scholarly article | Q13442814 |
P8978 | DBLP publication ID | journals/bioinformatics/HormozdiariKYPE15 |
P356 | DOI | 10.1093/BIOINFORMATICS/BTV240 |
P932 | PMC publication ID | 4542778 |
P698 | PubMed publication ID | 26072484 |
P5875 | ResearchGate publication ID | 278331929 |
P50 | author | Bogdan Pasaniuc | Q56555817 |
Eleazar Eskin | Q62673408 | ||
P2093 | author name string | Farhad Hormozdiari | |
Wen-Yun Yang | |||
Gleb Kichaev | |||
P2860 | cites work | Genome-wide association analyses identify 18 new loci associated with serum urate concentrations | Q24620065 |
Principal components analysis corrects for stratification in genome-wide association studies | Q27860975 | ||
Genome-wide association analysis identifies 13 new risk loci for schizophrenia | Q28297287 | ||
Genetic mapping in human disease | Q29614943 | ||
Linkage disequilibrium in the human genome | Q29616097 | ||
A high-resolution association mapping panel for the dissection of complex traits in mice | Q30435297 | ||
Linkage disequilibrium in humans: models and data | Q30654298 | ||
Integrating functional data to prioritize causal variants in statistical fine-mapping studies | Q30865659 | ||
Rapid and accurate multiple testing correction and power estimation for millions of correlated markers | Q33432685 | ||
Leveraging genetic variability across populations for the identification of causal variants. | Q33571814 | ||
Fast and accurate imputation of summary statistics enhances evidence of functional enrichment | Q34285337 | ||
Identifying causal variants at loci with multiple signals of association | Q34336624 | ||
A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene | Q34651283 | ||
Increasing power of groupwise association test with likelihood ratio test | Q35550128 | ||
Genome-wide association mapping of quantitative traits in outbred mice | Q35771644 | ||
Incorporating prior information into association studies | Q36022170 | ||
Efficient control of population structure in model organism association mapping | Q36515832 | ||
Increasing power in association studies by using linkage disequilibrium structure and molecular function as prior information | Q36517959 | ||
Conditional and joint multiple-SNP analysis of GWAS summary statistics identifies additional variants influencing complex traits | Q36670925 | ||
Improved linear mixed models for genome-wide association studies | Q36683291 | ||
Genome-wide association studies in mice | Q36763587 | ||
Elucidating the role of gonadal hormones in sexually dimorphic gene coexpression networks | Q37125958 | ||
Bayesian refinement of association signals for 14 loci in 3 common diseases | Q37217525 | ||
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis | Q37322100 | ||
Genome-wide efficient mixed-model analysis for association studies | Q41961596 | ||
DIST: direct imputation of summary statistics for unmeasured SNPs | Q42931079 | ||
FaST linear mixed models for genome-wide association studies | Q46661213 | ||
P275 | copyright license | Creative Commons Attribution-NonCommercial 4.0 International | Q34179348 |
P6216 | copyright status | copyrighted | Q50423863 |
P433 | issue | 12 | |
P407 | language of work or name | English | Q1860 |
P921 | main subject | complex trait | Q55608248 |
P304 | page(s) | i206-13 | |
P577 | publication date | 2015-06-01 | |
P1433 | published in | Bioinformatics | Q4914910 |
P1476 | title | Identification of causal genes for complex traits | |
P478 | volume | 31 |
Q38692856 | A Statistical Approach to Fine Mapping for the Identification of Potential Causal Variants Related to Bone Mineral Density |
Q89693028 | A Unifying Framework for Imputing Summary Statistics in Genome-Wide Association Studies |
Q92532286 | A statistical approach to fine-mapping for the identification of potential causal variants related to human intelligence |
Q38769896 | ASD restricted and repetitive behaviors associated at 17q21.33: genes prioritized by expression in fetal brains |
Q92267404 | Accurate estimation of SNP-heritability from biobank-scale data irrespective of genetic architecture |
Q42697286 | Applying meta-analysis to genotype-tissue expression data from multiple tissues to identify eQTLs and increase the number of eGenes |
Q60907336 | Biological relevance of computationally predicted pathogenicity of noncoding variants |
Q59792594 | Chromatin interactions and expression quantitative trait loci reveal genetic drivers of multimorbidities |
Q37480692 | Colocalization of GWAS and eQTL Signals Detects Target Genes |
Q52647745 | Determining Genetic Causal Variants Through Multivariate Regression Using Mixture Model Penalty. |
Q30241340 | Dissecting the genetics of complex traits using summary association statistics |
Q31138389 | Efficient and Accurate Multiple-Phenotype Regression Method for High Dimensional Data Considering Population Structure |
Q64240282 | Genetics and epigenetics of autism spectrum disorder-current evidence in the field |
Q57057122 | Improving Imputation Accuracy by Inferring Causal Variants in Genetic Studies |
Q37218478 | Imputing Phenotypes for Genome-wide Association Studies |
Q37336953 | Joint Bayesian inference of risk variants and tissue-specific epigenomic enrichments across multiple complex human diseases |
Q57030056 | Large-scale transcriptome-wide association study identifies new prostate cancer risk regions |
Q91959027 | Leveraging allelic imbalance to refine fine-mapping for eQTL studies |
Q36758653 | Multiple testing correction in linear mixed models |
Q28550282 | Network Analysis of Genome-Wide Selective Constraint Reveals a Gene Network Active in Early Fetal Brain Intolerant of Mutation |
Q52372478 | New considerations for hiPSC-based models of neuropsychiatric disorders. |
Q92709272 | Probabilistic fine-mapping of transcriptome-wide association studies |
Q52566012 | Prostate Cancer Genomics: Recent Advances and the Prevailing Underrepresentation from Racial and Ethnic Minorities. |
Q30827855 | Pure and Confounded Effects of Causal SNPs on Longevity: Insights for Proper Interpretation of Research Findings in GWAS of Populations with Different Genetic Structures |
Q92264369 | QTG-Finder: A Machine-Learning Based Algorithm To Prioritize Causal Genes of Quantitative Trait Loci in Arabidopsis and Rice |
Q42359790 | The SSV Evaluation System: A Tool to Prioritize Short Structural Variants for Studies of Possible Regulatory and Causal Variants |
Q36056569 | Transethnic Genetic-Correlation Estimates from Summary Statistics |
Q37005532 | Using genomic annotations increases statistical power to detect eGenes |
Q40213493 | Widespread Allelic Heterogeneity in Complex Traits |
Search more.