Gene mapping in the 20th and 21st centuries: statistical methods, data analysis, and experimental design.
about
Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigreesMapping the new frontier: complex genetic disorders.Prospects for admixture mapping of complex traitsDesign and analysis of admixture mapping studiesGenomewide scans of complex human diseases: true linkage is hard to findLinkage analysis in the next-generation sequencing eraThe genetics of rheumatoid arthritis and the need for animal models to find and understand the underlying genesScience, medicine, and the future. Genetic epidemiologyTilting at quixotic trait loci (QTL): an evolutionary perspective on genetic causationSize matters: just how big is BIG?: Quantifying realistic sample size requirements for human genome epidemiology"Are we there yet?": Deciding when one has demonstrated specific genetic causation in complex diseases and quantitative traits.Influence of leukotriene gene polymorphisms on chronic rhinosinusitis.Genome-wide linkage in Utah autism pedigreesNational Biobanks: Clinical Labor, Risk Production, and the Creation of BiovalueThe emperor's new methodsCombined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16qQuantitative-trait-locus analysis of body-mass index and of stature, by combined analysis of genome scans of five Finnish study groups.Large upward bias in estimation of locus-specific effects from genomewide scans.Two loci on chromosomes 2 and X for premature coronary heart disease identified in early- and late-settlement populations of Finland.A genome scan in families from Australia and New Zealand confirms the presence of a maternal susceptibility locus for pre-eclampsia, on chromosome 2Linkage 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 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.Genome scan for loci regulating HDL cholesterol levels in Finnish extended pedigrees with early coronary heart diseaseSingle nucleotide polymorphism seeking long term association with complex diseaseInbreeding and the genetic complexity of human hypertension.Optimal designs for linkage disequilibrium mapping and candidate gene association tests in livestock populationsA low COMT activity haplotype is associated with recurrent preeclampsia in a Norwegian population cohort (HUNT2)PSEUDOMARKER: a powerful program for joint linkage and/or linkage disequilibrium analysis on mixtures of singletons and related individuals.Neurocognitive function in an extended Afrikaner-ancestry family with affective illnessOn the statistical properties of family-based association tests in datasets containing both pedigrees and unrelated case-control samples.Estimation and visualization of identity-by-descent within pedigrees simplifies interpretation of complex trait analysis.Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families.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.A significant risk locus on 19q13 for bipolar disorder identified using a combined genome-wide linkage and copy number variation analysis.Translational research in central nervous system drug discovery.Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late-onset Alzheimer's disease.Dopamine genes and schizophrenia: case closed or evidence pending?Reflections on the Field of Human Genetics: A Call for Increased Disease Genetics Theory
P2860
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P2860
Gene mapping in the 20th and 21st centuries: statistical methods, data analysis, and experimental design.
description
2000 nî lūn-bûn
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2000 թուականի Փետրուարին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի փետրվարին 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
Gene mapping in the 20th and 2 ...... ysis, and experimental design.
@ast
Gene mapping in the 20th and 2 ...... ysis, and experimental design.
@en
type
label
Gene mapping in the 20th and 2 ...... ysis, and experimental design.
@ast
Gene mapping in the 20th and 2 ...... ysis, and experimental design.
@en
prefLabel
Gene mapping in the 20th and 2 ...... ysis, and experimental design.
@ast
Gene mapping in the 20th and 2 ...... ysis, and experimental design.
@en
P1433
P1476
Gene mapping in the 20th and 2 ...... lysis, and experimental design
@en
P2093
Terwilliger JD
P304
P577
2000-02-01T00:00:00Z