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Javier Simon-Sanchez

Showing results (1-10 of 21) with videos related to

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Human Mutation|November 13, 2007
Genomewide SNP assay reveals mutations underlying Parkinson diseaseJavier Simon-Sanchez, Sonja Scholz, Maria del Mar Matarin, et al.
Neuroscience Letters|May 25, 2005
Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's diseaseJavier Simon-Sanchez, Melissa Hanson, Amanda Singleton, et al.
Plos Genetics|March 14, 2009
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical geneticsMichael A Nalls, Javier Simon-Sanchez, J Raphael Gibbs, et al.
Human Molecular Genetics|November 23, 2006
Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individualsJavier Simon-Sanchez, Sonja Scholz, Hon-Chung Fung, et al.
Neurobiology of Aging|February 23, 2013
Regional differences in gene expression and promoter usage in aged human brainsLuba M Pardo, Patrizia Rizzu, Margherita Francescatto, et al.
Scientific Data|December 1, 2023
A multi-omics dataset for the analysis of frontotemporal dementia genetic subtypesKevin Menden, Margherita Francescatto, Tenzin Nyima, et al.
Neurogenetics|February 22, 2008
Structural genomic variation in ischemic strokeMar Matarin, Javier Simon-Sanchez, Hon-Chung Fung, et al.
Plos Genetics|June 26, 2007
Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humansJoyce van de Leemput, Jayanth Chandran, Melanie A Knight, et al.
Plos One|August 23, 2013
Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locusDaniah Trabzuni, Mina Ryten, Warren Emmett, et al.
Nature|February 22, 2008
Genotype, haplotype and copy-number variation in worldwide human populationsMattias Jakobsson, Sonja W Scholz, Paul Scheet, et al.
Pageof 3

Showing results (1-10 of 21) with videos related to

Sort By:
Pageof 3
Human Mutation|November 13, 2007
Genomewide SNP assay reveals mutations underlying Parkinson diseaseJavier Simon-Sanchez, Sonja Scholz, Maria del Mar Matarin, et al.
Neuroscience Letters|May 25, 2005
Analysis of SCA-2 and SCA-3 repeats in Parkinsonism: evidence of SCA-2 expansion in a family with autosomal dominant Parkinson's diseaseJavier Simon-Sanchez, Melissa Hanson, Amanda Singleton, et al.
Plos Genetics|March 14, 2009
Measures of autozygosity in decline: globalization, urbanization, and its implications for medical geneticsMichael A Nalls, Javier Simon-Sanchez, J Raphael Gibbs, et al.
Human Molecular Genetics|November 23, 2006
Genome-wide SNP assay reveals structural genomic variation, extended homozygosity and cell-line induced alterations in normal individualsJavier Simon-Sanchez, Sonja Scholz, Hon-Chung Fung, et al.
Neurobiology of Aging|February 23, 2013
Regional differences in gene expression and promoter usage in aged human brainsLuba M Pardo, Patrizia Rizzu, Margherita Francescatto, et al.
Scientific Data|December 1, 2023
A multi-omics dataset for the analysis of frontotemporal dementia genetic subtypesKevin Menden, Margherita Francescatto, Tenzin Nyima, et al.
Neurogenetics|February 22, 2008
Structural genomic variation in ischemic strokeMar Matarin, Javier Simon-Sanchez, Hon-Chung Fung, et al.
Plos Genetics|June 26, 2007
Deletion at ITPR1 underlies ataxia in mice and spinocerebellar ataxia 15 in humansJoyce van de Leemput, Jayanth Chandran, Melanie A Knight, et al.
Plos One|August 23, 2013
Fine-mapping, gene expression and splicing analysis of the disease associated LRRK2 locusDaniah Trabzuni, Mina Ryten, Warren Emmett, et al.
Nature|February 22, 2008
Genotype, haplotype and copy-number variation in worldwide human populationsMattias Jakobsson, Sonja W Scholz, Paul Scheet, et al.
Pageof 3