| review article | Q7318358 |
| scholarly article | Q13442814 |
| P50 | author | Frank Dudbridge | Q60878633 |
| P2093 | author name string | Frank Dudbridge | |
| P2860 | cites work | Heritability in the genomics era — concepts and misconceptions | Q22122010 |
| Genetic studies of body mass index yield new insights for obesity biology | Q22305005 | ||
| Biological insights from 108 schizophrenia-associated genetic loci | Q24561833 | ||
| Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis | Q24597718 | ||
| Five years of GWAS discovery | Q24610574 | ||
| Common polygenic variation contributes to risk of schizophrenia and bipolar disorder | Q28250609 | ||
| A comprehensive 1,000 Genomes-based genome-wide association meta-analysis of coronary artery disease | Q28267020 | ||
| Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs | Q28296286 | ||
| Large-scale genotyping identifies 41 new loci associated with breast cancer risk | Q29416989 | ||
| Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index | Q29547208 | ||
| Re: “Multivariable Mendelian Randomization: The Use of Pleiotropic Genetic Variants to Estimate Causal Effects” | Q61865038 | ||
| No evidence for shared genetic basis of common variants in multiple sclerosis and amyotrophic lateral sclerosis | Q37619291 | ||
| Bringing genome-wide association findings into clinical use. | Q38120138 | ||
| Adult height, coronary heart disease and stroke: a multi-locus Mendelian randomization meta-analysis | Q39313673 | ||
| A Fast Method that Uses Polygenic Scores to Estimate the Variance Explained by Genome-wide Marker Panels and the Proportion of Variants Affecting a Trait | Q39334653 | ||
| Linkage strategies for genetically complex traits. I. Multilocus models | Q40623210 | ||
| Mendelian randomization with invalid instruments: effect estimation and bias detection through Egger regression | Q40862437 | ||
| Multivariable Mendelian randomization: the use of pleiotropic genetic variants to estimate causal effects | Q41511077 | ||
| Prediction of individual genetic risk to prostate cancer using a polygenic score | Q41584352 | ||
| Using multiple genetic variants as instrumental variables for modifiable risk factors | Q41931960 | ||
| Genome-wide efficient mixed-model analysis for association studies | Q41961596 | ||
| Use of allele scores as instrumental variables for Mendelian randomization | Q42970966 | ||
| Bayesian inference analyses of the polygenic architecture of rheumatoid arthritis | Q44921278 | ||
| The heritability of prostate cancer—letter | Q46112463 | ||
| Celebrating the 30th anniversary of genetic epidemiology: how to define our scope? | Q48072440 | ||
| Common SNPs explain a large proportion of the heritability for human height | Q29547221 | ||
| Personal genomes: The case of the missing heritability | Q29614582 | ||
| Plasma HDL cholesterol and risk of myocardial infarction: a mendelian randomisation study | Q29615729 | ||
| Prediction of total genetic value using genome-wide dense marker maps | Q29619613 | ||
| Mendelian randomization of blood lipids for coronary heart disease | Q30407506 | ||
| Statistical power to detect genetic (co)variance of complex traits using SNP data in unrelated samples. | Q30798286 | ||
| Accuracy of predicting the genetic risk of disease using a genome-wide approach | Q33375729 | ||
| Prediction and interaction in complex disease genetics: experience in type 1 diabetes | Q33479555 | ||
| Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come | Q33772946 | ||
| A population genetic signal of polygenic adaptation | Q34015195 | ||
| A comprehensive model for familial breast cancer incorporating BRCA1, BRCA2 and other genes | Q34115258 | ||
| MultiBLUP: improved SNP-based prediction for complex traits | Q34153795 | ||
| Predicting human height by Victorian and genomic methods | Q34326904 | ||
| Power and predictive accuracy of polygenic risk scores. | Q34337027 | ||
| Prediction of individual genetic risk to disease from genome-wide association studies | Q34676890 | ||
| Polygenic dissection of the bipolar phenotype | Q34729917 | ||
| Most common 'sporadic' cancers have a significant germline genetic component | Q34736858 | ||
| Genome partitioning of genetic variation for complex traits using common SNPs | Q34973837 | ||
| Harnessing the information contained within genome-wide association studies to improve individual prediction of complex disease risk | Q34988777 | ||
| Mining the human phenome using allelic scores that index biological intermediates | Q35034381 | ||
| Genomic inflation factors under polygenic inheritance | Q35108650 | ||
| Massively expedited genome-wide heritability analysis (MEGHA). | Q35134802 | ||
| Sixty-five common genetic variants and prediction of type 2 diabetes | Q35532317 | ||
| Simultaneous discovery, estimation and prediction analysis of complex traits using a bayesian mixture model | Q35596725 | ||
| Implications of polygenic risk-stratified screening for prostate cancer on overdiagnosis | Q35602297 | ||
| Mendelian Randomization Study of Body Mass Index and Colorectal Cancer Risk | Q35815677 | ||
| LD Score regression distinguishes confounding from polygenicity in genome-wide association studies | Q35831121 | ||
| Mammographic breast density and breast cancer: evidence of a shared genetic basis | Q36043843 | ||
| Height and Breast Cancer Risk: Evidence From Prospective Studies and Mendelian Randomization | Q36276540 | ||
| Inherited determinants of Crohn's disease and ulcerative colitis phenotypes: a genetic association study | Q36468290 | ||
| Genome partitioning of genetic variation for height from 11,214 sibling pairs | Q36492176 | ||
