| P2093 | author name string | Brian L Browning | |
| | Yu Qian | |
| | Sharon R Browning | |
| P2860 | cites work | Biological, clinical and population relevance of 95 loci for blood lipids | Q24622541 |
| | Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans | Q24643492 |
| | A second generation human haplotype map of over 3.1 million SNPs | Q24651939 |
| | Genome-wide association analysis of metabolic traits in a birth cohort from a founder population | Q24654676 |
| | PLINK: a tool set for whole-genome association and population-based linkage analyses | Q24677407 |
| | Missing heritability and strategies for finding the underlying causes of complex disease | Q29614586 |
| | Sequence variations in PCSK9, low LDL, and protection against coronary heart disease | Q29616310 |
| | Improving the accuracy and efficiency of identity-by-descent detection in population data | Q30608038 |
| | Fast and flexible simulation of DNA sequence data | Q33386692 |
| | A groupwise association test for rare mutations using a weighted sum statistic | Q33408787 |
| | Discovery of rare variants via sequencing: implications for the design of complex trait association studies | Q33444638 |
| | Systematic interpretation of genetic interactions using protein networks | Q33622989 |
| | SPICi: a fast clustering algorithm for large biological networks | Q33785547 |
| | Rare-variant association testing for sequencing data with the sequence kernel association test | Q33954046 |
| | Common vs. rare allele hypotheses for complex diseases | Q34038820 |
| | Natural selection and the distribution of identity-by-descent in the human genome | Q34123495 |
| | The empirical power of rare variant association methods: results from sanger sequencing in 1,998 individuals | Q34154481 |
| | A method for detecting IBD regions simultaneously in multiple individuals--with applications to disease genetics | Q34178416 |
| | DASH: a method for identical-by-descent haplotype mapping uncovers association with recent variation | Q34188020 |
| | Detecting rare variant associations by identity-by-descent mapping in case-control studies | Q34248911 |
| | Identity-by-descent mapping to detect rare variants conferring susceptibility to multiple sclerosis | Q34331816 |
| | The geography of recent genetic ancestry across Europe | Q34344298 |
| | IBD-Groupon: an efficient method for detecting group-wise identity-by-descent regions simultaneously in multiple individuals based on pairwise IBD relationships | Q34354422 |
| | Population-based linkage analysis of schizophrenia and bipolar case-control cohorts identifies a potential susceptibility locus on 19q13. | Q34828678 |
| | Whole population, genome-wide mapping of hidden relatedness | Q34868594 |
| | How and when should interactome-derived clusters be used to predict functional modules and protein function? | Q35198634 |
| | Identity-by-descent-based heritability analysis in the Northern Finland Birth Cohort | Q36528366 |
| | Genome-wide characterization of shared and distinct genetic components that influence blood lipid levels in ethnically diverse human populations | Q36909249 |
| | Identity by descent between distant relatives: detection and applications | Q38044951 |
| | Approximating the coalescent with recombination | Q43239115 |
| P433 | issue | 7 | |
| P407 | language of work or name | English | Q1860 |
| P304 | page(s) | 915-922 | |
| P577 | publication date | 2013-12-19 | |
| P1433 | published in | Bioinformatics | Q4914910 |
| P1476 | title | Efficient clustering of identity-by-descent between multiple individuals | |
| P478 | volume | 30 | |