| scholarly article | Q13442814 |
| P6179 | Dimensions Publication ID | 1084758381 |
| P356 | DOI | 10.1038/EJHG.2017.50 |
| P932 | PMC publication ID | 5520063 |
| P698 | PubMed publication ID | 28401901 |
| P50 | author | Dirkje Postma | Q13135289 |
| Behrooz Z. Alizadeh | Q41265465 | ||
| Bruce H Wolffenbuttel | Q51331410 | ||
| Morris A Swertz | Q57065320 | ||
| Peter J. van der Most | Q58326268 | ||
| Harold Snieder | Q30437456 | ||
| P2093 | author name string | Marcel Bruinenberg | |
| Marianne G Rots | |||
| Ilja M Nolte | |||
| H Marike Boezen | |||
| Ronald P Stolk | |||
| Gerjan Navis | |||
| Paul Iw de Bakker | |||
| P2860 | cites work | A flexible and accurate genotype imputation method for the next generation of genome-wide association studies | Q21129496 |
| Potential etiologic and functional implications of genome-wide association loci for human diseases and traits | Q22066284 | ||
| Genetic studies of body mass index yield new insights for obesity biology | Q22305005 | ||
| The NHGRI GWAS Catalog, a curated resource of SNP-trait associations | Q24568334 | ||
| Five years of GWAS discovery | Q24610574 | ||
| Genome-wide association analyses identify 18 new loci associated with serum urate concentrations | Q24620065 | ||
| Genetic variants in novel pathways influence blood pressure and cardiovascular disease risk | Q24630394 | ||
| A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals | Q24644474 | ||
| PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
| The International HapMap Project | Q27860695 | ||
| Meta-analysis of the heritability of human traits based on fifty years of twin studies | Q28262090 | ||
| New genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes risk | Q28270700 | ||
| Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization | Q28654771 | ||
| Discovery and refinement of loci associated with lipid levels | Q28661470 | ||
| The mystery of missing heritability: Genetic interactions create phantom heritability | Q28732355 | ||
| GCTA: a tool for genome-wide complex trait analysis | Q29547216 | ||
| Integrating common and rare genetic variation in diverse human populations | Q29547220 | ||
| Common SNPs explain a large proportion of the heritability for human height | Q29547221 | ||
| Loci influencing blood pressure identified using a cardiovascular gene-centric array | Q36853815 | ||
| Identification of heart rate-associated loci and their effects on cardiac conduction and rhythm disorders | Q36968428 | ||
| Gene-centric meta-analysis in 87,736 individuals of European ancestry identifies multiple blood-pressure-related loci | Q37634121 | ||
| Gene-centric meta-analyses for central adiposity traits in up to 57 412 individuals of European descent confirm known loci and reveal several novel associations | Q37705562 | ||
| Evaluating the contribution of genetics and familial shared environment to common disease using the UK Biobank. | Q39590896 | ||
| Low levels of vitamin D are associated with multimorbidity: results from the LifeLines Cohort Study | Q41412454 | ||
| Cohort Profile: LifeLines, a three-generation cohort study and biobank | Q41696801 | ||
| Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height | Q56457854 | ||
| Genetic associations at 53 loci highlight cell types and biological pathways relevant for kidney function | Q30277642 | ||
| Genome-wide association analysis identifies six new loci associated with forced vital capacity | Q30408891 | ||
| Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. | Q30427183 | ||
| CUBN is a gene locus for albuminuria | Q30428102 | ||
| Genome-wide association study of PR interval | Q33772170 | ||
| Gene-centric association signals for haemostasis and thrombosis traits identified with the HumanCVD BeadChip | Q33794493 | ||
| Pitfalls of predicting complex traits from SNPs | Q33896815 | ||
| Novel genes for QTc interval. How much heritability is explained, and how much is left to find? | Q33918840 | ||
| Multiple loci are associated with white blood cell phenotypes | Q33954440 | ||
| Genetic loci influencing kidney function and chronic kidney disease | Q34109552 | ||
| Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction | Q34149773 | ||
