Artículos de la revista "BMC Genetics"
385 artículos en 20 páginas: 1 | 2 | 3 | 4 | 5 | 6 | 7 | 8 | 9 | 10 | 11 | 12 | 13 | 14 | 15 | 16 ... 20
- Are there mappable genes for family resemblance for the magnitude of intra-individual variation in systolic blood pressure?2003; 4(Suppl 1): S11
- Genome-wide linkage analysis of longitudinal phenotypes using σ2A random effects (SSARs) fitted by Gibbs sampling2003; 4(Suppl 1): S12
- Genome-wide linkage analysis of systolic blood pressure: a comparison of two approaches to phenotype definition2003; 4(Suppl 1): S13
- The genetics of cross-sectional and longitudinal body mass index2003; 4(Suppl 1): S14
- Empíricamente derivados fenotípica subgrupos - composición cualitativa y cuantitativa rasgo análisisEmpirically derived phenotypic subgroups – qualitative and quantitative trait analyses2003; 4(Suppl 1): S15
- Power of maximum HLOD tests to detect linkage to obesity genes2003; 4(Suppl 1): S16
- Comparison of longitudinal variance components and regression-based approaches for linkage detection on chromosome 17 for systolic blood pressure2003; 4(Suppl 1): S17
- Analysis of gene × environment interactions in sibships using mixed models2003; 4(Suppl 1): S18
- Multilevel modeling for the analysis of longitudinal blood pressure data in the Framingham Heart Study pedigrees2003; 4(Suppl 1): S19
- Description of the Framingham Heart Study data for Genetic Analysis Workshop 132003; 4(Suppl 1): S2
- Comparison of the linkage results of two phenotypic constructs from longitudinal data in the Framingham Heart Study: analyses on data measured at three time points and on the average of three measurements2003; 4(Suppl 1): S20
- Segregation and linkage analysis for longitudinal measurements of a quantitative trait2003; 4(Suppl 1): S21
- Longitudinal variance-components analysis of the Framingham Heart Study data2003; 4(Suppl 1): S22
- Comparison of Haseman-Elston regression analyses using single, summary, and longitudinal measures of systolic blood pressure2003; 4(Suppl 1): S23
- Genetic linkage analysis of longitudinal hypertension phenotypes using three summary measures2003; 4(Suppl 1): S24
- Longitudinal variance components models for systolic blood pressure, fitted using Gibbs sampling2003; 4(Suppl 1): S25
- Linkage analysis of cross-sectional and longitudinally derived phenotypic measures to identify loci influencing blood pressure2003; 4(Suppl 1): S26
- Linkage analysis of longitudinal data2003; 4(Suppl 1): S27
- Power of linkage analysis using traits generated from simulated longitudinal data of the Framingham Heart Study2003; 4(Suppl 1): S28
- Genetic analyses of longitudinal phenotype data: a comparison of univariate methods and a multivariate approach2003; 4(Suppl 1): S29
- Genetic Analysis Workshop 13: Simulated longitudinal data on families for a system of oligogenic traits2003; 4(Suppl 1): S3
- Consistency of linkage results across exams and methods in the Framingham Heart Study2003; 4(Suppl 1): S30
- Age-Stratified QTL Genome Scan Analyses for Anthropometric Measures2003; 4(Suppl 1): S31
- Age-stratified heritability estimation in the Framingham Heart Study families2003; 4(Suppl 1): S32
- Sibling recurrence risk ratio analysis of the metabolic syndrome and its components over time2003; 4(Suppl 1): S33
- Genome-wide linkage analysis using cross-sectional and longitudinal traits for body mass index in a subsample of the Framingham Heart Study2003; 4(Suppl 1): S35
- Comparison of year-of-exam- and age-matched estimates of heritability in the Framingham Heart Study data2003; 4(Suppl 1): S36
- Lack of reproducibility of linkage results in serially measured blood pressure data2003; 4(Suppl 1): S37
- Stability of exploratory multivariate data modeling in longitudinal data2003; 4(Suppl 1): S38
- Bootstrap calibration of TRANSMIT for informative missingness of parental genotype data2003; 4(Suppl 1): S39
- Variance components linkage analysis for adjusted systolic blood pressure in the Framingham Heart Study2003; 4(Suppl 1): S4
- An examination of the genotyping error detection function of SIMWALK22003; 4(Suppl 1): S40
- Pedigree and genotype errors in the Framingham Heart Study2003; 4(Suppl 1): S41
- Imputation methods for missing data for polygenic models2003; 4(Suppl 1): S42
- Multiple imputation methods for longitudinal blood pressure measurements from the Framingham Heart Study2003; 4(Suppl 1): S43
