Back to Search
MD ASHIK ANSAR, M.D., PH.D
M.D., PH.D
Psychiatry Physician
NPI: 1952663775IndividualAccepts Medicare
Specialties, Licenses & Credentials
Psychiatry PhysicianPrimary
Psychiatry & Neurology — Psychiatry
Code: 2084P0800X
MD460858(PA)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
MT200917(PA)
CMS Specialties
PrimaryPSYCHIATRY
Education
OTHER
Class of 2000
Research & Publications (20)
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
Nitric oxide involvement in pancreatic beta cell apoptosis by glibenclamide.
PMID 16256381·Nitric Oxide·2006
7-preclinical
DFNB44, a novel autosomal recessive non-syndromic hearing impairment locus, maps to chromosome 7p14.1-q11.22.
PMID 15583425·Hum Hered·2004
8-other
Localization of a novel autosomal recessive non-syndromic hearing impairment locus (DFNB38) to 6q26-q27 in a consanguineous kindred from Pakistan.
PMID 12890929·Hum Hered·2003
8-other
A novel autosomal recessive non-syndromic deafness locus (DFNB35) maps to 14q24.1-14q24.3 in large consanguineous kindred from Pakistan.
PMID 12529709·Eur J Hum Genet·2003
8-other
Prevalence of hepatitis C virus infection in thalassemia and haemodialysis patients in north Iran-Rasht.
PMID 12225335·J Viral Hepat·2002
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
Novel missense mutations in lipase H (LIPH) gene causing autosomal recessive hypotrichosis (LAH2).
PMID 19167195·J Dermatol Sci·2009
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
Mapping of a new autosomal recessive non-syndromic hearing impairment locus (DFNB45) to chromosome 1q43-q44.
PMID 18325041·Clin Genet·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
Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene.
PMID 16901311·Clin Exp Dermatol·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
Genetic heterogeneity of synpolydactyly: a novel locus SPD3 maps to chromosome 14q11.2-q12.
PMID 16712704·Clin Genet·2006
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 · 2 locations total
- Address
- 1 MEDICAL CENTER BLVD
CHESTER, PA 19013 - Phone
- (610) 447-6003
Quick Facts
- NPI
- 1952663775
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 26
- Publications
- 20
Are you this provider?
Claim Your Profile