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Wendy H. Raskind · Study
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Author
Wendy H. Raskind
18 works
· latest 2016
· 2 institutions
cluster: provisional
ORCID 0000-0001-8141-9054
Works
18 shown
Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech
PLoS ONE
·
2016
·
9 authors
·
Open access
57
citations
Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech
Clinical Linguistics & Phonetics
·
2013
·
4 authors
·
Open access
44
citations
The Genetics of Reading Disabilities: From Phenotypes to Candidate Genes
Frontiers in Psychology
·
2013
·
5 authors
·
Open access
71
citations
Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample
Journal of Neurodevelopmental Disorders
·
2010
·
8 authors
·
Open access
117
citations
A Multidisciplinary Approach to Understanding Developmental Dyslexia Within Working-Memory Architecture: Genotypes, Phenotypes, Brain, and Instruction
Developmental Neuropsychology
·
2008
·
4 authors
149
citations
Evaluation of candidate genes for DYX1 and DYX2 in families with dyslexia
American Journal of Medical Genetics Part B Neuropsychiatric Genetics
·
2007
·
9 authors
89
citations
Gender differences in severity of writing and reading disabilities
Journal of School Psychology
·
2007
·
4 authors
189
citations
Writing problems in developmental dyslexia: Under-recognized and under-treated
Journal of School Psychology
·
2007
·
4 authors
·
Open access
356
citations
Converging Evidence for Triple Word Form Theory in Children With Dyslexia
Developmental Neuropsychology
·
2006
·
10 authors
106
citations
Modeling Phonological Core Deficits Within a Working Memory Architecture in Children and Adults With Developmental Dyslexia
Scientific Studies of Reading
·
2006
·
4 authors
153
citations
Genomewide scan for real‐word reading subphenotypes of dyslexia: Novel chromosome 13 locus and genetic complexity
American Journal of Medical Genetics Part B Neuropsychiatric Genetics
·
2005
·
10 authors
·
Open access
51
citations
A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency
Molecular Psychiatry
·
2005
·
9 authors
72
citations
Converging evidence for attentional influences on the orthographic word form in child dyslexics
Journal of Neurolinguistics
·
2005
·
6 authors
47
citations
Linkage analyses of four regions previously implicated in dyslexia: Confirmation of a locus on chromosome 15q
American Journal of Medical Genetics Part B Neuropsychiatric Genetics
·
2004
·
9 authors
91
citations
Current Understanding of the Genetic Basis of Reading and Spelling Disability
Learning Disability Quarterly
·
2001
·
1 author
48
citations
Language Phenotype for Reading and Writing Disability: A Family Approach
Scientific Studies of Reading
·
2001
·
3 authors
141
citations
Segregation Analysis of Phenotypic Components of Learning Disabilities. I. Nonword Memory and Digit Span
The American Journal of Human Genetics
·
2000
·
7 authors
·
Open access
76
citations
Familial Aggregation of Dyslexia Phenotypes
Behavior Genetics
·
2000
·
5 authors
71
citations