PubRank

Suzette J Bielinski

Author PubWeight™ 57.36‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Genetic variation in GIPR influences the glucose and insulin responses to an oral glucose challenge. Nat Genet 2010 6.66
2 Electronic medical records for genetic research: results of the eMERGE consortium. Sci Transl Med 2011 5.82
3 The interleukin-6 receptor as a target for prevention of coronary heart disease: a mendelian randomisation analysis. Lancet 2012 4.87
4 Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data. Nat Biotechnol 2013 4.85
5 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 2011 4.20
6 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 2011 3.85
7 NRXN3 is a novel locus for waist circumference: a genome-wide association study from the CHARGE Consortium. PLoS Genet 2009 3.18
8 Validation of electronic medical record-based phenotyping algorithms: results and lessons learned from the eMERGE network. J Am Med Inform Assoc 2013 3.00
9 Atrial fibrillation and death after myocardial infarction: a community study. Circulation 2011 2.63
10 Association of a fasting glucose genetic risk score with subclinical atherosclerosis: The Atherosclerosis Risk in Communities (ARIC) study. Diabetes 2010 1.71
11 Atrial fibrillation in myocardial infarction patients: Impact on health care utilization. Am Heart J 2013 1.40
12 Variation in TCF7L2 and increased risk of colon cancer: the Atherosclerosis Risk in Communities (ARIC) Study. Diabetes Care 2008 1.37
13 Impact of repeated measures and sample selection on genome-wide association studies of fasting glucose. Genet Epidemiol 2010 1.34
14 Pitfalls of merging GWAS data: lessons learned in the eMERGE network and quality control procedures to maintain high data quality. Genet Epidemiol 2011 1.26
15 Applying semantic web technologies for phenome-wide scan using an electronic health record linked Biobank. J Biomed Semantics 2012 1.20
16 An information extraction framework for cohort identification using electronic health records. AMIA Jt Summits Transl Sci Proc 2013 1.14
17 High density GWAS for LDL cholesterol in African Americans using electronic medical records reveals a strong protective variant in APOE. Clin Transl Sci 2012 1.13
18 Electrophysiological and hemodynamic characteristics associated with obesity in patients with atrial fibrillation. J Am Coll Cardiol 2012 1.01
19 Association of sICAM-1 and MCP-1 with coronary artery calcification in families enriched for coronary heart disease or hypertension: the NHLBI Family Heart Study. BMC Cardiovasc Disord 2007 1.00
20 Common coding variants of the HNF1A gene are associated with multiple cardiovascular risk phenotypes in community-based samples of younger and older European-American adults: the Coronary Artery Risk Development in Young Adults Study and The Cardiovascular Health Study. Circ Cardiovasc Genet 2009 0.96
21 Circulating soluble intercellular adhesion molecule 1 and subclinical atherosclerosis: the Coronary Artery Risk Development in Young Adults Study. Clin Chem 2011 0.93
22 Mining the human phenome using semantic web technologies: a case study for Type 2 Diabetes. AMIA Annu Symp Proc 2012 0.92
23 Genome-wide and gene-centric analyses of circulating myeloperoxidase levels in the charge and care consortia. Hum Mol Genet 2013 0.86
24 Hospitalizations and emergency department use in Mayo Clinic Biobank participants within the employee and community health medical home. Mayo Clin Proc 2013 0.81
25 Role of BMI in the Association of the TCF7L2 rs7903146 Variant with Coronary Heart Disease: The Atherosclerosis Risk in Communities (ARIC) Study. J Obes 2010 0.79
26 Multi-ethnic analysis reveals soluble L-selectin may be post-transcriptionally regulated by 3'UTR polymorphism: the Multi-Ethnic Study of Atherosclerosis (MESA). Hum Genet 2015 0.78
27 Genotype, echocardiography, and survival in familial transthyretin amyloidosis. Amyloid 2013 0.76
28 Association of TNFSF8 polymorphisms with peripheral neutrophil count. Mayo Clin Proc 2011 0.75