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MUHAMMAD ANSAR MD
MD
Endocrinology, Diabetes & Metabolism Physician
NPI: 1285918557IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
01084412A(IN)MD41877(IA)MT198966(PA)
Endocrinology, Diabetes & Metabolism PhysicianPrimary
Internal Medicine — Endocrinology, Diabetes & Metabolism
Code: 207RE0101X
063912(CT)01084412A(IN)
Education
OTHER
Class of 1997
Research & Publications (20)
Novel missense mutations in lipase H (LIPH) gene causing autosomal recessive hypotrichosis (LAH2).
PMID 19167195·J Dermatol Sci·2009
8-other
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
PMID 19576567·Am J Hum Genet·2009
7-preclinical
Recurrent mutations in functionally-related EDA and EDAR genes underlie X-linked isolated hypodontia and autosomal recessive hypohidrotic ectodermal dysplasia.
PMID 19551394·Arch Dermatol Res·2009
8-other
[Synthesis, chemical and toxicological study of a new benzimidazol derivative].
PMID 19298890·Ann Pharm Fr·2009
7-preclinical
Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3.
PMID 19229252·J Hum Genet·2009
8-other
Mapping of a new autosomal recessive non-syndromic hearing impairment locus (DFNB45) to chromosome 1q43-q44.
PMID 18325041·Clin Genet·2008
8-other
A novel insertion mutation in the cartilage-derived morphogenetic protein-1 (CDMP1) gene underlies Grebe-type chondrodysplasia in a consanguineous Pakistani family.
PMID 19038017·BMC Med Genet·2008
8-other
Contribution of BRCA1 germline mutation in patients with sporadic breast cancer.
PMID 18759965·Int Semin Surg Oncol·2008
8-other
Intragenic deletions in the dystrophin gene in 211 Pakistani Duchenne muscular dystrophy patients.
PMID 18353051·Pediatr Int·2008
8-other
Mutations of ESRRB encoding estrogen-related receptor beta cause autosomal-recessive nonsyndromic hearing impairment DFNB35.
PMID 18179891·Am J Hum Genet·2008
8-other
Genetic heterogeneity of synpolydactyly: a novel locus SPD3 maps to chromosome 14q11.2-q12.
PMID 16712704·Clin Genet·2006
8-other
Nitric oxide involvement in pancreatic beta cell apoptosis by glibenclamide.
PMID 16256381·Nitric Oxide·2006
7-preclinical
A novel autosomal recessive non-syndromic hearing impairment locus (DFNB47) maps to chromosome 2p25.1-p24.3.
PMID 16261342·Hum Genet·2006
8-other
Genetic studies of autosomal recessive primary microcephaly in 33 Pakistani families: Novel sequence variants in ASPM gene.
PMID 16673149·Neurogenetics·2006
8-other
Recurrent intragenic deletion mutation in desmoglein 4 gene underlies autosomal recessive hypotrichosis in two Pakistani families of Balochi and Sindhi origins.
PMID 16770573·Arch Dermatol Res·2006
8-other
Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene.
PMID 16901311·Clin Exp Dermatol·2006
8-other
Effect of linearization correction on statistical parametric mapping (SPM): a 99mTc-HMPAO brain perfusion SPECT study in mild Alzheimer's disease.
PMID 17134017·Ann Nucl Med·2006
8-other
Novel sequence variants in the TMC1 gene in Pakistani families with autosomal recessive hearing impairment.
PMID 16134132·Hum Mutat·2005
8-other
A novel autosomal recessive nonsyndromic hearing impairment locus (DFNB42) maps to chromosome 3q13.31-q22.3.
PMID 15641023·Am J Med Genet A·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
Via practice · 4 locations total
- Address
- 201 Pennsylvania Pkwy Ste 315
Carmel, IN 46280 - Phone
- (317) 817-1400
Quick Facts
- NPI
- 1285918557
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 5
- Locations
- 4
- Years in Practice
- 29
- Publications
- 20
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