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Daniel Brian Campbell, PhD
Assistant Professor of Psychiatry
Zilkha Neurogenetic Institute
ZNI 213 1501 San Pablo Street Health Sciences Campus Los Angeles
+1 323 442 2979


Campbell DB. Genetic investigation of autism-related social communication deficits. Am J Psychiatry. 2015 Mar 1; 172(3):212-3. View in: PubMed

Hecht PM, Ballesteros-Yanez I, Grepo N, Knowles JA, Campbell DB. Noncoding RNA in the transcriptional landscape of human neural progenitor cell differentiation. Front Neurosci. 2015; 9:392. View in: PubMed

Wilkinson B, Grepo N, Thompson BL, Kim J, Wang K, Evgrafov OV, Lu W, Knowles JA, Campbell DB. The autism-associated gene chromodomain helicase DNA-binding protein 8 (CHD8) regulates noncoding RNAs and autism-related genes. Transl Psychiatry. 2015; 5:e568. View in: PubMed

Volk HE, Kerin T, Lurmann F, Hertz-Picciotto I, McConnell R, Campbell DB. Autism Spectrum Disorder: Interaction of Air Pollution with the MET Receptor Tyrosine Kinase Gene. Epidemiology. 2014 Jan; 25(1):44-7. View in: PubMed

Wilkinson B, Campbell DB. Contribution of Long Noncoding RNAs to Autism Spectrum Disorder Risk. Int Rev Neurobiol. 2013; 113:35-59. View in: PubMed

Abrahams BS, Arking DE, Campbell DB, Mefford HC, Morrow EM, Weiss LA, Menashe I, Wadkins T, Banerjee-Basu S, Packer A. SFARI Gene 2. 0: a community-driven knowledgebase for the autism spectrum disorders (ASDs). Mol Autism. 2013; 4(1):36. View in: PubMed

Kerin T, Ramanathan A, Rivas K, Grepo N, Coetzee GA, Campbell DB. A noncoding RNA antisense to moesin at 5p14. 1 in autism. Sci Transl Med. 2012 Apr 4; 4(128):128ra40. View in: PubMed

Campbell DB, Datta D, Jones ST, Batey Lee E, Sutcliffe JS, Hammock EA, Levitt P. Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder. J Neurodev Disord. 2011 Jun; 3(2):101-12. View in: PubMed

Eagleson KL, Campbell DB, Thompson BL, Bergman MY, Levitt P. The autism risk genes MET and PLAUR differentially impact cortical development. Autism Res. 2011 Feb; 4(1):68-83. View in: PubMed

Sheng L, Ding X, Ferguson M, McCallister M, Rhoades R, Maguire M, Ramesh A, Aschner M, Campbell D, Levitt P, Hood DB. Prenatal polycyclic aromatic hydrocarbon exposure leads to behavioral deficits and downregulation of receptor tyrosine kinase, MET. Toxicol Sci. 2010 Dec; 118(2):625-34. View in: PubMed

Campbell DB, Warren D, Sutcliffe JS, Lee EB, Levitt P. Association of MET with social and communication phenotypes in individuals with autism spectrum disorder. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5; 153B(2):438-46. View in: PubMed

Buie T, Campbell DB, Fuchs GJ, Furuta GT, Levy J, Vandewater J, Whitaker AH, Atkins D, Bauman ML, Beaudet AL, Carr EG, Gershon MD, Hyman SL, Jirapinyo P, Jyonouchi H, Kooros K, Kushak R, Levitt P, Levy SE, Lewis JD, Murray KF, Natowicz MR, Sabra A, Wershil BK, Weston SC, Zeltzer L, Winter H. Evaluation, diagnosis, and treatment of gastrointestinal disorders in individuals with ASDs: a consensus report. Pediatrics. 2010 Jan; 125 Suppl 1:S1-18. View in: PubMed

Campbell DB. When linkage signal for autism MET candidate gene. Eur J Hum Genet. 2009 Jun; 17(6):699-700. View in: PubMed

Judson MC, Bergman MY, Campbell DB, Eagleson KL, Levitt P. Dynamic gene and protein expression patterns of the autism-associated met receptor tyrosine kinase in the developing mouse forebrain. J Comp Neurol. 2009 Apr 10; 513(5):511-31. View in: PubMed

Levitt P, Campbell DB. The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders. J Clin Invest. 2009 Apr; 119(4):747-54. View in: PubMed

