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

Genome Scan of a Nonword Repetition Phenotype in Families with Dyslexia: Evidence for Multiple Loci

Por Brkanac, Zoran, Chapman, Nicola H., Igo, Robert P., Matsushita, Mark M., Nielsen, Kathleen, Berninger, Virginia W., Wijsman, Ellen M., Raskind, Wendy H.
Publicado em 2008

Genetic Candidate Variants in Two Multigenerational Families with Childhood Apraxia of Speech

Por Peter, Beate, Wijsman, Ellen M., Nato, Alejandro Q., Matsushita, Mark M., Chapman, Kathy L., Stanaway, Ian B., Wolff, John, Oda, Kaori, Gabo, Virginia B., Raskind, Wendy H.
Publicado no PLoS One (2016)

Autosomal Dominant Familial Dyskinesia and Facial Myokymia: Single Exome Sequencing Identifies a Mutation in Adenylate Cyclase 5

Por Chen, Ying-Zhang, Matsushita, Mark M., Robertson, Peggy, Rieder, Mark, Girirajan, Santhosh, Antonacci, Francesca, Lipe, Hillary, Eichler, Evan E., Nickerson, Deborah A., Bird, Thomas D., Raskind, Wendy H.
Publicado em 2012