Faculty

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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

Publications

Transcriptional Gene Silencing of the Autism-Associated Long Noncoding RNA MSNP1AS in Human Neural Progenitor Cells. Dev Neurosci. 2016 Dec 29. View in: PubMed

Impact of the Autism-Associated Long Noncoding RNA MSNP1AS on Neuronal Architecture and Gene Expression in Human Neural Progenitor Cells. Genes (Basel). 2016 Sep 28; 7(10). View in: PubMed

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

Noncoding RNA in the transcriptional landscape of human neural progenitor cell differentiation. Front Neurosci. 2015; 9:392. View in: PubMed

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

Autism Spectrum Disorder: Interaction of Air Pollution with the MET Receptor Tyrosine Kinase Gene. Epidemiology. 2014 Jan; 25(1):44-7. View in: PubMed

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

SFARI Gene 2. 0: a community-driven knowledgebase for the autism spectrum disorders (ASDs). Mol Autism. 2013; 4(1):36. View in: PubMed

A noncoding RNA antisense to moesin at 5p14. 1 in autism. Sci Transl Med. 2012 Apr 4; 4(128):128ra40. View in: PubMed

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

The autism risk genes MET and PLAUR differentially impact cortical development. Autism Res. 2011 Feb; 4(1):68-83. View in: PubMed

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

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

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

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

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

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

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

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

Association of RGS2 and RGS5 variants with schizophrenia symptom severity. Schizophr Res. 2008 Apr; 101(1-3):67-75. View in: PubMed

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

Disruption of cerebral cortex MET signaling in autism spectrum disorder. Ann Neurol. 2007 Sep; 62(3):243-50. View in: PubMed

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

Bacterial artificial chromosome transgenic analysis of dynamic expression patterns of regulator of G-protein signaling 4 during development. I. Cerebral cortex. Neuroscience. 2006 Nov 3; 142(4):1145-61. View in: PubMed

Bacterial artificial chromosome transgenic analysis of dynamic expression patterns of regulator of G-protein signaling 4 during development. II. Subcortical regions. Neuroscience. 2006 Nov 3; 142(4):1163-81. View in: PubMed

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

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

Regulation of tyrosine hydroxylase expression in tottering mouse Purkinje cells. Neurotox Res. 2003; 5(7):521-8. View in: PubMed

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

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

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

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

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

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

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

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

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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