Wendy H Raskind
Internist
University Of Washington Medical Ctr 1959 Ne Pacific St Seattle WA, 98195About
Dr. Raskind is Professor of Medicine (Medical Genetics), Adjunct Professor of Genome Sciences, and Joint Professor of Psychiatry and Behavioral Sciences. Research Interests Dr. Raskind is a clinical and ...
Board Certification
Internal MedicineAmerican Board of Internal MedicineABIM
Provider Details
Expert Publications
Data provided by the National Library of Medicine- Evidence for a polyclonal etiology of palmar fibromatosis.
- Segregation analysis of phenotypic components of learning disabilities. I. Nonword memory and digit span.
- Familial aggregation of dyslexia phenotypes.
- In vitro analyses of known and novel RUNX1/AML1 mutations in dominant familial platelet disorder with predisposition to acute myelogenous leukemia: implications for mechanisms of pathogenesis.
- Autosomal dominant sensory/motor neuropathy with Ataxia (SMNA): Linkage to chromosome 7q22-q32.
- Familial aggregation of dyslexia phenotypes. II: paired correlated measures.
- X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction.
- Missense mutations in the regulatory domain of PKC gamma: a new mechanism for dominant nonepisodic cerebellar ataxia.
- Segregation analysis of phenotypic components of learning disabilities. II. Phonological decoding.
- Familial aggregation patterns in mathematical ability.
- Use of alpha interferon for the treatment of relapse of chronic myelogenous leukemia in chronic phase after allogeneic bone marrow transplantation.
- Linkage analyses of four regions previously implicated in dyslexia: confirmation of a locus on chromosome 15q.
- Loss of heterozygosity involving the APC and MCC genetic loci occurs in the majority of human esophageal cancers.
- A genome scan in multigenerational families with dyslexia: Identification of a novel locus on chromosome 2q that contributes to phonological decoding efficiency.
- Presence of alanine-to-valine substitutions in myofibrillogenesis regulator 1 in paroxysmal nonkinesigenic dyskinesia: confirmation in 2 kindreds.
Fellowships
- UW - Dept. of Genetics
Wendy H Raskind's Practice location
Practice At University Of Washington Medical Ctr 1959 Ne Pacific St
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