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PAUL LEVITT, M.D.
M.D.
Orthopaedic Surgery Physician
NPI: 1700163243Individual
Specialties, Licenses & Credentials
Orthopaedic Surgery PhysicianPrimary
Orthopaedic Surgery
Code: 207X00000X
GFE18550(CA)
Research & Publications (20)
Association of MET with social and communication phenotypes in individuals with autism spectrum disorder.
PMID 19548256·Am J Med Genet B Neuropsychiatr Genet·2010
8-other
The genetic and neurobiologic compass points toward common signaling dysfunctions in autism spectrum disorders.
PMID 19339766·J Clin Invest·2009
6-review
Genome maintenance defects in cultured cells and mice following partial inactivation of the essential cell cycle checkpoint gene Hus1.
PMID 17220276·Mol Cell Biol·2007
7-preclinical
Conditional inactivation of the mouse Hus1 cell cycle checkpoint gene.
PMID 15919177·Genomics·2005
7-preclinical
Distinct genetic risk based on association of MET in families with co-occurring autism and gastrointestinal conditions.
PMID 19255034·Pediatrics·2009
8-other
The organization of the transcriptional network in specific neuronal classes.
PMID 19638972·Mol Syst Biol·2009
7-preclinical
Dynamic gene and protein expression patterns of the autism-associated met receptor tyrosine kinase in the developing mouse forebrain.
PMID 19226509·J Comp Neurol·2009
7-preclinical
Prenatal exposure to drugs: effects on brain development and implications for policy and education.
PMID 19277053·Nat Rev Neurosci·2009
6-review
Three-dimensional high-resolution diffusion tensor imaging and tractography of the developing rabbit brain.
PMID 17962716·Dev Neurosci·2008
7-preclinical
It is time to take a stand for medical research and against terrorism targeting medical scientists.
PMID 18371494·Biol Psychiatry·2008
7-preclinical
Genetic deletion of Lsamp causes exaggerated behavioral activation in novel environments.
PMID 18199495·Behav Brain Res·2008
7-preclinical
Genetic evidence implicating multiple genes in the MET receptor tyrosine kinase pathway in autism spectrum disorder.
PMID 19360663·Autism Res·2008
8-other
Ethnic stratification of the association of RGS4 variants with antipsychotic treatment response in schizophrenia.
PMID 17588543·Biol Psychiatry·2008
3-trial
Linkage disequilibrium patterns and functional analysis of RGS4 polymorphisms in relation to schizophrenia.
PMID 17515439·Schizophr Bull·2008
8-other
Adaptive changes in gene expression patterns in the somatosensory cortex after deletion of ephrinA5.
PMID 18619851·Mol Cell Neurosci·2008
7-preclinical
Gene x environment effects: stress and memory dysfunctions caused by stress and gonadal factor irregularities during puberty in control and TGF-alpha hypomorphic mice.
PMID 17473839·Neuropsychopharmacology·2008
7-preclinical
Association of RGS2 and RGS5 variants with schizophrenia symptom severity.
PMID 18262772·Schizophr Res·2008
8-other
Disruption of Foxg1 expression by knock-in of cre recombinase: effects on the development of the mouse telencephalon.
PMID 17640820·Neuroscience·2007
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1020 WOODSTOCK LN
VENTURA, CA 93001 - Phone
- (805) 643-1543
Quick Facts
- NPI
- 1700163243
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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