A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other.
about
Genes to diseases (G2D) computational method to identify asthma candidate genesThe role of aldehyde dehydrogenase-1 (ALDH1A1) polymorphisms in harmful alcohol consumption in a Finnish populationAssociation of toll-interacting protein gene polymorphisms with atopic dermatitisGenome-wide analyses of borderline personality featuresThe Use of Multiplicity Corrections, Order Statistics and Generalized Family-Wise Statistics with Application to Genome-Wide StudiesPlacing epidemiological results in the context of multiplicity and typical correlations of exposuresSystematic identification of interaction effects between genome- and environment-wide associations in type 2 diabetes mellitusBipolar I disorder and schizophrenia: a 440-single-nucleotide polymorphism screen of 64 candidate genes among Ashkenazi Jewish case-parent triosDyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sampleJoint influence of small-effect genetic variants on human longevityA 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 schizophreniaAssociation between IRF6 and nonsyndromic cleft lip with or without cleft palate in four populationsBasic statistical analysis in genetic case-control studiesBlood pressure loci identified with a gene-centric arrayLinkage and association analysis of CACNG3 in childhood absence epilepsyExamination of association of genes in the serotonin system to autismAn ancestral variant of Secretogranin II confers regulation by PHOX2 transcription factors and association with hypertensionInteraction between interleukin 3 and dystrobrevin-binding protein 1 in schizophreniaA high-density association screen of 155 ion transport genes for involvement with common migraineHigh throughput SNP and expression analyses of candidate genes for non-syndromic oral cleftsCommon variants in the BMP2, BMP4, and HJV genes of the hepcidin regulation pathway modulate HFE hemochromatosis penetranceConvergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophreniaMultiple ADH genes modulate risk for drug dependence in both African- and European-AmericansCharacterization of the linkage disequilibrium structure and identification of tagging-SNPs in five DNA repair genes.Association of the OSCAR promoter polymorphism with BMD in postmenopausal womenDyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutationAssociation between the insulin-induced gene 2 (INSIG2) and weight gain in a German sample of antipsychotic-treated schizophrenic patients: perturbation of SREBP-controlled lipogenesis in drug-related metabolic adverse effects?Efficiency and power in genetic association studiesLinkage and association studies in African- and Caucasian-American populations demonstrate that SHC3 is a novel susceptibility locus for nicotine dependenceA single nucleotide polymorphism in APOA5 determines triglyceride levels in Hong Kong and Guangzhou ChineseGenetic variance in a component of the language acquisition device: ROBO1 polymorphisms associated with phonological buffer deficitsAssociation of Cardiometabolic Genes with Arsenic Metabolism Biomarkers in American Indian Communities: The Strong Heart Family Study (SHFS)Novel genetic locus implicated for HIV-1 acquisition with putative regulatory links to HIV replication and infectivity: a genome-wide association studyReceptor Polymorphism and Genomic Structure Interact to Shape Bitter Taste PerceptionAssociation of DCDC2 Polymorphisms with Normal Variations in Reading Abilities in a Chinese PopulationThe Growing Importance of CNVs: New Insights for Detection and Clinical InterpretationVariants located upstream of CHRNB4 on chromosome 15q25.1 are associated with age at onset of daily smoking and habitual smokingAssociation analysis of 94 candidate genes and schizophrenia-related endophenotypes.The effect of PCSK1 variants on waist, waist-hip ratio and glucose metabolism is modified by sex and glucose tolerance status
P2860
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P2860
A simple correction for multiple testing for single-nucleotide polymorphisms in linkage disequilibrium with each other.
description
2004 nî lūn-bûn
@nan
2004 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2004 թվականի մարտին 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
A simple correction for multip ...... isequilibrium with each other.
@ast
A simple correction for multip ...... isequilibrium with each other.
@en
type
label
A simple correction for multip ...... isequilibrium with each other.
@ast
A simple correction for multip ...... isequilibrium with each other.
@en
prefLabel
A simple correction for multip ...... isequilibrium with each other.
@ast
A simple correction for multip ...... isequilibrium with each other.
@en
P2860
P356
P1476
A simple correction for multip ...... isequilibrium with each other.
@en
P2860
P304
P356
10.1086/383251
P407
P577
2004-03-02T00:00:00Z