Back to Search
CHARLES GLATT, PHD
PHD
Clinical Psychologist
NPI: 1922278290Individual
Specialties, Licenses & Credentials
Clinical PsychologistPrimary
Psychologist — Clinical
Code: 103TC0700X
6301001601(MI)
Research & Publications (15)
Serotonin transporter polymorphisms, microstructural white matter abnormalities and remission of geriatric depression.
PMID 19375170·J Affect Disord·2009
8-other
Brain-derived neurotrophic factor as a model system for examining gene by environment interactions across development.
PMID 19358879·Neuroscience·2009
6-review
Glutathione S-transferase mu, omega, pi, and theta class variants and smoking in Parkinson's disease.
PMID 17194543·Neurosci Lett·2007
4-observational
Structural variants in the vesicular monoamine transporter do not contribute to sporadic Parkinson's disease.
PMID 16450345·Mov Disord·2006
8-other
Gain-of-function haplotypes in the vesicular monoamine transporter promoter are protective for Parkinson disease in women.
PMID 16339215·Hum Mol Genet·2006
4-observational
Response to Zhang et al. (2005): loss-of-function mutation in tryptophan hydroxylase-2 identified in unipolar major depression. Neuron 45, 11-16.
PMID 16337902·Neuron·2005
8-other
Molecular characterization of thyroid toxicity: anchoring gene expression profiles to biochemical and pathologic end points.
PMID 16203246·Environ Health Perspect·2005
7-preclinical
The effect of rare human sequence variants on the function of vesicular monoamine transporter 2.
PMID 15475732·Pharmacogenetics·2004
7-preclinical
Identification of genetic variants in the neuronal form of tryptophan hydroxylase (TPH2).
PMID 15167691·Psychiatr Genet·2004
8-other
A multi-laboratory evaluation of a common in vitro pepsin digestion assay protocol used in assessing the safety of novel proteins.
PMID 15041142·Regul Toxicol Pharmacol·2004
4-observational
Re-screening serotonin receptors for genetic variants identifies population and molecular genetic complexity.
PMID 14681923·Am J Med Genet B Neuropsychiatr Genet·2004
4-observational
Association analysis of candidate genes for neuropsychiatric disease: the perpetual campaign.
PMID 12044360·Trends Genet·2002
6-review
Fine-scale mapping of a locus for severe bipolar mood disorder on chromosome 18p11.3 in the Costa Rican population.
PMID 11572994·Proc Natl Acad Sci U S A·2001
8-other
Screening a large reference sample to identify very low frequency sequence variants: comparisons between two genes.
PMID 11279528·Nat Genet·2001
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
- 3040 WELLINGTON RD
KALAMAZOO, MI 49008 - Phone
- (269) 344-2365
Quick Facts
- NPI
- 1922278290
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 15
Are you this provider?
Claim Your Profile