Affected sib-pair tests for linkage: Type I errors with dependent sib-pairs |
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Apolipoprotein E epsilon4 allele and familial aggregation of Alzheimer disease. |
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Association between tumor necrosis factor receptor II and familial, but not sporadic, rheumatoid arthritis: evidence for genetic heterogeneity. |
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Association of rheumatoid arthritis with an amino acid allelic variation of the T cell receptor |
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Bases génétiques des troubles du contrôle des impulsions dans la maladie de Parkinson |
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Bivariate association analysis in selected samples: application to a GWAS of two bone mineral density phenotypes in males with high or low BMD. |
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Breast cancer risk modifying factors in hight risk women. |
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Chromosome 5 and Parkinson disease |
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Clases magistrales de macroeconomía I |
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Classification spatiale du déséquilibre de liaison pour les études d'association pangénomique. |
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Comparative study of statistical methods for detecting association with rare variants in exome-resequencing data |
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La consanguinité à l'ère du génome haut-débit : estimations et applications |
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Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease |
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Cuadernos metodológicos de macroecnomía |
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Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study |
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Étude des facteurs modificateurs du risque de cancer du sein des femmes à risque génétique élevé |
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Etudes d'association prenant en compte des mécanismes complexes : application à l'asthme |
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Evidence for apolipoprotein E epsilon 4 association in early-onset Alzheimer's patients with late-onset relatives. |
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Evidence for caveolin-1 as a new susceptibility gene regulating tissue fibrosis in systemic sclerosis |
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Further evidence for anticipation in schizophrenia |
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Further support for the association of GNPAT variant rs11558492 with severe iron overload in hemochromatosis |
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Genetic analysis of human breast cancer: Implications for family study designs |
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Genetic Association Studies Taking Into Account Complex Mechanisms In The Context Of Asthma. |
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Genetic comorbidities in Parkinson's disease |
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Genetic linkage mapping of the m4 human muscarinic receptor (CHRM4) |
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Genetic mapping of the Gs-alpha subunit gene (GNAS1) to the distal long arm of chromosome 20 using a polymorphism detected by denaturing gradient gel electrophoresis. |
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[Genetics of Alzheimer's disease]. |
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Genome wide association study design and statistical methods for complex traits : genome wide association study for Parkinson's disease. |
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Genome-Wide Linkage Screen of Bone Mineral Density (BMD) in European Pedigrees Ascertained through a Male Relative with Low BMD Values: Evidence for Quantitative Trait Loci on 17q21–23, 11q12–13, 13q12–14, and 22q11 |
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Genome-wide scan for autism susceptibility genes. Paris Autism Research International Sibpair Study |
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Genome-wide scan identifies TNIP1, PSORS1C1, and RHOB as novel risk loci for systemic sclerosis |
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Genomewide linkage scan of 409 European-ancestry and African American families with schizophrenia: suggestive evidence of linkage at 8p23.3-p21.2 and 11p13.1-q14.1 in the combined sample |
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How can maximum likelihood methods reveal candidate gene effects on a quantitative trait? |
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The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease |
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Is a single mutation at the same locus responsible for all affected cases in a large Alzheimer pedigree (FAD4)? |
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Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease |
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Linkage detection by the Affected-Pedigree-Member method: what is really tested? |
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Long-term stability of diagnosis and symptom dimensions in a systematic sample of patients with onset of schizophrenia in childhood and early adolescence. II: Postnegative distinction and childhood predictors of adult outcome. |
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Méthodes statistiques et stratégies d'études d'association de phénotypes complexes études pan-génomiques de la maladie de Parkinson |
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Modélisation de la composante génétique des maladies humaines : Données familiales et Modèles Mixtes |
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Modelisation of Genetic Risk in Human Diseases : Family Data and Mixed Model. |
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Multilocus Approach of the genome in the population genetics models. |
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El mutualismo de previsión social y los sistemas de protección complementarios |
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NeuroX, a fast and efficient genotyping platform for investigation of neurodegenerative diseases |
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New susceptibility locus for rheumatoid arthritis suggested by a genome-wide linkage study. |
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No founder effect in three novel Alzheimer's disease families with APP 717 Val-->Ile mutation. Clerget-darpoux. French Alzheimer's Disease Study Group. |
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No significant association of 14 candidate genes with schizophrenia in a large European ancestry sample: implications for psychiatric genetics |
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Noninherited maternal antigens do not play a role in rheumatoid arthritis susceptibility in Europe. European Consortium on Rheumatoid Arthritis Families |
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De novo presenilin 1 mutations are rare in clinically sporadic, early onset Alzheimer's disease cases. French Alzheimer's Disease Study Group. |
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The p.Asp216His TOR1A allele effect is not found in the French population |
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Performance of linkage analysis under misclassification error when the genetic model is unknown |
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El plan de vivienda 1992-1995: un estudio de su incidencia redistributiva |
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La política de vivienda en España : análisis de sus efectos redistributivos |
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Polymorphisms in the trace amine receptor 4 (TRAR4) gene on chromosome 6q23.2 are associated with susceptibility to schizophrenia |
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Posterior probability of linkage and maximal lod score. |
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Power of the linkage test for a heterogeneous disorder due to two independent inherited causes: a simulation study. |
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Proceedings of the Genetic Analysis Workshop 13: analysis of longitudinal family data for complex diseases and related risk factors. November 11-14, 2002. New Orleans, Louisiana, USA |
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La productividad del agua en el regadío andaluz |
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Pseudoautosomal region in schizophrenia: Linkage analysis of seven loci by sib-pair and lod-score methods |
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Regressive logistic models in linkage analysis of the cutaneous malignant melanoma-dysplastic nevus syndrome |
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Sampling strategies for linkage studies. |
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Segregation analysis of Alzheimer pedigrees: rare Mendelian dominant mutation(s) explain a minority of early-onset cases. French Alzheimer Collaborative Group. |
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Serotonin transporter gene polymorphism and schizophrenia: an association study |
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Single-marker and multi-marker mixed models for polygenic score analysis in family-based data |
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Spatial clustering of linkage disequilibrium blocks for genome-wide association studies |
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Statistical methods for genetic analysis of correlated quantitative traits : application to the study of bone mineral density. |
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Summary of contributions to GAW Group 15: family-based samples are useful in identifying common polymorphisms associated with complex traits |
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Transethnic meta-analysis identifies GSDMA and PRDM1 as susceptibility genes to systemic sclerosis. |
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Use of support vector machines for disease risk prediction in genome-wide association studies: concerns and opportunities. |
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Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease |
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The Val158Met COMT polymorphism is a modifier of the age at onset in Parkinson's disease with a sexual dimorphism |
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WES/WGS Reporting of Mutations from Cardiovascular "Actionable" Genes in Clinical Practice: A Key Role for UMD Knowledgebases in the Era of Big Databases. |
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