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

Joseph D. Buxbaum

Seaver Autism Center for Research and Treatment and Department of Psychiatry

Mount Sinai School of Medicine

New York



Name/email consistency: high



  • Seaver Autism Center for Research and Treatment and Department of Psychiatry, Mount Sinai School of Medicine, New York, USA. 2004 - 2010
  • Laboratory of Molecular Neuropsychiatry, Mount Sinai School of Medicine, One Gustave L Levy Place, New York, USA. 2004 - 2010


  1. Genetics in psychiatry: common variant association studies. Buxbaum, J.D., Baron-Cohen, S., Devlin, B. Mol. Autism (2010) [Pubmed]
  2. A large-scale survey of the novel 15q24 microdeletion syndrome in autism spectrum disorders identifies an atypical deletion that narrows the critical region. McInnes, L.A., Nakamine, A., Pilorge, M., Brandt, T., Jiménez González, P., Fallas, M., Manghi, E.R., Edelmann, L., Glessner, J., Hakonarson, H., Betancur, C., Buxbaum, J.D. Mol. Autism (2010) [Pubmed]
  3. Haploinsufficiency of the autism-associated Shank3 gene leads to deficits in synaptic function, social interaction, and social communication. Bozdagi, O., Sakurai, T., Papapetrou, D., Wang, X., Dickstein, D.L., Takahashi, N., Kajiwara, Y., Yang, M., Katz, A.M., Scattoni, M.L., Harris, M.J., Saxena, R., Silverman, J.L., Crawley, J.N., Zhou, Q., Hof, P.R., Buxbaum, J.D. Mol. Autism (2010) [Pubmed]
  4. Extensive proteomic screening identifies the obesity-related NYGGF4 protein as a novel LRP1-interactor, showing reduced expression in early Alzheimer's disease. Kajiwara, Y., Franciosi, S., Takahashi, N., Krug, L., Schmeidler, J., Taddei, K., Haroutunian, V., Fried, U., Ehrlich, M., Martins, R.N., Gandy, S., Buxbaum, J.D. Mol. Neurodegener (2010) [Pubmed]
  5. Multiple rare variants in the etiology of autism spectrum disorders. Buxbaum, J.D. Dialogues. Clinical. Neuroscience (2009) [Pubmed]
  6. Molecular dissection of NRG1-ERBB4 signaling implicates PTPRZ1 as a potential schizophrenia susceptibility gene. Buxbaum, J.D., Georgieva, L., Young, J.J., Plescia, C., Kajiwara, Y., Jiang, Y., Moskvina, V., Norton, N., Peirce, T., Williams, H., Craddock, N.J., Carroll, L., Corfas, G., Davis, K.L., Owen, M.J., Harroch, S., Sakurai, T., O'Donovan, M.C. Mol. Psychiatry (2008) [Pubmed]
  7. Mutation analysis of the NSD1 gene in patients with autism spectrum disorders and macrocephaly. Buxbaum, J.D., Cai, G., Nygren, G., Chaste, P., Delorme, R., Goldsmith, J., Råstam, M., Silverman, J.M., Hollander, E., Gillberg, C., Leboyer, M., Betancur, C. BMC Med. Genet. (2007) [Pubmed]
  8. Linkage analysis for autism in a subset families with obsessive-compulsive behaviors: evidence for an autism susceptibility gene on chromosome 1 and further support for susceptibility genes on chromosome 6 and 19. Buxbaum, J.D., Silverman, J., Keddache, M., Smith, C.J., Hollander, E., Ramoz, N., Reichert, J.G. Mol. Psychiatry (2004) [Pubmed]
  9. A role for calsenilin and related proteins in multiple aspects of neuronal function. Buxbaum, J.D. Biochem. Biophys. Res. Commun. (2004) [Pubmed]
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