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RACHEL MCGINNIS, DO
DO
Family Medicine Physician
NPI: 1083746119IndividualAccepts Medicare
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
N2631(TX)
CMS Specialties
PrimaryFAMILY PRACTICE
Education
NEW YORK COLLEGE OF OSTEO MEDICINE OF NEW YORK INSTITUTE OF TECHNOLOGY
Class of 2006
Research & Publications (20)
The largest prospective warfarin-treated cohort supports genetic forecasting.
PMID 18574025·Blood·2009
4-observational
Large scale association analysis of novel genetic loci for coronary artery disease.
PMID 19164808·Arterioscler Thromb Vasc Biol·2009
4-observational
A genome-wide association study confirms VKORC1, CYP2C9, and CYP4F2 as principal genetic determinants of warfarin dose.
PMID 19300499·PLoS Genet·2009
8-other
Detection of breast cancer with full-field digital mammography and computer-aided detection.
PMID 19155392·AJR Am J Roentgenol·2009
8-other
Haplotype-based search for SNPs associated with differential type 1 diabetes risk among chromosomes carrying a specific HLA DRB1-DQA1-DQB1 haplotype.
PMID 19143810·Diabetes Obes Metab·2009
8-other
Measurement of airborne particle concentrations near the Sunset Crater volcano, Arizona.
PMID 19131732·Health Phys·2009
8-other
Repeated replication and a prospective meta-analysis of the association between chromosome 9p21.3 and coronary artery disease.
PMID 18362232·Circulation·2008
4-observational
Global challenges in energy and water supply: the promise of engineered osmosis.
PMID 19192773·Environ Sci Technol·2008
8-other
Common variants near MC4R are associated with fat mass, weight and risk of obesity.
PMID 18454148·Nat Genet·2008
4-observational
Newly identified genetic risk variants for celiac disease related to the immune response.
PMID 18311140·Nat Genet·2008
7-preclinical
Interactions among genes in the ErbB-Neuregulin signalling network are associated with increased susceptibility to schizophrenia.
PMID 17598910·Behav Brain Funct·2007
8-other
Merging two universities: the Medical University of Ohio and the University of Toledo.
PMID 18046124·Acad Med·2007
8-other
Association scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variants.
PMID 17952073·Nat Genet·2007
2-rct
A genome-wide association study for celiac disease identifies risk variants in the region harboring IL2 and IL21.
PMID 17558408·Nat Genet·2007
7-preclinical
Association of warfarin dose with genes involved in its action and metabolism.
PMID 17048007·Hum Genet·2007
8-other
Characterization of common genetic variants in cathepsin K and testing for association with bone mineral density in a large cohort of perimenopausal women from Scotland.
PMID 14753734·J Bone Miner Res·2004
8-other
Effect of low-carbohydrate, unlimited calorie diet on the treatment of childhood obesity: a prospective controlled study.
PMID 18370665·Metab Syndr Relat Disord·2003
8-other
Power and efficiency of the TDT and case-control design for association scans.
PMID 12036111·Behav Genet·2002
4-observational
Data courtesy of the U.S. National Library of Medicine (NLM). Ltrl is not affiliated with or endorsed by NLM.
Contact & Hours
- Address
- 1340 WONDER WORLD DR STE 2300
SAN MARCOS, TX 78666 - Phone
- (512) 654-4900
Quick Facts
- NPI
- 1083746119
- Entity Type
- Individual
- Gender
- Female
- Medicare
- Accepted
- Specialties
- 1
- Locations
- 1
- Years in Practice
- 20
- Publications
- 20
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