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L CARDON, M.D.
M.D.
Family Medicine Physician
NPI: 1689608895Individual
Specialties, Licenses & Credentials
Family Medicine PhysicianPrimary
Family Medicine
Code: 207Q00000X
180572-1205(UT)
Research & Publications (20)
A large-scale genome-wide association study of Asian populations uncovers genetic factors influencing eight quantitative traits.
PMID 19396169·Nat Genet·2009
8-other
Risk prediction of prevalent diabetes in a Swiss population using a weighted genetic score--the CoLaus Study.
PMID 19139842·Diabetologia·2009
8-other
Repeat instability in the 27-39 CAG range of the HD gene in the Venezuelan kindreds: Counseling implications.
PMID 18712713·Am J Med Genet B Neuropsychiatr Genet·2009
8-other
Genome-wide association studies for complex traits: consensus, uncertainty and challenges.
PMID 18398418·Nat Rev Genet·2008
6-review
Fine mapping of the MHC Class III region demonstrates association of AIF1 and rheumatoid arthritis.
PMID 18835879·Rheumatology (Oxford)·2008
8-other
Goldsurfer2 (Gs2): a comprehensive tool for the analysis and visualization of genome wide association studies.
PMID 18318908·BMC Bioinformatics·2008
8-other
Genomewide linkage scan reveals novel loci modifying age of onset of Huntington's disease in the Venezuelan HD kindreds.
PMID 18481795·Genet Epidemiol·2008
8-other
Genetic determinants of ulcerative colitis include the ECM1 locus and five loci implicated in Crohn's disease.
PMID 18438406·Nat Genet·2008
4-observational
Population-based genome-wide association studies reveal six loci influencing plasma levels of liver enzymes.
PMID 18940312·Am J Hum Genet·2008
8-other
Genome-wide pharmacogenetic investigation of a hepatic adverse event without clinical signs of immunopathology suggests an underlying immune pathogenesis.
PMID 17505501·Pharmacogenomics J·2008
8-other
To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies?
PMID 18197186·Eur J Hum Genet·2008
8-other
The exon 1-8C/G SNP in the PSMA6 gene contributes only a small amount to the burden of myocardial infarction in 6946 cases and 2720 controls from a United Kingdom population.
PMID 18231128·Eur J Hum Genet·2008
8-other
Singleton SNPs in the human genome and implications for genome-wide association studies.
PMID 18197193·Eur J Hum Genet·2008
8-other
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease.
PMID 18587394·Nat Genet·2008
1-meta
Investigation of the fine structure of European populations with applications to disease association studies.
PMID 19020537·Eur J Hum Genet·2008
4-observational
Genetic susceptibility to cancer: the role of polymorphisms in candidate genes.
PMID 18505952·JAMA·2008
6-review
Evaluating the effects of imputation on the power, coverage, and cost efficiency of genome-wide SNP platforms.
PMID 18589396·Am J Hum Genet·2008
8-other
Designing candidate gene and genome-wide case-control association studies.
PMID 17947991·Nat Protoc·2007
8-other
Genome-wide detection and characterization of positive selection in human populations.
PMID 17943131·Nature·2007
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
- 975 CHAMBERS ST
SOUTH OGDEN, UT 84403 - Phone
- (801) 387-6200
Quick Facts
- NPI
- 1689608895
- Entity Type
- Individual
- Gender
- Male
- Medicare
- Not confirmed
- Specialties
- 1
- Locations
- 1
- Publications
- 20
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