Samuli Ripatti
Nature Genetics · 2008–2023
A researcher in the Science corpus: 38 papers; trusts 0 researchers and is trusted by 1 researcher here, as inferred from the citation graph.
Who trusts Samuli Ripatti
- Chris Wallace (in Genetics)
Papers from Samuli Ripatti's perspective
Ordered by how strongly the researchers Samuli Ripatti trusts endorse each paper. Same corpus, a different order for every researcher.
- Next-generation genotype imputation service and methods (Nature Genetics)
- A global reference for human genetic variation
- The support of human genetic evidence for approved drug indications (Nature Genetics)
- Clinical use of current polygenic risk scores may exacerbate health disparities
- Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood (Bioinform.)
- Assessing the impact of population stratification on genetic association studies (Nature Genetics)
- Fast and accurate long-range phasing in a UK Biobank cohort
- Partitioning heritability by functional annotation using genome-wide association summary statistics (Nature Genetics)
- THE CONTROL OF THE FALSE DISCOVERY RATE IN MULTIPLE TESTING UNDER DEPENDENCY
- The human genome browser at UCSC.
Their papers
- Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
- Systematic identification of trans-eQTLs as putative drivers of known disease associations (2013) — 1,732 citations
- FINEMAP: efficient variable selection using summary data from genome-wide association studies (2015) — 774 citations
- The transcriptional landscape of age in human peripheral blood (2015) — 654 citations
- Unraveling the polygenic architecture of complex traits using blood eQTL metaanalysis (2018) — 511 citations
- A comprehensive 1000 Genomes-based genome-wide association meta-analysis of coronary artery disease (2015) — 2,034 citations
- Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA (2016) — 691 citations
- Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression (2021) — 1,862 citations
- Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population (2014) — 412 citations
- Characterising the loss-of-function impact of 5’ untranslated region variants in 15,708 individuals (2019) — 162 citations
- FinnGen provides genetic insights from a well-phenotyped isolated population (2023) — 3,553 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
- Genetics of 35 blood and urine biomarkers in the UK Biobank (2021) — 673 citations
- Landscape of multi-nucleotide variants in 125,748 human exomes and 15,708 genomes (2020) — 126 citations
- A structural variation reference for medical and population genetics (2020) — 876 citations
- Evaluating drug targets through human loss-of-function genetic variation (2019) — 168 citations
- Genome-wide association analyses identify 143 risk variants and putative regulatory mechanisms for type 2 diabetes (2018) — 707 citations
- Analysis of shared heritability in common disorders of the brain (2018) — 1,836 citations
- Genetic analysis of over one million people identifies 535 new loci associated with blood pressure traits (2018) — 1,148 citations
- Geographic variation and bias in polygenic scores of complex diseases and traits in Finland (2018) — 32 citations