The Genetics of Reading Disabilities: From Phenotypes to Candidate Genes

by Raskind, Wendy H., Peter, Beate, Richards, Todd, Eckert, Mark M., Berninger, Virginia W.
Published 2013

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

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

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

by 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.
Published 2016

Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes

by Girirajan, Santhosh, Brkanac, Zoran, Coe, Bradley P., Baker, Carl, Vives, Laura, Vu, Tiffany H., Shafer, Neil, Bernier, Raphael, Ferrero, Giovanni B., Silengo, Margherita, Warren, Stephen T., Moreno, Carlos S., Fichera, Marco, Romano, Corrado, Raskind, Wendy H., Eichler, Evan E.
Published 2011

Evidence for Involvement of GNB1L in Autism

by Chen, Ying-Zhang, Matsushita, Mark, Girirajan, Santhosh, Lisowski, Mark, Sun, Elizabeth, Sul, Youngmee, Bernier, Raphael, Estes, Annette, Dawson, Geraldine, Minshew, Nancy, Shellenberg, Gerard D, Eichler, Evan E, Rieder, Mark J, Nickerson, Deborah A, Tsuang, Debby W, Tsuang, Ming T, Wijsman, Ellen M, Raskind, Wendy H, Brkanac, Zoran
Published 2012