|Evaluation, diagnosis, and treatment of gastrointestinal disorders in individuals with ASDs: a consensus report|
T Buie, DB Campbell, GJ Fuchs, GT Furuta, J Levy, J VandeWater, ...
Pediatrics 125 (Supplement 1), S1-S18, 2010
|A genetic variant that disrupts MET transcription is associated with autism|
DB Campbell, JS Sutcliffe, PJ Ebert, R Militerni, C Bravaccio, S Trillo, ...
Proceedings of the National Academy of Sciences 103 (45), 16834-16839, 2006
|SFARI Gene 2.0: a community-driven knowledgebase for the autism spectrum disorders (ASDs)|
BS Abrahams, DE Arking, DB Campbell, HC Mefford, EM Morrow, ...
Molecular autism 4 (1), 1-3, 2013
|Genetic disruption of cortical interneuron development causes region-and GABA cell type-specific deficits, epilepsy, and behavioral dysfunction|
EM Powell, DB Campbell, GD Stanwood, C Davis, JL Noebels, P Levitt
Journal of Neuroscience 23 (2), 622-631, 2003
|The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders|
P Levitt, DB Campbell
The Journal of clinical investigation 119 (4), 747-754, 2009
|Disruption of cerebral cortex MET signaling in autism spectrum disorder|
DB Campbell, R D'Oronzio, K Garbett, PJ Ebert, K Mirnics, P Levitt, ...
Annals of Neurology: Official Journal of the American Neurological …, 2007
|Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder|
DB Campbell, C Li, JS Sutcliffe, AM Persico, P Levitt
Autism Research 1 (3), 159-168, 2008
|Association of oxytocin receptor (OXTR) gene variants with multiple phenotype domains of autism spectrum disorder|
DB Campbell, D Datta, ST Jones, EB Lee, JS Sutcliffe, EAD Hammock, ...
Journal of neurodevelopmental disorders 3 (2), 101-112, 2011
|Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions|
DB Campbell, TM Buie, H Winter, M Bauman, JS Sutcliffe, JM Perrin, ...
Pediatrics 123 (3), 1018-1024, 2009
|Brief Report: Autism Spectrum Disorder: Interaction of Air Pollution with the MET Receptor Tyrosine Kinase Gene|
HE Volk, T Kerin, F Lurmann, I Hertz-Picciotto, R McConnell, ...
Epidemiology, 44-47, 2014
|A noncoding RNA antisense to moesin at 5p14. 1 in autism|
T Kerin, A Ramanathan, K Rivas, N Grepo, GA Coetzee, DB Campbell
Science translational medicine 4 (128), 128ra40-128ra40, 2012
|L-type calcium channels contribute to the tottering mouse dystonic episodes|
DB Campbell, EJ Hess
Molecular pharmacology 55 (1), 23-31, 1999
|Tottering mouse motor dysfunction is abolished on the Purkinje cell degeneration (pcd) mutant background|
DB Campbell, JB North, EJ Hess
Experimental neurology 160 (1), 268-278, 1999
|Use of Drosophila mutants to distinguish among volatile general anesthetics|
DB Campbell, HA Nash
Proceedings of the National Academy of Sciences 91 (6), 2135-2139, 1994
|The autism-associated gene chromodomain helicase DNA-binding protein 8 (CHD8) regulates noncoding RNAs and autism-related genes|
B Wilkinson, N Grepo, BL Thompson, J Kim, K Wang, OV Evgrafov, W Lu, ...
Translational psychiatry 5 (5), e568-e568, 2015
|Dynamic gene and protein expression patterns of the autism‐associated met receptor tyrosine kinase in the developing mouse forebrain|
MC Judson, MY Bergman, DB Campbell, KL Eagleson, P Levitt
Journal of Comparative Neurology 513 (5), 511-531, 2009
|Cerebellar circuitry is activated during convulsive episodes in the tottering (tg/tg) mutant mouse|
DB Campbell, EJ Hess
Neuroscience 85 (3), 773-783, 1998
|Association of a MET genetic variant with autism-associated maternal autoantibodies to fetal brain proteins and cytokine expression|
L Heuer, D Braunschweig, P Ashwood, J Van de Water, DB Campbell
Translational psychiatry 1 (10), e48-e48, 2011
|Prenatal polycyclic aromatic hydrocarbon exposure leads to behavioral deficits and downregulation of receptor tyrosine kinase, MET|
L Sheng, X Ding, M Ferguson, M McCallister, R Rhoades, M Maguire, ...
Toxicological Sciences 118 (2), 625-634, 2010
|Association of MET with social and communication phenotypes in individuals with autism spectrum disorder|
DB Campbell, D Warren, JS Sutcliffe, EB Lee, P Levitt
American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 153 …, 2010