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Genome-wide association study and meta-analysis find that over 40 loci affect risk of type 1 diabetesNADPH oxidase complex and IBD candidate gene studies: identification of a rare variant in NCF2 that results in reduced binding to RAC2Reappraisal of known malaria resistance loci in a large multicenter studyGenome-wide association study identifies multiple loci associated with bladder cancer riskA genome-wide association study of bladder cancer identifies a new susceptibility locus within SLC14A1, a urea transporter gene on chromosome 18q12.3A multi-stage genome-wide association study of bladder cancer identifies multiple susceptibility lociIdentification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-Wide Meta-analysisGenome-wide association study identifies three new melanoma susceptibility loci.Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans.Gene-centric approach identifies new and known loci for FVIII activity and VWF antigen levels in European Americans and African Americans.Multiple genetic variant association testing by collapsing and kernel methods with pedigree or population structured dataXWAS: A Software Toolset for Genetic Data Analysis and Association Studies of the X ChromosomeModeling X Chromosome Data Using Random Forests: Conquering Sex BiasTesting for genetic association taking into account phenotypic information of relatives.Whole-genome linkage and association scan in primary, nonsyndromic vesicoureteric refluxSex chromosomes and genetic association studies.The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes.Common variants on Xq28 conferring risk of schizophrenia in Han Chinese.Novel associations of multiple genetic loci with plasma levels of factor VII, factor VIII, and von Willebrand factor: The CHARGE (Cohorts for Heart and Aging Research in Genome Epidemiology) ConsortiumX-chromosome genetic association test accounting for X-inactivation, skewed X-inactivation, and escape from X-inactivation.GALNT14 SNP as a potential predictor of response to combination chemotherapy using 5-FU, mitoxantrone and cisplatin in advanced HCC.Adrenergic alpha-1 pathway is associated with hypertension among Nigerians in a pathway-focused analysis.X-inactivation informs variance-based testing for X-linked association of a quantitative trait.The association between the Angiotensin-Converting Enzyme-2 gene and blood pressure in a cohort study of adolescentsAccounting for eXentricities: analysis of the X chromosome in GWAS reveals X-linked genes implicated in autoimmune diseases.Association tests for X-chromosomal markers--a comparison of different test statistics.Statistical methods for genome-wide and sequencing association studies of complex traits in related samples.Simple strategies for haplotype analysis of the X chromosome with application to age-related macular degenerationGenetics of cardiovascular disease: Importance of sex and ethnicity.The Genotype of the Donor for the (GT)n Polymorphism in the Promoter/Enhancer of FOXP3 Is Associated with the Development of Severe Acute GVHD but Does Not Affect the GVL Effect after Myeloablative HLA-Identical Allogeneic Stem Cell Transplantation.Likelihood Ratio Test for Excess Homozygosity at Marker Loci on X Chromosome.Common Variants in CLDN2 and MORC4 Genes Confer Disease Susceptibility in Patients with Chronic Pancreatitis.Genotype-Based Score Test for Association Testing in Families.Evaluating the Calibration and Power of Three Gene-Based Association Tests of Rare Variants for the X ChromosomeHeterogeneous alleles comprising G6PD deficiency trait in West Africa exert contrasting effects on two major clinical presentations of severe malaria.eXclusion: toward integrating the X chromosome in genome-wide association analyses.An X chromosome-wide association analysis identifies variants in GPR174 as a risk factor for Graves' disease.XM: association testing on the X-chromosome in case-control samples with related individuals.Genome-wide association study suggests common variants within RP11-634B7.4 gene influencing severe pre-treatment pain in head and neck cancer patients.
P2860
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P2860
description
2008 nî lūn-bûn
@nan
2008年の論文
@ja
2008年論文
@yue
2008年論文
@zh-hant
2008年論文
@zh-hk
2008年論文
@zh-mo
2008年論文
@zh-tw
2008年论文
@wuu
2008年论文
@zh
2008年论文
@zh-cn
name
Testing for association on the X chromosome
@en
type
label
Testing for association on the X chromosome
@en
prefLabel
Testing for association on the X chromosome
@en
P2860
P356
P1433
P1476
Testing for association on the X chromosome
@en
P2093
David Clayton
P2860
P304
P356
10.1093/BIOSTATISTICS/KXN007
P577
2008-04-25T00:00:00Z