Linkage analysis in the presence of errors I: complex-valued recombination fractions and complex phenotypes.
about
Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigreesA linkage study of candidate loci in familial Parkinson's DiseaseStructures of isobutyryl-CoA dehydrogenase and enzyme-product complex: comparison with isovaleryl- and short-chain acyl-CoA dehydrogenasesA novel approach to the characterization of substrate specificity in short/branched chain Acyl-CoA dehydrogenaseA genome scan and follow-up study identify a bipolar disorder susceptibility locus on chromosome 1q42A 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.Comparison of linkage analysis methods for genome-wide scanning of extended pedigrees, with application to the TG/HDL-C ratio in the Framingham Heart StudyDetection of genotyping errors by Hardy-Weinberg equilibrium testing.On different approximations to multilocus identity-by-descent calculations and the resulting power of variance component-based linkage analysis.Comparing single-nucleotide polymorphism marker-based and microsatellite marker-based linkage analyses.Approaches to handling incomplete data in family-based association testing.Design considerations in a sib-pair study of linkage for susceptibility loci in cancer.No evidence of BRCA2 mutations in chromosome 13q-linked Utah high-risk prostate cancer pedigrees.Genome-wide linkage in Utah autism pedigreesA missense mutation in the aggrecan C-type lectin domain disrupts extracellular matrix interactions and causes dominant familial osteochondritis dissecans.Predisposition locus for major depression at chromosome 12q22-12q23.2.An application of the latent p value method to assess linkage in asthma pedigrees.Genomewide multipoint linkage analysis of seven extended Palauan pedigrees with schizophrenia, by a Markov-chain Monte Carlo method.Large upward bias in estimation of locus-specific effects from genomewide scans.Linkage analysis in the presence of errors II: marker-locus genotyping errors modeled with hypercomplex recombination fractionsLinkage analysis in the presence of errors III: marker loci and their map as nuisance parameters.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.Genotyping error detection through tightly linked markers.Fine mapping of candidate regions for bipolar disorder provides strong evidence for susceptibility loci on chromosomes 7qPSEUDOMARKER: a powerful program for joint linkage and/or linkage disequilibrium analysis on mixtures of singletons and related individuals.Evidence for pelvic organ prolapse predisposition genes on chromosomes 10 and 17.Factors affecting statistical power in the detection of genetic association.On the validity of the likelihood ratio test and consistency of resulting parameter estimates in joint linkage and linkage disequilibrium analysis under improperly specified parametric models.Utah family-based analysis: past, present and future.Further examination of the candidate genes in chromosome 12p13 locus for late-onset Alzheimer disease.Significant evidence for linkage to chromosome 5q13 in a genome-wide scan for asthma in an extended pedigree resource.A major predisposition locus for severe obesity, at 4p15-p14Detection and integration of genotyping errors in statistical geneticsGenome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disordersGenetic mapping in the presence of genotyping errors.Genome-wide linkage analysis for celiac disease in North American families.Convergent evolution of a 2-methylbutyryl-CoA dehydrogenase from isovaleryl-CoA dehydrogenase in Solanum tuberosum.Model-Free Linkage Analysis of a Binary Trait.An utter refutation of the "fundamental theorem of the HapMap".
P2860
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P2860
Linkage analysis in the presence of errors I: complex-valued recombination fractions and complex phenotypes.
description
2000 nî lūn-bûn
@nan
2000 թուականի Մարտին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի մարտին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Linkage analysis in the presen ...... ctions and complex phenotypes.
@ast
Linkage analysis in the presen ...... ctions and complex phenotypes.
@en
Linkage analysis in the presen ...... ctions and complex phenotypes.
@nl
type
label
Linkage analysis in the presen ...... ctions and complex phenotypes.
@ast
Linkage analysis in the presen ...... ctions and complex phenotypes.
@en
Linkage analysis in the presen ...... ctions and complex phenotypes.
@nl
prefLabel
Linkage analysis in the presen ...... ctions and complex phenotypes.
@ast
Linkage analysis in the presen ...... ctions and complex phenotypes.
@en
Linkage analysis in the presen ...... ctions and complex phenotypes.
@nl
P2860
P356
P1476
Linkage analysis in the presen ...... ctions and complex phenotypes.
@en
P2093
H H Göring
J D Terwilliger
P2860
P304
P356
10.1086/302797
P407
P577
2000-03-01T00:00:00Z