- Comparison of missing data approaches in linkage analysis2003; 4(Suppl 1): S44
- Interaction of gender and body mass index (BMI) reveals evidence of linkage for hypertension in the Framingham Heart Study2003; 4(Suppl 1): S45
- Comparison of significance level at the true location using two linkage approaches: LODPAL and GENEFINDER2003; 4(Suppl 1): S46
- Genome-wide scan on plasma triglyceride and high density lipoprotein cholesterol levels, accounting for the effects of correlated quantitative phenotypes2003; 4(Suppl 1): S47
- Transmission ratio distortion in families from the Framingham Heart Study2003; 4(Suppl 1): S48
- Susceptibility scoring in family-based association testing2003; 4(Suppl 1): S49
- Use of a random coefficient regression (RCR) model to estimate growth parameters2003; 4(Suppl 1): S5
- Adjusting for covariates on a slippery slope: linkage analysis of change over time2003; 4(Suppl 1): S50
- A statistical method for adjusting covariates in linkage analysis with sib pairs2003; 4(Suppl 1): S51
- Evidence for bivariate linkage of obesity and HDL-C levels in the Framingham Heart Study2003; 4(Suppl 1): S52
- Exploring pleiotropy using principal components2003; 4(Suppl 1): S53
- Pleiotropic effects on cardiovascular risk factors within and between the fourth and sixth decades of life: Implications for genotype × age interactions2003; 4(Suppl 1): S54
- Multivariate variance-components analysis of longitudinal blood pressure measurements from the Framingham Heart Study2003; 4(Suppl 1): S55
- Genetic analysis of common factors underlying cardiovascular disease-related traits2003; 4(Suppl 1): S56
- Localization of genes involved in the metabolic syndrome using multivariate linkage analysis2003; 4(Suppl 1): S57
- Identification of genes for complex disease using longitudinal phenotypes2003; 4(Suppl 1): S58
- Similarity by state/descent and genetic vector spaces: analysis of a longitudinal family study2003; 4(Suppl 1): S59
- Linkage analysis of a derived glucose phenotype in the Genetic Analysis Workshop 13 simulated data using a variety of Haseman-Elston based regression methods2003; 4(Suppl 1): S6
- Correlation between quantitative traits and correlation between corresponding LOD scores: detection of pleiotropic effects2003; 4(Suppl 1): S60
- Genome-wide linkage scan on estimated breeding values for a quantitative trait2003; 4(Suppl 1): S61
- Bivariate linkage analysis of cholesterol and triglyceride levels in the Framingham Heart Study2003; 4(Suppl 1): S62
- Screening the genome to detect an association with hypertension2003; 4(Suppl 1): S63
- Mapping complex traits using Random Forests2003; 4(Suppl 1): S64
- A genome-wide scan using tree-based association analysis for candidate loci related to fasting plasma glucose levels2003; 4(Suppl 1): S65
- Use of tree-based models to identify subgroups and increase power to detect linkage to cardiovascular disease traits2003; 4(Suppl 1): S66
- Risk factors for coronary artery disease and the use of neural networks to predict the presence or absence of high blood pressure2003; 4(Suppl 1): S67
- Multivariate sib-pair linkage analysis of longitudinal phenotypes by three step-wise analysis approaches2003; 4(Suppl 1): S68
- Acceso a la enfermedad utilizando genes Bayesiano variable con la selección Haseman método de ElstonLocating disease genes using Bayesian variable selection with the Haseman-Elston method2003; 4(Suppl 1): S69
- Quantitative trait linkage analysis of longitudinal change in body weight2003; 4(Suppl 1): S7
- Linkage analysis of the simulated data – evaluations and comparisons of methods2003; 4(Suppl 1): S70
- Approaches to mapping genetically correlated complex traits2003; 4(Suppl 1): S71
- On different approximations to multilocus identity-by-descent calculations and the resulting power of variance component-based linkage analysis2003; 4(Suppl 1): S72
- Importance sampling method of correction for multiple testing in affected sib-pair linkage analysis2003; 4(Suppl 1): S73
- Mapping loci influencing blood pressure in the Framingham pedigrees using model-free LOD score analysis of a quantitative trait2003; 4(Suppl 1): S74
- A model-integrated multipoint Bayesian analysis of hypertension in the Framingham Heart Study data finds little evidence of linkage2003; 4(Suppl 1): S75
- Linkage analysis of adult height with parent-of-origin effects in the Framingham Heart Study2003; 4(Suppl 1): S76
