| scholarly article | Q13442814 |
| P50 | author | Andrew G. Clark | Q4757042 |
| Stephen J. O'Brien | Q7609573 | ||
| P2093 | author name string | Yu Wang | |
| Sorin Istrail | |||
| Dennis A Gilbert | |||
| Francisco M De La Vega | |||
| Karl J Guegler | |||
| Yi Zheng | |||
| Mitsuo Itakura | |||
| Andrew Collins | |||
| Bjarni V Halldórsson | |||
| Xiaoping Su | |||
| Guy de Thé | |||
| Ross A Lippert | |||
| Junko F Stevens | |||
| Xiaoqing You | |||
| Francis Kalush | |||
| Ryan T Koehler | |||
| Janet S Ziegle | |||
| Charles R Scafe | |||
| Eugene G Spier | |||
| Hadar Isaac | |||
| Heinz G Hemken | |||
| Kyle M Leinen | |||
| Lewis T Wogan | |||
| Lily H Xu | |||
| Marion Laig-Webster | |||
| Michael W Hunkapiller | |||
| Sheri J Olson | |||
| P2860 | cites work | Genetic and fossil evidence for the origin of modern humans | Q22065529 |
| The Sequence of the Human Genome | Q22065842 | ||
| dbSNP: the NCBI database of genetic variation | Q24608672 | ||
| The structure of haplotype blocks in the human genome | Q27860500 | ||
| The International HapMap Project | Q27860695 | ||
| Intensely punctate meiotic recombination in the class II region of the major histocompatibility complex | Q28190352 | ||
| Impact of population structure, effective bottleneck time, and allele frequency on linkage disequilibrium maps | Q28770047 | ||
| A high-resolution recombination map of the human genome | Q29547815 | ||
| The Celera Discovery System. | Q30329281 | ||
| New generation pharmacogenomic tools: a SNP linkage disequilibrium Map, validated SNP assay resource, and high-throughput instrumentation system for large-scale genetic studies | Q30737171 | ||
| Haplotype diversity across 100 candidate genes for inflammation, lipid metabolism, and blood pressure regulation in two populations | Q33909698 | ||
| Human male recombination maps for individual chromosomes | Q33911027 | ||
| DNA synthesis errors associated with double-strand-break repair | Q33965497 | ||
| PharmGKB: the Pharmacogenetics Knowledge Base | Q34010656 | ||
| The first linkage disequilibrium (LD) maps: delineation of hot and cold blocks by diplotype analysis | Q34012852 | ||
| Lower-than-expected linkage disequilibrium between tightly linked markers in humans suggests a role for gene conversion | Q34044608 | ||
| Human genome sequence variation and the influence of gene history, mutation and recombination | Q34142742 | ||
| High levels of sequence polymorphism and linkage disequilibrium at the telomere of 12q: implications for telomere biology and human evolution. | Q34146140 | ||
| Variation of gene-based SNPs and linkage disequilibrium patterns in the human genome | Q34326176 | ||
| Localization of psoriasis-susceptibility locus PSORS1 to a 60-kb interval telomeric to HLA-C. | Q34390693 | ||
| Properties of linkage disequilibrium (LD) maps | Q34430510 | ||
| An automated computer system to support ultra high throughput SNP genotyping. | Q34584627 | ||
| Familial psoriasis and HLA-B: unambiguous support for linkage in 97 published families | Q34750227 | ||
| Human SNP variability and mutation rate are higher in regions of high recombination | Q34750287 | ||
| A SNP resource for human chromosome 22: extracting dense clusters of SNPs from the genomic sequence | Q35031627 | ||
| Recombination explains isochores in mammalian genomes | Q35076941 | ||
| The optimal measure of allelic association | Q35868910 | ||
| Gene map of the extended human MHC. | Q35968433 | ||
| Power calculations for genetic association studies using estimated probability distributions | Q37217339 | ||
| Ethnic-difference markers for use in mapping by admixture linkage disequilibrium | Q37361406 | ||
| Optimal haplotype block-free selection of tagging SNPs for genome-wide association studies | Q39817287 | ||
| Family-based analysis using a dense single-nucleotide polymorphism-based map defines genetic variation at PSORS1, the major psoriasis-susceptibility locus | Q40725419 | ||
| The impact of SNP density on fine-scale patterns of linkage disequilibrium | Q46454351 | ||
| A global survey of haplotype frequencies and linkage disequilibrium at the DRD2 locus | Q46793079 | ||
| A metric linkage disequilibrium map of a human chromosome | Q47356435 | ||
| Robustness of inference of haplotype block structure | Q47993569 | ||
| Does haplotype diversity predict power for association mapping of disease susceptibility? | Q48538210 | ||
| Is haplotype block identification useful for association mapping studies? | Q51996463 | ||
| Blocks of limited haplotype diversity revealed by high-resolution scanning of human chromosome 21. | Q52051237 | ||
| High-resolution haplotype structure in the human genome | Q56002085 | ||
| Chromosome-wide distribution of haplotype blocks and the role of recombination hot spots | Q56879657 | ||
| A first-generation linkage disequilibrium map of human chromosome 22 | Q56879659 | ||
| Patterns of linkage disequilibrium in the MHC region on human chromosome 6p | Q57568948 | ||
| The optimal measure of linkage disequilibrium reduces error in association mapping of affection status | Q62644506 | ||
| The genome-wide distribution of background linkage disequilibrium in a population isolate | Q73446646 | ||
| Recombination hotspots rather than population history dominate linkage disequilibrium in the MHC class II region | Q78685657 | ||
| Haplotype block structures show significant variation among populations | Q80609642 | ||
| P433 | issue | 4 | |
