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Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progressionHigh-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regionsGenetic differences between the determinants of lipid profile phenotypes in African and European Americans: the Jackson Heart StudyGenetic variation in healthy oldest-oldEvaluation 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 functionCYP2D6 gene variants: association with breast cancer specific survival in a cohort of breast cancer patients from the United Kingdom treated with adjuvant tamoxifenImplication of next-generation sequencing on association studiesAssociation between KCNJ6 (GIRK2) gene polymorphisms and postoperative analgesic requirements after major abdominal surgeryHLA-DRB1 reduces the risk of type 2 diabetes mellitus by increased insulin secretionAssociation of common variants in the human eyes shut ortholog (EYS) with statin-induced myopathy: evidence for additional functions of EYSGenetic association analysis of 13 nuclear-encoded mitochondrial candidate genes with type II diabetes mellitus: the DAMAGE studyA systematic gene-based screen of chr4q22-q32 identifies association of a novel susceptibility gene, DKK2, with the quantitative trait of alcohol dependence symptom countsReplication of association between working memory and Reelin, a potential modifier gene in schizophreniaAPOE/C1/C4/C2 gene cluster genotypes, haplotypes and lipid levels in prospective coronary heart disease risk among UK healthy menConfirmation of association between multiple sclerosis and CYP27B1High-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate geneGenome-wide and fine-resolution association analysis of malaria in West AfricaIdentification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypesCLOCK in breast tumorigenesis: genetic, epigenetic, and transcriptional profiling analysesMaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypesLinkage and association analysis of CACNG3 in childhood absence epilepsyA genome-wide analysis identifies genetic variants in the RELN gene associated with otosclerosisGenome-wide association study identifies novel breast cancer susceptibility lociNo evidence for association between 19 cholinergic genes and bipolar disorderAssociation of the proprotein convertase subtilisin/kexin-type 2 (PCSK2) gene with type 2 diabetes in an African American population.African Americans with asthma: genetic insightsInterpopulation linkage disequilibrium patterns of GABRA2 and GABRG1 genes at the GABA cluster locus on human chromosome 4A second generation human haplotype map of over 3.1 million SNPsIdentification of common variants in the SHBG gene affecting sex hormone-binding globulin levels and breast cancer risk in postmenopausal womenSingle nucleotide differences (SNDs) in the dbSNP database may lead to errors in genotyping and haplotyping studiesCommon variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetranceBone morphogenetic protein 7 (BMP7) gene polymorphisms are associated with inverse relationships between vascular calcification and BMD: the Diabetes Heart StudyTRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide studyCommon genetic variation in candidate genes and susceptibility to subtypes of breast cancerSingapore Genome Variation Project: a haplotype map of three Southeast Asian populationsComprehensive testing of positionally cloned asthma genes in two populationsGenetic mapping at 3-kilobase resolution reveals inositol 1,4,5-triphosphate receptor 3 as a risk factor for type 1 diabetes in SwedenA haplotype map of the human genomeA genetic association study of chromosome 11q22-24 in two different samples implicates the FXYD6 gene, encoding phosphohippolin, in susceptibility to schizophrenia
P2860
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P2860
description
2005 nî lūn-bûn
@nan
2005 թուականի Նոյեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի նոյեմբերին 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
Efficiency and power in genetic association studies
@ast
Efficiency and power in genetic association studies
@en
Efficiency and power in genetic association studies
@nl
type
label
Efficiency and power in genetic association studies
@ast
Efficiency and power in genetic association studies
@en
Efficiency and power in genetic association studies
@nl
prefLabel
Efficiency and power in genetic association studies
@ast
Efficiency and power in genetic association studies
@en
Efficiency and power in genetic association studies
@nl
P2860
P50
P3181
P356
P1433
P1476
Efficiency and power in genetic association studies
@en
P2093
Paul I W de Bakker
Roman Yelensky
P2860
P2888
P304
P3181
P356
10.1038/NG1669
P407
P577
2005-11-01T00:00:00Z