| scholarly article | Q13442814 |
| P8978 | DBLP publication ID | journals/bioinformatics/QiaoCFBGSL14 |
| P356 | DOI | 10.1093/BIOINFORMATICS/BTT654 |
| P932 | PMC publication ID | 3892690 |
| P698 | PubMed publication ID | 24262215 |
| P5875 | ResearchGate publication ID | 258827650 |
| P2093 | author name string | Christoph Lange | |
| Edwin K Silverman | |||
| Michael H Cho | |||
| Amund Gulsvik | |||
| Per S Bakke | |||
| Dandi Qiao | |||
| Heide Fier | |||
| P2860 | cites work | Heritability in the genomics era — concepts and misconceptions | Q22122010 |
| The allelic architecture of human disease genes: common disease-common variant... or not? | Q22337148 | ||
| Hundreds of variants clustered in genomic loci and biological pathways affect human height | Q24630979 | ||
| Rare variants of IFIH1, a gene implicated in antiviral responses, protect against type 1 diabetes | Q24651119 | ||
| PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 | ||
| Real time spatial cluster detection using interpoint distances among precise patient locations | Q24812843 | ||
| A method and server for predicting damaging missense mutations | Q27860835 | ||
| A HapMap harvest of insights into the genetics of common disease | Q29614875 | ||
| Rare variants create synthetic genome-wide associations | Q29614955 | ||
| Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function. | Q30427183 | ||
| Imputation-based analysis of association studies: candidate regions and quantitative traits | Q30833155 | ||
| Optimal tests for rare variant effects in sequencing association studies | Q31065241 | ||
| Methods for detecting associations with rare variants for common diseases: application to analysis of sequence data | Q33359015 | ||
| A groupwise association test for rare mutations using a weighted sum statistic | Q33408787 | ||
| A genome-wide association study in chronic obstructive pulmonary disease (COPD): identification of two major susceptibility loci. | Q33419815 | ||
| A genome-wide association study of pulmonary function measures in the Framingham Heart Study | Q33419839 | ||
| Variants in FAM13A are associated with chronic obstructive pulmonary disease | Q33687879 | ||
| A Novel Adaptive Method for the Analysis of Next-Generation Sequencing Data to Detect Complex Trait Associations with Rare Variants Due to Gene Main Effects and Interactions | Q33728642 | ||
| A new testing strategy to identify rare variants with either risk or protective effect on disease | Q33815362 | ||
| The future of association studies: gene-based analysis and replication | Q33910011 | ||
| Rare-variant association testing for sequencing data with the sequence kernel association test | Q33954046 | ||
| A versatile gene-based test for genome-wide association studies | Q33960489 | ||
| Gene-based tests of association | Q33987507 | ||
| Genetic epidemiology of COPD (COPDGene) study design | Q34074731 | ||
| Multiple rare variants in NPC1L1 associated with reduced sterol absorption and plasma low-density lipoprotein levels | Q34478587 | ||
| Genomewide association studies and human disease | Q34606556 | ||
| Most rare missense alleles are deleterious in humans: implications for complex disease and association studies | Q35752568 | ||
| A genome-wide association study of COPD identifies a susceptibility locus on chromosome 19q13. | Q35816887 | ||
| Pathway-based approaches for analysis of genomewide association studies | Q36512103 | ||
| The Choice of the Number of Bins for the M Statistic. | Q37244492 | ||
| Genome-wide association analysis by lasso penalized logistic regression | Q37319644 | ||
| Multiple rare variants in different genes account for multifactorial inherited susceptibility to colorectal adenomas | Q37619454 | ||
| A strategy to discover genes that carry multi-allelic or mono-allelic risk for common diseases: a cohort allelic sums test (CAST). | Q51928874 | ||
| P433 | issue | 2 | |
| P407 | language of work or name | English | Q1860 |
| P1104 | number of pages | 8 | |
| P304 | page(s) | 157-164 | |
| P577 | publication date | 2013-11-20 | |
| P1433 | published in | Bioinformatics | Q4914910 |
| P1476 | title | On the simultaneous association analysis of large genomic regions: a massive multi-locus association test | |
| P478 | volume | 30 |
| Q29052362 | Critical Assessment of Small Molecule Identification 2016: automated methods |
| Q35784927 | Discriminating precursors of common fragments for large-scale metabolite profiling by triple quadrupole mass spectrometry |
| Q54234994 | Multi-locus Test and Correction for Confounding Effects in Genome-Wide Association Studies. |
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