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ERIC MAHER, D.O.
D.O.
Family Medicine Physician
NPI: 1487094280IndividualAccepts Medicare
Specialties, Licenses & Credentials
Student in an Organized Health Care Education/Training Program
Student in an Organized Health Care Education/Training Program
Code: 390200000X
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
20A13765(CA)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
OTHER
Class of 2013
Research & Publications (20)
Brain metastasis: opportunities in basic and translational research.
PMID 19638593·Cancer Res·2009
7-preclinical
Preschool child care participation and obesity at the start of kindergarten.
PMID 18676550·Pediatrics·2008
4-observational
Survivorship, late effects and cancer of the cervix.
PMID 18515052·Clin Oncol (R Coll Radiol)·2008
6-review
An integrated support and information centre in a large U.K. Cancer Centre established in 1993 and replicated in more than 60 units across the United Kingdom and Australia.
PMID 18769579·Curr Oncol·2008
8-other
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
The pressure rises: update on the genetics of phaeochromocytoma.
PMID 12351569·Hum Mol Genet·2002
6-review
Beckwith-Wiedemann syndrome: imprinting in clusters revisited.
PMID 10675349·J Clin Invest·2000
6-review
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
RAN GTPase is a RASSF1A effector involved in controlling microtubule organization.
PMID 19559616·Curr Biol·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
CpG methylation profiling in VHL related and VHL unrelated renal cell carcinoma.
PMID 19493342·Mol Cancer·2009
8-other
Frequent epigenetic inactivation of the SLIT2 gene in chronic and acute lymphocytic leukemia.
PMID 19550140·Epigenetics·2009
8-other
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
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
The novel RASSF6 and RASSF10 candidate tumour suppressor genes are frequently epigenetically inactivated in childhood leukaemias.
PMID 19570220·Mol Cancer·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
- 685 MORRO AVE STE C
MORRO BAY, CA 93442 - Phone
- (805) 772-7313
Quick Facts
- NPI
- 1487094280
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 1
- Years in Practice
- 13
- Publications
- 20
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