Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium
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The diploid genome sequence of an individual humanGender differences in genetic risk profiles for cardiovascular diseaseVariation in LPA is associated with Lp(a) levels in three populations from the Third National Health and Nutrition Examination SurveyEvaluation of candidate stromal epithelial cross-talk genes identifies association between risk of serous ovarian cancer and TERT, a cancer susceptibility "hot-spot"Implication of next-generation sequencing on association studiesAsthma and genes encoding components of the vitamin D pathwayAssociation between KCNJ6 (GIRK2) gene polymorphisms and postoperative analgesic requirements after major abdominal surgeryProspects for admixture mapping of complex traitsGenetic variation in soluble epoxide hydrolase (EPHX2) and risk of coronary heart disease: The Atherosclerosis Risk in Communities (ARIC) studyGenetic susceptibility to occupational exposuresFunctional polymorphism in human CYP4F2 decreases 20-HETE productionNovel genetic variants contributing to left ventricular hypertrophy: the HyperGEN study.Identification of risk and age-at-onset genes on chromosome 1p in Parkinson disease.High-resolution whole-genome association study of Parkinson disease.Support for the homeobox transcription factor gene ENGRAILED 2 as an autism spectrum disorder susceptibility locusDevelopmentally restricted genetic determinants of human arsenic metabolism: association between urinary methylated arsenic and CYT19 polymorphisms in children.Variation in the gene encoding the serotonin 2A receptor is associated with outcome of antidepressant treatmentGerm line variation in nucleotide excision repair genes and lung cancer risk in smokersNovel susceptibility loci for second primary tumors/recurrence in head and neck cancer patients: large-scale evaluation of genetic variantsAssociation between genetic variants in VEGF, ERCC3 and occupational benzene haematotoxicityAssociations of 9p21 variants with cutaneous malignant melanoma, nevi, and pigmentation phenotypes in melanoma-prone families with and without CDKN2A mutationsSex-specific association of the Reelin gene with bipolar disorderMaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypesIntegrative predictive model of coronary artery calcification in atherosclerosis.No evidence for association between 19 cholinergic genes and bipolar disorderVariation in eicosanoid genes, non-fatal myocardial infarction and ischemic stroke.Polymorphisms in mitochondrial genes and prostate cancer riskPolymorphism in the IL18 gene and epithelial ovarian cancer in non-Hispanic white womenInterpopulation linkage disequilibrium patterns of GABRA2 and GABRG1 genes at the GABA cluster locus on human chromosome 4Signals of recent positive selection in a worldwide sample of human populationsA high-density association screen of 155 ion transport genes for involvement with common migraineNo associations of human pulmonary tuberculosis with Sp110 variantsRapid and accurate haplotype phasing and missing-data inference for whole-genome association studies by use of localized haplotype clusteringQuantitative trait loci predicting circulating sex steroid hormones in men from the NCI-Breast and Prostate Cancer Cohort Consortium (BPC3)Genetic mapping at 3-kilobase resolution reveals inositol 1,4,5-triphosphate receptor 3 as a risk factor for type 1 diabetes in SwedenDevelopmental and genetic modulation of arsenic biotransformation: a gene by environment interaction?A haplotype map of the human genomeComprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association.Common ERBB2 polymorphisms and risk of breast cancer in a white British population: a case-control studyERBB2 in cat mammary neoplasias disclosed a positive correlation between RNA and protein low expression levels: a model for erbB-2 negative human breast cancer
P2860
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P2860
Selecting a maximally informative set of single-nucleotide polymorphisms for association analyses using linkage disequilibrium
description
2004 nî lūn-bûn
@nan
2004 թուականի Յունուարին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի հունվարին հրատարակված գիտական հոդված
@hy
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
name
Selecting a maximally informat ...... s using linkage disequilibrium
@ast
Selecting a maximally informat ...... s using linkage disequilibrium
@en
type
label
Selecting a maximally informat ...... s using linkage disequilibrium
@ast
Selecting a maximally informat ...... s using linkage disequilibrium
@en
prefLabel
Selecting a maximally informat ...... s using linkage disequilibrium
@ast
Selecting a maximally informat ...... s using linkage disequilibrium
@en
P2093
P2860
P3181
P356
P1476
Selecting a maximally informat ...... s using linkage disequilibrium
@en
P2093
P2860
P304
P3181
P356
10.1086/381000
P407
P577
2004-01-01T00:00:00Z