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KIMBERLY FRAZER MD
MD
Family Medicine Physician
NPI: 1396713285IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
35071528F(OH)
Education
OHIO STATE UNIVERSITY COLLEGE OF MEDICINE
Class of 1995
Research & Publications (20)
Human genetic variation and its contribution to complex traits.
PMID 19293820·Nat Rev Genet·2009
6-review
Genomewide SNP variation reveals relationships among landraces and modern varieties of rice.
PMID 19597147·Proc Natl Acad Sci U S A·2009
8-other
Common vs. rare allele hypotheses for complex diseases.
PMID 19481926·Curr Opin Genet Dev·2009
6-review
Evaluation of next generation sequencing platforms for population targeted sequencing studies.
PMID 19327155·Genome Biol·2009
8-other
Method for improving sequence coverage uniformity of targeted genomic intervals amplified by LR-PCR using Illumina GA sequencing-by-synthesis technology.
PMID 19317667·Biotechniques·2009
8-other
Genome-wide scan identifies variation in MLXIPL associated with plasma triglycerides.
PMID 18193046·Nat Genet·2008
4-observational
The Zebrafish Information Network: the zebrafish model organism database provides expanded support for genotypes and phenotypes.
PMID 17991680·Nucleic Acids Res·2008
7-preclinical
A genome-wide approach to identifying novel-imprinted genes.
PMID 17955261·Hum Genet·2008
4-observational
Evaluation of the SNP tagging approach in an independent population sample--array-based SNP discovery in Sami.
PMID 17554563·Hum Genet·2007
4-observational
Genome-wide detection and characterization of positive selection in human populations.
PMID 17943131·Nature·2007
8-other
New models of collaboration in genome-wide association studies: the Genetic Association Information Network.
PMID 17728769·Nat Genet·2007
8-other
In vitro human keratinocyte migration rates are associated with SNPs in the KRT1 interval.
PMID 17668073·PLoS One·2007
8-other
Common sequence polymorphisms shaping genetic diversity in Arabidopsis thaliana.
PMID 17641193·Science·2007
8-other
A sequence-based variation map of 8.27 million SNPs in inbred mouse strains.
PMID 17660834·Nature·2007
7-preclinical
Common deletions and SNPs are in linkage disequilibrium in the human genome.
PMID 16327809·Nat Genet·2006
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
- 990 GALLOWAY RD
GALLOWAY, OH 43119 - Phone
- (614) 533-6770
Quick Facts
- NPI
- 1396713285
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 31
- Publications
- 20
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