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Exome sequencing identifies high-impact trait-associated alleles enriched in Finns
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/ajmg.a.36866openalex-snapshot
Clinical features associated with copy number variations of the 14q32 imprinted gene cluster
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Many Phenotypes Without Many False Discoveries: Error Controlling Strategies for Multitrait Association Studies
inferredcites →https://doi.org/10.1002/humu.22389openalex-snapshot
The Finnish Disease Heritage Database (FinDis) Update-A Database for the Genes Mutated in the Finnish Disease Heritage Brought to the Next-Generation Sequencing Era
inferredcites →https://doi.org/10.1002/sim.2165openalex-snapshot
Adjusting for treatment effects in studies of quantitative traits: antihypertensive therapy and systolic blood pressure
inferredcites →https://doi.org/10.1007/978-3-319-09665-0_15openalex-snapshot
HDL in Infectious Diseases and Sepsis
inferredcites →https://doi.org/10.1007/s00125-009-1291-1openalex-snapshot
Interaction between prenatal growth and high-risk genotypes in the development of type 2 diabetes
inferredcites →https://doi.org/10.1007/s00439-002-0875-3openalex-snapshot
Finnish Disease Heritage I:
inferredcites →https://doi.org/10.1016/j.ahj.2003.12.013openalex-snapshot
Replication of the association between the thrombospondin-4 A387P polymorphism and myocardial infarction
inferredcites →https://doi.org/10.1016/j.ahj.2006.06.002openalex-snapshot
Thrombospondin-4 1186G>C (A387P) is a sex-dependent risk factor for myocardial infarction: A large replication study with increased sample size from the same population
inferredcites →https://doi.org/10.1016/j.ajhg.2008.06.005openalex-snapshot
Long-Range LD Can Confound Genome Scans in Admixed Populations
inferredcites →https://doi.org/10.1016/j.ajhg.2008.11.005openalex-snapshot
The Genome-wide Patterns of Variation Expose Significant Substructure in a Founder Population
inferredcites →https://doi.org/10.1016/j.ajhg.2012.06.007openalex-snapshot
Optimal Unified Approach for Rare-Variant Association Testing with Application to Small-Sample Case-Control Whole-Exome Sequencing Studies
inferredcites →https://doi.org/10.1016/j.ajhg.2012.09.004openalex-snapshot
Detecting and Estimating Contamination of Human DNA Samples in Sequencing and Array-Based Genotype Data
inferredcites →https://doi.org/10.1016/j.ajhg.2018.05.002openalex-snapshot
Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum
inferredcites →https://doi.org/10.1016/j.ajog.2017.05.002openalex-snapshot
The placental imprinted DLK1-DIO3 domain: a new link to prenatal and postnatal growth in humans
inferredcites →https://doi.org/10.1016/j.amjhyper.2005.01.011openalex-snapshot
A Summary of the Effects of Antihypertensive Medications on Measured Blood Pressure
inferredcites →https://doi.org/10.1016/j.bbagen.2011.06.020openalex-snapshot
The T/NK cell co-stimulatory molecule SECTM1 is an IFN “early response gene” that is negatively regulated by LPS in Human monocytic cells
inferredcites →https://doi.org/10.1016/j.cell.2018.06.021openalex-snapshot
Molecular Architecture of the Mouse Nervous System
inferredcites →https://doi.org/10.1016/j.jacc.2012.08.001openalex-snapshot
Third Universal Definition of Myocardial Infarction
inferredcites →https://doi.org/10.1016/j.neuron.2017.06.029openalex-snapshot
Neural Circuit-Specialized Astrocytes: Transcriptomic, Proteomic, Morphological, and Functional Evidence
inferredcites →https://doi.org/10.1016/j.thromres.2015.04.019openalex-snapshot
Association between single nucleotide polymorphisms in thrombospondins genes and coronary artery disease: A meta-analysis
inferredcites →https://doi.org/10.1038/35042049openalex-snapshot
Use of population isolates for mapping complex traits
inferredcites →https://doi.org/10.1038/ejhg.2017.91openalex-snapshot
New insights into the imprinted MEG8-DMR in 14q32 and clinical and molecular description of novel patients with Temple syndrome
inferredcites →https://doi.org/10.1038/nature08494openalex-snapshot
Finding the missing heritability of complex diseases
inferredcites →https://doi.org/10.1038/nature13545openalex-snapshot
Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche
inferredcites →https://doi.org/10.1038/nature14132openalex-snapshot
New genetic loci link adipose and insulin biology to body fat distribution
inferredcites →https://doi.org/10.1038/nature14177openalex-snapshot
Genetic studies of body mass index yield new insights for obesity biology
inferredcites →https://doi.org/10.1038/nature14230openalex-snapshot
The fine-scale genetic structure of the British population
inferredcites →https://doi.org/10.1038/nature18309openalex-snapshot
Acetate mediates a microbiome–brain–β-cell axis to promote metabolic syndrome
inferredcites →https://doi.org/10.1038/ncomms11122openalex-snapshot
Genome-wide study for circulating metabolites identifies 62 loci and reveals novel systemic effects of LPA
inferredcites →https://doi.org/10.1038/ncomms15606openalex-snapshot
Whole genome sequencing and imputation in isolated populations identify genetic associations with medically-relevant complex traits
inferredcites →https://doi.org/10.1038/ncomms15927openalex-snapshot
Enrichment of low-frequency functional variants revealed by whole-genome sequencing of multiple isolated European populations
inferredcites →https://doi.org/10.1038/ng.1073openalex-snapshot
Genome-wide association study identifies multiple loci influencing human serum metabolite levels
inferredcites →https://doi.org/10.1038/ng.271openalex-snapshot
Genome-wide association analysis of metabolic traits in a birth cohort from a founder population
inferredcites →https://doi.org/10.1038/ng.2892openalex-snapshot
A general framework for estimating the relative pathogenicity of human genetic variants
inferredcites →https://doi.org/10.1038/ng.3097openalex-snapshot
Defining the role of common variation in the genomic and biological architecture of adult human height
inferredcites →https://doi.org/10.1038/ng.3247openalex-snapshot
Large-scale whole-genome sequencing of the Icelandic population
inferredcites →https://doi.org/10.1038/ng.3643openalex-snapshot
A reference panel of 64,976 haplotypes for genotype imputation
inferredcites →https://doi.org/10.1038/ng.3654openalex-snapshot
Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension
inferredcites →https://doi.org/10.1038/ng.3656openalex-snapshot
Next-generation genotype imputation service and methods
inferredcites →https://doi.org/10.1038/ng.3660openalex-snapshot
Meta-analysis identifies common and rare variants influencing blood pressure and overlapping with metabolic trait loci
inferredcites →https://doi.org/10.1038/ng.3679openalex-snapshot
Reference-based phasing using the Haplotype Reference Consortium panel
inferredcites →https://doi.org/10.1038/ng.3699openalex-snapshot
Fetus-derived DLK1 is required for maternal metabolic adaptations to pregnancy and is associated with fetal growth restriction
inferredcites →https://doi.org/10.1038/ng.3841openalex-snapshot
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
inferredcites →https://doi.org/10.1038/ng.3977openalex-snapshot
Exome-wide association study of plasma lipids in >300,000 individuals
inferredcites →https://doi.org/10.1038/ng.493openalex-snapshot
The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes
inferredcites →https://doi.org/10.1038/ng.548openalex-snapshot
Variance component model to account for sample structure in genome-wide association studies
inferredcites →https://doi.org/10.1038/ng.806openalex-snapshot
A framework for variation discovery and genotyping using next-generation DNA sequencing data
inferredcites →https://doi.org/10.1038/ng1770openalex-snapshot
Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies
inferredcites →https://doi.org/10.1038/nmeth.2307openalex-snapshot
Improved whole-chromosome phasing for disease and population genetic studies
inferredcites →https://doi.org/10.1038/nmeth.2890openalex-snapshot
MutationTaster2: mutation prediction for the deep-sequencing age
inferredcites →https://doi.org/10.1038/nmeth0410-248openalex-snapshot
A method and server for predicting damaging missense mutations
inferredcites →https://doi.org/10.1038/nprot.2009.86openalex-snapshot
Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm
