Mapping complex disease loci in whole-genome association studies.
about
Genotyping DNA pools on microarrays: tackling the QTL problem of large samples and large numbers of SNPsEpistasis--the essential role of gene interactions in the structure and evolution of genetic systemsGenetics of autism spectrum disorderProgress in genetic studies of pain and analgesiaFine mapping versus replication in whole-genome association studiesGenotyping pooled DNA using 100K SNP microarrays: a step towards genomewide association scans.Learning Abilities and Disabilities: Generalist Genes, Specialist EnvironmentsGenetic dissection and prognostic modeling of overt stroke in sickle cell anemiaHigh-density SNP association study of the 17q21 chromosomal region linked to autism identifies CACNA1G as a novel candidate geneRuns of homozygosity in European populationsGenetics of obsessive-compulsive disorderIdentification of EpCAM as the gene for congenital tufting enteropathyTranslation research: from accurate diagnosis to appropriate treatmentIdentification of disease causing loci using an array-based genotyping approach on pooled DNA.Effects of DNA mass on multiple displacement whole genome amplification and genotyping performance.Approximation properties of haplotype taggingBTA, a novel reagent for DNA attachment on glass and efficient generation of solid-phase amplified DNA colonies.New insights from monogenic diabetes for "common" type 2 diabetesGenetic causation of neointimal hyperplasia in hemodialysis vascular access dysfunctionPathway-based analysis tools for complex diseases: a reviewCentral role of gimap5 in maintaining peripheral tolerance and T cell homeostasis in the gutUGMDR: a unified conceptual framework for detection of multifactor interactions underlying complex traits.Genetic & epigenetic approach to human obesityPathways to gene identification in rheumatoid arthritis: PTPN22 and beyondAutism: the quest for the genesEfficiency and power in genetic association studiesCalmodulin-binding transcription activator 1 (CAMTA1) alleles predispose human episodic memory performanceGene-gene Interaction Analyses for Atrial FibrillationHaplotype Analysis and Linkage Disequilibrium at Five Loci in Eragrostis tefGenome-wide association study identifies susceptibility loci for polycystic ovary syndrome on chromosome 2p16.3, 2p21 and 9q33.3Genome-wide association studies for common diseases and complex traitsIL-13 R130Q, a common variant associated with allergy and asthma, enhances effector mechanisms essential for human allergic inflammation.Molecular nutrition research: the modern way of performing nutritional scienceA model-based approach to selection of tag SNPsFastANOVA: an Efficient Algorithm for Genome-Wide Association Study.High-throughput single nucleotide polymorphism genotyping using nanofluidic Dynamic ArraysAn evaluation of HapMap sample size and tagging SNP performance in large-scale empirical and simulated data sets.A forest-based feature screening approach for large-scale genome data with complex structures.Power and type I error rate of false discovery rate approaches in genome-wide association studies.How well do HapMap SNPs capture the untyped SNPs?
P2860
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P2860
Mapping complex disease loci in whole-genome association studies.
description
2004 nî lūn-bûn
@nan
2004年の論文
@ja
2004年論文
@yue
2004年論文
@zh-hant
2004年論文
@zh-hk
2004年論文
@zh-mo
2004年論文
@zh-tw
2004年论文
@wuu
2004年论文
@zh
2004年论文
@zh-cn
name
Mapping complex disease loci in whole-genome association studies.
@ast
Mapping complex disease loci in whole-genome association studies.
@en
type
label
Mapping complex disease loci in whole-genome association studies.
@ast
Mapping complex disease loci in whole-genome association studies.
@en
prefLabel
Mapping complex disease loci in whole-genome association studies.
@ast
Mapping complex disease loci in whole-genome association studies.
@en
P2093
P2860
P356
P1433
P1476
Mapping complex disease loci in whole-genome association studies.
@en
P2093
Christopher S Carlson
Deborah A Nickerson
Leonid Kruglyak
Michael A Eberle
P2860
P2888
P304
P356
10.1038/NATURE02623
P407
P577
2004-05-01T00:00:00Z
P5875
P6179
1017921358