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BRIAN GLASER, MD

MD

Family Medicine Physician

NPI: 1689171225Individual

Specialties, Licenses & Credentials

Family Medicine PhysicianPrimary

Family Medicine

Code: 207Q00000X

32362(NE)201810(CA)

Research & Publications (20)

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
Insulin mutations in diabetes: the clinical spectrum.
PMID 18375443·Diabetes·2008
8-other
LRET-based HTS of a small-compound library for inhibitors of bacterial RNA polymerase.
PMID 18052851·Assay Drug Dev Technol·2007
8-other
Structural changes to the fusiform gyrus: a cerebral marker for social impairments in 22q11.2 deletion syndrome?
PMID 17826962·Schizophr Res·2007
8-other
Analyses of single marker and pairwise effects of candidate loci for rheumatoid arthritis using logistic regression and random forests.
PMID 18466554·BMC Proc·2007
8-other
Type 2 diabetes: hypoinsulinism, hyperinsulinism, or both?
PMID 17407388·PLoS Med·2007
7-preclinical
No evidence for an effect of COMT Val158Met genotype on executive function in patients with 22q11 deletion syndrome.
PMID 16513880·Am J Psychiatry·2006
4-observational
Analysis of ProDH, COMT and ZDHHC8 risk variants does not support individual or interactive effects on schizophrenia susceptibility.
PMID 16860541·Schizophr Res·2006
8-other
Attitudes of academic and clinical researchers toward financial ties in research: a systematic review.
PMID 16279755·Sci Eng Ethics·2005
1-meta
No association between the putative functional ZDHHC8 single nucleotide polymorphism rs175174 and schizophrenia in large European samples.
PMID 15992527·Biol Psychiatry·2005
8-other
Identification of a potential bipolar risk haplotype in the gene encoding the winged-helix transcription factor RFX4.
PMID 15940297·Mol Psychiatry·2005
8-other
Linkage disequilibrium mapping of bipolar affective disorder at 12q23-q24 provides evidence for association at CUX2 and FLJ32356.
PMID 15389760·Am J Med Genet B Neuropsychiatr Genet·2005
8-other
Biological and environmental contributions to adaptive behavior in fragile X syndrome.
PMID 12548736·Am J Med Genet A·2003
8-other
Pendred syndrome.
PMID 16444159·Pediatr Endocrinol Rev·2003
6-review
Dominant SUR1 mutation causing autosomal dominant type 2 diabetes.
PMID 12559857·Lancet·2003
8-other
Language skills in children with velocardiofacial syndrome (deletion 22q11.2).
PMID 12072882·J Pediatr·2002
8-other
Hyperinsulinism of the newborn.
PMID 10805170·Semin Perinatol·2000
6-review
[Hyperinsulinemia, a heterogeneous illness].
PMID 10932866·Journ Annu Diabetol Hotel Dieu·2000
6-review
Genetics of neonatal hyperinsulinism.
PMID 10685979·Arch Dis Child Fetal Neonatal Ed·2000
6-review
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

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
5342 DUDLEY BLVD
MCCLELLAN, CA 95652

Locations (3)

Practice Location

5342 DUDLEY BLVD, MCCLELLAN, CA
(916) 561-7793

Practice Location

3100 DOUGLAS BLVD STE 220, ROSEVILLE, CA
(916) 774-8300

Practice Location

101 BODIN CIR, TRAVIS AFB, CA
(707) 423-3000

Quick Facts

NPI
1689171225
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
2
Locations
3
Publications
20

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