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WASEEM AHMAD MD
MD
Nephrology Physician
NPI: 1366520108IndividualAccepts Medicare
Specialties, Licenses & Credentials
Nephrology PhysicianPrimary
Internal Medicine — Nephrology
Code: 207RN0300X
A73846(CA)
Education
OTHER
Class of 1988
Research & Publications (20)
Detection of FLT3 oncogene mutations in acute myeloid leukemia using conformation sensitive gel electrophoresis.
PMID 19330068·Int J Mol Sci·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
A novel deletion mutation in CENPJ gene in a Pakistani family with autosomal recessive primary microcephaly.
PMID 16900296·J Hum Genet·2006
5-case
A novel missense mutation in MSX1 underlies autosomal recessive oligodontia with associated dental anomalies in Pakistani families.
PMID 16932841·J Hum Genet·2006
8-other
Being deaf and being other things: young Asian people negotiating identities.
PMID 12383460·Soc Sci Med·2002
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
Noncoding mutations of HGF are associated with nonsyndromic hearing loss, DFNB39.
PMID 19576567·Am J Hum Genet·2009
7-preclinical
A novel splice-site mutation in the CDH3 gene in hypotrichosis with juvenile macular dystrophy.
PMID 19076794·Clin Exp Dermatol·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
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
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
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
Ectodermal dysplasia-cutaneous syndactyly syndrome maps to chromosome 7p21.1-p14.3.
PMID 19221800·Hum Genet·2009
5-case
Mutations in the P2RY5 gene underlie autosomal recessive hypotrichosis in 13 Pakistani families.
PMID 19292720·Br J Dermatol·2009
8-other
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
A syndromic form of autosomal recessive congenital microcephaly (Jawad syndrome) maps to chromosome 18p11.22-q11.2.
PMID 18071751·Hum Genet·2008
8-other
Novel mutations in G protein-coupled receptor gene (P2RY5) in families with autosomal recessive hypotrichosis (LAH3).
PMID 18461368·Hum 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
- Address
- 975 SERENO DR
VALLEJO, CA 94589 - Phone
- (707) 651-1000
Quick Facts
- NPI
- 1366520108
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 38
- Publications
- 20
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