| Recombination fraction estimate of zero in the presence of apparent recombinants: Effects of incomplete penetrance and sporadic cases |
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| Segregation analysis of human red blood cell thiopurine methyltransferase activity |
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| Comparison of analysis of variance and maximum likelihood based path analysis of twin data: Partitioning genetic and environmental sources of covariance |
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| Extended HLA profile of an inbred isolate: The Schmiedeleut Hutterites of South Dakota |
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| Detection of a recessive major gene for high IgE levels acting independently of specific response to allergens |
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| Use of robust statistical methods to determine the effect of fragile X on means and variance components of a quantitative trait |
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| Method for calculating risk associated with family history of a disease |
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| Population genetic study of the human dopamine transporter gene (DAT1) |
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✓ |
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✓ |
✓ |
black Americans; Hispanics |
| Dementia among elderly apolipoprotein E type 4/4 homozygotes: A prospective study |
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| Masthead |
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| Maximum‐likelihood estimation in linkage heterogeneity models including additional information via the EM algorithm |
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| Announcements |
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| Data simulation for GAW9 problems 1 and 2 |
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| Comparing the power of linkage detection by the transmission disequilibrium test and the identity‐by‐descent test |
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| Two‐locus approach of segregation and linkage analysis in the study of complex traits |
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| ARCAD: A method for estimating age‐dependent disease risk associated with mutation carrier status from family data |
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| Physician to the gene pool, James V. Neel. New York: John Wiley & Sons, 1994, 457 pages, $24.95 |
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| Sex‐specific effects for body mass index in the new Norwegian twin panel |
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| Evaluating a new algorithm for linking maternal and newborn medical records |
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| Epidemiologic and genetic follo‐up study of 544 Minnesota breast cancer families: Design and methods |
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| Cystic fibrosis: Current topics, J.A. Dodge, D.J.H. Brock, and J.H. Widdicombe, eds., New York: John Wiley & Sons, 1994, 354 pages, $99.95 |
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| Major gene with sex‐specific effects influences fat mass in Mexican Americans |
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✓ |
✓ |
Mexican American |
| Underexpression of the apolipoprotein E2 and E4 alleles in the Greek Cypriot population of Cyprus |
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✓ |
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✓ |
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general Caucasian European pattern; European populations compared; clustered with populations mainly |
| Epidemiology: The logic of medicine, Milos Jenicek. Montreal: EPIMED International, 1995 |
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| Acknowledgments |
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| An oliogenic disease displaying weak marker assocations: A summary of contributions to problem 1 of GAW9 |
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| Genetic analysis workshop 9: Development of problem 1 |
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| Use of sibling risk ratios and components of genetic variance in the characterization of a simulated oligogenic disease |
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| Systematic search of susceptibility loci with methods using gametic disequilibrium |
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| Modeling the role of two susceptibility loci by the MASC method |
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| Screening for linkage and association in nuclear families |
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| Detection of vulnerability loci by association and sib‐pair methods |
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| Genome scanning for complex disease genes using the transmission/disequilibrium test and haplotype‐based haplotype relative risk |
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| Interval mapping of quantitative trait loci using a sib‐pair linkage method |
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| A genetic analysis of common disease data |
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| Weighted pairwise correlation and transmission disequilibrium in a common oligogenic disease |
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| Analysis of quantitative risk factors for a common oligogenic disease |
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| Association and linkage with quantitative traits |
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| Screening for linkage using a multipoint identity‐by‐descent method |
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| How can maximum likelihood methods reveal candidate gene effects on a quantitative trait? |
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| Multivariate genetic analysis of an oligogenic disease |
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| An investigation to determine whether clusters of cancer types exist in nine breast‐ovary families |
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| Variability of genotype‐specific penetrance probabilities in the calculation of risk support intervals |
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| Gain in efficiency from using generalized least squares in the Haseman‐Elston test |
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| Announcement |
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| Robust multipoint linkage analysis: An extension of the Haseman‐Elston method |
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| Causes of diabetes: Genetic and environmental factors, R.D.G. Leslie, ed. Chichester: John Wiley & Sons, 1993, 355 pages, $149.95 |
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| Announcement |
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| Masthead |
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| Complex segregation analysis of familial diseases with variable age of onset: Comparison of different methods by a simulation study |
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| Blastogenesis: Normal and abnormal, John M. Opitz and Natalie W. Paul, eds. New York: Wiley‐Liss, 1993, 424 pp, $185.95 |
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| Masthead |
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| Polymorphism at VNTR Locus 3′ to the apolipoprotein B gene in a tunisian population: Difference from other ethnic groups |
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✓ |
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✓ |
✓ |
Caucasoid populations; Tunisian population; black and white American populations; black African grou |
| Segregation analysis of breast cancer in a population‐based sample of postmenopausal probands: The Iowa women's health study |
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| Genetic analysis of durations: Correlated frailty model applied to survival of Danish twins |
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✓ |
✓ |
Danish |
| Screening a 2 cM genetic map for allelic association: A simulated oligogenic trait |
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| Logistic transmission modeling of simulated data |
