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BRITTANY GLASER, LAPC, MDIV, MA, NCC
LAPC, MDIV, MA, NCC
Mental Health Counselor
NPI: 1710407978Individual
Specialties, Licenses & Credentials
Mental Health CounselorPrimary
Counselor — Mental Health
Code: 101YM0800X
Research & Publications (20)
Preliminary evidence that a functional polymorphism in type 1 deiodinase is associated with enhanced potentiation of the antidepressant effect of sertraline by triiodothyronine.
PMID 19064291·J Affect Disord·2009
8-other
Parental diabetes status reveals association of mitochondrial DNA haplogroup J1 with type 2 diabetes.
PMID 19534826·BMC Med Genet·2009
8-other
Minimal promoter systems reveal the importance of conserved residues in the B-finger of human transcription factor IIB.
PMID 19590095·J Biol Chem·2009
8-other
Genetic variation in LIN28B is associated with the timing of puberty.
PMID 19448623·Nat Genet·2009
8-other
Studying the salt dependence of the binding of sigma70 and sigma32 to core RNA polymerase using luminescence resonance energy transfer.
PMID 19649256·PLoS One·2009
8-other
Common variants in the region around Osterix are associated with bone mineral density and growth in childhood.
PMID 19181680·Hum Mol Genet·2009
8-other
Activated VEGF receptor shed into the vitreous in eyes with wet AMD: a new class of biomarkers in the vitreous with potential for predicting the treatment timing and monitoring response.
PMID 19433709·Arch Ophthalmol·2009
8-other
Congenital heart disease affects local gyrification in 22q11.2 deletion syndrome.
PMID 19416334·Dev Med Child Neurol·2009
8-other
Comparison of methods for combining case-control and family-based association studies.
PMID 19365137·Hum Hered·2009
4-observational
Cingulate gyral reductions are related to low executive functioning and psychotic symptoms in 22q 11.2 deletion syndrome.
PMID 18616958·Neuropsychologia·2008
8-other
Analysis of copy number variation using quantitative interspecies competitive PCR.
PMID 18697816·Nucleic Acids Res·2008
7-preclinical
Post genome-wide association studies of novel genes associated with type 2 diabetes show gene-gene interaction and high predictive value.
PMID 18461161·PLoS One·2008
8-other
Novel de novo mutation in sulfonylurea receptor 1 presenting as hyperinsulinism in infancy followed by overt diabetes in early adolescence.
PMID 18390792·Diabetes·2008
5-case
The H syndrome: a genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations.
PMID 18410979·J Am Acad Dermatol·2008
5-case
Differences in mtDNA haplogroup distribution among 3 Jewish populations alter susceptibility to T2DM complications.
PMID 18445251·BMC Genomics·2008
8-other
Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies.
PMID 18728231·Diabetes·2008
8-other
Impact of polymorphisms in WFS1 on prediabetic phenotypes in a population-based sample of middle-aged people with normal and abnormal glucose regulation.
PMID 18568334·Diabetologia·2008
8-other
Long-acting somatostatin analogues are an effective treatment for type 1 gastric carcinoid tumours.
PMID 18662970·Eur J Endocrinol·2008
3-trial
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 2750 OLD ALABAMA RD, C/O THE SUMMIT COUNSELING
ALPHARETTA, GA 30022 - Phone
- (678) 893-5300
Quick Facts
- NPI
- 1710407978
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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