| P921 | main subject | linkage disequilibrium | Q2064311 |
| demographics | Q2725376 | ||
| disequilibrium | Q5282160 | ||
| P304 | page(s) | 454-462 | |
| P577 | publication date | 2005-03-21 | |
| P1433 | published in | Genome Research | Q5533485 |
| P1476 | title | The linkage disequilibrium maps of three human chromosomes across four populations reflect their demographic history and a common underlying recombination pattern | |
| P478 | volume | 15 |
| Q51706663 | A comparison of methods to detect recombination hotspots. |
| Q35038722 | A first-generation metric linkage disequilibrium map of bovine chromosome 6 |
| Q40598773 | A multifaceted computational report on the variants effect on KIR2DL3 and IFNL3 candidate gene in HCV clearance |
| Q57310432 | A predominant role for the HLA class II region in the association of the MHC region with multiple sclerosis |
| Q42743358 | A primary assembly of a bovine haplotype block map based on a 15,036-single-nucleotide polymorphism panel genotyped in holstein-friesian cattle. |
| Q83201548 | Association of NRAMP 1 gene polymorphism with susceptibility to tuberculosis in Taiwanese aboriginals |
| Q82077227 | Comparative study of the linkage disequilibrium of an ENCODE region, chromosome 7p15, in Korean, Japanese, and Han Chinese samples |
| Q40192727 | Comparison of ENCODE region SNPs between Cebu Filipino and Asian HapMap samples |
| Q33578165 | Comparison of linkage disequilibrium patterns between the HapMap CEPH samples and a family-based cohort of Northern European descent |
| Q36585409 | Constructing a linkage-linkage disequilibrium map using dominant-segregating markers |
| Q34307396 | Contrasting methods of quantifying fine structure of human recombination. |
| Q37270473 | Designing pharmacogenetic projects in industry: practical design perspectives from the Industry Pharmacogenomics Working Group |
| Q31120402 | Evaluation of genome-wide power of genetic association studies based on empirical data from the HapMap project |
| Q57297733 | Evaluation of the SNP tagging approach in an independent population sample—array-based SNP discovery in Sami |
| Q51645904 | Extensive linkage disequilibrium in a wild bird population. |
| Q38738916 | GeneImp: Fast Imputation to Large Reference Panels Using Genotype Likelihoods from Ultralow Coverage Sequencing. |
| Q40148417 | Genetic association of single nucleotide polymorphisms in endonuclease G-like 1 gene with type 2 diabetes in a Japanese population. |
| Q33747077 | Genomic and geographic distribution of private SNPs and pathways in human populations |
| Q21562491 | High differentiation among eight villages in a secluded area of Sardinia revealed by genome-wide high density SNPs analysis |
| Q33250071 | Human imprinted chromosomal regions are historical hot-spots of recombination. |
| Q34091093 | Identifying highly conserved and highly differentiated gene ontology categories in human populations |
| Q36388041 | Immunogenomics: molecular hide and seek |
| Q24288730 | Is replication the gold standard for validating genome-wide association findings? |
| Q42741267 | Joint Prediction of the Effective Population Size and the Rate of Fixation of Deleterious Mutations. |
| Q33325802 | Lack of association of genetic variation in chromosome region 15q14-22.1 with type 2 diabetes in a Japanese population |
| Q37799282 | Leprosy as a genetic disease |
| Q37735223 | Linkage disequilibrium mapping in domestic dog breeds narrows the progressive rod-cone degeneration interval and identifies ancestral disease-transmitting chromosome |
| Q80218672 | Long contiguous stretches of homozygosity in the human genome |
| Q46468372 | Magnitude and distribution of linkage disequilibrium in population isolates and implications for genome-wide association studies |
| Q89495287 | On the Extent of Linkage Disequilibrium in the Genome of Farm Animals |
| Q79360348 | Pairwise linkage disequilibrium under disease models |
| Q57909497 | Patterns of Linkage Disequilibrium between SNPs in a Sardinian Population Isolate and the Selection of Markers for Association Studies |
| Q47369948 | Power and sample size calculations for genetic case/control studies using gene-centric SNP maps: application to human chromosomes 6, 21, and 22 in three populations |
| Q39856829 | Pronounced inter- and intrachromosomal variation in linkage disequilibrium across the zebra finch genome |
| Q35009487 | Rare variant APOC3 R19X is associated with cardio-protective profiles in a diverse population-based survey as part of the Epidemiologic Architecture for Genes Linked to Environment Study |
| Q33417666 | Recombinational landscape and population genomics of Caenorhabditis elegans |
| Q48085245 | SNP identification, linkage disequilibrium, and haplotype analysis for a 200-kb genomic region in a Korean population |
| Q33379607 | Strong signature of natural selection within an FHIT intron implicated in prostate cancer risk |
| Q36057890 | Temporal dynamics of linkage disequilibrium in two populations of bighorn sheep. |
| Q24656569 | The SNPlex genotyping system: a flexible and scalable platform for SNP genotyping |
| Q43252157 | The portability of tagSNPs across populations: a worldwide survey |
| Q40969514 | Visualizing chromosome mosaicism and detecting ethnic outliers by the method of "rare" heterozygotes and homozygotes (RHH) |
| Q21283781 | Worldwide distribution of NAT2 diversity: implications for NAT2 evolutionary history |
Search more.