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WAQAAR AHMAD, M.D.
M.D.
Vascular & Interventional Radiology Physician
NPI: 1639515034IndividualAccepts Medicare
Specialties, Licenses & Credentials
Internal Medicine Physician
Internal Medicine
Code: 207R00000X
4301103802(MI)
Diagnostic Radiology Physician
Radiology — Diagnostic Radiology
Code: 2085R0202X
58702(AZ)
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
4301103802(MI)
Vascular & Interventional Radiology PhysicianPrimary
Radiology — Vascular & Interventional Radiology
Code: 2085R0204X
20193(NV)
CMS Specialties
PrimaryINTERVENTIONAL RADIOLOGY
Education
OTHER
Class of 2013
Research & Publications (20)
Novel missense mutations in lipase H (LIPH) gene causing autosomal recessive hypotrichosis (LAH2).
PMID 19167195·J Dermatol Sci·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
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
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
The applicability of measures of socioeconomic position to different ethnic groups within the UK.
PMID 19250528·Int J Equity Health·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
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
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
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
Coronary artery anomaly with congenital factor V deficiency.
PMID 19024144·J Pak Med Assoc·2008
5-case
Detection of FLT3 oncogene mutations in acute myeloid leukemia using conformation sensitive gel electrophoresis.
PMID 19330068·Int J Mol Sci·2008
8-other
Diagnostic transgastric flexible peritoneoscopy: is pure natural orifice transluminal endoscopic surgery a fantasy?
PMID 19122940·Singapore Med J·2008
5-case
Identification of AGE-precursors and AGE formation in glycation-induced BSA peptides.
PMID 18682035·BMB Rep·2008
8-other
New antibacterial pentacyclic triterpenes from Myricaria elegans Royle. (tamariscineae).
PMID 18608775·J Enzyme Inhib Med Chem·2008
8-other
Norditerpenoid alkaloids from the roots of Aconitum heterophyllum Wall with antibacterial activity.
PMID 18608773·J Enzyme Inhib Med Chem·2008
8-other
[Discoid lateral meniscus as the cause of limping in children].
PMID 18940172·Ugeskr Laeger·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
- 10381 DOUBLE R BLVD
RENO, NV 89521 - Phone
- (775) 348-8800
Quick Facts
- NPI
- 1639515034
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 4
- Locations
- 1
- Years in Practice
- 13
- Publications
- 20
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