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Jose Bras

Showing results (81-90 of 118) with videos related to

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JAMA Neurology|May 8, 2013
Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R geneRita Guerreiro, Eleanna Kara, Isabelle Le Ber, et al.
Neurobiology of Aging|December 31, 2022
TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patientsMarco Foddis, Sonja Blumenau, Manuel Holtgrewe, et al.
Human Molecular Genetics|November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritanceSteven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.
Neurobiology of Aging|March 17, 2018
Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3Celeste Sassi, Michael A Nalls, Perry G Ridge, et al.
Human Molecular Genetics|August 16, 2012
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's diseaseMargaux F Keller, Mohamad Saad, Jose Bras, et al.
Scientific Reports|March 17, 2021
PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J miceClemens Messerschmidt, Marco Foddis, Sonja Blumenau, et al.
JAMA Neurology|July 25, 2018
Frequency of Loss of Function Variants in LRRK2 in Parkinson DiseaseCornelis Blauwendraat, Xylena Reed, Demis A Kia, et al.
Neurobiology of Aging|December 3, 2014
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseasesMike A Nalls, Jose Bras, Dena G Hernandez, et al.
Neurobiology of Aging|June 13, 2016
ABCA7 p.G215S as potential protective factor for Alzheimer's diseaseCeleste Sassi, Michael A Nalls, Perry G Ridge, et al.
Genome Medicine|November 30, 2017
Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resiliencePerry G Ridge, Celeste M Karch, Simon Hsu, et al.
Pageof 12

Showing results (81-90 of 118) with videos related to

Sort By:
Pageof 12
JAMA Neurology|May 8, 2013
Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R geneRita Guerreiro, Eleanna Kara, Isabelle Le Ber, et al.
Neurobiology of Aging|December 31, 2022
TREX1 p.A129fs and p.Y305C variants in a large multi-ethnic cohort of CADASIL-like unrelated patientsMarco Foddis, Sonja Blumenau, Manuel Holtgrewe, et al.
Human Molecular Genetics|November 1, 2016
Additional rare variant analysis in Parkinson's disease cases with and without known pathogenic mutations: evidence for oligogenic inheritanceSteven J Lubbe, Valentina Escott-Price, J Raphael Gibbs, et al.
Neurobiology of Aging|March 17, 2018
Mendelian adult-onset leukodystrophy genes in Alzheimer's disease: critical influence of CSF1R and NOTCH3Celeste Sassi, Michael A Nalls, Perry G Ridge, et al.
Human Molecular Genetics|August 16, 2012
Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's diseaseMargaux F Keller, Mohamad Saad, Jose Bras, et al.
Scientific Reports|March 17, 2021
PHACTR1 genetic variability is not critical in small vessel ischemic disease patients and PcomA recruitment in C57BL/6J miceClemens Messerschmidt, Marco Foddis, Sonja Blumenau, et al.
JAMA Neurology|July 25, 2018
Frequency of Loss of Function Variants in LRRK2 in Parkinson DiseaseCornelis Blauwendraat, Xylena Reed, Demis A Kia, et al.
Neurobiology of Aging|December 3, 2014
NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseasesMike A Nalls, Jose Bras, Dena G Hernandez, et al.
Neurobiology of Aging|June 13, 2016
ABCA7 p.G215S as potential protective factor for Alzheimer's diseaseCeleste Sassi, Michael A Nalls, Perry G Ridge, et al.
Genome Medicine|November 30, 2017
Linkage, whole genome sequence, and biological data implicate variants in RAB10 in Alzheimer's disease resiliencePerry G Ridge, Celeste M Karch, Simon Hsu, et al.
Pageof 12