DanielBruceCampbellMD

PubMed

• 13 citations
  Smek1/2 Is a Nuclear Chaperone and Cofactor for Cleaved Wnt Receptor Ryk, Regulating Cortical Neurogenesis
  Wen-Hsuan Chang, Si Ho Choi, Byoung-San Moon, Mingyang Cai, Jungmook Lyu, Jinlun Bai, Fan Gao, Ibrahim Hajjali, Zhongfang Zhao, Daniel B. Campbell, Leslie P. Weiner, W...> ;Proceedings of the National Academy of Sciences of the United States of America. 2017 Dec 12
• Autism Spectrum Disorder: Interaction of Air Pollution with the MET Receptor Tyrosine Kinase Gene.
  Volk, H. E.,Kerin, T.,Lurmann, F.,Hertz-Picciotto, I.,McConnell, R.,Campbell, D. B.> ;Epidemiology. 2013 Nov 19
• 38 citations
  The autism risk genes MET and PLAUR differentially impact cortical development
  Kathie L. Eagleson, Daniel B. Campbell, Mica Y. Bergman, Pat Levitt> ;Autism Research. 2011 Feb 1
• 120 citations
  Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder
  Daniel B. Campbell, Dibyadeep Datta, Shaine T. Jones, Evon Batey Lee, James S. Sutcliffe, Elizabeth A. D. Hammock, Pat Levitt> ;Journal of Neurodevelopmental Disorders. 2011 Jan 6
• The autism risk genes MET and PLAUR differentially impact cortical development.
  Eagleson, K.L., Campbell, D.B., Thompson, B.L., Bergman, M.Y., Levitt, P.> ;Autism Res. 2010-12-03
• 37 citations
  Association of MET with social and communication phenotypes in individuals with autism spectrum disorder
  Daniel B. Campbell, Dana E. Warren, James S. Sutcliffe, Evon Batey Lee, Pat Levitt> ;American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics. 2010 Mar 1
• 448 citations
  Evaluation, Diagnosis, and Treatment of Gastrointestinal Disorders in Individuals With ASDs: A Consensus Report
  Timothy Buie, Daniel B. Campbell, George J. Fuchs, Glenn T. Furuta, Joseph Levy, Judy VandeWater, Agnes H. Whitaker, Dan Atkins, Margaret L. Bauman, Arthur L. Beaudet,...> ;Pediatrics. 2010 Jan 1
• 66 citations
  Dynamic gene and protein expression patterns of the autism-associated met receptor tyrosine kinase in the developing mouse forebrain.
  Matthew C. Judson, Mica Y. Bergman, Daniel B. Campbell, Kathie L. Eagleson, Pat Levitt> ;The Journal of Comparative Neurology. 2009 Apr 10
• 172 citations
  The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders
  Pat Levitt, Daniel B. Campbell> ;The Journal of Clinical Investigation. 2009 Apr 1
• 97 citations
  Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions.
  Daniel B. Campbell, Timothy Buie, Harland S. Winter, Margaret L. Bauman, James S. Sutcliffe, James M. Perrin, Pat Levitt> ;Pediatrics. 2009 Mar 1
• 111 citations
  Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder
  Daniel B. Campbell, Chun Li, James S. Sutcliffe, Antonio M. Persico, Pat Levitt> ;Autism Research. 2008 Jun 1
• 47 citations
  Ethnic Stratification of the Association of RGS4 Variants with Antipsychotic Treatment Response in Schizophrenia
  Daniel B. Campbell, Philip J. Ebert, Tara Skelly, T. Scott Stroup, Jeffrey A. Lieberman, Pat Levitt, Patrick F. Sullivan> ;Biological Psychiatry. 2008 Jan 1
• 143 citations
  Disruption of cerebral cortex MET signaling in autism spectrum disorder
  Daniel B. Campbell, Rosanna D'Oronzio, Krassi Garbett, Philip J. Ebert, Karoly Mirnics, Pat Levitt, Antonio M. Persico> ;Annals of Neurology. 2007 Sep 1
• 301 citations
  A genetic variant that disrupts MET transcription is associated with autism
  Daniel B. Campbell, James S. Sutcliffe, Philip J. Ebert, Roberto Militerni, Carmela Bravaccio, Simona Trillo, Maurizio Elia, Cindy Schneider, Raun Melmed, Roberto Sacc...> ;Proceedings of the National Academy of Sciences of the United States of America. 2006 Nov 7
• 18 citations
  Regionally restricted expression of the transcription factor c-myc intron 1 binding protein during brain development.
  Daniel B. Campbell, Pat Levitt> ;The Journal of Comparative Neurology. 2003 Dec 22
• 262 citations
  Genetic disruption of cortical interneuron development causes region- and GABA cell type-specific deficits, epilepsy, and behavioral dysfunction.
  Elizabeth M. Powell, Daniel B. Campbell, Gregg D. Stanwood, Caleb F. Davis, Pat Levitt> ;The Journal of Neuroscience. 2003 Jan 15
• 9 citations
  Regulation of tyrosine hydroxylase expression in tottering mouse Purkinje cells.
  Brandy E. Fureman, Daniel B. Campbell, Ellen J. Hess> ;Neurotoxicity Research. 2003 Jan 1
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