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| Segregation and linkage analysis of the complex trait Q1 |
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| Relative‐risk regression models using cases and their parents |
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| Identification and mapping of mendelian subtypes of disease |
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| The GAW9 breast cancer linkage data set |
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| Analysis of breast cancer pedigrees using affected sibship methods |
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| Detection of genome similarity as an exploratory tool for mapping complex traits |
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| Epidemiology of retinitis pigmentosa in the valencian community (Spain) |
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| Apolipoprotein E4 allele and Alzheimer disease: Examination of Allelic association and effect on age at onset in both early‐and late‐onset cases |
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| Masthead |
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| Statistical validity for testing associations between genetic markers and quantitative traits in family data |
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| Asymptotic distributions of polylocus test statistics |
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| Statistical methodology for estimating twin similarity with respect to a dichotomous trait |
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| Abstracts from the fourth annual meeting of the international genetic epidemiology society |
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| No association of apolipoprotein A‐IV codon 347 and 360 variation with atherosclerosis and lipid transport in a sample of mixed hyperlipidemics |
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| Announcement |
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| Variation in HLA‐associated risks of childhood insulin‐dependent diabetes in the finnish population: II. Haplotype effects |
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|
✓ |
✓ |
Finnish population; Finnish diabetics |
| Association of childhood rhabdomyosarcoma with neurofibromatosis type i and birth defects |
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| Masthead |
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| Preface |
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| Model‐free association analysis of a rare Disease |
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| Identification of susceptibility loci contributing to a complex disease using conventional segregation, linkage, and association methods |
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| Effects of marker information on sib‐pair linkage analysis of a rare disease |
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| Sequential analysis of marker data for a rare oligogenic disease |
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| Integration of linkage analyses and disease association studies |
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| TDT with covariates and genomic screens with mod scores: Their behavior on simulated data |
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| Genetic analysis of a common oligogenic trait with quantitative correlates: Summary of GAW9 results |
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| A brute force dichotomization approach to quantitative trait linkage analysis |
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| Linkage analysis of a common oligogenic disease using selected sib pairs |
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| Genetic epidemiologic analysis of quantitative phenotypes using gibbs sampling |
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| Use of exact and adjusted liability scores to detect genes affecting common traits |
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| A graphical approach for presenting linkage results from a genomic screen |
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| Analysis of familial breast cancer in genetic analysis workshop 9: Summary of findings |
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| Development of the WPC approach and application to linkage analysis of breast cancer |
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| A Chromosome‐based method to infer IBD scores for missing and ambiguous markers |
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| Masthead |
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| Complex segregation analysis of leprosy in Southern Vietnam |
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✓ |
✓ |
Vietnamese origin; Chinese origin |
| Phenotypic assortative mating in segregation analysis |
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| Segregation analysis of plasma lipoprotein(a) levels in pedigrees with molecularly defined familial hypercholesterolemia |
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✓ |
✓ |
Druze, Christian‐Arabs, Ashkenazi, Sephardic Jews |
| Guess LOD approach: Sufficient conditions for robustness |
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| General purpose model and a computer program for combined segregation and path analysis (SEGPATH): Automatically creating computer programs from symbolic language model specifications |
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| Announcement |
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| Using loss of heterozygosity data in affected pedigree member linkage tests |
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| Simulation study comparing interval estimates for the recombination fraction |
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| Angiotensin‐converting enzyme genotypes in the high‐ and low‐risk area for coronary heart disease in Finland |
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| Assessing genetic risks. Implications for health and social policy, Lori B. Andrews, Jane E. Fullarton, Neil A. Holtzman, and Arno G. Motulsky, eds., Washington, DC: National Academy Press, 1994, 307 |
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| Variation in HLA‐associated risks of childhood insulin‐dependent diabetes in the finnish population: I. Allele effects at A, B, and DR Loci |
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|
✓ |
✓ |
Finnish population |
| Apolipoprotein B gene DNA polymorphisms (<i>Eco</i>RI and <i>Msp</i>I) and serum lipid levels in the serbian healthy population: Interaction of rare alleles and smoking and cholesterol levels |
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✓ |
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✓ |
✓ |
serbian healthy population; Belgrade area |
| Genome scan for association and linkage |
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| The TDT reveals linkage and linkage disequilibrium in a rare disease |
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| Evaluation of screening strategies to detect an oligogenic disease |
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| Precision of marker heterozygosity estimates |
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| Sib‐based detection of QTLs |
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| Measuring gene‐disease association using a general pair method |
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| Simulation of a common oligogenic disease with quantitative risk factors. GAW9 problem 2: The answers |
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| Evaluation of genetic and environmental effects using GEE and APM methods |
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| Statistical genetics of normal variation in family data for oligogenic diseases |
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| The influence of response bias on segregation and linkage analysis |
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| Statistical properties of the allelic and genotypic transmission/disequilibrium test for multiallelic markers |
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| Computing conditional recombination probabilities given marker information |
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