A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission.
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Mega2: validated data-reformatting for linkage and association analysesExamination of NRCAM, LRRN3, KIAA0716, and LAMB1 as autism candidate genesControl of confounding of genetic associations in stratified populationsFamily-based association study of synapsin II and schizophreniaThe Ile198Thr and Ala379Val variants of plasmatic PAF-acetylhydrolase impair catalytical activities and are associated with atopy and asthmaFunctional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence.Variants in the SP110 gene are associated with genetic susceptibility to tuberculosis in West AfricaGenetic variation in the 6p22.3 gene DTNBP1, the human ortholog of the mouse dysbindin gene, is associated with schizophreniaT-bet polymorphisms are associated with asthma and airway hyperresponsivenessAryl hydrocarbon receptor nuclear translocator-like (BMAL1) is associated with susceptibility to hypertension and type 2 diabetesEvidence for association of schizophrenia with genetic variation in the 8p21.3 gene, PPP3CC, encoding the calcineurin gamma subunitVariants in the vitamin D receptor gene and asthmaTapasin gene polymorphism in systemic onset juvenile rheumatoid arthritis: a family-based case-control study.Evaluation of SLC11A1 as an inflammatory bowel disease candidate geneUsing ancestry matching to combine family-based and unrelated samples for genome-wide association studiesAssociation of polymorphisms in the apolipoprotein E region with susceptibility to and progression of multiple sclerosisReplication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia familiesAssociation of GABRG3 with alcohol dependenceAssociation of DLG5 R30Q variant with inflammatory bowel diseaseAssociation of the homeobox transcription factor, ENGRAILED 2, 3, with autism spectrum disorderGene expression and association analyses of LIM (PDLIM5) in bipolar disorder and schizophreniaEvaluating association and transmission of eight inflammatory genes with Viliuisk encephalomyelitis susceptibilityAssociation of the glutamate receptor subunit gene GRIN2B with attention-deficit/hyperactivity disorderSupport for EKN1 as the susceptibility locus for dyslexia on 15q21A dinucleotide deletion in CD24 confers protection against autoimmune diseasesA Mal functional variant is associated with protection against invasive pneumococcal disease, bacteremia, malaria and tuberculosisA generalized family-based association test for dichotomous traits.Review and evaluation of methods correcting for population stratification with a focus on underlying statistical principlesHandling missing data in transmission disequilibrium test in nuclear families with one affected offspring.Detection of disease genes by use of family data. I. Likelihood-based theoryA unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetesTests for genetic association using family data.Association of familial and sporadic rheumatoid arthritis with a single corticotropin-releasing hormone genomic region (8q12.3) haplotype.Identification of two independent risk factors for lupus within the MHC in United Kingdom families.Bootstrap calibration of TRANSMIT for informative missingness of parental genotype dataFine mapping functional sites or regions from case-control data using haplotypes of multiple linked SNPs.High resolution T association tests of complex diseases based on family data.Identification of polymorphisms explaining a linkage signal: application to the GAW14 simulated dataAllowing for missing data at highly polymorphic genes when testing for maternal, offspring and maternal-fetal genotype incompatibility effects.An evaluation of power and type I error of single-nucleotide polymorphism transmission/disequilibrium-based statistical methods under different family structures, missing parental data, and population stratification.
P2860
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P2860
A generalization of the transmission/disequilibrium test for uncertain-haplotype transmission.
description
1999 nî lūn-bûn
@nan
1999年の論文
@ja
1999年学术文章
@wuu
1999年学术文章
@zh-cn
1999年学术文章
@zh-hans
1999年学术文章
@zh-my
1999年学术文章
@zh-sg
1999年學術文章
@yue
1999年學術文章
@zh
1999年學術文章
@zh-hant
name
A generalization of the transm ...... ertain-haplotype transmission.
@en
A generalization of the transm ...... ertain-haplotype transmission.
@nl
type
label
A generalization of the transm ...... ertain-haplotype transmission.
@en
A generalization of the transm ...... ertain-haplotype transmission.
@nl
prefLabel
A generalization of the transm ...... ertain-haplotype transmission.
@en
A generalization of the transm ...... ertain-haplotype transmission.
@nl
P2860
P356
P1476
A generalization of the transm ...... ertain-haplotype transmission.
@en
P2093
P2860
P304
P356
10.1086/302577
P407
P577
1999-10-01T00:00:00Z