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ELLEN MAHER, M.D.
M.D.
Internal Medicine Physician
NPI: 1447637038IndividualAccepts Medicare
Specialties, Licenses & Credentials
Pediatrics Physician
Pediatrics
Code: 208000000X
2019-01266(NC)88889(SC)
Internal Medicine PhysicianPrimary
Internal Medicine
Code: 207R00000X
2019-01266(NC)88889(SC)
CMS Specialties
PrimaryINTERNAL MEDICINE
Education
MEDICAL UNIVERSITY OF SOUTH CAROLINA COLLEGE OF MEDICINE
Class of 2015
Research & Publications (20)
Preschool child care participation and obesity at the start of kindergarten.
PMID 18676550·Pediatrics·2008
4-observational
Marked genomic differences characterize primary and secondary glioblastoma subtypes and identify two distinct molecular and clinical secondary glioblastoma entities.
PMID 17114236·Cancer Res·2006
4-observational
Epigenetic risks related to assisted reproductive technologies: epigenetics, imprinting, ART and icebergs?
PMID 14645164·Hum Reprod·2003
8-other
Social status determinants of control in individuals' accounts of their mental illness.
PMID 12220096·Soc Sci Med·2002
8-other
The pressure rises: update on the genetics of phaeochromocytoma.
PMID 12351569·Hum Mol Genet·2002
6-review
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
RAN GTPase is a RASSF1A effector involved in controlling microtubule organization.
PMID 19559616·Curr Biol·2009
7-preclinical
The novel RASSF6 and RASSF10 candidate tumour suppressor genes are frequently epigenetically inactivated in childhood leukaemias.
PMID 19570220·Mol Cancer·2009
8-other
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
CpG methylation profiling in VHL related and VHL unrelated renal cell carcinoma.
PMID 19493342·Mol Cancer·2009
8-other
EGFRvIII and DNA double-strand break repair: a molecular mechanism for radioresistance in glioblastoma.
PMID 19435898·Cancer Res·2009
7-preclinical
Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataract.
PMID 19461930·Mol Vis·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
Patterns of complementary and alternative medicine use among patients undergoing cancer treatment.
PMID 19432919·Eur J Cancer Care (Engl)·2009
8-other
Brain metastasis: opportunities in basic and translational research.
PMID 19638593·Cancer Res·2009
7-preclinical
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
Frequent epigenetic inactivation of the SLIT2 gene in chronic and acute lymphocytic leukemia.
PMID 19550140·Epigenetics·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
Via practice · 2 locations total
- Address
- 171 ASHLEY AVE
CHARLESTON, SC 29425 - Phone
- (843) 792-1414
Quick Facts
- NPI
- 1447637038
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 4
- Locations
- 2
- Years in Practice
- 11
- Publications
- 20
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