Mapping disease genes: family-based association studies.
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- Type
- article
- Published
- 1995-08-01
- Cited by
- 377
- References
- 44
- Access
- Open access
- OpenAlex
- https://openalex.org/W2013869066
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:35606840
Keywords
Genetics, Biology, Allele, Population, Genetic marker
References
- Comparing the Classification of Subjects by Two Independent Judges
- Relative predispositional effects (RPEs) of marker alleles with disease: HLA-DR alleles and Graves disease.
- The transmission/disequilibrium test detects cosegregation and linkage.
- Linkage analysis versus association analysis: distinguishing between two models that explain disease-marker associations.
- Genetic analysis of IDDM: Summary of GAW5 IDDM results
- Genetic heterogeneity, modes of inheritance, and risk estimates for a joint study of Caucasians with insulin-dependent diabetes mellitus.
- Linkage disequilibrium predicts physical distance in the adenomatous polyposis coli region.
- HLA and insulin gene associations with IDDM
- Charateristics of a multiplex IDDM sample: Unexplained differences with other samples
- Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM).
- Mapping by admixture linkage disequilibrium in human populations: limits and guidelines.
- Genotype relative risks: methods for design and analysis of candidate-gene association studies.
- The haplotype-relative-risk (HRR) method for analysis of association in nuclear families.
- Maximum-likelihood estimation of gene location by linkage disequilibrium.
- Polymorphic admixture typing in human ethnic populations.
- Comparison of statistics for candidate-gene association studies using cases and parents.
- Genes predisposing to IDDM in multiplex families
- Case-parental control method in the search for disease-susceptibility genes.
- A haplotype-based 'haplotype relative risk' approach to detecting allelic associations.
- HLA‐DR effects in a large German IDDM dataset
Cited by
- Novel polymorphisms in the IL-10 related AK155 gene (chromosome 12q15)
- Additional factor in some HLA DR3/DQ2 haplotypes confers a fourfold increased genetic risk of celiac disease.
- Juvenile rheumatoid arthritis affected sibpairs: extent of clinical phenotype concordance.
- Genes outside The Hla Region affecting Susceptibility to Type 1 Diabetes - The Role of Iddm2 and Iddm9 in the Finnish Population
- Logistic regression protects against population structure in genetic association studies.
- Family-based designs in the age of large-scale gene-association studies
- Including Measured Genotypes in Statistical Models to Study the Interplay of Multiple Factors Affecting Complex Traits
- Review of statistical methodologies for the detection of parent-of-origin effects in family trio genome-wide association data with binary disease traits
- Investigation of Candidate Genes and HLA-Related Risk Factors in a Genetic Study of Autoimmune Disease
- Molecular genetic investigation of autosomal dominant muscular dystrophy
- Introduction and overview
- Detecting disease-predisposing variants: the haplotype method.
- A Comparison Between Different Designs and Tests to Detect QTLs in Association Studies
- Analysis of Allelic Association: Estimation of the Power of the TDT
- Examining cleft lip and palate as a lifelong disease: genetic investigation of causes and outcomes
- Selected Methodological Issues in Meiotic Mapping of Obesity Genes in Humans: Issues of Power and Efficiency
- From Basic Immunology to Immune-Mediated Demyelination
- Linkage disequilibrium between an allele at the dopamine D4 receptor locus and Tourette syndrome, by the transmission-disequilibrium test.
- A polygenic model of inherited predisposition to cancer
- Admixture mapping and the role of population structure for localizing disease genes.
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