Genetic Epidemiology - 1998

68 articles | Last updated: 2025-12-03 14:12:56
Caucasian
4
White
0
European
0
Other
2
Article Title Cauc. White Euro. Other Phrases Used
T A T A T A T A
Semiparametric estimation of major gene effects for age of onset
Abstracts from the seventh annual meeting of the International Genetic Epidemiology Society
FRAXA and FRAXE prevalence in patients with nonspecific mental retardation in the Hellenic population
CAT scans, PET scans, and genomic scans
Inheritance of the shared epitope and long-term outcomes of rheumatoid arthritis among community-based Caucasian females
Method and computer program for controlling the family-wise alpha rate in gene association studies involving multiple phenotypes
Logistic regression model for analyzing extended haplotype data
Identifying influential families using regression diagnostics for generalized estimating equations
Segregation analysis of cutaneous melanoma in Queensland
HLA haplotype sharing in rheumatoid arthritis sibships: Risk estimates subdivided by proband genotype
Testing for contributions of mitochondrial DNA mutations to complex diseases
Relative predispositional effects and mode of inheritance of HLA-DRB1 alleles among community-based Caucasian females with rheumatoid arthritis
Using information from both parents when testing for association between marker and disease loci
National database of familial cancer in Sweden
Two-locus developments of the weighted pairwise correlation method for linkage analysis
Abstracts from the seventh annual meeting of the International Genetic Epidemiology Society
Congenital limb deficiences in Hungary by Czeizel et al. Akademial Kiado, Budapest, 1994
Increased risk for familial ovarian cancer among Jewish women: A population-based case-control study
Segregation analysis of two-locus models regulating apolipoprotein-A1 levels
Univariate genetic analyses of epilepsy and seizures in a population-based twin study: The Virginia twin registry
Parental genotype reconstruction: Applications of haplotype relative risk to incomplete parental data
Meta-analysis methodology for combining non-parametric sibpair linkage results: Genetic homogeneity and identical markers
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
Major locus influencing plasma APO-A1 levels also controls plasma HDL3-C concentrations
Increased risk for familial ovarian cancer among Jewish women: A population‐based case‐control study Jewish women
Sib‐pair collection strategies for complex diseases
CAT scans, PET scans, and genomic scans
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
Analysis of Swedish male breast cancer family data: A simple way to incorporate a common sibling effect
Environmental factors can confound identification of a major gene effect: Results from a segregation analysis of a simulated population of lung cancer families
Comparison of four sib-pair linkage methods for analyzing sibships with more than two affecteds: Interest of the binomial maximum likelihood approach
Letter to the editor
Review of inference procedures for the interclass correlation coefficient with emphasis on applications to family studies
Human malaria: Segregation analysis of blood infection levels in a suburban area and a rural area in Burkina Faso
Syndrome X: Is it for real?
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
Pedigree analysis package (PAP) vs. MORGAN: Model selection and hypothesis testing on a large pedigree
Abstracts from the seventh annual meeting of the International Genetic Epidemiology Society
Linkage and association
Analytic strategies to detect linkage to a common disorder with genetically determined age of onset: Diabetes mellitus in Pima Indians
Testing causal hypotheses in multivariate linkage analysis of quantitative traits: General formulation and application to sibpair data
Modelling the major histocompatibility complex susceptibility to RA using the MASC method
Familial correlation of dietary intakes among postmenopausal women
Segregation analysis of cutaneous melanoma in Queensland
Sample size calculations for linkage analysis using extreme sib pairs based on segregation analysis with the quantitative phenotype body weight as an example
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
Validity of family history for the diagnosis of dementia among siblings of patients with late-onset Alzheimer's disease
Genotypic relative risks under ordered restriction
Logistic regression model for analyzing extended haplotype data
Using family history information to distinguish true and false positive model-free linkage results
Strategy for mapping minor histocompatibility genes involved in graft-versus-host disease: A novel application of discordant sib pair methodology