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THOMAS WASSINK, MD

MD

Psychiatry Physician

NPI: 1760470637IndividualAccepts Medicare

Specialties, Licenses & Credentials

Psychiatry PhysicianPrimary

Psychiatry & Neurology — Psychiatry

Code: 2084P0800X

31837(IA)

CMS Specialties

PrimaryPSYCHIATRY

Education

UNIVERSITY OF ILLINOIS COLLEGE OF MED (CHI/PEOR/ROCK/CHM-URB)

Class of 1993

Research & Publications (20)

Posterior probability of linkage analysis of autism dataset identifies linkage to chromosome 16.
PMID 18349700·Psychiatr Genet·2008
8-other
Systematic screening for subtelomeric anomalies in a clinical sample of autism.
PMID 17004120·J Autism Dev Disord·2007
5-case
Evaluation of the chromosome 2q37.3 gene CENTG2 as an autism susceptibility gene.
PMID 15892143·Am J Med Genet B Neuropsychiatr Genet·2005
8-other
A case of autism and uniparental disomy of chromosome 1.
PMID 15887000·Hum Genet·2005
5-case
The search for autism disease genes.
PMID 15666342·Ment Retard Dev Disabil Res Rev·2004
6-review
Examination of AVPR1a as an autism susceptibility gene.
PMID 15098001·Mol Psychiatry·2004
4-observational
NOTCH4 and the frontal lobe in schizophrenia.
PMID 12627456·Am J Med Genet B Neuropsychiatr Genet·2003
8-other
Evaluation of FOXP2 as an autism susceptibility gene.
PMID 12116195·Am J Med Genet·2002
8-other
Chromosomal abnormalities in a clinic sample of individuals with autistic disorder.
PMID 11525418·Psychiatr Genet·2001
6-review
Evidence supporting WNT2 as an autism susceptibility gene.
PMID 11449391·Am J Med Genet·2001
8-other
Tumor necrosis factor receptor-II: heritability and effect on brain morphology in schizophrenia.
PMID 11126399·Mol Psychiatry·2000
8-other
The molecular genetics of autism.
PMID 11122951·Curr Psychiatry Rep·2000
6-review
Cerebral cortical gray matter overgrowth and functional variation of the serotonin transporter gene in autism.
PMID 17548752·Arch Gen Psychiatry·2007
4-observational
Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes.
PMID 19557195·PLoS Genet·2009
8-other
Autism genome-wide copy number variation reveals ubiquitin and neuronal genes.
PMID 19404257·Nature·2009
8-other
Common genetic variants on 5p14.1 associate with autism spectrum disorders.
PMID 19404256·Nature·2009
8-other
MTHFR 677C --> T genotype disrupts prefrontal function in schizophrenia through an interaction with COMT 158Val --> Met.
PMID 18988738·Proc Natl Acad Sci U S A·2008
4-observational
Basic helix-loop-helix transcription factor NEUROG1 and schizophrenia: effects on illness susceptibility, MRI brain morphometry and cognitive abilities.
PMID 18799289·Schizophr Res·2008
8-other
Cortical enlargement in autism is associated with a functional VNTR in the monoamine oxidase A gene.
PMID 18361446·Am J Med Genet B Neuropsychiatr Genet·2008
8-other
Pax6 3' deletion results in aniridia, autism and mental retardation.
PMID 18322702·Hum Genet·2008
5-case

Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.

Contact & Hours

Address
200 HAWKINS DR, 1-191 MEB
IOWA CITY, IA 52242

Location

Practice Location

200 HAWKINS DR, IOWA CITY, IA
(319) 335-7743

Quick Facts

NPI
1760470637
Entity Type
Individual
Gender
Male
Medicare
Accepted
Specialties
1
Locations
1
Years in Practice
33
Publications
20

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