PubRank

Sarah A Pendergrass

Author PubWeight™ 32.90‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data. Nat Biotechnol 2013 4.85
2 Molecular subsets in the gene expression signatures of scleroderma skin. PLoS One 2008 2.66
3 A core MYC gene expression signature is prominent in basal-like breast cancer but only partially overlaps the core serum response. PLoS One 2009 2.29
4 Genetic determinants of lipid traits in diverse populations from the population architecture using genomics and epidemiology (PAGE) study. PLoS Genet 2011 2.13
5 A phenomics-based strategy identifies loci on APOC1, BRAP, and PLCG1 associated with metabolic syndrome phenotype domains. PLoS Genet 2011 1.35
6 Consistent directions of effect for established type 2 diabetes risk variants across populations: the population architecture using Genomics and Epidemiology (PAGE) Consortium. Diabetes 2012 1.31
7 Genome-wide analysis of mRNAs bound to the histone stem-loop binding protein. RNA 2006 1.25
8 Genomic analyses with biofilter 2.0: knowledge driven filtering, annotation, and model development. BioData Min 2013 1.15
9 Visualizing genomic information across chromosomes with PhenoGram. BioData Min 2013 1.08
10 Leveraging Epidemiologic and Clinical Collections for Genomic Studies of Complex Traits. Hum Hered 2015 1.00
11 Comparative evaluation of strain-based and model-based modulus elastography. Ultrasound Med Biol 2005 0.98
12 Environment-wide association study (EWAS) for type 2 diabetes in the Marshfield Personalized Medicine Research Project Biobank. Pac Symp Biocomput 2014 0.98
13 Antagonistic effect of the matricellular signaling protein CCN3 on TGF-beta- and Wnt-mediated fibrillinogenesis in systemic sclerosis and Marfan syndrome. J Invest Dermatol 2010 0.97
14 Characterization of mitochondrial haplogroups in a large population-based sample from the United States. Hum Genet 2014 0.96
15 Association of the FTO obesity risk variant rs8050136 with percentage of energy intake from fat in multiple racial/ethnic populations: the PAGE study. Am J Epidemiol 2013 0.94
16 Enabling high-throughput genotype-phenotype associations in the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) project as part of the Population Architecture using Genomics and Epidemiology (PAGE) study. Pac Symp Biocomput 2013 0.93
17 ATHENA: the analysis tool for heritable and environmental network associations. Bioinformatics 2013 0.90
18 BioBin: a bioinformatics tool for automating the binning of rare variants using publicly available biological knowledge. BMC Med Genomics 2013 0.90
19 Genetic variants associated with fasting glucose and insulin concentrations in an ethnically diverse population: results from the Population Architecture using Genomics and Epidemiology (PAGE) study. BMC Med Genet 2013 0.84
20 Genomic architecture of pharmacological efficacy and adverse events. Pharmacogenomics 2014 0.83
21 Using BioBin to explore rare variant population stratification. Pac Symp Biocomput 2013 0.81
22 Polygenic heritability estimates in pharmacogenetics: focus on asthma and related phenotypes. Pharmacogenet Genomics 2013 0.80
23 The detection and characterization of pleiotropy: discovery, progress, and promise. Brief Bioinform 2015 0.78
24 Multiancestral analysis of inflammation-related genetic variants and C-reactive protein in the population architecture using genomics and epidemiology study. Circ Cardiovasc Genet 2014 0.77
25 PHENOME-WIDE INTERACTION STUDY (PheWIS) IN AIDS CLINICAL TRIALS GROUP DATA (ACTG). Pac Symp Biocomput 2016 0.75
26 INTEGRATING CLINICAL LABORATORY MEASURES AND ICD-9 CODE DIAGNOSES IN PHENOME-WIDE ASSOCIATION STUDIES. Pac Symp Biocomput 2016 0.75
27 Multiphenotype association study of patients randomized to initiate antiretroviral regimens in AIDS Clinical Trials Group protocol A5202. Pharmacogenet Genomics 2017 0.75
28 IDENTIFYING GENETIC ASSOCIATIONS WITH VARIABILITY IN METABOLIC HEALTH AND BLOOD COUNT LABORATORY VALUES: DIVING INTO THE QUANTITATIVE TRAITS BY LEVERAGING LONGITUDINAL DATA FROM AN EHR. Pac Symp Biocomput 2016 0.75
29 OPENING THE DOOR TO THE LARGE SCALE USE OF CLINICAL LAB MEASURES FOR ASSOCIATION TESTING: EXPLORING DIFFERENT METHODS FOR DEFINING PHENOTYPES. Pac Symp Biocomput 2016 0.75
30 Next-generation analysis of cataracts: determining knowledge driven gene-gene interactions using biofilter, and gene-environment interactions using the Phenx Toolkit*. Pac Symp Biocomput 2015 0.75
31 PATTERNS IN BIOMEDICAL DATA-HOW DO WE FIND THEM? Pac Symp Biocomput 2016 0.75