A statistical method for identification of polymorphisms that explain a linkage result.
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GAD2 on chromosome 10p12 is a candidate gene for human obesityVariants in CPT1A, FADS1, and FADS2 are Associated with Higher Levels of Estimated Plasma and Erythrocyte Delta-5 Desaturases in Alaskan EskimosCombined linkage and family-based association analysis improves candidate gene detection in Genetic Analysis Workshop 18 simulation data.Identifying the susceptibility gene(s) in a set of trait-linked genes using genotype data.Joint linkage and association analysis for identification of potentially causal polymorphisms in GAW15 data.A new score statistic to test for association given linkage in affected sibling pair-control designs.No evidence for multiple loci affecting rheumatoid arthritis risk on chromosome 6p21.Assessing whether an allele can account in part for a linkage signal: the Genotype-IBD Sharing Test (GIST).Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21Joint modeling of linkage and association: identifying SNPs responsible for a linkage signalA method to detect single-nucleotide polymorphisms accounting for a linkage signal using covariate-based affected relative pair linkage analysis.Evaluation of approaches to identify associated SNPs that explain the linkage evidence in nuclear families with affected siblingsGenetic approaches to the molecular understanding of type 2 diabetes.Complex pedigrees in the sequencing era: to track transmissions or decorrelate?Case-control association testing with related individuals: a more powerful quasi-likelihood score test.Calpains and their multiple roles in diabetes mellitus.Genome-wide association studies: implications for multiethnic samples.Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13?Common and rare variants of DAOA in bipolar disorderEvidence that multiple genetic variants of MC4R play a functional role in the regulation of energy expenditure and appetite in Hispanic children.G-STRATEGY: Optimal Selection of Individuals for Sequencing in Genetic Association Studies.A composite-likelihood approach for identifying polymorphisms that are potentially directly associated with disease.Exploring causality via identification of SNPs or haplotypes responsible for a linkage signal.Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin.Developmental dysplasia of the hip: linkage mapping and whole exome sequencing identify a shared variant in CX3CR1 in all affected members of a large multigeneration family.Findings in an independent sample support an association between bipolar affective disorder and the G72/G30 locus on chromosome 13q33Characterizing the Extent of Human Genetic Variation for Performance-Related TraitsDesign and Analysis of Genetic Association Studies to Finely Map a Locus Identified by Linkage Analysis: Assessment of the Extent to Which an Association Can Account for the Linkage
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P2860
A statistical method for identification of polymorphisms that explain a linkage result.
description
article científic
@ca
article scientifique
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articolo scientifico
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artigo científico
@pt
bilimsel makale
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scientific article published on 08 January 2002
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
A statistical method for identification of polymorphisms that explain a linkage result.
@en
A statistical method for identification of polymorphisms that explain a linkage result.
@nl
type
label
A statistical method for identification of polymorphisms that explain a linkage result.
@en
A statistical method for identification of polymorphisms that explain a linkage result.
@nl
prefLabel
A statistical method for identification of polymorphisms that explain a linkage result.
@en
A statistical method for identification of polymorphisms that explain a linkage result.
@nl
P2860
P356
P1476
A statistical method for identification of polymorphisms that explain a linkage result.
@en
P2093
Mary Sara McPeek
P2860
P304
P356
10.1086/338660
P407
P50
P577
2002-01-08T00:00:00Z