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SHELBY BLANTON DO
DO
Family Medicine Physician
NPI: 1376293613IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
34.017814(OH)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Education
UNIVERSITY OF PIKEVILLE, KENTUCKY COLLEGE OF OSTEOPATHIC MED
Class of 2022
Research & Publications (20)
A Community's Awareness and Perceptions of Genomic Medicine.
PMID 19439917·Public Health Genomics·2010
8-other
Genomic screening identifies novel linkages and provides further evidence for a role of MYH9 in nonsyndromic cleft lip and palate.
PMID 18716610·Eur J Hum Genet·2009
8-other
Heritability and linkage analysis for carotid intima-media thickness: the family study of stroke risk and carotid atherosclerosis.
PMID 19498180·Stroke·2009
8-other
Novel quantitative trait locus is mapped to chromosome 12p11 for left ventricular mass in Dominican families: the Family Study of Stroke Risk and Carotid Atherosclerosis.
PMID 19627612·BMC Med Genet·2009
8-other
Mutations in STIL, encoding a pericentriolar and centrosomal protein, cause primary microcephaly.
PMID 19215732·Am J Hum Genet·2009
8-other
Minimal detectable change scores for the Wolf Motor Function Test.
PMID 19498013·Neurorehabil Neural Repair·2009
8-other
International Family, Adult, and Child Enhancement Services (FACES): a community-based comprehensive services model for refugee children in resettlement.
PMID 18444734·Am J Orthopsychiatry·2008
8-other
A comparative analysis of the genetic epidemiology of deafness in the United States in two sets of pedigrees collected more than a century apart.
PMID 18656178·Am J Hum Genet·2008
4-observational
Retention of upper limb function in stroke survivors who have received constraint-induced movement therapy: the EXCITE randomised trial.
PMID 18077218·Lancet Neurol·2008
2-rct
Constraint-induced movement therapy in stroke rehabilitation: perspectives on future clinical applications.
PMID 18356586·NeuroRehabilitation·2008
6-review
Variation in WNT genes is associated with non-syndromic cleft lip with or without cleft palate.
PMID 18413325·Hum Mol Genet·2008
8-other
Apoptotic gene analysis in idiopathic talipes equinovarus (clubfoot).
PMID 17534194·Clin Orthop Relat Res·2007
8-other
NAT2 variation and idiopathic talipes equinovarus (clubfoot).
PMID 17726690·Am J Med Genet A·2007
8-other
The Excite Trial: relationship of intensity of constraint induced movement therapy to improvement in the wolf motor function test.
PMID 18334772·Restor Neurol Neurosci·2007
4-observational
Lessons learned in participant recruitment and retention: the EXCITE trial.
PMID 17079752·Phys Ther·2006
4-observational
Attempting to improve function and quality of life using the FTM Protocol: case report.
PMID 17029658·J Neurol Phys Ther·2006
5-case
A novel locus for autosomal dominant non-syndromic deafness, DFNA53, maps to chromosome 14q11.2-q12.
PMID 15958501·J Med Genet·2006
8-other
Genomic rearrangements of the PRPF31 gene account for 2.5% of autosomal dominant retinitis pigmentosa.
PMID 17003455·Invest Ophthalmol Vis Sci·2006
8-other
Canine RPGRIP1 mutation establishes cone-rod dystrophy in miniature longhaired dachshunds as a homologue of human Leber congenital amaurosis.
PMID 16806805·Genomics·2006
7-preclinical
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
Via TRIHEALTH G LLC · 2 locations total
- Address
- 379 DIXMYTH AVE
CINCINNATI, OH 45220 - Phone
- (513) 246-7000
Quick Facts
- NPI
- 1376293613
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 4
- Publications
- 20
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