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NANCY HAMEL, M.D.
M.D.
Family Medicine Physician
NPI: 1427250521Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
153905(MA)
Research & Publications (20)
Mixed ovarian germ cell tumor in a BRCA2 mutation carrier.
PMID 17413983·Int J Gynecol Pathol·2007
5-case
Founder mutations in BRCA1/2 are not frequent in Canadian Ashkenazi Jewish men with prostate cancer.
PMID 12911837·BMC Med Genet·2003
8-other
Relationship between angiotensin-converting enzyme gene polymorphism and body composition, functional performance, and blood biomarkers in advanced cancer patients.
PMID 19258445·Clin Cancer Res·2009
7-preclinical
Equity-oriented toolkit for health technology assessment and knowledge translation: application to scaling up of training and education for health workers.
PMID 19656381·Hum Resour Health·2009
8-other
Brain-specific proteins decline in the cerebrospinal fluid of humans with Huntington disease.
PMID 18984577·Mol Cell Proteomics·2009
7-preclinical
Is research working for you? Validating a tool to examine the capacity of health organizations to use research.
PMID 19627601·Implement Sci·2009
8-other
Analysis of the gene coding for the BRCA2-interacting protein PALB2 in familial and sporadic pancreatic cancer.
PMID 19635604·Gastroenterology·2009
8-other
Frequency of the CHEK2 1100delC mutation among women with breast cancer: an international study.
PMID 18381420·Cancer Res·2008
8-other
Pathogenicity of the BRCA1 missense variant M1775K is determined by the disruption of the BRCT phosphopeptide-binding pocket: a multi-modal approach.
PMID 18285836·Eur J Hum Genet·2008
8-other
[Enucleations and eviscerations in a large medical center between the years 1981 and 2007].
PMID 19039900·Harefuah·2008
8-other
Identification and characterization of novel SNPs in CHEK2 in Ashkenazi Jewish men with prostate cancer.
PMID 18571837·Cancer Lett·2008
8-other
Identification of a novel CHEK2 variant and assessment of its contribution to the risk of breast cancer in French Canadian women.
PMID 18706089·BMC Cancer·2008
8-other
Multiple novel prostate cancer predisposition loci confirmed by an international study: the PRACTICAL Consortium.
PMID 18708398·Cancer Epidemiol Biomarkers Prev·2008
4-observational
Analysis of PALB2/FANCN-associated breast cancer families.
PMID 17420451·Proc Natl Acad Sci U S A·2007
8-other
Identification of a novel truncating PALB2 mutation and analysis of its contribution to early-onset breast cancer in French-Canadian women.
PMID 18053174·Breast Cancer Res·2007
8-other
The frequent BRCA1 mutation 1135insA has multiple origins: a haplotype study in different populations.
PMID 16509964·BMC Med Genet·2006
8-other
The HNPCC associated MSH2*1906G-->C founder mutation probably originated between 1440 CE and 1715 CE in the Ashkenazi Jewish population.
PMID 16199548·J Med Genet·2005
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
- 272 MAIN ST
WALPOLE, MA 02081 - Phone
- (508) 668-7600
Quick Facts
- NPI
- 1427250521
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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