A multigenerational family study of oral and hand motor sequencing ability provides evidence for a familial speech sound disorder subtype

Por Peter, Beate, Raskind, Wendy H.
Publicado em 2011

Motor sequencing deficit as an endophenotype of speech sound disorder: A genome-wide linkage analysis in a multigenerational family

Por Peter, Beate, Matsushita, Mark, Raskind, Wendy H.
Publicado em 2012

Global Processing Speed in Children With Low Reading Ability and in Children and Adults With Typical Reading Ability: Exploratory Factor Analytic Models

Por Peter, Beate, Matsushita, Mark, Raskind, Wendy H.
Publicado em 2010

Pharmacology and genetics of autism: implications for diagnosis and treatment

Por Brkanac, Zoran, Raskind, Wendy H, King, Bryan H
Publicado em 2008

Human Phenotypes Associated with GATA-1 Mutations

Por Ciovacco, Wendy A., Raskind, Wendy H., Kacena, Melissa A.
Publicado em 2008

Associations among measures of sequential processing in motor and linguistics tasks in adults with and without a family history of childhood apraxia of speech: A replication study

Por BUTTON, LE, PETER, BEATE, STOEL-GAMMON, CAROL, RASKIND, WENDY H.
Publicado em 2013

Mutations in the SIGMAR1 gene cause a distal hereditary motor neuropathy phenotype mimicking ALS: report of two novel variants

Por Ma, Maxwell T., Chen, Dong-Hui, Raskind, Wendy H., Bird, Thomas D.
Publicado no Neuromuscul Disord (2020)

Sensorineural Deafness, Distinctive Facial Features and Abnormal Cranial Bones: a New Variant of Waardenburg Syndrome?

Por Gad, Alona, Laurino, Mercy, Maravilla, Kenneth R., Matsushita, Mark, Raskind, Wendy H.
Publicado em 2008

Deficits in sequential processing manifest in motor and linguistic tasks in a multigenerational family with childhood apraxia of speech

Por PETER, BEATE, BUTTON, LE, STOEL-GAMMON, CAROL, CHAPMAN, KATHY, RASKIND, WENDY H.
Publicado em 2013

Genome Scan for Spelling Deficits: Effects of Verbal IQ on Models of Transmission and Trait Gene Localization

Por Rubenstein, Kevin, Matsushita, Mark, Berninger, Virginia W., Raskind, Wendy H., Wijsman, Ellen M.
Publicado em 2010

The Genetics of Reading Disabilities: From Phenotypes to Candidate Genes

Por Raskind, Wendy H., Peter, Beate, Richards, Todd, Eckert, Mark M., Berninger, Virginia W.
Publicado em 2013

Genome scan for cognitive trait loci of dyslexia: rapid naming and rapid switching of letters, numbers, and colors

Por Rubenstein, Kevin, Raskind, Wendy H., Berninger, Virginia W., Matsushita, Mark M., Wijsman, Ellen M.
Publicado em 2014

ADCY5–Related Dyskinesia: Improving Clinical Detection of an Evolving Disorder

Por Vijiaratnam, Nirosen, Bhatia, Kailash P., Lang, Anthony E., Raskind, Wendy H., Espay, Alberto J.
Publicado no Mov Disord Clin Pract (2019)

X-linked thrombocytopenia with thalassemia from a mutation in the amino finger of GATA-1 affecting DNA binding rather than FOG-1 interaction

Por Yu, Channing, Niakan, Kathy K., Matsushita, Mark, Stamatoyannopoulos, George, Orkin, Stuart H., Raskind, Wendy H.
Publicado em 2002

Pancreatic intraductal papillary mucinous neoplasm in a patient with Lynch syndrome

Por Flanagan, Meghan R, Jayaraj, Arjun, Xiong, Wei, Yeh, Matthew M, Raskind, Wendy H, Pillarisetty, Venu G
Publicado no World J Gastroenterol (2015)

ADCY5-Related Dyskinesia: Comments on Characteristic Manifestations and Variant-Associated Severity

Por Raskind, Wendy H., Friedman, Jennifer R., Roze, Emmanuel, Méneret, Aurélie, Chen, Dong-Hui, Bird, Thomas D.
Publicado no Mov Disord (2016)

Patterns of biomarkers for three phenotype profiles of persisting specific learning disabilities during middle childhood and early adolescence: A preliminary study

Por Abbott, Robert D., Raskind, Wendy H., Matsushita, Mark, Price, Nathan D., Richards, Todd, Berninger, Virginia W.
Publicado no Biomark Genes (2017)

ADCY5 Mutation Carriers Display Pleiotropic Paroxysmal Day and Nighttime Dyskinesias

Por Friedman, Jennifer R, Méneret, Aurélie, Chen, Dong-Hui, Trouillard, Oriane, Vidailhet, Marie, Raskind, Wendy H., Roze, Emmanuel
Publicado no Mov Disord (2015)

Familial Dyskinesia and Facial Myokymia (FDFM): Follow-up of a large family and linkage to chromosome 3p21-3q21

Por Raskind, Wendy H., Matsushita, Mark, Peter, Beate, Biberston, Jeffrey, Wolff, John, Lipe, Hillary, Burbank, Ruben, Bird, Thomas D.
Publicado em 2009

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample

Por Peter, Beate, Raskind, Wendy H., Matsushita, Mark, Lisowski, Mark, Vu, Tiffany, Berninger, Virginia W., Wijsman, Ellen M., Brkanac, Zoran
Publicado em 2010