Mapping disease genes: family-based association studies.
about
High-density SNP screening of the major histocompatibility complex in systemic lupus erythematosus demonstrates strong evidence for independent susceptibility regionsControl of confounding of genetic associations in stratified populationsTests and estimates of allelic association in complex inheritanceAssociation of MSX1 and TGFB3 with nonsyndromic clefting in humansSeveral loci in the HLA class III region are associated with T1D risk after adjusting for DRB1-DQB1HLA-DR-DQ haplotypes and genotypes in Finnish patients with rheumatoid arthritisThe TDT and other family-based tests for linkage disequilibrium and associationRisk for rheumatic disease in relation to ethnicity and admixture.The HLA class I A locus affects susceptibility to type 1 diabetesHLA DPA1, DPB1 alleles and haplotypes contribute to the risk associated with type 1 diabetes: analysis of the type 1 diabetes genetics consortium families.HLA DR-DQ haplotypes and genotypes and type 1 diabetes risk: analysis of the type 1 diabetes genetics consortium familiesNext generation sequencing reveals the association of DRB3*02:02 with type 1 diabetes.HLA class I and genetic susceptibility to type 1 diabetes: results from the Type 1 Diabetes Genetics Consortiumrs2476601 T allele (R620W) defines high-risk PTPN22 type I diabetes-associated haplotypes with preliminary evidence for an additional protective haplotype.A unified stepwise regression procedure for evaluating the relative effects of polymorphisms within a gene using case/control or family data: application to HLA in type 1 diabetesAbsence of linkage of phonological coding dyslexia to chromosome 6p23-p21.3 in a large family data set.A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting.Modeling of PTPN22 and HLA-DRB1 susceptibility to rheumatoid arthritisConditional genotype analysis: detecting secondary disease loci in linkage disequilibrium with a primary disease locusPower of the 2-locus TDT for testing the interaction of two susceptibility genes.Combined haplotype relative risk (CHRR): a general and simple genetic association test that combines trios and unrelated case-controls.Genetic variation within the HLA class III influences T1D susceptibility conferred by high-risk HLA haplotypes.CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis.HLA-DR2 dose effect on susceptibility to multiple sclerosis and influence on disease course.Association of specific language impairment (SLI) to the region of 7q31.Linkage analysis of a complex disease through use of admixed populations.Small duct primary sclerosing cholangitis without inflammatory bowel disease is genetically different from large duct disease.Improving the estimation of celiac disease sibling risk by non-HLA genes.Multipoint linkage-disequilibrium-mapping approach based on the case-parent trio design.Transmission/disequilibrium tests using multiple tightly linked markers.Analytical methods for disease association studies with immunogenetic data.Susceptibility to relapsing-progressive multiple sclerosis is associated with inheritance of genes linked to the variable region of the TcR beta locus: use of affected family-based controlsGenetic association mapping based on discordant sib pairs: the discordant-alleles test.Association and linkage of the dopamine transporter gene and attention-deficit hyperactivity disorder in children: heterogeneity owing to diagnostic subtype and severity.Assessing genuine parents-offspring trios for genetic association studies.Conditional meta-analysis stratifying on detailed HLA genotypes identifies a novel type 1 diabetes locus around TCF19 in the MHCDosage transmission disequilibrium test (dTDT) for linkage and association detection.The HLA-B 3906 allele imparts a high risk of diabetes only on specific HLA-DR/DQ haplotypes.Uncoupling the roles of HLA-DRB1 and HLA-DRB5 genes in multiple sclerosis.Power studies for the transmission/disequilibrium tests with multiple alleles.
P2860
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P2860
Mapping disease genes: family-based association studies.
description
1995 nî lūn-bûn
@nan
1995年の論文
@ja
1995年論文
@yue
1995年論文
@zh-hant
1995年論文
@zh-hk
1995年論文
@zh-mo
1995年論文
@zh-tw
1995年论文
@wuu
1995年论文
@zh
1995年论文
@zh-cn
name
Mapping disease genes: family-based association studies.
@en
Mapping disease genes: family-based association studies.
@nl
type
label
Mapping disease genes: family-based association studies.
@en
Mapping disease genes: family-based association studies.
@nl
prefLabel
Mapping disease genes: family-based association studies.
@en
Mapping disease genes: family-based association studies.
@nl
P2860
P1476
Mapping disease genes: family-based association studies.
@en
P2093
P2860
P304
P407
P577
1995-08-01T00:00:00Z