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CLAIR A FRANCOMANO MD
MD
Clinical Molecular Genetics Physician
NPI: 1083657613IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
D25334(MD)01082750A(IN)
Clinical Genetics (M.D.) Physician
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
D025334(MD)01082750A(IN)
Clinical Molecular Genetics PhysicianPrimary
Medical Genetics — Clinical Molecular Genetics
Code: 207SG0203X
D025334(MD)01082750A(IN)
Education
JOHNS HOPKINS UNIVERSITY SCHOOL OF MEDICINE
Class of 1980
Research & Publications (20)
Medical genetic studies in the Amish: historical perspective.
PMID 12888981·Am J Med Genet C Semin Med Genet·2003
8-other
Association of Chiari malformation type I and tethered cord syndrome: preliminary results of sectioning filum terminale.
PMID 19559924·Surg Neurol·2009
8-other
Syndrome of occipitoatlantoaxial hypermobility, cranial settling, and chiari malformation type I in patients with hereditary disorders of connective tissue.
PMID 18074684·J Neurosurg Spine·2007
8-other
Echocardiographic findings in classical and hypermobile Ehlers-Danlos syndromes.
PMID 16353246·Am J Med Genet A·2006
4-observational
Comparison of gene expression profile between human chondrons and chondrocytes: a cDNA microarray study.
PMID 16414292·Osteoarthritis Cartilage·2006
4-observational
Complementary medicine and genetic medicine: polar disciplines or dynamic partners?
PMID 15865502·J Altern Complement Med·2005
6-review
Growth and integration of neocartilage with native cartilage in vitro.
PMID 15734259·J Orthop Res·2005
7-preclinical
Stickler syndrome: clinical characteristics and diagnostic criteria.
PMID 16152640·Am J Med Genet A·2005
8-other
Hyaline cartilage engineered by chondrocytes in pellet culture: histological, immunohistochemical and ultrastructural analysis in comparison with cartilage explants.
PMID 15379928·J Anat·2004
4-observational
Klotho gene variation and expression in 20 inbred mouse strains.
PMID 15520879·Mamm Genome·2004
7-preclinical
Living with achondroplasia: quality of life evaluation following cervico-medullary decompression.
PMID 15487008·Am J Med Genet A·2004
8-other
The effects of pulsed low-intensity ultrasound on chondrocyte viability, proliferation, gene expression and matrix production.
PMID 14654159·Ultrasound Med Biol·2003
4-observational
Clinico-pathogenetic findings and management of chondrodystrophic myotonia (Schwartz-Jampel syndrome): a case report.
PMID 12839625·BMC Neurol·2003
5-case
A study of linkage and association of body mass index in the Old Order Amish.
PMID 12888987·Am J Med Genet C Semin Med Genet·2003
8-other
The major mutation in the RMRP gene causing CHH among the Amish is the same as that found in most Finnish cases.
PMID 12888988·Am J Med Genet C Semin Med Genet·2003
4-observational
A central nervous system specific mouse model for thanatophoric dysplasia type II.
PMID 12966031·Hum Mol Genet·2003
7-preclinical
Gene expression profile of human bone marrow stromal cells: high-throughput expressed sequence tag sequencing analysis.
PMID 11827452·Genomics·2002
8-other
Structural and functional mutations of the perlecan gene cause Schwartz-Jampel syndrome, with myotonic myopathy and chondrodysplasia.
PMID 11941538·Am J Hum Genet·2002
5-case
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
- 1002 WISHARD BLVD
INDIANAPOLIS, IN 46202 - Phone
- (317) 944-3966
Quick Facts
- NPI
- 1083657613
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 6
- Locations
- 3
- Years in Practice
- 46
- Publications
- 20
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