The world's first wiki where authorship really matters (Nature Genetics, 2008). Due credit and reputation for authors. Imagine a global collaborative knowledge base for original thoughts. Search thousands of articles and collaborate with scientists around the globe.

wikigene or wiki gene protein drug chemical gene disease author authorship tracking collaborative publishing evolutionary knowledge reputation system wiki2.0 global collaboration genes proteins drugs chemicals diseases compound
Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)

Daniel H. Geschwind

Program in Neurogenetics

Department of Neurology

and the Center for Neurobehavioral Genetics

Neuropsychiatric Institute



Name/email consistency: high



  • Program in Neurogenetics, Department of Neurology, and the Center for Neurobehavioral Genetics, Neuropsychiatric Institute, USA. 2003 - 2009
  • Program in Neurogenetics, Department of Neurology and Semel Institute, David Geffen School of Medicine at University of California Los Angeles, 710 Westwood Plaza, USA. 2007 - 2009
  • Neurogenetics Program, UCLA School of Medicine, Los Angeles, CA 90095-1769, USA. 1999 - 2008
  • Neurogenetics Program, Department of Neurology and Center for Autism Research and Treatment, Geffen School of Medicine at UCLA, Los Angeles, USA. 2007
  • Department of Neurology, University of California, Los Angeles, School of Medicine, USA. 1997 - 2004
  • The Neuropsychiatric Institute, David Geffen School of Medicine, University of California, Los Angeles, USA. 2003
  • Department of Neurology and Program in Neurogenetics, UCLA School of Medicine, Los Angeles, California90095-1769, USA. 2000
  • Reed Neurological Research Center, Department of Neurology, UCLA School of Medicine, USA. 1996


  1. Neuroscience in the era of functional genomics and systems biology. Geschwind, D.H., Konopka, G. Nature (2009) [Pubmed]
  2. Autism: the ups and downs of neuroligin. Geschwind, D.H. Biol. Psychiatry (2009) [Pubmed]
  3. Autism: many genes, common pathways?. Geschwind, D.H. Cell (2008) [Pubmed]
  4. Autism spectrum disorders: developmental disconnection syndromes. Geschwind, D.H., Levitt, P. Curr. Opin. Neurobiol. (2007) [Pubmed]
  5. Autism: searching for coherence. Geschwind, D. Biol. Psychiatry (2007) [Pubmed]
  6. GENSAT: a genomic resource for neuroscience research. Geschwind, D. Lancet. Neurol (2004) [Pubmed]
  7. DNA microarrays: translation of the genome from laboratory to clinic. Geschwind, D.H. Lancet. Neurol (2003) [Pubmed]
  8. Tau phosphorylation, tangles, and neurodegeneration: the chicken or the egg?. Geschwind, D.H. Neuron (2003) [Pubmed]
  9. Heritability of lobar brain volumes in twins supports genetic models of cerebral laterality and handedness. Geschwind, D.H., Miller, B.L., DeCarli, C., Carmelli, D. Proc. Natl. Acad. Sci. U.S.A. (2002) [Pubmed]
  10. A genetic analysis of neural progenitor differentiation. Geschwind, D.H., Ou, J., Easterday, M.C., Dougherty, J.D., Jackson, R.L., Chen, Z., Antoine, H., Terskikh, A., Weissman, I.L., Nelson, S.F., Kornblum, H.I. Neuron (2001) [Pubmed]
  11. Sharing gene expression data: an array of options. Geschwind, D.H. Nat. Rev. Neurosci. (2001) [Pubmed]
  12. Molecular approaches to cerebral laterality: development and neurodegeneration. Geschwind, D.H., Miller, B.L. Am. J. Med. Genet. (2001) [Pubmed]
  13. Dementia and neurodevelopmental predisposition: cognitive dysfunction in presymptomatic subjects precedes dementia by decades in frontotemporal dementia. Geschwind, D.H., Robidoux, J., Alarcón, M., Miller, B.L., Wilhelmsen, K.C., Cummings, J.L., Nasreddine, Z.S. Ann. Neurol. (2001) [Pubmed]
  14. Neurobehavioral phenotype of Klinefelter syndrome. Geschwind, D.H., Boone, K.B., Miller, B.L., Swerdloff, R.S. Ment. Retard. Dev. Disabil. Res. Rev (2000) [Pubmed]
  15. Mice, microarrays, and the genetic diversity of the brain. Geschwind, D.H. Proc. Natl. Acad. Sci. U.S.A. (2000) [Pubmed]
  16. Identification of a locus on chromosome 14q for idiopathic basal ganglia calcification (Fahr disease). Geschwind, D.H., Loginov, M., Stern, J.M. Am. J. Hum. Genet. (1999) [Pubmed]
  17. Klinefelter's syndrome as a model of anomalous cerebral laterality: testing gene dosage in the X chromosome pseudoautosomal region using a DNA microarray. Geschwind, D.H., Gregg, J., Boone, K., Karrim, J., Pawlikowska-Haddal, A., Rao, E., Ellison, J., Ciccodicola, A., D'Urso, M., Woods, R., Rappold, G.A., Swerdloff, R., Nelson, S.F. Dev. Genet. (1998) [Pubmed]
  18. The prevalence and wide clinical spectrum of the spinocerebellar ataxia type 2 trinucleotide repeat in patients with autosomal dominant cerebellar ataxia. Geschwind, D.H., Perlman, S., Figueroa, C.P., Treiman, L.J., Pulst, S.M. Am. J. Hum. Genet. (1997) [Pubmed]
  19. Identification and characterization of novel developmentally regulated proteins in rat spinal cord. Geschwind, D.H., Kelly, G.M., Fryer, H., Feeser-Bhatt, H., Hockfield, S. Brain Res. Dev. Brain Res. (1996) [Pubmed]
WikiGenes - Universities