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ELIZABETH MAINA, M.D.
M.D.
Internal Medicine Physician
NPI: 1790041960IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
279547(NY)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
TULANE UNIVERSITY SCHOOL OF MEDICINE
Class of 2012
Research & Publications (13)
The ATM tumour suppressor gene is down-regulated in EBV-associated nasopharyngeal carcinoma.
PMID 19142888·J Pathol·2009
8-other
Stratification of pediatric ALL by in vitro cellular responses to DNA double-strand breaks provides insight into the molecular mechanisms underlying clinical response.
PMID 18941120·Blood·2009
8-other
In search of the psychosis gene in people with Prader-Willi syndrome.
PMID 18324689·Am J Med Genet A·2008
8-other
The phenomenology and diagnosis of psychiatric illness in people with Prader-Willi syndrome.
PMID 18177526·Psychol Med·2008
8-other
Effectiveness and safety of hypnotic drugs in the treatment of insomnia in over 70-year old people.
PMID 17317444·Arch Gerontol Geriatr·2007
8-other
Analysis of candidate imprinted genes in PWS subjects with atypical genetics: a possible inactivating mutation in the SNURF/SNRPN minimal promoter.
PMID 17262171·J Hum Genet·2007
8-other
The course and outcome of psychiatric illness in people with Prader-Willi syndrome: implications for management and treatment.
PMID 17181601·J Intellect Disabil Res·2007
8-other
Identification of novel VHL targets that are associated with the development of renal cell carcinoma.
PMID 17001320·Oncogene·2007
8-other
The transmembrane protein meckelin (MKS3) is mutated in Meckel-Gruber syndrome and the wpk rat.
PMID 16415887·Nat Genet·2006
7-preclinical
Tumor suppressor activity and epigenetic inactivation of hepatocyte growth factor activator inhibitor type 2/SPINT2 in papillary and clear cell renal cell carcinoma.
PMID 15930277·Cancer Res·2005
7-preclinical
Identification of novel VHL target genes and relationship to hypoxic response pathways.
PMID 15824735·Oncogene·2005
8-other
Mutations of the catalytic subunit of RAB3GAP cause Warburg Micro syndrome.
PMID 15696165·Nat Genet·2005
8-other
Molecular genetic analysis of FIH-1, FH, and SDHB candidate tumour suppressor genes in renal cell carcinoma.
PMID 15220362·J Clin Pathol·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 10065 - Phone
- (212) 639-2000
Quick Facts
- NPI
- 1790041960
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 14
- Publications
- 13
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