Matthew W. State
Program on Neurogenetics
Departments of Child Psychiatry and Genetics
Yale University School of Medicine
230 South Frontage Road
USA
Name/email consistency: high
- Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome. Fernandez, T., Morgan, T., Davis, N., Klin, A., Morris, A., Farhi, A., Lifton, R.P., State, M.W. Am. J. Hum. Genet. (2008)
- A surprising METamorphosis: autism genetics finds a common functional variant. State, M.W. Proc. Natl. Acad. Sci. U.S.A. (2006)
- Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype. State, M.W., Greally, J.M., Cuker, A., Bowers, P.N., Henegariu, O., Morgan, T.M., Gunel, M., DiLuna, M., King, R.A., Nelson, C., Donovan, A., Anderson, G.M., Leckman, J.F., Hawkins, T., Pauls, D.L., Lifton, R.P., Ward, D.C. Proc. Natl. Acad. Sci. U.S.A. (2003)
- Obsessive-compulsive symptoms in Prader-Willi and "Prader-Willi-Like" patients. State, M.W., Dykens, E.M., Rosner, B., Martin, A., King, B.H. J. Am. Acad. Child. Adolesc. Psychiatry (1999)