Back to Search
DAVID EASTON, D.O
D.O
Family Medicine Physician
NPI: 1053354589Individual
Specialties, Licenses & Credentials
Research & Publications (20)
Consortium analysis of 7 candidate SNPs for ovarian cancer.
PMID 18431743·Int J Cancer·2008
4-observational
A systematic genetic assessment of 1,433 sequence variants of unknown clinical significance in the BRCA1 and BRCA2 breast cancer-predisposition genes.
PMID 17924331·Am J Hum Genet·2007
8-other
Genome-wide association study identifies novel breast cancer susceptibility loci.
PMID 17529967·Nature·2007
8-other
Where are the prostate cancer genes?--A summary of eight genome wide searches.
PMID 14601022·Prostate·2003
8-other
Prostate cancer segregation analyses using 4390 families from UK and Australian population-based studies.
PMID 19492347·Genet Epidemiol·2010
8-other
Common germline polymorphisms in COMT, CYP19A1, ESR1, PGR, SULT1E1 and STS and survival after a diagnosis of breast cancer.
PMID 19551860·Int J Cancer·2009
4-observational
Younger age-at-diagnosis for familial malignant testicular germ cell tumor.
PMID 19609727·Fam Cancer·2009
4-observational
Eligibility for magnetic resonance imaging screening in the United Kingdom: effect of strict selection criteria and anonymous DNA testing on breast cancer incidence in the MARIBS Study.
PMID 19567506·Cancer Epidemiol Biomarkers Prev·2009
4-observational
Five polymorphisms and breast cancer risk: results from the Breast Cancer Association Consortium.
PMID 19423537·Cancer Epidemiol Biomarkers Prev·2009
4-observational
Seq4SNPs: new software for retrieval of multiple, accurately annotated DNA sequences, ready formatted for SNP assay design.
PMID 19523221·BMC Bioinformatics·2009
8-other
Risk of estrogen receptor-positive and -negative breast cancer and single-nucleotide polymorphism 2q35-rs13387042.
PMID 19567422·J Natl Cancer Inst·2009
4-observational
Genetic variation in the chromosome 17q23 amplicon and breast cancer risk.
PMID 19454617·Cancer Epidemiol Biomarkers Prev·2009
8-other
A genome-wide association study identifies a new ovarian cancer susceptibility locus on 9p22.2.
PMID 19648919·Nat Genet·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
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation.
PMID 19377476·Nat Genet·2009
8-other
Association between common germline genetic variation in 94 candidate genes or regions and risks of invasive epithelial ovarian cancer.
PMID 19543528·PLoS One·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
- 8767 GRATIOT RD
SAGINAW, MI 48609 - Phone
- (989) 781-1124
Quick Facts
- NPI
- 1053354589
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
Are you this provider?
Claim Your Profile