| Semiparametric estimation of major gene effects for age of onset |
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| Abstracts from the seventh annual meeting of the International Genetic Epidemiology Society |
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| FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population |
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| CAT scans, PET scans, and genomic scans |
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| Inheritance of the shared epitope and long-term outcomes of rheumatoid arthritis among community-based Caucasian females |
✓ |
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| Method and computer program for controlling the family-wise alpha rate in gene association studies involving multiple phenotypes |
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| Logistic regression model for analyzing extended haplotype data |
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| Identifying influential families using regression diagnostics for generalized estimating equations |
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| Segregation analysis of cutaneous melanoma in Queensland |
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| HLA haplotype sharing in rheumatoid arthritis sibships: Risk estimates subdivided by proband genotype |
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| Testing for contributions of mitochondrial DNA mutations to complex diseases |
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| Relative predispositional effects and mode of inheritance of HLA-DRB1 alleles among community-based Caucasian females with rheumatoid arthritis |
✓ |
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| Using information from both parents when testing for association between marker and disease loci |
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| National database of familial cancer in Sweden |
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| Two-locus developments of the weighted pairwise correlation method for linkage analysis |
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| Abstracts from the seventh annual meeting of the International Genetic Epidemiology Society |
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| Congenital limb deficiences in Hungary by Czeizel et al. Akademial Kiado, Budapest, 1994 |
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| Increased risk for familial ovarian cancer among Jewish women: A population-based case-control study |
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| Segregation analysis of two-locus models regulating apolipoprotein-A1 levels |
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| Univariate genetic analyses of epilepsy and seizures in a population-based twin study: The Virginia twin registry |
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| Parental genotype reconstruction: Applications of haplotype relative risk to incomplete parental data |
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| Meta-analysis methodology for combining non-parametric sibpair linkage results: Genetic homogeneity and identical markers |
|
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| Inheritance of the shared epitope and long‐term outcomes of rheumatoid arthritis among community‐based Caucasian females |
✓ |
|
|
|
|
|
|
|
|
| Identifying influential families using regression diagnostics for generalized estimating equations |
|
|
|
|
|
|
|
|
|
| HLA haplotype sharing in rheumatoid arthritis sibships: Risk estimates subdivided by proband genotype |
|
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| Major locus influencing plasma APO-A1 levels also controls plasma HDL3-C concentrations |
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| Increased risk for familial ovarian cancer among Jewish women: A population‐based case‐control study |
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|
✓ |
|
Jewish women |
| Sib‐pair collection strategies for complex diseases |
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| CAT scans, PET scans, and genomic scans |
|
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|
|
|
|
|
|
| Congenital limb deficiences in Hungary by Czeizel et al. Akademial Kiado, Budapest, 1994 |
|
|
|
|
|
|
|
|
|
| FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population |
|
|
|
|
|
|
✓ |
|
Hellenic population |
| Parental genotype reconstruction: Applications of haplotype relative risk to incomplete parental data |
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| Analysis of Swedish male breast cancer family data: A simple way to incorporate a common sibling effect |
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| Environmental factors can confound identification of a major gene effect: Results from a segregation analysis of a simulated population of lung cancer families |
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| Comparison of four sib-pair linkage methods for analyzing sibships with more than two affecteds: Interest of the binomial maximum likelihood approach |
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| Letter to the editor |
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| Review of inference procedures for the interclass correlation coefficient with emphasis on applications to family studies |
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| Human malaria: Segregation analysis of blood infection levels in a suburban area and a rural area in Burkina Faso |
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| Syndrome X: Is it for real? |
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| Method and computer program for controlling the family‐wise alpha rate in gene association studies involving multiple phenotypes |
|
|
|
|
|
|
|
|
|
| National database of familial cancer in Sweden |
|
|
|
|
|
|
|
|
|
| Semiparametric estimation of major gene effects for age of onset |
|
|
|
|
|
|
|
|
|
| Abstracts from the seventh annual meeting of the International Genetic Epidemiology Society |
|
|
|
|
|
|
|
|
|
| Segregation analysis of two‐locus models regulating apolipoprotein‐A1 levels |
|
|
|
|
|
|
|
|
|
| Using information from both parents when testing for association between marker and disease loci |
|
|
|
|
|
|
|
|
|
| Testing for contributions of mitochondrial DNA mutations to complex diseases |
|
|
|
|
|
|
|
|
|
| Abstracts from the seventh annual meeting of the International Genetic Epidemiology Society |
|
|
|
|
|
|
|
|
|
| Meta‐analysis methodology for combining non‐parametric sibpair linkage results: Genetic homogeneity and identical markers |
|
|
|
|
|
|
|
|
|
| Modeling hazard functions in families |
|
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| Pedigree analysis package (PAP) vs. MORGAN: Model selection and hypothesis testing on a large pedigree |
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| Abstracts from the seventh annual meeting of the International Genetic Epidemiology Society |
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| Linkage and association |
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| Analytic strategies to detect linkage to a common disorder with genetically determined age of onset: Diabetes mellitus in Pima Indians |
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| Testing causal hypotheses in multivariate linkage analysis of quantitative traits: General formulation and application to sibpair data |
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| Modelling the major histocompatibility complex susceptibility to RA using the MASC method |
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| Familial correlation of dietary intakes among postmenopausal women |
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| Segregation analysis of cutaneous melanoma in Queensland |
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| Sample size calculations for linkage analysis using extreme sib pairs based on segregation analysis with the quantitative phenotype body weight as an example |
|
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|
|
|
|
| Univariate genetic analyses of epilepsy and seizures in a population‐based twin study: The Virginia twin registry |
|
|
|
|
|
|
|
|
|
| Abstracts from the seventh annual meeting of the International Genetic Epidemiology Society |
|
|
|
|
|
|
|
|
|
| Relative predispositional effects and mode of inheritance of HLA‐DRB1 alleles among community‐based Caucasian females with rheumatoid arthritis |
✓ |
|
|
|
|
|
|
|
|
| Two‐locus developments of the weighted pairwise correlation method for linkage analysis |
|
|
|
|
|
|
|
|
|
| APO B 3′ HVR polymorphism in healthy population: Relationships to serum lipid levels |
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| Validity of family history for the diagnosis of dementia among siblings of patients with late-onset Alzheimer's disease |
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| Genotypic relative risks under ordered restriction |
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| Logistic regression model for analyzing extended haplotype data |
|
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| Using family history information to distinguish true and false positive model-free linkage results |
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| Strategy for mapping minor histocompatibility genes involved in graft-versus-host disease: A novel application of discordant sib pair methodology |
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