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

John B. Vincent

Centre for Addiction and Mental Health





Name/email consistency: high



  • Centre for Addiction and Mental Health, Toronto, Ontario, Canada. 2004 - 2009
  • Molecular Psychiatry Laboratory, Department of Psychiatry and Behavioural Sciences, Windeyer Institute of Medical Science, University College London, London. 2005
  • Program in Genetics and Genomic Biology, The Hospital for Sick Children, Toronto, ON M5G 1X8, Canada. 2004


  1. Characterization of a de novo translocation t(5;18)(q33.1;q12.1) in an autistic boy identifies a breakpoint close to SH3TC2, ADRB2, and HTR4 on 5q, and within the desmocollin gene cluster on 18q. Vincent, J.B., Noor, A., Windpassinger, C., Gianakopoulos, P.J., Schwarzbraun, T., Alfred, S.E., Stachowiak, B., Scherer, S.W., Roberts, W., Wagner, K., Kroisel, P.M., Petek, E. Am. J. Med. Genet. B Neuropsychiatr. Genet. (2009) [Pubmed]
  2. A translocation t(6;7)(p11-p12;q22) associated with autism and mental retardation: localization and identification of candidate genes at the breakpoints. Vincent, J.B., Choufani, S., Horike, S., Stachowiak, B., Li, M., Dill, F.J., Marshall, C., Hrynchak, M., Pewsey, E., Ukadike, K.C., Friedman, J.M., Srivastava, A.K., Scherer, S.W. Psychiatr. Genet. (2008) [Pubmed]
  3. Genetic linkage analysis of the X chromosome in autism, with emphasis on the fragile X region. Vincent, J.B., Melmer, G., Bolton, P.F., Hodgkinson, S., Holmes, D., Curtis, D., Gurling, H.M. Psychiatr. Genet. (2005) [Pubmed]
  4. Association and transmission analysis of the FMR1 IVS10 + 14C-T variant in autism. Vincent, J.B., Thevarkunnel, S., Kolozsvari, D., Paterson, A.D., Roberts, W., Scherer, S.W. Am. J. Med. Genet. B Neuropsychiatr. Genet. (2004) [Pubmed]
  5. Mutation screening of X-chromosomal neuroligin genes: no mutations in 196 autism probands. Vincent, J.B., Kolozsvari, D., Roberts, W.S., Bolton, P.F., Gurling, H.M., Scherer, S.W. Am. J. Med. Genet. B Neuropsychiatr. Genet. (2004) [Pubmed]
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