma Kinsella, et al.
Neurobiology of Aging|October 26, 2016
Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX arrayImelda S Barber, Anne Braae, Naomi Clement, et al.
Journal of Alzheimer'S Disease : JAD|June 10, 2011
APOE and AβPP gene variation in cortical and cerebrovascular amyloid-β pathology and Alzheimer's disease: a population-based analysisTerhi Peuralinna, Maarit Tanskanen, Mira Mäkelä, et al.
The International Journal of Neuropsychopharmacology|December 21, 2012
Age-modulated association between prefrontal NAA and the BDNF geneBasira Salehi, Nora Preuss, Jan Willem van der Veen, et al.
American Journal of Human Genetics|April 21, 2009
A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial diseaseAndrew J Duncan, Maria Bitner-Glindzicz, Brigitte Meunier, et al.
Genomics|October 15, 2014
Whole blood gene expression and interleukin-6 levelsHonghuang Lin, Roby Joehanes, Luke C Pilling, et al.
Neurology. Genetics|April 12, 2016
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson diseaseSuzanne Lesage, Jose Bras, Florence Cormier-Dequaire, et al.
Annals of Neurology|May 23, 2022
Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk FactorsHui Liu, Mohammad Dehestani, Cornelis Blauwendraat, et al.
Pageof 29

Showing results (131-140 of 286) with videos related to

Sort By:
Pageof 29
Stroke|September 24, 2011
Siblings with ischemic stroke study: results of a genome-wide scan for stroke lociJames F Meschia, Michael Nalls, Mar Matarin, et al.
Plos One|September 30, 2011
Genomic risk profiling of ischemic stroke: results of an international genome-wide association meta-analysisJames F Meschia, Andrew Singleton, Michael A Nalls, et al.
Neurobiology of Aging|December 14, 2011
Exome sequencing reveals an unexpected genetic cause of disease: NOTCH3 mutation in a Turkish family with Alzheimer's diseaseRita João Guerreiro, Ebba Lohmann, Emma Kinsella, et al.
Neurobiology of Aging|October 26, 2016
Mutation analysis of sporadic early-onset Alzheimer's disease using the NeuroX arrayImelda S Barber, Anne Braae, Naomi Clement, et al.
Journal of Alzheimer'S Disease : JAD|June 10, 2011
APOE and AβPP gene variation in cortical and cerebrovascular amyloid-β pathology and Alzheimer's disease: a population-based analysisTerhi Peuralinna, Maarit Tanskanen, Mira Mäkelä, et al.
The International Journal of Neuropsychopharmacology|December 21, 2012
Age-modulated association between prefrontal NAA and the BDNF geneBasira Salehi, Nora Preuss, Jan Willem van der Veen, et al.
American Journal of Human Genetics|April 21, 2009
A nonsense mutation in COQ9 causes autosomal-recessive neonatal-onset primary coenzyme Q10 deficiency: a potentially treatable form of mitochondrial diseaseAndrew J Duncan, Maria Bitner-Glindzicz, Brigitte Meunier, et al.
Genomics|October 15, 2014
Whole blood gene expression and interleukin-6 levelsHonghuang Lin, Roby Joehanes, Luke C Pilling, et al.
Neurology. Genetics|April 12, 2016
Loss-of-function mutations in RAB39B are associated with typical early-onset Parkinson diseaseSuzanne Lesage, Jose Bras, Florence Cormier-Dequaire, et al.
Annals of Neurology|May 23, 2022
Polygenic Resilience Modulates the Penetrance of Parkinson Disease Genetic Risk FactorsHui Liu, Mohammad Dehestani, Cornelis Blauwendraat, et al.
Pageof 29