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JEFFREY BELMONT, MD, MPH
MD, MPH
General Practice Physician
NPI: 1467915074Individual
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
General Practice PhysicianPrimary
General Practice
Code: 208D00000X
36832(NE)
Research & Publications (20)
Complex phenotypes and complex genetics: an introduction to genetic studies of complex traits.
PMID 15811251·Curr Atheroscler Rep·2005
6-review
Congenital sucrase-isomaltase deficiency presenting with failure to thrive, hypercalcemia, and nephrocalcinosis.
PMID 12014995·BMC Pediatr·2002
5-case
The futility of genomic counseling: essential role of electronic health records.
PMID 19439060·Genome Med·2009
8-other
BCOR analysis in patients with OFCD and Lenz microphthalmia syndromes, mental retardation with ocular anomalies, and cardiac laterality defects.
PMID 19367324·Eur J Hum Genet·2009
7-preclinical
20p12.3 microdeletion predisposes to Wolff-Parkinson-White syndrome with variable neurocognitive deficits.
PMID 18812404·J Med Genet·2009
7-preclinical
Linkage analysis of left ventricular outflow tract malformations (aortic valve stenosis, coarctation of the aorta, and hypoplastic left heart syndrome).
PMID 19142209·Eur J Hum Genet·2009
8-other
Ancestry informative marker sets for determining continental origin and admixture proportions in common populations in America.
PMID 18683858·Hum Mutat·2009
8-other
An ancestry informative marker set for determining continental origin: validation and extension using human genome diversity panels.
PMID 19630973·BMC Genet·2009
8-other
Identification and functional characterization of NODAL rare variants in heterotaxy and isolated cardiovascular malformations.
PMID 19064609·Hum Mol Genet·2009
8-other
Microduplications of 22q11.2 are frequently inherited and are associated with variable phenotypes.
PMID 18414210·Genet Med·2008
4-observational
Low-level mosaicism of trisomy 14: phenotypic and molecular characterization.
PMID 18412278·Am J Med Genet A·2008
5-case
NOTCH1 mutations in individuals with left ventricular outflow tract malformations reduce ligand-induced signaling.
PMID 18593716·Hum Mol Genet·2008
7-preclinical
Human milk intake and retinopathy of prematurity in extremely low birth weight infants.
PMID 18762549·Pediatrics·2008
8-other
22q11.2 distal deletion: a recurrent genomic disorder distinct from DiGeorge syndrome and velocardiofacial syndrome.
PMID 18179902·Am J Hum Genet·2008
8-other
Analysis of East Asia genetic substructure using genome-wide SNP arrays.
PMID 19057645·PLoS One·2008
8-other
Reduced NODAL signaling strength via mutation of several pathway members including FOXH1 is linked to human heart defects and holoprosencephaly.
PMID 18538293·Am J Hum Genet·2008
7-preclinical
Recurrent reciprocal 1q21.1 deletions and duplications associated with microcephaly or macrocephaly and developmental and behavioral abnormalities.
PMID 19029900·Nat Genet·2008
8-other
Amerindian ancestry in Argentina is associated with increased risk for systemic lupus erythematosus.
PMID 18401351·Genes Immun·2008
8-other
Effectiveness of teaching cardiac auscultation to residents during an elective pediatric cardiology rotation.
PMID 18648718·Pediatr Cardiol·2008
8-other
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 7703 FLOYD CURL DR
SAN ANTONIO, TX 78229 - Phone
- (210) 567-4509
Quick Facts
- NPI
- 1467915074
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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