Campbell DB, Buie TM, Winter H, Bauman M, Sutcliffe JS, Perrin JM, Levitt P. Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions. Pediatrics. 2009 Mar; 123(3):1018-24. View in: PubMed

Campbell DB, Li C, Sutcliffe JS, Persico AM, Levitt P. Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder. Autism Res. 2008 Jun; 1(3):159-68. View in: PubMed

Campbell DB, Levitt P. Future of individualized psychiatric treatment. Pharmacogenomics. 2008 May; 9(5):493-5. View in: PubMed

Campbell DB, Lange LA, Skelly T, Lieberman J, Levitt P, Sullivan PF. Association of RGS2 and RGS5 variants with schizophrenia symptom severity. Schizophr Res. 2008 Apr; 101(1-3):67-75. View in: PubMed

Campbell DB, Ebert PJ, Skelly T, Stroup TS, Lieberman J, Levitt P, Sullivan PF. Ethnic stratification of the association of RGS4 variants with antipsychotic treatment response in schizophrenia. Biol Psychiatry. 2008 Jan 1; 63(1):32-41. View in: PubMed

Campbell DB, D'Oronzio R, Garbett K, Ebert PJ, Mirnics K, Levitt P, Persico AM. Disruption of cerebral cortex MET signaling in autism spectrum disorder. Ann Neurol. 2007 Sep; 62(3):243-50. View in: PubMed

Campbell DB, Sutcliffe JS, Ebert PJ, Militerni R, Bravaccio C, Trillo S, Elia M, Schneider C, Melmed R, Sacco R, Persico AM, Levitt P. A genetic variant that disrupts MET transcription is associated with autism. Proc Natl Acad Sci U S A. 2006 Nov 7; 103(45):16834-9. View in: PubMed

Campbell DB, Levitt P. Regionally restricted expression of the transcription factor c-myc intron 1 binding protein during brain development. J Comp Neurol. 2003 Dec 22; 467(4):581-92. View in: PubMed

Powell EM, Campbell DB, Stanwood GD, Davis C, Noebels JL, Levitt P. Genetic disruption of cortical interneuron development causes region- and GABA cell type-specific deficits, epilepsy, and behavioral dysfunction. J Neurosci. 2003 Jan 15; 23(2):622-31. View in: PubMed

Fureman BE, Campbell DB, Hess EJ. Regulation of tyrosine hydroxylase expression in tottering mouse Purkinje cells. Neurotox Res. 2003; 5(7):521-8. View in: PubMed

Campbell DB, North JB, Hess EJ. Tottering mouse motor dysfunction is abolished on the Purkinje cell degeneration (pcd) mutant background. Exp Neurol. 1999 Nov; 160(1):268-78. View in: PubMed

Fureman BE, Campbell DB, Hess EJ. L-type calcium channel regulation of abnormal tyrosine hydroxylase expression in cerebella of tottering mice. Ann N Y Acad Sci. 1999 Apr 30; 868:217-9. View in: PubMed

Campbell DB, Hess EJ. L-type calcium channels contribute to the tottering mouse dystonic episodes. Mol Pharmacol. 1999 Jan; 55(1):23-31. View in: PubMed

Campbell DB, Hess EJ. Cerebellar circuitry is activated during convulsive episodes in the tottering (tg/tg) mutant mouse. Neuroscience. 1998 Aug; 85(3):773-83. View in: PubMed

Campbell DB, Hess EJ. Rapid genotyping of mutant mice using dried blood spots for polymerase chain reaction (PCR) analysis. Brain Res Brain Res Protoc. 1997 May; 1(2):117-23. View in: PubMed

Campbell DB, Hess EJ. Chromosomal localization of the neurological mouse mutations tottering (tg), Purkinje cell degeneration (pcd), and nervous (nr). Brain Res Mol Brain Res. 1996 Apr; 37(1-2):79-84. View in: PubMed

Leibovitch BA, Campbell DB, Krishnan KS, Nash HA. Mutations that affect ion channels change the sensitivity of Drosophila melanogaster to volatile anesthetics. J Neurogenet. 1995 Apr; 10(1):1-13. View in: PubMed

Campbell DB, Nash HA. Use of Drosophila mutants to distinguish among volatile general anesthetics. Proc Natl Acad Sci U S A. 1994 Mar 15; 91(6):2135-9. View in: PubMed

Nash HA, Campbell DB, Krishnan KS. New mutants of Drosophila that are resistant to the anesthetic effects of halothane. Ann N Y Acad Sci. 1991; 625:540-4. View in: PubMed

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