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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 

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

Name/email consistency: high

 
 
 
 
 
 
 

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

  1. 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]
  2. A surprising METamorphosis: autism genetics finds a common functional variant. State, M.W. Proc. Natl. Acad. Sci. U.S.A. (2006) [Pubmed]
  3. 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]
  4. 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]
 
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