| Heritability and genetic correlations explained by common SNPs for metabolic syndrome traits | Q34221082 | ||
| Genome-wide association study identifies loci influencing concentrations of liver enzymes in plasma | Q34224637 | ||
| Common variants at 10 genomic loci influence hemoglobin A₁(C) levels via glycemic and nonglycemic pathways | Q34355379 | ||
| Defining the role of common variation in the genomic and biological architecture of adult human height | Q34441746 | ||
| Meta-analysis of Dense Genecentric Association Studies Reveals Common and Uncommon Variants Associated with Height | Q34458862 | ||
| Universal risk factors for multifactorial diseases: LifeLines: a three-generation population-based study | Q34724620 | ||
| Using extended genealogy to estimate components of heritability for 23 quantitative and dichotomous traits | Q34758236 | ||
| Genome partitioning of genetic variation for complex traits using common SNPs | Q34973837 | ||
| New genetic loci link adipose and insulin biology to body fat distribution | Q35114362 | ||
| Meta-analysis of genome-wide association studies in >80 000 subjects identifies multiple loci for C-reactive protein levels | Q35138365 | ||
| Dominance genetic variation contributes little to the missing heritability for human complex traits | Q35221899 | ||
| Representativeness of the LifeLines Cohort Study | Q35762658 | ||
| New gene functions in megakaryopoiesis and platelet formation | Q35909375 | ||
| Improving Phenotypic Prediction by Combining Genetic and Epigenetic Associations | Q36066696 | ||
| Genetic variance estimation with imputed variants finds negligible missing heritability for human height and body mass index | Q36109132 | ||
| Large-scale association analyses identify new loci influencing glycemic traits and provide insight into the underlying biological pathways | Q36207326 | ||
| Gene-centric meta-analyses of 108 912 individuals confirm known body mass index loci and reveal three novel signals | Q36467059 | ||
| Seventy-five genetic loci influencing the human red blood cell | Q36758500 | ||
| P433 | issue | 7 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | heritability | Q1503548 |
| complex trait | Q55608248 | ||
| P304 | page(s) | 877-885 | |
| P577 | publication date | 2017-04-12 | |
| P1433 | published in | European Journal of Human Genetics | Q2155433 |
| P1476 | title | Missing heritability: is the gap closing? An analysis of 32 complex traits in the Lifelines Cohort Study | |
| P478 | volume | 25 |
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| Q40047414 | Assessing genetic risk of hypertension at an early age: future research directions |
| Q90658220 | Deconstructing the sources of genotype-phenotype associations in humans |
| Q45870909 | Deriving genomic diagnoses without revealing patient genomes |
| Q60300466 | Detecting the dominance component of heritability in isolated and outbred human populations |
| Q89798942 | Efficient Estimation and Applications of Cross-Validated Genetic Predictions to Polygenic Risk Scores and Linear Mixed Models |
| Q47100859 | Evaluating the glucose raising effect of established loci via a genetic risk score |
| Q50123812 | Full genetic analysis for genome-wide association study of Fangji: a powerful approach for effectively dissecting the molecular architecture of personalized traditional Chinese medicine. |
| Q92178716 | GWEHS: A Genome-Wide Effect Sizes and Heritability Screener |
| Q64969525 | Genetic Susceptibility to Chronic Kidney Disease - Some More Pieces for the Heritability Puzzle. |
| Q47195395 | Genetic and Environmental Effects on Gene Expression Signatures of Blood Pressure: A Transcriptome-Wide Twin Study |
| Q30313100 | Genetic loci associated with heart rate variability and their effects on cardiac disease risk |
| Q88738754 | Genetics of Resistant Hypertension: the Missing Heritability and Opportunities |
| Q113227714 | REGENS: an open source Python package for simulating realistic autosomal genotypes |
| Q64091430 | The genetics of depression: successful genome-wide association studies introduce new challenges |
| Q96347990 | Validating the doubly weighted genetic risk score for the prediction of type 2 diabetes in the Lifelines and Estonian Biobank cohorts |
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