Wendy H. Raskind

Relative Burden of Large CNVs on a Range of Neurodevelopmental Phenotypes

Carlos S. Moreno, Carl Baker, Evan E. Eichler, 2011, PLoS genetics.

Erratum: Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (American Journal of Human Genetics (2016) 98(6) (1067–1076) (S0002929716301069) (10.1016/j.ajhg.2016.04.011))

Sara Chandros Hull, Robert C. Green, Sean D. Mooney, 2016 .

Language Phenotype for Reading and Writing Disability: A Family Approach

Virginia W. Berninger, Robert D. Abbott, R. Abbott, 2001 .

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

Ellen M. Wijsman, Virginia W. Berninger, Beate Peter, 2010, Journal of Neurodevelopmental Disorders.