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SHANTI THIRUMALAI, MD
MD
Neurology with Special Qualifications in Child Neurology Physician
NPI: 1528155132Individual
Specialties, Licenses & Credentials
Neurology with Special Qualifications in Child Neurology PhysicianPrimary
Psychiatry & Neurology — Neurology with Special Qualifications in Child Neurology
Code: 2084N0402X
24452(NV)MD-37167(IA)MD70047140(WA)
Pediatric Neurodevelopmental Disabilities Physician
Pediatrics — Neurodevelopmental Disabilities
Code: 2080P0008X
ME99791(FL)
Research & Publications (17)
A threonine to isoleucine missense mutation in the pericentriolar material 1 gene is strongly associated with schizophrenia.
PMID 19048012·Mol Psychiatry·2010
8-other
Evidence for the association of the DAOA (G72) gene with schizophrenia and bipolar disorder but not for the association of the DAO gene with schizophrenia.
PMID 19586533·Behav Brain Funct·2009
8-other
DISC1 association, heterogeneity and interplay in schizophrenia and bipolar disorder.
PMID 18317464·Mol Psychiatry·2009
8-other
Confirmation of the genetic association between the U2AF homology motif (UHM) kinase 1 (UHMK1) gene and schizophrenia on chromosome 1q23.3.
PMID 18414510·Eur J Hum Genet·2008
8-other
Failure to confirm allelic and haplotypic association between markers at the chromosome 6p22.3 dystrobrevin-binding protein 1 (DTNBP1) locus and schizophrenia.
PMID 17888175·Behav Brain Funct·2007
8-other
A genetic association study of chromosome 11q22-24 in two different samples implicates the FXYD6 gene, encoding phosphohippolin, in susceptibility to schizophrenia.
PMID 17357072·Am J Hum Genet·2007
4-observational
Fine mapping by genetic association implicates the chromosome 1q23.3 gene UHMK1, encoding a serine/threonine protein kinase, as a novel schizophrenia susceptibility gene.
PMID 16978587·Biol Psychiatry·2007
4-observational
Failure to confirm genetic association between schizophrenia and markers on chromosome 1q23.3 in the region of the gene encoding the regulator of G-protein signaling 4 protein (RGS4).
PMID 16508931·Am J Med Genet B Neuropsychiatr Genet·2006
4-observational
Genetic association and brain morphology studies and the chromosome 8p22 pericentriolar material 1 (PCM1) gene in susceptibility to schizophrenia.
PMID 16894060·Arch Gen Psychiatry·2006
4-observational
Failure to confirm allelic association between markers at the CAPON gene locus and schizophrenia in a British sample.
PMID 16202394·Biol Psychiatry·2006
2-rct
Citalopram associated with acute angle-closure glaucoma: case report.
PMID 16202173·BMC Ophthalmol·2005
5-case
The Epsin 4 gene on chromosome 5q, which encodes the clathrin-associated protein enthoprotin, is involved in the genetic susceptibility to schizophrenia.
PMID 15793701·Am J Hum Genet·2005
8-other
NS-398, a selective cyclooxygenase-2 blocker, acutely inhibits receptor-mediated contractions of rat aorta: role of endothelium.
PMID 12498919·Eur J Pharmacol·2003
7-preclinical
A double-blind, randomised comparative trial of amisulpride versus olanzapine in the treatment of schizophrenia: short-term results at two months.
PMID 12442883·Curr Med Res Opin·2002
3-trial
Rapid eye movement sleep behavior disorder in children with autism.
PMID 12026231·J Child Neurol·2002
5-case
Video-EEG in the diagnosis of paroxysmal events in children with mental retardation and in children with normal intelligence.
PMID 11730145·Dev Med Child Neurol·2001
8-other
Successful treatment for stroke in a child using recombinant tissue plasminogen activator.
PMID 10961797·J Child Neurol·2000
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via practice · 3 locations total
- Address
- 330 LAUREL ST STE 1200
DES MOINES, IA 50314 - Phone
- (515) 643-6290
Quick Facts
- NPI
- 1528155132
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 4
- Locations
- 3
- Publications
- 17
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