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WAQAR AHMAD, MD
Internal Medicine Physician
NPI: 1215077482IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
24488(OK)N2363(TX)
Education
OTHER
Class of 1998
Research & Publications (20)
A novel splice-site mutation in the CDH3 gene in hypotrichosis with juvenile macular dystrophy.
PMID 19076794·Clin Exp Dermatol·2009
8-other
Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.
PMID 19292720·Br J Dermatol·2009
8-other
A mutation in CTSK gene in an autosomal recessive pycnodysostosis family of Pakistani origin.
PMID 19674475·BMC Med Genet·2009
8-other
Ectodermal dysplasia-cutaneous syndactyly syndrome maps to chromosome 7p21.1-p14.3.
PMID 19221800·Hum Genet·2009
5-case
Mutation in the HPGD gene encoding NAD+ dependent 15-hydroxyprostaglandin dehydrogenase underlies isolated congenital nail clubbing (ICNC).
PMID 18805827·J Med 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
The applicability of measures of socioeconomic position to different ethnic groups within the UK.
PMID 19250528·Int J Equity Health·2009
8-other
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
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
PMID 19576567·Am J Hum Genet·2009
7-preclinical
A novel deletion mutation in the phospholipase H (LIPH) gene in a consanguineous Pakistani family with autosomal recessive hypotrichosis (LAH2).
PMID 18795930·Br J Dermatol·2009
5-case
Novel autosomal recessive non-syndromic hearing impairment locus (DFNB71) maps to chromosome 8p22-21.3.
PMID 19229252·J Hum Genet·2009
8-other
A novel locus for ectodermal dysplasia of hairs, nails and teeth type maps to chromosome 18q22.1-22.3.
PMID 18184143·Ann Hum 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
The moral economy of selfhood and caring: negotiating boundaries of personal care as embodied moral practice.
PMID 18298630·Sociol Health Illn·2008
8-other
Splice-site mutations in the TRIC gene underlie autosomal recessive nonsyndromic hearing impairment in Pakistani families.
PMID 18084694·J Hum Genet·2008
4-observational
Identification of AGE-precursors and AGE formation in glycation-induced BSA peptides.
PMID 18682035·BMB Rep·2008
8-other
A novel missense mutation in the TRPS1 gene underlies trichorhinophalangeal syndrome type III.
PMID 18544079·Br J Dermatol·2008
5-case
A novel missense mutation in RSPO4 gene underlies autosomal recessive congenital anonychia in a consanguineous Pakistani family.
PMID 18070203·Br J Dermatol·2008
5-case
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 755 N 11TH ST, SUITE D1001, CHRISTUS ST. ELIZABETH WOUND CARE/HYPERBARICS
BEAUMONT, TX 77702 - Phone
- (409) 924-6975
Quick Facts
- NPI
- 1215077482
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Publications
- 20
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