Ruth J. F. Loos
Nature Genetics · 2006–2021
A researcher in the Science corpus: 39 papers; trusts 0 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Whom Ruth J. F. Loos trusts overall
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Who trusts Ruth J. F. Loos overall
Papers from Ruth J. F. Loos's perspective
Ordered by how strongly the researchers Ruth J. F. Loos trusts endorse each paper. Same corpus, a different order for every researcher.
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- Comparison of abdominal adiposity and overall obesity in predicting risk of type 2 diabetes among men. (American Journal of Clinical Nutrition)
- Defining the role of common variation in the genomic and biological architecture of adult human height
- Estimating Effects and Making Predictions from Genome-Wide Marker Data
- General and abdominal adiposity and risk of death in Europe. (New England Journal of Medicine)
- Acquired and inherited lipodystrophies. (New England Journal of Medicine)
- Finding the missing heritability of complex diseases (Nature)
- Efficient Bayesian mixed model analysis increases association power in large cohorts
- Assumption-Free Estimation of Heritability from Genome-Wide Identity-by-Descent Sharing between Full Siblings (PLoS Genetics)
- Fast and accurate long-range phasing in a UK Biobank cohort
Their papers
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) — 1,941 citations
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease (2015) — 2,034 citations
- Association analyses based on false discovery rate implicate new loci for coronary artery disease (2017) — 631 citations
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations
- The genetics of obesity: from discovery to biology (2021) — 971 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
- Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
- A structural variation reference for medical and population genetics (2020) — 876 citations
- The Polygenic and Monogenic Basis of Blood Traits and Diseases (2020) — 602 citations
- Recovery of trait heritability from whole genome sequence data (2019) — 222 citations
- Human loss-of-function variants suggest that partial LRRK2 inhibition is a safe therapeutic strategy for Parkinson’s disease (2019) — 13 citations
- Genomic Risk Prediction of Coronary Artery Disease in 480,000 Adults Implications for Primary Prevention (2019)
- Genetic analyses of diverse populations improves discovery for complex traits (2019) — 901 citations
- Evaluating drug targets through human loss-of-function genetic variation (2019) — 168 citations
- Associations of autozygosity with a broad range of human phenotypes (2019) — 112 citations
- A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) — 744 citations
- Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry (2018) — 1,022 citations
- Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traits (2018) — 1,148 citations