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MATTHEW STATE, MD
MD
Child & Adolescent Psychiatry Physician
NPI: 1457370066Individual
Specialties, Licenses & Credentials
Child & Adolescent Psychiatry PhysicianPrimary
Psychiatry & Neurology — Child & Adolescent Psychiatry
Code: 2084P0804X
037357(CT)
Research & Publications (20)
Rare independent mutations in renal salt handling genes contribute to blood pressure variation.
PMID 18391953·Nat Genet·2008
8-other
A surprising METamorphosis: autism genetics finds a common functional variant.
PMID 17075042·Proc Natl Acad Sci U S A·2006
8-other
Epigenetic abnormalities associated with a chromosome 18(q21-q22) inversion and a Gilles de la Tourette syndrome phenotype.
PMID 12682296·Proc Natl Acad Sci U S A·2003
5-case
Tourette's syndrome and related disorders.
PMID 11351801·Child Adolesc Psychiatr Clin N Am·2001
6-review
The genetics of childhood psychiatric disorders: a decade of progress.
PMID 10939224·J Am Acad Child Adolesc Psychiatry·2000
6-review
Genetics of childhood disorders: XV. Prader-Willi syndrome: genes, brain, and behavior.
PMID 10846317·J Am Acad Child Adolesc Psychiatry·2000
6-review
Autism and autism spectrum disorders: diagnostic issues for the coming decade.
PMID 19220594·J Child Psychol Psychiatry·2009
6-review
Functional and evolutionary insights into human brain development through global transcriptome analysis.
PMID 19477152·Neuron·2009
8-other
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
PMID 19404256·Nature·2009
8-other
Developmentally regulated and evolutionarily conserved expression of SLITRK1 in brain circuits implicated in Tourette syndrome.
PMID 19105198·J Comp Neurol·2009
7-preclinical
Haplotype evolution of SLITRK1, a candidate gene for Gilles de la Tourette syndrome.
PMID 18004766·Am J Med Genet B Neuropsychiatr Genet·2008
8-other
Susceptibility loci for intracranial aneurysm in European and Japanese populations.
PMID 18997786·Nat Genet·2008
8-other
Molecular characterization of a patient with 3p deletion syndrome and a review of the literature.
PMID 18837054·Am J Med Genet A·2008
5-case
Disruption of Contactin 4 (CNTN4) results in developmental delay and other features of 3p deletion syndrome.
PMID 18551756·Am J Hum Genet·2008
5-case
Novel NTRK1 mutations cause hereditary sensory and autonomic neuropathy type IV: demonstration of a founder mutation in the Turkish population.
PMID 18322713·Neurogenetics·2008
5-case
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders.
PMID 18179895·Am J Hum Genet·2008
7-preclinical
A novel syndrome of cerebral cavernous malformation and Greig cephalopolysyndactyly. Laboratory investigation.
PMID 18154020·J Neurosurg·2007
5-case
Rapid identification of disease-causing mutations using copy number analysis within linkage intervals.
PMID 17676595·Hum Mutat·2007
8-other
Mapping autism risk loci using genetic linkage and chromosomal rearrangements.
PMID 17322880·Nat Genet·2007
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 800 HOWARD AVE, YALE PHYSICIANS BLDG
NEW HAVEN, CT 06519 - Phone
- (203) 785-2140
Quick Facts
- NPI
- 1457370066
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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