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GEORGE LATHROP, MD
MD
Emergency Medicine Physician
NPI: 1265526222Individual
Specialties, Licenses & Credentials
Emergency Medicine PhysicianPrimary
Emergency Medicine
Code: 207P00000X
01058752(IN)
Research & Publications (20)
U.S. allopathic emergency medicine residency programs: a descriptive review.
PMID 12896896·Acad Emerg Med·2003
6-review
Genome-wide association study identifies three loci associated with melanoma risk.
PMID 19578364·Nat Genet·2009
8-other
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distribution.
PMID 19557161·PLoS Genet·2009
1-meta
Genome-wide association study identifies eight loci associated with blood pressure.
PMID 19430483·Nat Genet·2009
8-other
Polymorphisms in the WNK1 gene are associated with blood pressure variation and urinary potassium excretion.
PMID 19347040·PLoS One·2009
8-other
Genome-wide scan reveals association of psoriasis with IL-23 and NF-kappaB pathways.
PMID 19169254·Nat Genet·2009
8-other
Newly identified loci that influence lipid concentrations and risk of coronary artery disease.
PMID 18193043·Nat Genet·2008
1-meta
Genome-wide association study identifies genes for biomarkers of cardiovascular disease: serum urate and dyslipidemia.
PMID 18179892·Am J Hum Genet·2008
1-meta
Genetic and haplotypic structure in 14 European and African cattle breeds.
PMID 17720924·Genetics·2007
7-preclinical
Genetic variants regulating ORMDL3 expression contribute to the risk of childhood asthma.
PMID 17611496·Nature·2007
8-other
Linkage analysis using co-phenotypes in the BRIGHT study reveals novel potential susceptibility loci for hypertension.
PMID 16826522·Am J Hum Genet·2006
8-other
Two-dimensional genome-scan identifies novel epistatic loci for essential hypertension.
PMID 16543358·Hum Mol Genet·2006
8-other
Haplotypes of the WNK1 gene associate with blood pressure variation in a severely hypertensive population from the British Genetics of Hypertension study.
PMID 15888480·Hum Mol Genet·2005
8-other
A variant in the CD209 promoter is associated with severity of dengue disease.
PMID 15838506·Nat Genet·2005
8-other
Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity.
PMID 15220213·Diabetes·2004
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
- 2001 W 86TH ST
INDIANAPOLIS, IN 46260 - Phone
- (317) 802-3140
Quick Facts
- NPI
- 1265526222
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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