Haploview: analysis and visualization of LD and haplotype maps
about
Ensembl variation resourcesFetal alcohol exposure and IQ at age 8: evidence from a population-based birth-cohort studySystematic association mapping identifies NELL1 as a novel IBD disease geneGenetic variants in EPAS1 contribute to adaptation to high-altitude hypoxia in SherpasMaternal and fetal genetic associations of PTGER3 and PON1 with preterm birthHippocampal atrophy as a quantitative trait in a genome-wide association study identifying novel susceptibility genes for Alzheimer's diseasePolymorphisms within the novel type 2 diabetes risk locus MTNR1B determine beta-cell functionGender differences in genetic risk profiles for cardiovascular diseasePreterm birth in Caucasians is associated with coagulation and inflammation pathway gene variantsGenes to diseases (G2D) computational method to identify asthma candidate genesCanine population structure: assessment and impact of intra-breed stratification on SNP-based association studiesGenome-wide gene-environment study identifies glutamate receptor gene GRIN2A as a Parkinson's disease modifier gene via interaction with coffeeHigh-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regionsGenetic association and expression studies indicate a role of toll-like receptor 8 in pulmonary tuberculosisNon-synonymous polymorphisms in the FCN1 gene determine ligand-binding ability and serum levels of M-ficolinCentrosomal localization of the psoriasis candidate gene product, CCHCR1, supports a role in cytoskeletal organizationAssociation between FGFR1OP2/wit3.0 polymorphisms and residual ridge resorption of mandible in Korean populationPolymorphisms in RYBP and AOAH genes are associated with chronic rhinosinusitis in a Chinese population: a replication studyThe PLIN4 variant rs8887 modulates obesity related phenotypes in humans through creation of a novel miR-522 seed siteGenome-wide association study identifies single nucleotide polymorphism in DYRK1A associated with replication of HIV-1 in monocyte-derived macrophagesIntegrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locusA conserved role for syndecan family members in the regulation of whole-body energy metabolismSelection for genetic variation inducing pro-inflammatory responses under adverse environmental conditions in a Ghanaian populationGenetic structure of Europeans: a view from the North-EastGenome-wide association study of young-onset hypertension in the Han Chinese population of TaiwanCommon variants within MECP2 confer risk of systemic lupus erythematosusA high density SNP array for the domestic horse and extant Perissodactyla: utility for association mapping, genetic diversity, and phylogeny studiesGermline genetic variants disturbing the Let-7/LIN28 double-negative feedback loop alter breast cancer susceptibilityGenome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosisIdentifying signatures of natural selection in Tibetan and Andean populations using dense genome scan dataEvaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot"Functional polymorphisms in PRODH are associated with risk and protection for schizophrenia and fronto-striatal structure and functionGenetic analysis of completely sequenced disease-associated MHC haplotypes identifies shuffling of segments in recent human history.Lipoprotein genotype and conserved pathway for exceptional longevity in humansMega2: validated data-reformatting for linkage and association analysesThe cushion-star Parvulastra exigua in South Africa: one species or more?Common NFKBIL2 polymorphisms and susceptibility to pneumococcal disease: a genetic association studyPolymorphisms in leucine-rich repeat genes are associated with autism spectrum disorder susceptibility in populations of European ancestryCardioGxE, a catalog of gene-environment interactions for cardiometabolic traitsDeep resequencing of the voltage-gated potassium channel subunit KCNE3 gene in chronic tinnitus
P2860
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P2860
Haploview: analysis and visualization of LD and haplotype maps
description
2005 nî lūn-bûn
@nan
2005 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Haploview: analysis and visualization of LD and haplotype maps
@ast
Haploview: analysis and visualization of LD and haplotype maps
@en
Haploview: analysis and visualization of LD and haplotype maps
@nl
type
label
Haploview: analysis and visualization of LD and haplotype maps
@ast
Haploview: analysis and visualization of LD and haplotype maps
@en
Haploview: analysis and visualization of LD and haplotype maps
@nl
prefLabel
Haploview: analysis and visualization of LD and haplotype maps
@ast
Haploview: analysis and visualization of LD and haplotype maps
@en
Haploview: analysis and visualization of LD and haplotype maps
@nl
P3181
P356
P1433
P1476
Haploview: analysis and visualization of LD and haplotype maps
@en
P2093
P3181
P356
10.1093/BIOINFORMATICS/BTH457
P407
P577
2005-01-15T00:00:00Z