Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified.

Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified.

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http://www.wikidata.org/entity/Q34145564

Q34145564

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How many diseases does it take to map a gene with SNPs?Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus A genomewide screen of 345 families for autism-susceptibility loci.Identification of a new candidate locus for uric acid nephrolithiasis.The genetics of rheumatoid arthritis and the need for animal models to find and understand the underlying genes Evidence for allelic association on chromosome 3q25-27 in families with autism spectrum disorders originating from a subisolate of Finland Replication of linkage on chromosome 7q22 and association of the regional Reelin gene with working memory in schizophrenia families A genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42 A transmission/disequilibrium test that allows for genotyping errors in the analysis of single-nucleotide polymorphism data.Simple tests to detect errors in high-throughput genotype data in the molecular laboratory.Combined linkage and family-based association analysis improves candidate gene detection in Genetic Analysis Workshop 18 simulation data.Effects of updating linkage evidence across subsets of data: reanalysis of the autism genetic resource exchange data set.Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data.Detection of genotyping errors by Hardy-Weinberg equilibrium testing.Approaches to handling incomplete data in family-based association testing.Identifying single-nucleotide polymorphisms responsible for the linkage signal of rheumatoid arthritis on chromosome 6 by joint modeling of linkage and association.Two candidate genes for low platelet count identified in an Asian Indian kindred by genome-wide linkage analysis: glycoprotein IX and thrombopoietin.Allelic variants of IL1R1 gene associate with severe hand osteoarthritis.In vitro vs in silico detected SNPs for the development of a genotyping array: what can we learn from a non-model species?Role of nicotine dependence in the association between the dopamine receptor gene DRD3 and major depressive disorder Mapping a new spontaneous preterm birth susceptibility gene, IGF1R, using linkage, haplotype sharing, and association analysis.Linkage analysis of schizophrenia controlling for population substructure.Localization of a novel melanoma susceptibility locus to 1p22 Linkage disequilibrium mapping of schizophrenia susceptibility to the CAPON region of chromosome 1q22.Genomewide scan in families with schizophrenia from the founder population of Afrikaners reveals evidence for linkage and uniparental disomy on chromosome 1 Assessing the contribution family data can make to case-control studies of rare variants.Association testing in a linked region using large pedigrees Joint modeling of linkage and association: identifying SNPs responsible for a linkage signal Large upward bias in estimation of locus-specific effects from genomewide scans.Statistical approaches to gene mapping Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland.Linkage analysis in the presence of errors I: complex-valued recombination fractions and complex phenotypes.Linkage analysis in the presence of errors II: marker-locus genotyping errors modeled with hypercomplex recombination fractions Linkage analysis in the presence of errors III: marker loci and their map as nuisance parameters.Disease-related mutations among Caribbean Hispanics with familial dementia.A novel test of informative missingness using inconsistent linkage disequilibrium signals between case-parent triads and incomplete data.A potential novel spontaneous preterm birth gene, AR, identified by linkage and association analysis of X chromosomal markers.Families with the risk allele of DISC1 reveal a link between schizophrenia and another component of the same molecular pathway, NDE1.Genotyping error detection through tightly linked markers.Complex pedigrees in the sequencing era: to track transmissions or decorrelate?

P2860

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P2860

Linkage analysis in the presence of errors IV: joint pseudomarker analysis of linkage and/or linkage disequilibrium on a mixture of pedigrees and singletons when the mode of inheritance cannot be accurately specified.

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http://www.wikidata.org/entity/Q34145564

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2000 nî lūn-bûn

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2000 թուականի Մարտին հրատարակուած գիտական յօդուած

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2000 թվականի մարտին հրատարակված գիտական հոդված

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2000年の論文

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