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ELIZABETH MAHER, MD
MD
Ophthalmic Plastic and Reconstructive Surgery Physician
NPI: 1275547945IndividualAccepts Medicare
Specialties, Licenses & Credentials
Ophthalmology Physician
Ophthalmology
Code: 207W00000X
162782(NY)
Ophthalmic Plastic and Reconstructive Surgery PhysicianPrimary
Ophthalmology — Ophthalmic Plastic and Reconstructive Surgery
Code: 207WX0200X
162782-1(NY)
CMS Specialties
PrimaryOPHTHALMOLOGY
Education
HARVARD MEDICAL SCHOOL
Class of 1984
Research & Publications (20)
An immunohistochemical procedure to detect patients with paraganglioma and phaeochromocytoma with germline SDHB, SDHC, or SDHD gene mutations: a retrospective and prospective analysis.
PMID 19576851·Lancet Oncol·2009
3-trial
The novel RASSF6 and RASSF10 candidate tumour suppressor genes are frequently epigenetically inactivated in childhood leukaemias.
PMID 19570220·Mol Cancer·2009
8-other
Brain metastasis: opportunities in basic and translational research.
PMID 19638593·Cancer Res·2009
7-preclinical
Analysis of germline variants in CDH1, IGFBP3, MMP1, MMP3, STK15 and VEGF in familial and sporadic renal cell carcinoma.
PMID 19551141·PLoS One·2009
8-other
Frequent epigenetic inactivation of the SLIT2 gene in chronic and acute lymphocytic leukemia.
PMID 19550140·Epigenetics·2009
8-other
CpG methylation profiling in VHL related and VHL unrelated renal cell carcinoma.
PMID 19493342·Mol Cancer·2009
8-other
Homozygous loss-of-function mutations in the gene encoding the dopamine transporter are associated with infantile parkinsonism-dystonia.
PMID 19478460·J Clin Invest·2009
7-preclinical
RAN GTPase is a RASSF1A effector involved in controlling microtubule organization.
PMID 19559616·Curr Biol·2009
7-preclinical
EGFRvIII and DNA double-strand break repair: a molecular mechanism for radioresistance in glioblastoma.
PMID 19435898·Cancer Res·2009
7-preclinical
Patterns of complementary and alternative medicine use among patients undergoing cancer treatment.
PMID 19432919·Eur J Cancer Care (Engl)·2009
8-other
X-linked cataract and Nance-Horan syndrome are allelic disorders.
PMID 19414485·Hum Mol Genet·2009
8-other
Increased colorectal cancer incidence in obligate carriers of heterozygous mutations in MUTYH.
PMID 19394335·Gastroenterology·2009
4-observational
Automating Giemsa banding of chromosomes: protocol for and evaluation of the use of a programmable, high-throughput automatic stainer.
PMID 19384744·Biotech Histochem·2009
8-other
Proteomic identification of differentially expressed plasma membrane proteins in renal cell carcinoma by stable isotope labelling of a von Hippel-Lindau transfectant cell line model.
PMID 19337990·Proteomics·2009
8-other
Germline mutation in NLRP2 (NALP2) in a familial imprinting disorder (Beckwith-Wiedemann Syndrome).
PMID 19300480·PLoS Genet·2009
8-other
Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataract.
PMID 19461930·Mol Vis·2009
8-other
Germline mutation in DOK7 associated with fetal akinesia deformation sequence.
PMID 19261599·J Med Genet·2009
8-other
Excision of periocular basal cell carcinoma with stereoscopic microdissection of surgical margins for frozen-section control: report of 200 cases.
PMID 19667338·Arch Ophthalmol·2009
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
- 36 E 36TH ST
NEW YORK, NY 10016 - Phone
- (212) 353-0030
Quick Facts
- NPI
- 1275547945
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 42
- Publications
- 20
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