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R Gruen

Showing results (121-130 of 160) with videos related to

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Human Genetics|September 4, 2017
Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNCAndrew K Adams, Shelley D Smith, Dongnhu T Truong, et al.
Journal of Biotechnology|November 7, 2006
Striptease on glass: validation of an improved stripping procedure for in situ microarraysKarin Hahnke, Marc Jacobsen, Andreas Gruetzkau, et al.
Human Mutation|April 11, 2001
Human GABA(B) receptor 1 gene: eight novel sequence variantsF M Hisama, J R Gruen, J Choi, et al.
Biological Psychiatry|October 20, 2025
KIAA0319 Plays a Critical Role in Cortical Neuronal Maturation and Synaptic Development Through a Dyslexia-Associated Gene NetworkMichael J Scandura, Mu Seog Choe, Ferdi Ridvan Kiral, et al.
Developmental Neuroscience|June 29, 2021
Identifying Dyslexia: Link between Maze Learning and Dyslexia Susceptibility Gene, DCDC2, in Young ChildrenLisa A Gabel, Kelsey Voss, Evelyn Johnson, et al.
Genes|September 28, 2023
The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive TraitStephen A Petrill, Brett G Klamer, Steven Buyske, et al.
American Journal of Human Genetics|June 1, 1997
Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomesR S Ajioka, L B Jorde, J R Gruen, et al.
Neuroimage|July 4, 2012
Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disabilityNatalie Cope, John D Eicher, Haiying Meng, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|June 14, 2014
The DCDC2/intron 2 deletion and white matter disorganization: focus on developmental dyslexiaCecilia Marino, Paola Scifo, Pasquale A Della Rosa, et al.
Journal of Medical Genetics|December 15, 2015
The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective allelesNatalie R Powers, John D Eicher, Laura L Miller, et al.
Pageof 16

Showing results (121-130 of 160) with videos related to

Sort By:
Pageof 16
Human Genetics|September 4, 2017
Enrichment of putatively damaging rare variants in the DYX2 locus and the reading-related genes CCDC136 and FLNCAndrew K Adams, Shelley D Smith, Dongnhu T Truong, et al.
Journal of Biotechnology|November 7, 2006
Striptease on glass: validation of an improved stripping procedure for in situ microarraysKarin Hahnke, Marc Jacobsen, Andreas Gruetzkau, et al.
Human Mutation|April 11, 2001
Human GABA(B) receptor 1 gene: eight novel sequence variantsF M Hisama, J R Gruen, J Choi, et al.
Biological Psychiatry|October 20, 2025
KIAA0319 Plays a Critical Role in Cortical Neuronal Maturation and Synaptic Development Through a Dyslexia-Associated Gene NetworkMichael J Scandura, Mu Seog Choe, Ferdi Ridvan Kiral, et al.
Developmental Neuroscience|June 29, 2021
Identifying Dyslexia: Link between Maze Learning and Dyslexia Susceptibility Gene, DCDC2, in Young ChildrenLisa A Gabel, Kelsey Voss, Evelyn Johnson, et al.
Genes|September 28, 2023
The Rosetta Phenotype Harmonization Method Facilitates Finding a Relationship Quantitative Trait Locus for a Complex Cognitive TraitStephen A Petrill, Brett G Klamer, Steven Buyske, et al.
American Journal of Human Genetics|June 1, 1997
Haplotype analysis of hemochromatosis: evaluation of different linkage-disequilibrium approaches and evolution of disease chromosomesR S Ajioka, L B Jorde, J R Gruen, et al.
Neuroimage|July 4, 2012
Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disabilityNatalie Cope, John D Eicher, Haiying Meng, et al.
Cortex; a Journal Devoted to the Study of the Nervous System and Behavior|June 14, 2014
The DCDC2/intron 2 deletion and white matter disorganization: focus on developmental dyslexiaCecilia Marino, Paola Scifo, Pasquale A Della Rosa, et al.
Journal of Medical Genetics|December 15, 2015
The regulatory element READ1 epistatically influences reading and language, with both deleterious and protective allelesNatalie R Powers, John D Eicher, Laura L Miller, et al.
Pageof 16