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MARC GREENBLATT, MD
MD
Medical Oncology Physician
NPI: 1770654550IndividualAccepts Medicare
Specialties, Licenses & Credentials
Medical Oncology PhysicianPrimary
Internal Medicine — Medical Oncology
Code: 207RX0202X
042-0009106(VT)
Education
JEFFERSON MEDICAL COLLEGE OF THOMAS JEFFERSON UNIVERSITY
Class of 1983
Research & Publications (20)
Locus-specific databases and recommendations to strengthen their contribution to the classification of variants in cancer susceptibility genes.
PMID 18951438·Hum Mutat·2008
8-other
Detailed computational study of p53 and p16: using evolutionary sequence analysis and disease-associated mutations to predict the functional consequences of allelic variants.
PMID 12606942·Oncogene·2003
7-preclinical
TP53 mutations in breast cancer associated with BRCA1 or BRCA2 germ-line mutations: distinctive spectrum and structural distribution.
PMID 11358831·Cancer Res·2001
8-other
TAK1 is an essential regulator of BMP signalling in cartilage.
PMID 19536134·EMBO J·2009
7-preclinical
Electronic properties, band structure, and fermi surface instabilities of Ni1+/Ni2+ nickelate La3Ni2O6, isoelectronic with superconducting cuprates.
PMID 19257449·Phys Rev Lett·2009
8-other
Assessment of functional effects of unclassified genetic variants.
PMID 18951449·Hum Mutat·2008
8-other
Sequence variant classification and reporting: recommendations for improving the interpretation of cancer susceptibility genetic test results.
PMID 18951446·Hum Mutat·2008
8-other
In silico analysis of missense substitutions using sequence-alignment based methods.
PMID 18951440·Hum Mutat·2008
8-other
Genetic evidence and integration of various data sources for classifying uncertain variants into a single model.
PMID 18951437·Hum Mutat·2008
8-other
Assessing pathogenicity: overview of results from the IARC Unclassified Genetic Variants Working Group.
PMID 18951436·Hum Mutat·2008
8-other
Uncertain pathogenicity of MSH2 variants N127S and G322D challenges their classification.
PMID 18470917·Int J Cancer·2008
8-other
Crystal structures of Ln4Ni3O8 (Ln = La, Nd) triple layer T'-type nickelates.
PMID 17985874·Inorg Chem·2007
8-other
A structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases.
PMID 17726697·Hum Mutat·2007
8-other
Founder and recurrent CDH1 mutations in families with hereditary diffuse gastric cancer.
PMID 17545690·JAMA·2007
8-other
Interpreting missense variants: comparing computational methods in human disease genes CDKN2A, MLH1, MSH2, MECP2, and tyrosinase (TYR).
PMID 17370310·Hum Mutat·2007
4-observational
Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated protein.
PMID 17101317·Gastroenterology·2006
7-preclinical
An automated procedure to identify biomedical articles that contain cancer-associated gene variants.
PMID 16865690·Hum Mutat·2006
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
- 111 COLCHESTER AVE
BURLINGTON, VT 05401 - Phone
- (802) 847-8400
Quick Facts
- NPI
- 1770654550
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 43
- Publications
- 20
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