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Mar Matarin

Showing results (11-20 of 41) with videos related to

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CNS Neuroscience & Therapeutics|June 29, 2018
The impact of brain-derived neurotrophic factor Val66Met polymorphism on cognition and functional brain networks in patients with intractable partial epilepsyMeneka K Sidhu, Pamela J Thompson, Britta Wandschneider, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 10, 2009
The TOR1A polymorphism rs1182 and the risk of spread in primary blepharospasmGiovanni Defazio, Mar Matarin, Elizabeth L Peckham, et al.
Brain : a Journal of Neurology|April 2, 2019
Transcriptomic and genetic analyses reveal potential causal drivers for intractable partial epilepsySebastian Guelfi, Juan A Botia, Maria Thom, 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.
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.
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.
Epilepsy Research|November 23, 2015
Variants in KCNJ11 and BAD do not predict response to ketogenic dietary therapies for epilepsyNatasha E Schoeler, Costin Leu, Jon White, et al.
European Journal of Human Genetics : EJHG|September 23, 2010
Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophyFrancesca I Arrigoni, Mar Matarin, Pamela J Thompson, et al.
Human Molecular Genetics|December 24, 2013
Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequenceJacqueline K Rainger, Shipra Bhatia, Hemant Bengani, 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.
Pageof 5

Showing results (11-20 of 41) with videos related to

Sort By:
Pageof 5
CNS Neuroscience & Therapeutics|June 29, 2018
The impact of brain-derived neurotrophic factor Val66Met polymorphism on cognition and functional brain networks in patients with intractable partial epilepsyMeneka K Sidhu, Pamela J Thompson, Britta Wandschneider, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|February 10, 2009
The TOR1A polymorphism rs1182 and the risk of spread in primary blepharospasmGiovanni Defazio, Mar Matarin, Elizabeth L Peckham, et al.
Brain : a Journal of Neurology|April 2, 2019
Transcriptomic and genetic analyses reveal potential causal drivers for intractable partial epilepsySebastian Guelfi, Juan A Botia, Maria Thom, 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.
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.
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.
Epilepsy Research|November 23, 2015
Variants in KCNJ11 and BAD do not predict response to ketogenic dietary therapies for epilepsyNatasha E Schoeler, Costin Leu, Jon White, et al.
European Journal of Human Genetics : EJHG|September 23, 2010
Extended extraocular phenotype of PROM1 mutation in kindreds with known autosomal dominant macular dystrophyFrancesca I Arrigoni, Mar Matarin, Pamela J Thompson, et al.
Human Molecular Genetics|December 24, 2013
Disruption of SATB2 or its long-range cis-regulation by SOX9 causes a syndromic form of Pierre Robin sequenceJacqueline K Rainger, Shipra Bhatia, Hemant Bengani, 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.
Pageof 5