COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome (original) (raw)

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Acknowledgements

We thank L. Xiaoyan and J.F. Hallmayer for DNA extraction, and J. Keller for cognitive assessments. This work was supported by US National Institutes of Health grants MH50047, HD31715 and MH19908 (A.L.R.) and by the Swiss National Science Foundation, the European Union Federal Office of Education and the 'Child Care' Foundation (S.E.A.).

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Authors and Affiliations

  1. Center for Interdisciplinary Brain Sciences Research, Stanford University School of Medicine, 401 Quarry Road, Stanford, 94305–5795, California, USA
    Doron Gothelf, Tracy Thompson, Lauren Penniman, Carl Feinstein, Shuting Jin, Booil Jo & Allan L Reiss
  2. Sackler Faculty of Medicine, Tel Aviv University, Ramat Aviv, Israel
    Doron Gothelf
  3. Department of Psychiatry, University of Geneva School of Medicine, 41 Ch. des Crêts-de-Champel, Geneva, CH-1206, Switzerland
    Stephan Eliez
  4. Medical Genetics Service, University Hospitals, 1 Rue Michel Servet, Geneva, 1211, Switzerland
    Christine Hinard & Michael A Morris
  5. Department of Psychiatry and Behavioral Sciences, University of Washington, Box 359911, Seattle, 98104, Washington, USA
    Hower Kwon
  6. Department of Genetic Medicine and Development, University Medical School, Centre Medicale Universitaire, 1 Rue Michel Servet, Geneva, 1211, Switzerland
    Stylianos E Antonarakis

Authors

  1. Doron Gothelf
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  2. Stephan Eliez
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  3. Tracy Thompson
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  4. Christine Hinard
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  5. Lauren Penniman
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  6. Carl Feinstein
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  7. Hower Kwon
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  8. Shuting Jin
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  9. Booil Jo
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  10. Stylianos E Antonarakis
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  11. Michael A Morris
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  12. Allan L Reiss
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Correspondence toAllan L Reiss.

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The authors declare no competing financial interests.

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Gothelf, D., Eliez, S., Thompson, T. et al. COMT genotype predicts longitudinal cognitive decline and psychosis in 22q11.2 deletion syndrome.Nat Neurosci 8, 1500–1502 (2005). https://doi.org/10.1038/nn1572

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