| Prediction of breast cancer risk based on profiling with common genetic variants | Q36583004 | ||
| An atlas of genetic correlations across human diseases and traits | Q36701237 | ||
| Projecting the performance of risk prediction based on polygenic analyses of genome-wide association studies | Q37059182 | ||
| P275 | copyright license | Creative Commons Attribution | Q6905323 |
| P6216 | copyright status | copyrighted | Q50423863 |
| P433 | issue | 4 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | genetics | Q7162 |
| epidemiology | Q133805 | ||
| biomedical investigative technique | Q66648976 | ||
| multifactorial inheritance | Q67200773 | ||
| P304 | page(s) | 268-272 | |
| P577 | publication date | 2016-04-07 | |
| 2016-05-01 | |||
| P1433 | published in | Genetic Epidemiology | Q5532864 |
| P1476 | title | Polygenic Epidemiology | |
| P478 | volume | 40 |
| Q92066484 | A flexible and parallelizable approach to genome-wide polygenic risk scores |
| Q57050769 | A polygenic p factor for major psychiatric disorders |
| Q96822534 | A systematic review of gene-by-intervention studies of alcohol and other substance use |
| Q52372349 | A tutorial on conducting genome-wide association studies: Quality control and statistical analysis. |
| Q98465031 | Association Between FoxO1, A2M, and TGF-β1, Environmental Factors, and Major Depressive Disorder |
| Q47425592 | Association Between Schizophrenia-Related Polygenic Liability and the Occurrence and Level of Mood-Incongruent Psychotic Symptoms in Bipolar Disorder |
| Q55463277 | Cardiovascular Risk Stratification: From Phenotype to Genotype? |
| Q64058600 | Combining Sparse Group Lasso and Linear Mixed Model Improves Power to Detect Genetic Variants Underlying Quantitative Traits |
| Q50301210 | Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection. |
| Q47094762 | Comparison of weighting approaches for genetic risk scores in gene-environment interaction studies |
| Q89798942 | Efficient Estimation and Applications of Cross-Validated Genetic Predictions to Polygenic Risk Scores and Linear Mixed Models |
| Q92008549 | Exome chip-driven association study of lipidemia in >14,000 Koreans and evaluation of genetic effect on identified variants between different ethnic groups |
| Q39448284 | Genes, Environments, and Sex Differences in Alcohol Research |
| Q90480219 | Genetic Variants Detection Based on Weighted Sparse Group Lasso |
| Q93154106 | Genetic risk, body mass index, and weight control behaviors: Unlocking the triad |
| Q90618568 | Genome-Wide Association Study of Latent Cognitive Measures in Adolescence: Genetic Overlap With Intelligence and Education |
| Q92599298 | Genome-wide association studies of severe P. falciparum malaria susceptibility: progress, pitfalls and prospects |
| Q38752201 | Genome-wide association study identifies four novel loci associated with Alzheimer's endophenotypes and disease modifiers |
| Q46419306 | Genomics of Posttraumatic Stress Disorder: Sequencing Stress and Modeling Misfortune. |
| Q41978253 | Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations |
| Q42145797 | Improving polygenic risk prediction from summary statistics by an empirical Bayes approach |
| Q90453214 | Investigation of prediction accuracy and the impact of sample size, ancestry, and tissue in transcriptome-wide association studies |
| Q40259459 | Letter to the Editor: Posttraumatic stress disorder has genetic overlap with cardiometabolic traits. |
| Q90341162 | Missing single nucleotide polymorphisms in Genetic Risk Scores: A simulation study |
| Q38840593 | Mortality selection in a genetic sample and implications for association studies |
| Q47703297 | No Genetic Overlap Between Circulating Iron Levels and Alzheimer's Disease |
| Q50100394 | Novel Insights into the Pathogenesis of Monogenic Congenital Anomalies of the Kidney and Urinary Tract. |
| Q54079923 | On the use of genetic risk scores to predict cardiovascular disease in the general population. |
| Q90685954 | Polygenic Risk Scores for Psychiatric Disorders Reveal Novel Clues About the Genetics of Disordered Gambling |
| Q52630895 | Polygenic Risk Scores in Clinical Psychology: Bridging Genomic Risk to Individual Differences. |
| Q92859182 | Polygenic risk scores in psychiatry: Will they be useful for clinicians? |
| Q38798713 | Polygenic scores via penalized regression on summary statistics |
| Q57471049 | Prediction of treatment response in rheumatoid arthritis patients using genome-wide SNP data |
| Q47409320 | Predictive accuracy of combined genetic and environmental risk scores |
| Q58564518 | Provider bias as a function of patient genotype: polygenic score analysis among diabetics from the Health and Retirement Study |
| Q91989992 | Quick assessment for systematic test statistic inflation/deflation due to null model misspecifications in genome-wide environment interaction studies |
| Q91337965 | Rigor and reproducibility in genetic research on eating disorders |
| Q61755960 | The Genetic Sphygmomanometer: an argument for routine genome-wide genotyping in the population and a new view on its use to inform clinical practice |
| Q57789969 | The Role of Emergence in Genetically Informed Relationships Research: A Methodological Analysis |
| Q47619056 | The iPSYCH2012 case-cohort sample: new directions for unravelling genetic and environmental architectures of severe mental disorders. |
| Q57170901 | Trans-Ethnic Polygenic Analysis Supports Genetic Overlaps of Lumbar Disc Degeneration With Height, Body Mass Index, and Bone Mineral Density |
| Q97692972 | Tutorial: a guide to performing polygenic risk score analyses |
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