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WAQAS AHMAD MD
MD
Internal Medicine Physician
NPI: 1316300247IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
036152963(IL)
Education
OTHER
Class of 2015
Research & Publications (20)
[Discoid lateral meniscus as the cause of limping in children].
PMID 18940172·Ugeskr Laeger·2008
5-case
Linkage mapping of a nonspecific form of X-linked mental retardation (MRX53) in a large Pakistani family.
PMID 11337751·Am J Med Genet·2001
8-other
Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.
PMID 19292720·Br J Dermatol·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
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
Ectodermal dysplasia-cutaneous syndactyly syndrome maps to chromosome 7p21.1-p14.3.
PMID 19221800·Hum Genet·2009
5-case
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
A novel splice-site mutation in the CDH3 gene in hypotrichosis with juvenile macular dystrophy.
PMID 19076794·Clin Exp Dermatol·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
A mutation in CTSK gene in an autosomal recessive pycnodysostosis family of Pakistani origin.
PMID 19674475·BMC Med Genet·2009
8-other
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
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
PMID 19576567·Am J Hum Genet·2009
7-preclinical
Antifungal and antibacterial activities of Taxus wallichiana Zucc.
PMID 18343912·J Enzyme Inhib Med Chem·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
Intragenic deletions in the dystrophin gene in 211 Pakistani Duchenne muscular dystrophy patients.
PMID 18353051·Pediatr Int·2008
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
A novel deletion mutation in LIPH gene causes autosomal recessive hypotrichosis (LAH2).
PMID 18445047·Clin Genet·2008
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
- 1500 OGLETHORPE AVE, SUITE 200D
ATHENS, GA 30606 - Phone
- (706) 389-3875
Quick Facts
- NPI
- 1316300247
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 2
- Years in Practice
- 11
- Publications
- 20
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