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NORALANE LINDOR, M.D.
M.D.
NPI: 1205806601Individual
Specialties, Licenses & Credentials
Family Medicine Physician
Family Medicine
Code: 207Q00000X
19576(AZ)
Clinical Genetics (M.D.) PhysicianPrimary
Medical Genetics — Clinical Genetics (M.D.)
Code: 207SG0201X
27910(MN)19576(AZ)
Research & Publications (20)
Desmoid tumors in familial adenomatous polyposis: a pilot project evaluating efficacy of treatment with pirfenidone.
PMID 12907346·Am J Gastroenterol·2003
8-other
Germline MutY human homologue mutations and colorectal cancer: a multisite case-control study.
PMID 19245865·Gastroenterology·2009
4-observational
Hereditary colorectal cancer: MYH-associated polyposis and other newly identified disorders.
PMID 19258188·Best Pract Res Clin Gastroenterol·2009
6-review
The association of tumor microsatellite instability phenotype with family history of colorectal cancer.
PMID 19258475·Cancer Epidemiol Biomarkers Prev·2009
4-observational
No evidence that GATA3 rs570613 SNP modifies breast cancer risk.
PMID 19082709·Breast Cancer Res Treat·2009
8-other
Making a case for surveillance colonoscopy in Lynch syndrome.
PMID 19160466·Colorectal Dis·2009
8-other
Concise handbook of familial cancer susceptibility syndromes - second edition.
PMID 18559331·J Natl Cancer Inst Monogr·2008
8-other
Ready reference to common segmental aneusomies by syndromic names, major features and chromosomal locations.
PMID 18322350·J Assoc Genet Technol·2008
8-other
The clinical phenotype of Lynch syndrome due to germ-line PMS2 mutations.
PMID 18602922·Gastroenterology·2008
4-observational
Germline duplication of chromosomes 10p15.3 and Yp11.32 in a man with learning disability and early onset cutaneous malignant melanoma.
PMID 18671282·Am J Med Genet A·2008
5-case
Molecular characterization of MSI-H colorectal cancer by MLHI promoter methylation, immunohistochemistry, and mismatch repair germline mutation screening.
PMID 18990764·Cancer Epidemiol Biomarkers Prev·2008
4-observational
Further clinical description of duplication of Williams-Beuren region presenting with congenital glaucoma and brachycephaly.
PMID 18266245·Am J Med Genet A·2008
8-other
AURKA F31I polymorphism and breast cancer risk in BRCA1 and BRCA2 mutation carriers: a consortium of investigators of modifiers of BRCA1/2 study.
PMID 17627006·Cancer Epidemiol Biomarkers Prev·2007
8-other
Pathology features in Bethesda guidelines predict colorectal cancer microsatellite instability: a population-based study.
PMID 17631130·Gastroenterology·2007
4-observational
Predicting BRCA1 and BRCA2 gene mutation carriers: comparison of LAMBDA, BRCAPRO, Myriad II, and modified Couch models.
PMID 17636425·Fam Cancer·2007
4-observational
Colorectal cancer risks in relatives of young-onset cases: is risk the same across all first-degree relatives?
PMID 17702662·Clin Gastroenterol Hepatol·2007
4-observational
Colon Cancer Family Registry: an international resource for studies of the genetic epidemiology of colon cancer.
PMID 17982118·Cancer Epidemiol Biomarkers Prev·2007
4-observational
Variants on 9p24 and 8q24 are associated with risk of colorectal cancer: results from the Colon Cancer Family Registry.
PMID 18056436·Cancer Res·2007
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 13400 E SHEA BLVD, MAYO CLINIC
SCOTTSDALE, AZ 85259 - Phone
- (480) 301-6817
Quick Facts
- NPI
- 1205806601
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 3
- Locations
- 1
- Publications
- 20
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