- Linkage analysis of systolic blood pressure: a score statistic and computer implementation2003; 4(Suppl 1): S77
- Genoma en todo el análisis de ligamiento de la presión arterial en virtud de la heterogeneidad locusGenome-wide linkage analysis of blood pressure under locus heterogeneity2003; 4(Suppl 1): S78
- Segregation analysis comparing liability and quantitative trait models for hypertension using the Genetic Analysis Workshop 13 simulated data2003; 4(Suppl 1): S79
- An autosome-wide search using longitudinal data for loci linked to type 2 diabetes progression2003; 4(Suppl 1): S8
- Age-of-onset of hypertension vs. a single measurement of systolic blood pressure in a combined linkage and segregation analysis2003; 4(Suppl 1): S80
- Bivariate variance-component analysis, with application to systolic blood pressure and total cholesterol levels in the Framingham Heart Study2003; 4(Suppl 1): S81
- Genome-wide linkage scan for genes affecting longitudinal trends in systolic blood pressure2003; 4(Suppl 1): S82
- Genome scan linkage results for longitudinal systolic blood pressure phenotypes in subjects from the Framingham Heart Study2003; 4(Suppl 1): S83
- Using an age-at-onset phenotype with interval censoring to compare methods of segregation and linkage analysis in a candidate region for elevated systolic blood pressure2003; 4(Suppl 1): S84
- Nonparametric longitudinal allele-sharing model2003; 4(Suppl 1): S85
- Genome-wide linkage analysis of systolic blood pressure slope using the Genetic Analysis Workshop 13 data sets2003; 4(Suppl 1): S86
- Longitudinal familial analysis of blood pressure involving parametric (co)variance functions2003; 4(Suppl 1): S87
- Genome-wide linkage analysis of the tracking of systolic blood pressure using a mixed model2003; 4(Suppl 1): S88
- A cautionary note on the appropriateness of using a linkage resource for an association study2003; 4(Suppl 1): S89
- Detecting susceptibility genes in case-control studies using set association2003; 4(Suppl 1): S9
- Comparison between two analytic strategies to detect linkage to obesity with genetically determined age of onset: the Framingham Heart Study2003; 4(Suppl 1): S90
- Genome scan for body mass index and height in the Framingham Heart Study2003; 4(Suppl 1): S91
- Linkage mapping of total cholesterol level in a young cohort via nonparametric regression2003; 4(Suppl 1): S92
- Comparison of linkage analysis methods for genome-wide scanning of extended pedigrees, with application to the TG/HDL-C ratio in the Framingham Heart Study2003; 4(Suppl 1): S93
- Familial aggregation of components of the multiple metabolic syndrome in the Framingham Heart and Offspring Cohorts: Genetic Analysis Workshop Problem 12003; 4(Suppl 1): S94
- Phenotypic, genetic, and genome-wide structure in the metabolic syndrome2003; 4(Suppl 1): S95
- A QTL genome scan of the metabolic syndrome and its component traits2003; 4(Suppl 1): S96
- A genome-wide linkage scan for body mass index on Framingham Heart Study families2003; 4(Suppl 1): S97
- HDL cholesterol in females in the Framingham Heart Study is linked to a region of chromosome 2q2003; 4(Suppl 1): S98
- Structural equation model-based genome scan for the metabolic syndrome2003; 4(Suppl 1): S99
- Strategy and model building in the fourth dimension: a null model for genotype × age interaction as a Gaussian stationary stochastic process2003; 4(Suppl 1): S34
- Using mixture models to characterize disease-related traits2005; 6(Suppl 1): S99
- Comparing strategies for association mapping in samples with related individuals2005; 6(Suppl 1): S98
- Identifying genetic variation affecting a complex trait in simulated data: a comparison of meta-analysis with pooled data analysis2005; 6(Suppl 1): S97
- Comparison of linkage and association strategies for quantitative traits using the COGA dataset2005; 6(Suppl 1): S96
- A regression based transmission/disequilibrium test for binary traits: the power of joint tests for linkage and association2005; 6(Suppl 1): S95
- Microsatellite linkage analysis, single-nucleotide polymorphisms, and haplotype associations with ECB21 in the COGA data2005; 6(Suppl 1): S94
- Selection of single-nucleotide polymorphisms in disease association data2005; 6(Suppl 1): S93
- Analysis of binary traits: testing association in the presence of linkage2005; 6(Suppl 1): S92
