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JAMA Neurology
|
May 8, 2013
Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R gene
Rita 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 patients
Marco 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 inheritance
Steven 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 NOTCH3
Celeste 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 disease
Margaux 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 mice
Clemens Messerschmidt, Marco Foddis, Sonja Blumenau, et al.
JAMA Neurology
|
July 25, 2018
Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease
Cornelis 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 diseases
Mike 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 disease
Celeste 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 resilience
Perry G Ridge, Celeste M Karch, Simon Hsu, et al.
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of 12
Search research articles
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Showing results (81-90 of 118) with videos related to
Sort By:
Page
of 12
JAMA Neurology
|
May 8, 2013
Genetic analysis of inherited leukodystrophies: genotype-phenotype correlations in the CSF1R gene
Rita 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 patients
Marco 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 inheritance
Steven 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 NOTCH3
Celeste 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 disease
Margaux 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 mice
Clemens Messerschmidt, Marco Foddis, Sonja Blumenau, et al.
JAMA Neurology
|
July 25, 2018
Frequency of Loss of Function Variants in LRRK2 in Parkinson Disease
Cornelis 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 diseases
Mike 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 disease
Celeste 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 resilience
Perry G Ridge, Celeste M Karch, Simon Hsu, et al.
Page
of 12