inferredcites →https://doi.org/10.1038/s41467-019-08936-1openalex-snapshot
Assessing the causal association of glycine with risk of cardio-metabolic diseases
inferredcites →https://doi.org/10.1038/s41586-018-0566-4openalex-snapshot
Common genetic variants contribute to risk of rare severe neurodevelopmental disorders
inferredcites →https://doi.org/10.1038/s41588-017-0011-xopenalex-snapshot
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
inferredcites →https://doi.org/10.1038/s41588-018-0084-1openalex-snapshot
Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes
inferredcites →https://doi.org/10.1038/s41588-018-0215-8openalex-snapshot
Genomic history of the Sardinian population
inferredcites →https://doi.org/10.1056/nejmp1500523openalex-snapshot
A New Initiative on Precision Medicine
inferredcites →https://doi.org/10.1073/pnas.1322563111openalex-snapshot
Searching for missing heritability: Designing rare variant association studies
inferredcites →https://doi.org/10.1074/mcp.m113.035600openalex-snapshot
Analysis of the Human Tissue-specific Expression by Genome-wide Integration of Transcriptomics and Antibody-based Proteomics
inferredcites →https://doi.org/10.1093/aje/kwx016openalex-snapshot
Quantitative Serum Nuclear Magnetic Resonance Metabolomics in Large-Scale Epidemiology: A Primer on -Omic Technologies
inferredcites →https://doi.org/10.1093/bioinformatics/btq559openalex-snapshot
Robust relationship inference in genome-wide association studies
inferredcites →https://doi.org/10.1093/bioinformatics/btv112openalex-snapshot
Unified representation of genetic variants
inferredcites →https://doi.org/10.1093/bioinformatics/btx166openalex-snapshot
biMM: efficient estimation of genetic variances and covariances for cohorts with high-dimensional phenotype measurements
inferredcites →https://doi.org/10.1093/biomet/73.3.751openalex-snapshot
An Improved Bonferroni Procedure for Multiple Tests of Significance
inferredcites →https://doi.org/10.1093/clinchem/18.6.499openalex-snapshot
Estimation of the Concentration of Low-Density Lipoprotein Cholesterol in Plasma, Without Use of the Preparative Ultracentrifuge
inferredcites →https://doi.org/10.1093/eurheartj/ehw450openalex-snapshot
Genomic prediction of coronary heart disease
inferredcites →https://doi.org/10.1093/eurpub/cku174openalex-snapshot
Forty-year trends in cardiovascular risk factors in Finland
inferredcites →https://doi.org/10.1093/hmg/ddy067openalex-snapshot
Identification of seven novel loci associated with amino acid levels using single-variant and gene-based tests in 8545 Finnish men from the METSIM study
inferredcites →https://doi.org/10.1093/hmg/ddy271openalex-snapshot
Meta-analysis of genome-wide association studies for height and body mass index in ∼700000 individuals of European ancestry
inferredcites →https://doi.org/10.1093/hmg/ddy327openalex-snapshot
Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry
inferredcites →https://doi.org/10.1093/ije/dyx239openalex-snapshot
Cohort Profile: The National FINRISK Study
inferredcites →https://doi.org/10.1093/nar/gkw1133openalex-snapshot
The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog)
inferredcites →https://doi.org/10.1101/080770openalex-snapshot
The rate of false polymorphisms introduced when imputing genotypes from global imputation panels
inferredcites →https://doi.org/10.1101/457960openalex-snapshot
Genetics of human plasma lipidome: Understanding lipid metabolism and its link to diseases beyond traditional lipids
inferredcites →https://doi.org/10.1101/gr.092619.109openalex-snapshot
Identification of deleterious mutations within three human genomes
inferredcites →https://doi.org/10.1111/mec.13743openalex-snapshot
Genomic variation at the tips of the adaptive radiation of Darwin's finches
inferredcites →https://doi.org/10.1111/rssb.12028openalex-snapshot
Selective Inference on Multiple Families of Hypotheses
inferredcites →https://doi.org/10.1126/science.aal4043openalex-snapshot
Phenotype risk scores identify patients with unrecognized Mendelian disease patterns
inferredcites →https://doi.org/10.1159/000072554openalex-snapshot
European Stroke Initiative Recommendations for Stroke Management – Update 2003
