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Wendy H Raskind

Showing results (11-20 of 82) with videos related to

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Clinical Linguistics & Phonetics|January 24, 2013
Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speechBeate Peter, Le Button, Carol Stoel-Gammon, et al.
Neuromuscular Disorders : NMD|July 1, 2020
Mutations in the SIGMAR1 gene cause a distal hereditary motor neuropathy phenotype mimicking ALS: Report of two novel variantsMaxwell T Ma, Dong-Hui Chen, Wendy H Raskind, et al.
Behavior Genetics|September 21, 2010
Genome scan for spelling deficits: effects of verbal IQ on models of transmission and trait gene localizationKevin Rubenstein, Mark Matsushita, Virginia W Berninger, et al.
Frontiers in Psychology|January 12, 2013
The genetics of reading disabilities: from phenotypes to candidate genesWendy H Raskind, Beate Peter, Todd Richards, et al.
Movement Disorders Clinical Practice|September 21, 2019
ADCY5-Related Dyskinesia: Improving Clinical Detection of an Evolving DisorderNirosen Vijiaratnam, Kailash P Bhatia, Anthony E Lang, et al.
American Journal of Medical Genetics|May 7, 2002
Familial aggregation of dyslexia phenotypes. II: paired correlated measuresLi Hsu, Ellen M Wijsman, Virginia W Berninger, et al.
Blood|August 30, 2002
X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interactionChanning Yu, Kathy K Niakan, Mark Matsushita, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 5, 2003
Segregation analysis of phenotypic components of learning disabilities. II. Phonological decodingNicola H Chapman, Wendy H Raskind, Jennifer B Thomson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 9, 2014
Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colorsKevin B Rubenstein, Wendy H Raskind, Virginia W Berninger, et al.
Biorxiv : the Preprint Server for Biology|July 15, 2024
Joint exome and metabolome analysis in individuals with dyslexia: Evidence for associated dysregulations of olfactory perception and autoimmune functionsRohit Nandakumar, Xiaojian Shi, Haiwei Gu, et al.
Pageof 9

Showing results (11-20 of 82) with videos related to

Sort By:
Pageof 9
Clinical Linguistics & Phonetics|January 24, 2013
Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speechBeate Peter, Le Button, Carol Stoel-Gammon, et al.
Neuromuscular Disorders : NMD|July 1, 2020
Mutations in the SIGMAR1 gene cause a distal hereditary motor neuropathy phenotype mimicking ALS: Report of two novel variantsMaxwell T Ma, Dong-Hui Chen, Wendy H Raskind, et al.
Behavior Genetics|September 21, 2010
Genome scan for spelling deficits: effects of verbal IQ on models of transmission and trait gene localizationKevin Rubenstein, Mark Matsushita, Virginia W Berninger, et al.
Frontiers in Psychology|January 12, 2013
The genetics of reading disabilities: from phenotypes to candidate genesWendy H Raskind, Beate Peter, Todd Richards, et al.
Movement Disorders Clinical Practice|September 21, 2019
ADCY5-Related Dyskinesia: Improving Clinical Detection of an Evolving DisorderNirosen Vijiaratnam, Kailash P Bhatia, Anthony E Lang, et al.
American Journal of Medical Genetics|May 7, 2002
Familial aggregation of dyslexia phenotypes. II: paired correlated measuresLi Hsu, Ellen M Wijsman, Virginia W Berninger, et al.
Blood|August 30, 2002
X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interactionChanning Yu, Kathy K Niakan, Mark Matsushita, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|August 5, 2003
Segregation analysis of phenotypic components of learning disabilities. II. Phonological decodingNicola H Chapman, Wendy H Raskind, Jennifer B Thomson, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|May 9, 2014
Genome scan for cognitive trait loci of dyslexia: Rapid naming and rapid switching of letters, numbers, and colorsKevin B Rubenstein, Wendy H Raskind, Virginia W Berninger, et al.
Biorxiv : the Preprint Server for Biology|July 15, 2024
Joint exome and metabolome analysis in individuals with dyslexia: Evidence for associated dysregulations of olfactory perception and autoimmune functionsRohit Nandakumar, Xiaojian Shi, Haiwei Gu, et al.
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