- The quantitative trait linkage disequilibrium test: a more powerful alternative to the quantitative transmission disequilibrium test for use in the absence of population stratification2005; 6(Suppl 1): S91
- Impact of non-ignorable missingness on genetic tests of linkage and/or association using case-parent trios2005; 6(Suppl 1): S90
- Whole-genome association studies of alcoholism with loci linked to schizophrenia susceptibility2005; 6(Suppl 1): S9
- A comparison in association and linkage genome-wide scans for alcoholism susceptibility genes using single-nucleotide polymorphisms2005; 6(Suppl 1): S89
- Identification of polymorphisms explaining a linkage signal: application to the GAW14 simulated data2005; 6(Suppl 1): S88
- Modeling the effect of a genetic factor for a complex trait in a simulated population2005; 6(Suppl 1): S87
- Linkage disequilibrium across two different single-nucleotide polymorphism genome scans2005; 6(Suppl 1): S86
- Evaluation of linkage disequilibrium and its effect on non-parametric multipoint linkage analysis using two high density single-nucleotide polymorphism mapping panels2005; 6(Suppl 1): S85
- The efficacy of short tandem repeat polymorphisms versus single-nucleotide polymorphisms for resolving population structure2005; 6(Suppl 1): S84
- Examining the effect of linkage disequilibrium on multipoint linkage analysis2005; 6(Suppl 1): S83
- Bias of allele-sharing linkage statistics in the presence of intermarker linkage disequilibrium2005; 6(Suppl 1): S82
- An exploration of sex-specific linkage disequilibrium on chromosome X in Caucasians from the COGA study2005; 6(Suppl 1): S81
- Accuracy of haplotype estimation in a region of low linkage disequilibrium2005; 6(Suppl 1): S80
- Genome-wide linkage analysis for alcohol dependence: a comparison between single-nucleotide polymorphism and microsatellite marker assays2005; 6(Suppl 1): S8
- Haplotype sharing correlation of alcohol dependence on chromosomes 1–6 in 93 nuclear families2005; 6(Suppl 1): S79
- Comparison of type I error for multiple test corrections in large single-nucleotide polymorphism studies using principal components versus haplotype blocking algorithms2005; 6(Suppl 1): S78
- Haplotypic structure of the X chromosome in the COGA population sample and the quality of its reconstruction by extant software packages2005; 6(Suppl 1): S77
- Comparisons of methods for linkage analysis and haplotype reconstruction using extended pedigree data2005; 6(Suppl 1): S76
- Haplotype-sharing analysis for alcohol dependence based on quantitative traits and the Mantel statistic2005; 6(Suppl 1): S75
- Fine-scale mapping in case-control samples using locus scoring and haplotype-sharing methods2005; 6(Suppl 1): S74
- Identification of tag single-nucleotide polymorphisms in regions with varying linkage disequilibrium2005; 6(Suppl 1): S73
- Strategies for selecting subsets of single-nucleotide polymorphisms to genotype in association studies2005; 6(Suppl 1): S72
- A comparison of five methods for selecting tagging single-nucleotide polymorphisms2005; 6(Suppl 1): S71
- Haplotype-sharing analysis using Mantel statistics for combined genetic effects2005; 6(Suppl 1): S70
- Comparison of the power between microsatellite and single-nucleotide polymorphism markers for linkage and linkage disequilibrium mapping of an electrophysiological phenotype2005; 6(Suppl 1): S7
- Robust testing of haplotype/disease association2005; 6(Suppl 1): S69
- Application of family-based association testing to assess the genotype-phenotype association involved in complex traits using single-nucleotide polymorphisms2005; 6(Suppl 1): S68
- Fine-mapping using the weighted average method for a case-control study2005; 6(Suppl 1): S67
- Will the real disease gene please stand up?2005; 6(Suppl 1): S66
- Comparison of genotype- and haplotype-based approaches for fine-mapping of alcohol dependence using COGA data2005; 6(Suppl 1): S65
- Potts model for haplotype associations2005; 6(Suppl 1): S64
- Fine mapping – 19th century style2005; 6(Suppl 1): S63
- Comparison of family-based association tests in chromosome regions selected by linkage-based confidence intervals2005; 6(Suppl 1): S62
- Optimizing the evidence for linkage by permuting marker order2005; 6(Suppl 1): S61
- Locally weighted transmission/disequilibrium test for genetic association analysis2005; 6(Suppl 1): S60