Novel common and rare genetic determinants of paraoxonase activity: FTO, SERPINA12, and ITGAL.
J. Lipid Res., Nov (2012)
High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE.
Clin Transl Sci., Oct;5(5):394-9 (2012)
Large-Scale Gene-Centric Meta-analysis across 32 Studies Identifies Multiple Lipid Loci.
Am. J. Hum. Genet., Nov;91(5):823-38 (2012)
Results of genome-wide analyses on neurodevelopmental phenotypes at four-year follow-up following cardiac surgery in infancy.
PLoS ONE., 7(9):e45936 (2012)
Leveraging the electronic health record to implement genomic medicine.
Genet. Med., Sep (2012)
Beneficence, clinical urgency, and the return of individual research results to relatives.
Am J Bioeth., 12(10):9-10 (2012)
Dietary cholesterol increases paraoxonase 1 enzyme activity.
J. Lipid Res., Nov;53(11):2450-8 (2012)
Additional Common Polymorphisms in the PON Gene Cluster Predict PON1 Activity but Not Vascular Disease.
J Lipids., 2012:476316 (2012)
ColoSeq provides comprehensive lynch and polyposis syndrome mutational analysis using massively parallel sequencing.
J Mol Diagn., Jul;14(4):357-66 (2012)
Detectable clonal mosaicism from birth to old age and its relationship to cancer.
Nat. Genet., Jun;44(6):642-50 (2012)
Genetic Loci implicated in erythroid differentiation and cell cycle regulation are associated with red blood cell traits.
Mayo Clin. Proc., May;87(5):461-74 (2012)
Return of individual research results from genome-wide association studies: experience of the Electronic Medical Records and Genomics (eMERGE) Network.
Genet. Med., Apr;14(4):424-31 (2012)
Large-scale gene-centric meta-analysis across 39 studies identifies type 2 diabetes loci.
Am. J. Hum. Genet., Mar;90(3):410-25 (2012)
Technical desiderata for the integration of genomic data into Electronic Health Records.
J Biomed Inform., Jun;45(3):419-22 (2012)
Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality.
Genet. Epidemiol., Dec;35(8):887-98 (2011)
Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study.
J Am Med Inform Assoc., 19(2):212-8 (2012 Mar-Apr)
Genetic variants associated with the white blood cell count in 13,923 subjects in the eMERGE Network.
Hum. Genet., Apr;131(4):639-52 (2012)
Variants near FOXE1 are associated with hypothyroidism and other thyroid conditions: using electronic medical records for genome- and phenome-wide studies.
Am. J. Hum. Genet., Oct;89(4):529-42 (2011)
Follow-up of carriers of BRCA1 and BRCA2 variants of unknown significance: variant reclassification and surgical decisions.
Genet. Med., Dec;13(12):998-1005 (2011)
Linkage and association of phospholipid transfer protein activity to LASS4.
J. Lipid Res., Oct;52(10):1837-46 (2011)