inferredcites →https://doi.org/10.1160/th11-03-0206openalex-snapshot
Thrombospondin-4 polymorphism (A387P) predicts cardiovascular risk in postinfarction patients with high HDL cholesterol and C-reactive protein levels
inferredcites →https://doi.org/10.1161/circgenetics.114.000216openalex-snapshot
Quantitative Serum Nuclear Magnetic Resonance Metabolomics in Cardiovascular Epidemiology and Genetics
inferredcites →https://doi.org/10.1161/circulationaha.114.013116openalex-snapshot
Metabolite Profiling and Cardiovascular Event Risk
inferredcites →https://doi.org/10.1161/jaha.115.002621openalex-snapshot
Plasma Glycine and Risk of Acute Myocardial Infarction in Patients With Suspected Stable Angina Pectoris
inferredcites →https://doi.org/10.1172/jci5343openalex-snapshot
Exocrine pancreatic disorders in transsgenic mice expressing human keratin 8
inferredcites →https://doi.org/10.1186/s13059-016-0974-4openalex-snapshot
The Ensembl Variant Effect Predictor
inferredcites →https://doi.org/10.1186/s13742-015-0047-8openalex-snapshot
Second-generation PLINK: rising to the challenge of larger and richer datasets
inferredcites →https://doi.org/10.1194/jlr.o072629openalex-snapshot
The Metabolic Syndrome in Men study: a resource for studies of metabolic and cardiovascular diseases
inferredcites →https://doi.org/10.1198/016214502760047131openalex-snapshot
Model-Based Clustering, Discriminant Analysis, and Density Estimation
inferredcites →https://doi.org/10.1371/journal.pgen.1000529openalex-snapshot
A Flexible and Accurate Genotype Imputation Method for the Next Generation of Genome-Wide Association Studies
inferredcites →https://doi.org/10.1371/journal.pgen.1002453openalex-snapshot
Inference of Population Structure using Dense Haplotype Data
inferredcites →https://doi.org/10.1371/journal.pgen.1002907openalex-snapshot
Novel Loci for Metabolic Networks and Multi-Tissue Expression Studies Reveal Genes for Atherosclerosis
inferredcites →https://doi.org/10.1371/journal.pgen.1004147openalex-snapshot
Re-sequencing Expands Our Understanding of the Phenotypic Impact of Variants at GWAS Loci
inferredcites →https://doi.org/10.1371/journal.pgen.1004494openalex-snapshot
Distribution and Medical Impact of Loss-of-Function Variants in the Finnish Founder Population
inferredcites →https://doi.org/10.1371/journal.pgen.1006916openalex-snapshot
Statistical correction of the Winner’s Curse explains replication variability in quantitative trait genome-wide association studies
inferredcites →https://doi.org/10.1371/journal.pgen.1007079openalex-snapshot
Common, low-frequency, and rare genetic variants associated with lipoprotein subclasses and triglyceride measures in Finnish men from the METSIM study
inferredcites →https://doi.org/10.1371/journal.pgen.1007329openalex-snapshot
Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population
inferredcites →https://doi.org/10.1534/g3.117.300217openalex-snapshot
Fine-Scale Genetic Structure in Finland
inferredcites →https://doi.org/10.1534/genetics.116.193987openalex-snapshot
Controlling the Rate of GWAS False Discoveries
inferredcites →https://doi.org/10.1534/genetics.117.300551openalex-snapshot
Relaxed Selection During a Recent Human Expansion
inferredcites →https://doi.org/10.2337/db08-1607openalex-snapshot
Changes in Insulin Sensitivity and Insulin Release in Relation to Glycemia and Glucose Tolerance in 6,414 Finnish Men
inferredcites →https://doi.org/10.2337/db16-1329openalex-snapshot
A Low-Frequency Inactivating AKT2 Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk
inferredcites →https://doi.org/10.2337/db17-1142openalex-snapshot
A Partial Loss-of-Function Variant in AKT2 Is Associated With Reduced Insulin-Mediated Glucose Uptake in Multiple Insulin-Sensitive Tissues: A Genotype-Based Callback Positron Emission Tomography Study
inferredcites →https://doi.org/10.7554/elife.15266openalex-snapshot
Admixture into and within sub-Saharan Africa
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Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1038/s41588-021-00892-1openalex-snapshot
Whole-exome imputation within UK Biobank powers rare coding variant association and fine-mapping analyses
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