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KHEDOUDJA NAFA, PHD
PHD
Clinical Molecular Genetics Physician
NPI: 1730256330Individual
Specialties, Licenses & Credentials
Clinical Molecular Genetics PhysicianPrimary
Medical Genetics — Clinical Molecular Genetics
Code: 207SG0203X
NAFAK1(NY)
Research & Publications (20)
cDNA analysis demonstrates that the BRCA2 intronic variant IVS4-12del5 is a deleterious mutation.
PMID 19070627·Mutat Res·2009
8-other
CpG methylation analysis--current status of clinical assays and potential applications in molecular diagnostics: a report of the Association for Molecular Pathology.
PMID 19541921·J Mol Diagn·2009
8-other
KRAS mutational testing in the selection of patients for EGFR-targeted therapies.
PMID 19013894·Semin Diagn Pathol·2008
6-review
Frequency and distinctive spectrum of KRAS mutations in never smokers with lung adenocarcinoma.
PMID 18794081·Clin Cancer Res·2008
8-other
EWSR1-CREB1 is the predominant gene fusion in angiomatoid fibrous histiocytoma.
PMID 17724745·Genes Chromosomes Cancer·2007
8-other
Single-amplicon MSH2 A636P mutation testing in Ashkenazi Jewish patients with colorectal cancer: role in presurgical management.
PMID 17414604·Ann Surg·2007
8-other
EWS-CREB1: a recurrent variant fusion in clear cell sarcoma--association with gastrointestinal location and absence of melanocytic differentiation.
PMID 17000668·Clin Cancer Res·2006
5-case
Prediction of germline mutations and cancer risk in the Lynch syndrome.
PMID 17003396·JAMA·2006
4-observational
Increased frequency of disease-causing MYH mutations in colon cancer families.
PMID 16774938·Carcinogenesis·2006
8-other
Localization of breast cancer susceptibility loci by genome-wide SNP linkage disequilibrium mapping.
PMID 16206141·Genet Epidemiol·2006
8-other
The TP53 mutational spectrum and frequency of CHEK2*1100delC in Li-Fraumeni-like kindreds.
PMID 15951970·Fam Cancer·2005
8-other
Functional and genomic approaches reveal an ancient CHEK2 allele associated with breast cancer in the Ashkenazi Jewish population.
PMID 15649950·Hum Mol Genet·2005
8-other
Value of immunohistochemical detection of DNA mismatch repair proteins in predicting germline mutation in hereditary colorectal neoplasms.
PMID 15613860·Am J Surg Pathol·2005
8-other
Colorectal cancer risk in individuals with biallelic or monoallelic mutations of MYH.
PMID 15578699·Int J Cancer·2005
8-other
Pleomorphic characteristics of a germ-line KIT mutation in a large kindred with gastrointestinal stromal tumors, hyperpigmentation, and dysphagia.
PMID 14977822·Clin Cancer Res·2004
8-other
Localization of cancer susceptibility genes by genome-wide single-nucleotide polymorphism linkage-disequilibrium mapping.
PMID 15520224·Cancer Res·2004
8-other
BRCA mutations and risk of prostate cancer in Ashkenazi Jews.
PMID 15131025·Clin Cancer Res·2004
4-observational
Loss of the tumor suppressor PML in human cancers of multiple histologic origins.
PMID 14970276·J Natl Cancer Inst·2004
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
- 1275 YORK AVE
NEW YORK, NY 10021 - Phone
- (646) 227-3275
Quick Facts
- NPI
- 1730256330
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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