Teri Manolio
Genetics · 2003–2017
A researcher in the Science corpus: 15 papers; trusts 5 researchers and is trusted by 17 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 220 citations into it; #757 of 6,854 by trust here, #114 by citations
- Molecular Biology — 133 citations into it; #16,241 of 17,773 by trust here, #1,185 by citations
- Rheumatology — 15 citations into it
- Plant Science — 14 citations into it
Whom Teri Manolio trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Michael Olivier
- John Hardy
- David Reich
- J. K. Pritchard
- David B. Goldstein
- Peter M. Visscher
- Joel Hirschhorn
- Eric S. Lander
Who trusts Teri Manolio overall
- Yan V. Sun
- Yijuan Hu
- Peter M. Visscher
- Or Zuk
- Jian Yang
- Naomi R. Wray
- Sang Hong Lee
- Wei-Qi Wei
- Greg Gibson
- Jishnu Das
Papers from Teri Manolio's perspective
Ordered by how strongly the researchers Teri Manolio trusts endorse each paper. Same corpus, a different order for every researcher.
- A frameshift mutation in NOD2 associated with susceptibility to Crohn's disease (Nature)
- Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn's disease (Nature)
- Principal components analysis corrects for stratification in genome-wide association studies
- A genome-wide association study identifies novel risk loci for type 2 diabetes (Nature)
- PLINK: a tool set for whole-genome association and population-based linkage analyses.
- The human genome browser at UCSC.
- Complement Factor H Variant Increases the Risk of Age-Related Macular Degeneration (Science)
- Hepatocyte Nuclear Factor 4α (Nuclear Receptor 2A1) Is Essential for Maintenance of Hepatic Gene Expression and Lipid Homeostasis (Molecular and Cellular Biology)
- Large-scale association analyses identifies 13 new susceptibility loci for coronary artery disease (Nature Genetics)
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
Their papers
- Potential etiologic and functional implications of genome-wide association loci for human diseases and traits (2009) — 4,227 citations
- The NHGRI GWAS Catalog, a curated resource of SNP-trait associations (2013) — 2,838 citations
- Electronic Medical Records for Genetic Research: Results of the eMERGE Consortium (2011) — 351 citations
- Replicating genotype–phenotype associations (2007) — 1,394 citations
- Systematic comparison of phenome-wide association study of electronic medical record data and genome-wide association study data (2013) — 986 citations
- Prioritizing diversity in human genomics research (2017) — 332 citations
- Genome- and Phenome-Wide Analysis of Cardiac Conduction Identifies Markers of Arrhythmia Risk (2013) — 177 citations
- Human polymorphism at microRNAs and microRNA target sites. (2013) — 605 citations
- Assuring the quality of next-generation sequencing in clinical laboratory practice (2012) — 463 citations
- Genomewide association studies and assessment of the risk of disease. (2010) — 1,615 citations
- Finding the missing heritability of complex diseases (2009) — 8,360 citations
- A HapMap harvest of insights into the genetics of common disease. (2008) — 956 citations
- Heart disease and stroke statistics--2006 update: a report from the American Heart Association Statistics Committee and Stroke Statistics Subcommittee. (2006) — 3,353 citations
- Cardiovascular mortality risk in chronic kidney disease: comparison of traditional and novel risk factors. (2005) — 776 citations
- Elevations of Inflammatory and Procoagulant Biomarkers in Elderly Persons With Renal Insufficiency (2003) — 802 citations