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Andrew B Singleton

Showing results (191-200 of 397) with videos related to

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Plos One|May 23, 2013
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputationAndrew R Wood, John R B Perry, Toshiko Tanaka, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 8, 2017
Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern ItalyRosa Capozzo, Celeste Sassi, Monia B Hammer, et al.
Human Molecular Genetics|June 23, 2012
MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathiesDaniah Trabzuni, Selina Wray, Jana Vandrovcova, et al.
Annals of Clinical and Translational Neurology|September 25, 2015
Genome-wide association study of neocortical Lewy-related pathologyTerhi Peuralinna, Liisa Myllykangas, Minna Oinas, et al.
Brain : a Journal of Neurology|May 31, 2022
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's diseaseWilliam Zhu, Xiaoping Huang, Esther Yoon, et al.
JAMA Neurology|July 9, 2014
A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlationsEleanna Kara, Aoife P Kiely, Christos Proukakis, et al.
Science Translational Medicine|October 15, 2020
LRRK2 mediates microglial neurotoxicity via NFATc2 in rodent models of synucleinopathiesChangyoun Kim, Alexandria Beilina, Nathan Smith, et al.
Plos Genetics|May 21, 2010
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brainJ Raphael Gibbs, Marcel P van der Brug, Dena G Hernandez, et al.
Neurobiology of Aging|September 5, 2017
Establishing the role of rare coding variants in known Parkinson's disease risk lociIris E Jansen, J Raphael Gibbs, Mike A Nalls, et al.
Cell Reports|June 21, 2016
Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and HumansYubin Wang, Joshua Hersheson, Dulce Lopez, et al.
Pageof 40

Showing results (191-200 of 397) with videos related to

Sort By:
Pageof 40
Plos One|May 23, 2013
Imputation of variants from the 1000 Genomes Project modestly improves known associations and can identify low-frequency variant-phenotype associations undetected by HapMap based imputationAndrew R Wood, John R B Perry, Toshiko Tanaka, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|March 8, 2017
Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern ItalyRosa Capozzo, Celeste Sassi, Monia B Hammer, et al.
Human Molecular Genetics|June 23, 2012
MAPT expression and splicing is differentially regulated by brain region: relation to genotype and implication for tauopathiesDaniah Trabzuni, Selina Wray, Jana Vandrovcova, et al.
Annals of Clinical and Translational Neurology|September 25, 2015
Genome-wide association study of neocortical Lewy-related pathologyTerhi Peuralinna, Liisa Myllykangas, Minna Oinas, et al.
Brain : a Journal of Neurology|May 31, 2022
Heterozygous PRKN mutations are common but do not increase the risk of Parkinson's diseaseWilliam Zhu, Xiaoping Huang, Esther Yoon, et al.
JAMA Neurology|July 9, 2014
A 6.4 Mb duplication of the α-synuclein locus causing frontotemporal dementia and Parkinsonism: phenotype-genotype correlationsEleanna Kara, Aoife P Kiely, Christos Proukakis, et al.
Science Translational Medicine|October 15, 2020
LRRK2 mediates microglial neurotoxicity via NFATc2 in rodent models of synucleinopathiesChangyoun Kim, Alexandria Beilina, Nathan Smith, et al.
Plos Genetics|May 21, 2010
Abundant quantitative trait loci exist for DNA methylation and gene expression in human brainJ Raphael Gibbs, Marcel P van der Brug, Dena G Hernandez, et al.
Neurobiology of Aging|September 5, 2017
Establishing the role of rare coding variants in known Parkinson's disease risk lociIris E Jansen, J Raphael Gibbs, Mike A Nalls, et al.
Cell Reports|June 21, 2016
Defects in the CAPN1 Gene Result in Alterations in Cerebellar Development and Cerebellar Ataxia in Mice and HumansYubin Wang, Joshua Hersheson, Dulce Lopez, et al.
Pageof 40