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SHARON BALCELLS, M.D.
M.D.
Internal Medicine Physician
NPI: 1730148693Individual
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
K6809(TX)
Research & Publications (20)
Polymorphisms and haplotypes across the osteoprotegerin gene associated with bone mineral density and osteoporotic fractures.
PMID 19436932·Osteoporos Int·2010
8-other
A haplotype-based analysis of the LRP5 gene in relation to osteoporosis phenotypes in Spanish postmenopausal women.
PMID 18684085·J Bone Miner Res·2008
8-other
Large-scale analysis of association between LRP5 and LRP6 variants and osteoporosis.
PMID 18349089·JAMA·2008
8-other
Large-scale analysis of association between polymorphisms in the transforming growth factor beta 1 gene (TGFB1) and osteoporosis: the GENOMOS study.
PMID 18284942·Bone·2008
4-observational
Polymorphisms in the interleukin-6 receptor gene are associated with bone mineral density and body mass index in Spanish postmenopausal women.
PMID 17984249·Eur J Endocrinol·2007
4-observational
Promoter 2 -1025 T/C polymorphism in the RUNX2 gene is associated with femoral neck bmd in Spanish postmenopausal women.
PMID 17878995·Calcif Tissue Int·2007
8-other
A CBS haplotype and a polymorphism at the MSR gene are associated with cardiovascular disease in a Spanish case-control study.
PMID 17553479·Clin Biochem·2007
8-other
Simvastatin and atorvastatin enhance gene expression of collagen type 1 and osteocalcin in primary human osteoblasts and MG-63 cultures.
PMID 17252541·J Cell Biochem·2007
8-other
COL1A1, ESR1, VDR and TGFB1 polymorphisms and haplotypes in relation to BMD in Spanish postmenopausal women.
PMID 17021946·Osteoporos Int·2007
8-other
Haplotypes defined by promoter and intron 1 polymorphisms of the COLIA1 gene regulate bone mineral density in women.
PMID 16804049·J Clin Endocrinol Metab·2006
8-other
The p.T191M mutation of the CBS gene is highly prevalent among homocystinuric patients from Spain, Portugal and South America.
PMID 16479318·J Hum Genet·2006
4-observational
Large-scale evidence for the effect of the COLIA1 Sp1 polymorphism on osteoporosis outcomes: the GENOMOS study.
PMID 16475872·PLoS Med·2006
4-observational
High prevalence of CBS p.T191M mutation in homocystinuric patients from Colombia.
PMID 16470595·Hum Mutat·2006
8-other
Functional assays testing pathogenicity of 14 cystathionine-beta synthase mutations.
PMID 16429402·Hum Mutat·2006
8-other
A new SNP in a negative regulatory region of the CYP19A1 gene is associated with lumbar spine BMD in postmenopausal women.
PMID 16344016·Bone·2006
8-other
Functional analysis of the I.3, I.6, pII and I.4 promoters of CYP19 (aromatase) gene in human osteoblasts and their role in vitamin D and dexamethasone stimulation.
PMID 16322405·Eur J Endocrinol·2005
8-other
A folate-rich diet is as effective as folic acid from supplements in decreasing plasma homocysteine concentrations.
PMID 15968341·Int J Med Sci·2005
8-other
Polymorphisms of genes involved in homocysteine metabolism in preeclampsia and in uncomplicated pregnancies.
PMID 15866085·Eur J Obstet Gynecol Reprod Biol·2005
8-other
In vitro functional assay of alleles and haplotypes of two COL1A1-promoter SNPs.
PMID 15814304·Bone·2005
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
- 4501 S GENERAL BRUCE DR, STE 75
TEMPLE, TX 76502 - Phone
- (254) 743-1628
Quick Facts
- NPI
- 1730148693
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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