| scholarly article | Q13442814 |
| P356 | DOI | 10.1371/JOURNAL.PGEN.1006493 |
| P8608 | Fatcat ID | release_c24gi3hanjckjc6y6gd5tfw3fe |
| P932 | PMC publication ID | 5201242 |
| P698 | PubMed publication ID | 28036406 |
| P50 | author | Nilanjan Chatterjee | Q21526241 |
| Paolo Vineis | Q25999450 | ||
| Stephen Chanock | Q27662321 | ||
| Nathaniel Rothman | Q28050622 | ||
| Montserrat García-Closas | Q28356305 | ||
| Nuria Malats | Q28360608 | ||
| Maria Teresa Landi | Q28606990 | ||
| Hermann Brenner | Q28958315 | ||
| Victoria Cortessis | Q46581470 | ||
| Douglas F Levinson | Q59748818 | ||
| Alan R. Sanders | Q67652837 | ||
| Jonine Figueroa | Q71778357 | ||
| Eric Jacobs | Q85550629 | ||
| Yun-Chul Hong | Q85715844 | ||
| Margaret Karagas | Q88162936 | ||
| Alison P Klein | Q89907184 | ||
| Jubao Duan | Q90172397 | ||
| Gloria M Petersen | Q95972100 | ||
| Harvey A. Risch | Q97531829 | ||
| Debra T. Silverman | Q103839499 | ||
| Neil Caporaso | Q107095573 | ||
| Brian M. Wolpin | Q110920101 | ||
| Pablo V Gejman | Q114270584 | ||
| Adeline Seow | Q114328035 | ||
| Baosen Zhou | Q114328051 | ||
| Winton Moy | Q114441101 | ||
| Rachael Z. Stolzenberg-Solomon | Q30002268 | ||
| Laufey T. Amundadottir | Q30093106 | ||
| Keitaro Matsuo | Q30506416 | ||
| P2093 | author name string | Kai Yu | |
| William Wheeler | |||
| Donghui Li | |||
| Jianxin Shi | |||
| Ju-Hyun Park | |||
| Qing Lan | |||
| Lei Song | |||
| Dongxin Lin | |||
| Robert E Schoen | |||
| Chao Agnes Hsiung | |||
| Li Hsu | |||
| Xing Hua | |||
| I-Shou Chang | |||
| Sonja T Berndt | |||
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| Genome-wide association study identifies multiple susceptibility loci for pancreatic cancer | Q34314018 | ||
| Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors | Q34325802 | ||
| Power and predictive accuracy of polygenic risk scores. | Q34337027 | ||
| Defining the role of common variation in the genomic and biological architecture of adult human height | Q34441746 | ||
| Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases | Q34478075 | ||
| Lung eQTLs to help reveal the molecular underpinnings of asthma | Q34499419 | ||
| All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs | Q34699776 | ||
| Joint analysis of psychiatric disorders increases accuracy of risk prediction for schizophrenia, bipolar disorder, and major depressive disorder | Q35059381 | ||
| A meta-analysis of 87,040 individuals identifies 23 new susceptibility loci for prostate cancer | Q35248192 | ||
| Genome-wide association analysis of more than 120,000 individuals identifies 15 new susceptibility loci for breast cancer | Q35996692 | ||
| Modeling Linkage Disequilibrium Increases Accuracy of Polygenic Risk Scores | Q36133352 | ||
| Estimation of effect size distribution from genome-wide association studies and implications for future discoveries | Q36191121 | ||
| Partitioning heritability by functional annotation using genome-wide association summary statistics | Q36225291 | ||
| Prediction of breast cancer risk based on profiling with common genetic variants | Q36583004 | ||
| Bias-reduced estimators and confidence intervals for odds ratios in genome-wide association studies | Q36877035 | ||
| Projecting the performance of risk prediction based on polygenic analyses of genome-wide association studies | Q37059182 | ||
| Mapping cis- and trans-regulatory effects across multiple tissues in twins | Q37200482 | ||
| Global analysis of DNA methylation variation in adipose tissue from twins reveals links to disease-associated variants in distal regulatory elements | Q37298169 | ||
| Comprehensive functional annotation of 77 prostate cancer risk loci | Q37533894 | ||
| Characterizing the genetic basis of methylome diversity in histologically normal human lung tissue | Q37696685 | ||
| P275 | copyright license | Creative Commons CC0 License | Q6938433 |
| P6216 | copyright status | copyrighted, dedicated to the public domain by copyright holder | Q88088423 |
| P4510 | describes a project that uses | genome-wide association study | Q1098876 |
| P433 | issue | 12 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | genome-wide association study | Q1098876 |
| P304 | page(s) | e1006493 | |
| P577 | publication date | 2016-12-01 | |
| P1433 | published in | PLOS Genetics | Q1893441 |
| P1476 | title | Winner's Curse Correction and Variable Thresholding Improve Performance of Polygenic Risk Modeling Based on Genome-Wide Association Study Summary-Level Data | |
| P478 | volume | 12 |
| Q92066484 | A flexible and parallelizable approach to genome-wide polygenic risk scores |
| Q90600031 | Annotations capturing cell-type-specific TF binding explain a large fraction of disease heritability |
| Q52576610 | Association of polygenic risk score with the risk of chronic lymphocytic leukemia and monoclonal B-cell lymphocytosis. |
| Q55306707 | Beginning at the ends: telomeres and human disease. |
| Q64458461 | Combining common genetic variants and non-genetic risk factors to predict risk of cutaneous melanoma |
| Q90257889 | Contemporary Issues in Depressive Disorders |
| Q47321577 | Critical research gaps and recommendations to inform research prioritisation for more effective prevention and improved outcomes in colorectal cancer. |
| Q92578476 | Disease Heritability Enrichment of Regulatory Elements Is Concentrated in Elements with Ancient Sequence Age and Conserved Function across Species |
| Q55443199 | Enrichment of B cell receptor signaling and epidermal growth factor receptor pathways in monoclonal gammopathy of undetermined significance: a genome-wide genetic interaction study. |
| Q93161870 | Functional disease architectures reveal unique biological role of transposable elements |
| Q58707538 | Gene × Environment Interaction in Developmental Disorders: Where Do We Stand and What's Next? |
| Q58122265 | Generalizing polygenic risk scores from Europeans to Hispanics/Latinos |
| Q59340592 | Genetic disease risks can be misestimated across global populations |
| Q41978253 | Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations |
| Q61443957 | Imputation to whole-genome sequence using multiple pig populations and its use in genome-wide association studies |
| Q38652895 | Leveraging Multi-ethnic Evidence for Risk Assessment of Quantitative Traits in Minority Populations |
| Q40047884 | Linkage disequilibrium-dependent architecture of human complex traits shows action of negative selection. |
| Q46496028 | Multiethnic polygenic risk scores improve risk prediction in diverse populations. |
| Q40054865 | Non-parametric genetic prediction of complex traits with latent Dirichlet process regression models. |
| Q92907278 | Pharmacogenetics and Depression: A Critical Perspective |
| Q62583133 | Polygenic Risk Scores for Prediction of Breast Cancer and Breast Cancer Subtypes |
| Q52630895 | Polygenic Risk Scores in Clinical Psychology: Bridging Genomic Risk to Individual Differences. |
| Q64109912 | Polygenic prediction via Bayesian regression and continuous shrinkage priors |
| Q53692090 | The Genetics of Treatment-Resistant Depression: A Critical Review and Future Perspectives. |
| Q97692972 | Tutorial: a guide to performing polygenic risk score analyses |
| Q90027616 | Validity of polygenic risk scores: are we measuring what we think we are? |
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