A genomic pathway approach to a complex disease: axon guidance and Parkinson diseaseHigh-resolution whole-genome association study of Parkinson disease.Lower cancer incidence in Amsterdam-I criteria families without mismatch repair deficiency: familial colorectal cancer type XTrans-ethnic meta-analysis identifies common and rare variants associated with hepatocyte growth factor levels in the Multi-Ethnic Study of Atherosclerosis (MESA).Interferon gamma allelic variants: sex-biased multiple sclerosis susceptibility and gene expressionCohort profile: the Baependi Heart Study—a family-based, highly admixed cohort study in a rural Brazilian townThe ATXN2-SH2B3 locus is associated with peripheral arterial disease: an electronic medical record-based genome-wide association study.Multi-ethnic analysis reveals soluble L-selectin may be post-transcriptionally regulated by 3'UTR polymorphism: the Multi-Ethnic Study of Atherosclerosis (MESA).Plasma and serum L-selectin and clinical and subclinical cardiovascular disease: the Multi-Ethnic Study of Atherosclerosis (MESA).Clinical outcomes and changes in lung function after segmentectomy versus lobectomy for lung cancer cases.Extension of variance components approach to incorporate temporal trends and longitudinal pedigree data analysis.Using item response theory to model multiple phenotypes and their joint heritability in family data.Using the theory of added-variable plot for linear mixed models to decompose genetic effects in family data.Random-effects Cox proportional hazards model: general variance components methods for time-to-event data.Global Individual Ancestry Using Principal Components for Family DataGenetic analyses of smoking initiation, persistence, quantity, and age-at-onset of regular cigarette use in Brazilian families: the Baependi Heart Study.Missing phenotype data imputation in pedigree data analysis.Comparison of variable and model selection methods for genetic association studies using the GAW15 simulated data.Linkage analysis using principal components of gene expression data.Comparison of longitudinal variance components and regression-based approaches for linkage detection on chromosome 17 for systolic blood pressureLocalization of genes involved in the metabolic syndrome using multivariate linkage analysis.Screening the genome to detect an association with hypertensionIdentification of genes involved in alcohol consumption and cigarettes smoking.Autosomal mutations affecting Y chromosome loops in Drosophila melanogaster.Analysis of variation in NF-kappaB genes and expression levels of NF-kappaB-regulated moleculesThe genetics of gene expression: comparison of linkage scans using two phenotype normalization methodsComparison of tagging single-nucleotide polymorphism methods in association analysesAdjusting for HLA-DRbeta1 in a genome-wide association analysis of rheumatoid arthritis and related biomarkers.Assessment of genotype imputation methodsIdentification of genes and haplotypes that predict rheumatoid arthritis using random forests.Identification of gene-gene interaction using principal componentsEvaluating gene by sex and age interactions on cardiovascular risk factors in Brazilian families.Biochemical response to ursodeoxycholic acid predicts survival in a North American cohort of primary biliary cirrhosis patients.Leukocyte DNA methylation signature differentiates pancreatic cancer patients from healthy controlsFamilial aggregation of irritable bowel syndrome: a family case-control study.Reduced coffee consumption among individuals with primary sclerosing cholangitis but not primary biliary cirrhosis.Software comparison for evaluating genomic copy number variation for Affymetrix 6.0 SNP array platform.Clinical features of bronchioloalveolar carcinoma with new histologic and staging definitionsHeritability of physical activity traits in Brazilian families: the Baependi Heart Study.Obesity adversely affects survival in pancreatic cancer patients.
P50
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