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Matthew W. State

Program on Neurogenetics

Departments of Child Psychiatry and Genetics

Yale University School of Medicine

230 South Frontage Road

USA

[email]@yale.edu

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Affiliations

Program on Neurogenetics, Departments of Child Psychiatry and Genetics, Yale University School of Medicine, 230 South Frontage Road, USA. 2006
Child Study Center, Yale University School of Medicine, New Haven, CT 06520, USA. 1999 - 2003

References

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) [Pubmed]
A surprising METamorphosis: autism genetics finds a common functional variant. State, M.W. Proc. Natl. Acad. Sci. U.S.A. (2006) [Pubmed]
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) [Pubmed]
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) [Pubmed]