Genetic dissection of complex diseases;Dissection génétique des maladies à hérédité complexe

Medecine/Sciences

Volumn 17, Issue 11, 2001, Pages 1139-1148

  Campion, D ^a  

^a INSERM   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ALZHEIMER DISEASE; GENE MUTATION; GENETIC ANALYSIS; GENETIC ASSOCIATION; GENETIC LINKAGE; GENETIC RISK; GENETIC SUSCEPTIBILITY; GENOME; GENOTYPE; HUMAN; MENTAL DISEASE; PHENOTYPE; REVIEW; RISK FACTOR; SINGLE NUCLEOTIDE POLYMORPHISM;

EID: 0035201518     PISSN: 07670974     EISSN: None     Source Type: Journal    
DOI: 10.1051/medsci/200117111139     Document Type: Review

References (35)

1. The inheritance of liability to certain diseases
2. Genetic dissection of complex traits
3. Effects of misspecifying genetic parameters in lod score analysis
4. Linkage strategies for genetically complex traits
5. Genetic analysis of complex diseases
6. Susceptibility locus for Alzheimer's disease on chromosome 10
7. A sibship based test for linkage in the presence of association: The sib transmission/disequilibrium test
8. Le déséquilibre de liaison
9. Mapping genes by drift-generated linkage disequilibrium
10. Population choice in mapping genes for complex diseases
11. Prospects for whole-genome linkage disequilibrium mapping of common disease genes
12. Population structure in admixed populations: Effect of admixture dynamics on the pattern of linkage disequilibrium
13. A look at linkage disequilibrium
14. Association of an apolipoprotein CII allele with familial dementia of the Alzheimer type
15. The apolipoprotein E/CI/CII gene cluster and late-onset Alzheimer disease
16. Apolipoprotein E and Alzheimer's disease
17. Linkage studies in familial Alzheimer disease: Evidence for chromosome 19 linkage
18. Apolipoprotein E and Alzheimer disease: Genotype-specific risks by age and sex
19. Single nucleotide polymorphisms as tools in human genetics
20. Characterization of single-nucleotide polymorphisms in coding regions of human genes
21. The future of genetic studies of complex human diseases
22. Variations on a theme: Cataloging human DNA sequence variation
23. Linkage disequilibrium as a gene mapping tool
24. SNPing away at complex diseases: Analysis of single-nucleotide polymorphisms around APOE in Alzheimer's disease
25. Genetic dissection of complex traits: Guidelines for interpreting and reporting linkage results
26. Phenotypes of patients with «simple» mendelian disorders are complex traits: Thresholds, modifiers, and systems dynamics
27. Complexity in a monogenic disease
28. Mapping mendelian factors underlying quantitative traits using RFLP linkage maps
29. The roads from phenotypic variation to gene discovery: Mutagenesis versus QTL
30. A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains
31. Untangling tau-related dementia
32. Deficit in sensory gating in schizophrenic patients and their relatives
33. Nicotinic receptor function in schizophrenia
34. Searching for genetic determinants in the new millennium
35. How many diseases does it take to map a gene with SNP?