COMT Val108/158Met Modifies Mismatch Negativity and Cognitive Function in 22q11 Deletion Syndrome

Effect of COMT Val ^108/158 Met genotype on frontal lobe function and risk for schizophrenia

Michael Egan, Terry E. Goldberg, Bhaskar Kolachana et al. · Proceedings of the National Academy of Sciences · 2001 · 2.4K citations · Full text

Life Sciences, Genetics, Psychiatry +16

Functional Analysis of Genetic Variation in Catechol-O-Methyltransferase (COMT): Effects on mRNA, Protein, and Enzyme Activity in Postmortem Human Brain

Jingshan Chen, Barbara K. Lipska, Nader D. Halim et al. · The American Journal of Human Genetics · 2004 · 1.7K citations · Full text

Life Sciences, Genetics, Neuroscience +10

Spectrum of clinical features associated with interstitial chromosome 22q11 deletions: a European collaborative study.

A K Ryan, Judith A. Goodship, David I. Wilson et al. · Journal of Medical Genetics · 1997 · 1.2K citations · Full text

Life Sciences, Genetics, Molecular Genetics +16

Genome Scan Meta-Analysis of Schizophrenia and Bipolar Disorder, Part II: Schizophrenia

Cathryn M. Lewis, Douglas F. Levinson, Lesley H. Wise et al. · The American Journal of Human Genetics · 2003 · 1.1K citations · Full text

Life Sciences, Genetics, Psychiatry +16

Tbx1 haploinsufficiency in the DiGeorge syndrome region causes aortic arch defects in mice

Elizabeth A. Lindsay, Francesca Vitelli, Hong Hua Su et al. · Nature · 2001 · 1K citations

Medicine, Genetics, Molecular Genetics +15