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MICHAEL GREENBLATT, MD

MD

Internal Medicine Physician

NPI: 1750483483Individual

Specialties, Licenses & Credentials

Internal Medicine PhysicianPrimary

Internal Medicine

Code: 207R00000X

092850(NY)

Research & Publications (20)

Planning the human variome project: the Spain report.
PMID 19306394·Hum Mutat·2009
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
GENETICS. The Human Variome Project.
PMID 18988827·Science·2008
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
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
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
Recommendations for locus-specific databases and their curation.
PMID 18157828·Hum Mutat·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
An automated procedure to identify biomedical articles that contain cancer-associated gene variants.
PMID 16865690·Hum Mutat·2006
8-other
Pathogenicity of MSH2 missense mutations is typically associated with impaired repair capability of the mutated protein.
PMID 17101317·Gastroenterology·2006
7-preclinical
La3Ni2O6: a new double T'-type nickelate with infinite Ni1+/2+O2 layers.
PMID 16834375·J Am Chem Soc·2006
8-other
Germ line mutations of mismatch repair genes in hereditary nonpolyposis colorectal cancer patients with small bowel cancer: International Society for Gastrointestinal Hereditary Tumours Collaborative Study.
PMID 16740762·Clin Cancer Res·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
100 EAST 77TH STREET
NEW YORK, NY 10021

Location

Practice Location

100 EAST 77TH STREET, NEW YORK, NY
(212) 434-2972

Quick Facts

NPI
1750483483
Entity Type
Individual
Gender
Male
Medicare
Not confirmed
Specialties
1
Locations
1
Publications
20

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