The use of measured genotype information in the analysis of quantitative phenotypes in man. I. Models and analytical methods.
about
Novel genetic loci identified for the pathophysiology of childhood obesity in the Hispanic populationVariations in GABRA2, encoding the alpha 2 subunit of the GABA(A) receptor, are associated with alcohol dependence and with brain oscillations.Wide disparity in genetic admixture among Mexican Americans from San Antonio, TXGenetic studies of human apolipoproteins. X. The effect of the apolipoprotein E polymorphism on quantitative levels of lipoproteins in Nigerian blacksAssociation of neuropeptide Y receptor Y5 polymorphisms with dyslipidemia in Mexican AmericansGenetic variation underlying renal uric acid excretion in Hispanic children: the Viva La Familia StudyA genome-wide association study of the Protein C anticoagulant pathwayThe characterization of Abelson helper integration site-1 in skeletal muscle and its links to the metabolic syndromeGenome-wide pleiotropy of osteoporosis-related phenotypes: the Framingham StudyGenome wide signatures of positive selection: the comparison of independent samples and the identification of regions associated to traitsHypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality.Genotype imputationGenetic variation in SH3-domain GRB2-like (endophilin)-interacting protein 1 has a major impact on fat mass.Single-nucleotide polymorphisms in corticotropin releasing hormone receptor 1 gene (CRHR1) are associated with quantitative trait of event-related potential and alcohol dependenceGenetic variation in APOJ, LPL, and TNFRSF10B affects plasma fatty acid distribution in Alaskan Eskimos.Genome-wide association of an integrated osteoporosis-related phenotype: is there evidence for pleiotropic genes?Variants in CPT1A, FADS1, and FADS2 are Associated with Higher Levels of Estimated Plasma and Erythrocyte Delta-5 Desaturases in Alaskan EskimosComparison of methods to account for relatedness in genome-wide association studies with family-based data.Single-marker and multi-marker mixed models for polygenic score analysis in family-based dataExome Sequence Data From Multigenerational Families Implicate AMPA Receptor Trafficking in Neurocognitive Impairment and Schizophrenia Risk.Polymorphisms in the SOCS7 gene and glucose homeostasis traits.An analysis of genotype effects and their interactions by using the apolipoprotein E polymorphism and longitudinal data.Linkage disequilibrium interval mapping of quantitative trait loci.A genomic background based method for association analysis in related individualsRapid and robust association mapping of expression quantitative trait loci.Gene x gene and gene x environment interactions for complex disordersA comparative study of three methods for detecting association of quantitative traits in samples of related subjectsFAM-MDR: a flexible family-based multifactor dimensionality reduction technique to detect epistasis using related individuals.Prioritizing GWAS results: A review of statistical methods and recommendations for their application.Differences in the heritability of growth and growth velocity during infancy and associations with FTO variants.A kernel of truth: statistical advances in polygenic variance component models for complex human pedigrees.Association of functional polymorphism rs2231142 (Q141K) in the ABCG2 gene with serum uric acid and gout in 4 US populations: the PAGE Study.Genetic variation at the FTO locus influences RBL2 gene expression.Genetic variation in PARL influences mitochondrial content.Genetic and molecular functional characterization of variants within TNFSF13B, a positional candidate preeclampsia susceptibility gene on 13qFine mapping of the alpha-T catenin gene to a quantitative trait locus on chromosome 10 in late-onset Alzheimer's disease pedigrees.Replication of the effect of SLC2A9 genetic variation on serum uric acid levels in American IndiansChemerin, a novel adipokine in the regulation of angiogenesis.The positive association of obesity variants with adulthood adiposity strengthens over an 80-year period: a gene-by-birth year interaction.Linkage and association analyses identify a candidate region for apoB level on chromosome 4q32.3 in FCHL families.
P2860
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P2860
The use of measured genotype information in the analysis of quantitative phenotypes in man. I. Models and analytical methods.
description
1986 nî lūn-bûn
@nan
1986年の論文
@ja
1986年学术文章
@wuu
1986年学术文章
@zh
1986年学术文章
@zh-cn
1986年学术文章
@zh-hans
1986年学术文章
@zh-my
1986年学术文章
@zh-sg
1986年學術文章
@yue
1986年學術文章
@zh-hant
name
The use of measured genotype i ...... Models and analytical methods.
@en
The use of measured genotype i ...... Models and analytical methods.
@nl
type
label
The use of measured genotype i ...... Models and analytical methods.
@en
The use of measured genotype i ...... Models and analytical methods.
@nl
prefLabel
The use of measured genotype i ...... Models and analytical methods.
@en
The use of measured genotype i ...... Models and analytical methods.
@nl
P2860
P1476
The use of measured genotype i ...... Models and analytical methods.
@en
P2093
Chakraborty R
P2860
P304
P356
10.1111/J.1469-1809.1986.TB01037.X
P407
P577
1986-05-01T00:00:00Z