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PETER RADICE, M.D.
M.D.
Hospice and Palliative Medicine (Internal Medicine) Physician
NPI: 1356339170IndividualAccepts Medicare
Specialties, Licenses & Credentials
Hospice and Palliative Medicine (Internal Medicine) PhysicianPrimary
Internal Medicine — Hospice and Palliative Medicine
Code: 207RH0002X
35.135935(OH)ME38243(FL)
Education
GEORGE WASHINGTON UNIVERSITY SCHOOL OF MEDICINE
Class of 1974
Research & Publications (20)
Lynch syndrome--related endometrial carcinomas show a high frequency of nonendometrioid types and of high FIGO grade endometrioid types.
PMID 19443869·Int J Surg Pathol·2010
8-other
Analysis of a set of missense, frameshift, and in-frame deletion variants of BRCA1.
PMID 18992264·Mutat Res·2009
8-other
Common variants in LSP1, 2q35 and 8q24 and breast cancer risk for BRCA1 and BRCA2 mutation carriers.
PMID 19656774·Hum Mol Genet·2009
4-observational
Evidences for association of the CASP8 -652 6N del promoter polymorphism with age at diagnosis in familial breast cancer cases.
PMID 18343995·Breast Cancer Res Treat·2009
8-other
SNPs in ultraconserved elements and familial breast cancer risk.
PMID 19126653·Carcinogenesis·2009
8-other
Nonfluorescent denaturing HPLC-based primer-extension method for allele-specific expression: application to analysis of mismatch repair genes.
PMID 19628660·Clin Chem·2009
4-observational
Reproductive and hormonal factors, and ovarian cancer risk for BRCA1 and BRCA2 mutation carriers: results from the International BRCA1/2 Carrier Cohort Study.
PMID 19190154·Cancer Epidemiol Biomarkers Prev·2009
4-observational
A novel WT1 mutation in a 46,XY boy with congenital bilateral cryptorchidism, nystagmus and Wilms tumor.
PMID 19048299·Pediatr Nephrol·2009
5-case
Common breast cancer-predisposition alleles are associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers.
PMID 18355772·Am J Hum Genet·2008
4-observational
Functional inactivation of the WTX gene is not a frequent event in Wilms' tumors.
PMID 18391980·Oncogene·2008
8-other
Cyclin D1 expression analysis in familial breast cancers may discriminate BRCAX from BRCA2-linked cases.
PMID 18327210·Mod Pathol·2008
8-other
The BOADICEA model of genetic susceptibility to breast and ovarian cancers: updates and extensions.
PMID 18349832·Br J Cancer·2008
8-other
BRCA1 p.Val1688del is a deleterious mutation that recurs in breast and ovarian cancer families from Northeast Italy.
PMID 18165637·J Clin Oncol·2008
4-observational
Reconstructing the genealogy of a BRCA1 founder mutation by phylogenetic analysis.
PMID 18215206·Ann Hum Genet·2008
8-other
Prediction and assessment of splicing alterations: implications for clinical testing.
PMID 18951448·Hum Mutat·2008
8-other
The p53 Arg72Pro and Ins16bp polymorphisms and their haplotypes are not associated with breast cancer risk in BRCA-mutation negative familial cases.
PMID 18640791·Cancer Detect Prev·2008
8-other
Molecular evidence of the independent origin of multiple Wilms tumors in a case of WAGR syndrome.
PMID 18293378·Pediatr Blood Cancer·2008
5-case
Re: Molecular basis for estrogen receptor alpha deficiency in BRCA1-linked breast cancer.
PMID 18477803·J Natl Cancer Inst·2008
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 · 3 locations total
- Address
- 4031 COLONEL GLENN HWY, SUITE 133
BEAVERCREEK, OH 45431 - Phone
- (855) 232-0644
Quick Facts
- NPI
- 1356339170
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Accepted
- Specialties
- 2
- Locations
- 3
- Years in Practice
- 52
- Publications
- 20
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