1. Jansen R. Studying complex biological systems using multifactorial perturbation. Nature Rev Genet. 2003;4:145-151.
2. Tregouet D, Escolano S, Tiret L, Mallet A, Golmard J. A new algorithm for haplotype-based association analysis: the Stochastic-EM algorithm. Ann Hum Genet. 2004;68:165-177.
3. Tahri-Daizadeh N, Tregouet D, Nicaud V, Manuel N, Cambien F, Tiret L. Automated detection of informative combined effects in genetic association studies of complex traits. Genome Res. 2003;13:1952-1960.
4. BIOMED EC-funded project. Dissecting complex diseases with FINESSE. Genet Epidemiol. 1998;15:521.
5. Patterson S, Aebersold R. Proteomics: the first decade and beyond. Nature Genet suppl. 2003;33:311-323.
6. Blankenberg S, Barbaux S, Tiret L. Adhesion molecules and atherosclerosis. Atherosclerosis. 2003;170:191-203.
7. Orita M, Iwahana H, Kanazawa H, Hayashi K, Sekiya T. Detection of polymorphisms of human DNA by gel electrophoresis as single-strand conformation polymorphism. Proc Natl Acad Sci USA. 1989;86:2766-2770.
8. Cambien F, Poirier O, Nicaud V, Herrmann S, Mallet C, Ricard S, Behague I, Hallet H, Blanc H, Loukaci V, Thillet J, Evans, Ruidavets J, Arveiler D, Luc G, Tiret L. Sequence diversity in 36 candidate genes for cardiovascular disorders. Am J Hum Genet. 1999;65:183-191.
9. Tiret L, Poirier O, Nicaud V, Barbaux S, Herrmann S, Perret C, Raoux S, Francomme C, Lebard G, Trégouët D, Cambien F. Heterogeneity of linkage disequilibrium in human genes has implications for association studies of common diseases. Hum Mol Genet. 2002;11:419-429.
10. Collins F, Guyer M, Chakravarti A. Variations on a theme: Cataloging human DNA sequence variation. Science. 1997;278:1580-1581.
11. Collins FS, Patrinos A, Jordan E, Chakravarti A, Gesteland R, Walters L. New goals for the U.S. Human Genome Project: 1998-2003. Science. 1998;282:682-9.
12. Kruglyak L. Prospects for whole-genome linkage disequilibrium mapping of common disease genes. Nature Genet. 1999;22:139-144.
13. Schneider S, Roessli D, Excouffier L. Arlequin ver.2.000: A software for population genetics data analysis. In. University of Geneva, Switzerland: Genetics and Biometry Laboratory; 2000.
14. Stephens M, Smith N, Donnelly P. A new statistical method for haplotype reconstruction from population data. Am J Hum Genet. 2001;68:978-989.
15. Trégouët D, Barbaux S, Escolano S, Tahri N, Golmard J, Tiret L, Cambien F. Specific haplotypes of the P-selectin gene are associated with myocardial infarction. Hum Mol Genet. 2002;11:2015-2023.
16. Tregouet D, Barbaux S, Poirier O, Blankenberg S, Bickel C, Escolano S, Rupprecht H, Meyer J, Cambien F, Tiret L. SELPLG gene polymorphisms in relation to plasma SELPLG levels and coronary artery disease. Ann Hum Genet. 2003;67:504-511.
17. Tahri-Daizadeh N, Tregouet D, Nicaud V, Poirier O, Cambien F, Tiret L. Exploration of Multilocus Effects in a Highly Polymorphic Gene, the Apolipoprotein (APOB) Gene, in Relation to Plasma ApoB Levels. Ann Hum Genet. 2004;68:405-418.
18. Zhang H, Bonney G. Use of classification trees for association studies. Genet Epidemiol. 2000;19:323-32.
19. Province MA, Shannon WD, Rao DC. Classification methods for confronting heterogeneity. Adv Genet. 2001;42:273-86.
20. Nelson MR, Kardia SL, Ferrell RE, Sing CF. A combinatorial partitioning method to identify multilocus genotypic partitions that predict quantitative trait variation. Genome Res. 2001;11:458-70.
21. Ritchie MD, Hahn LW, Roodi N, Bailey LR, Dupont WD, Parl FF, Moore JH. Multifactor-dimensionality reduction reveals high-order interactions among estrogen-metabolism genes in sporadic breast cancer. Am J Hum Genet. 2001;69:138-47.
22. Sherriff A, Ott J. Applications of neural networks for gene finding. Adv Genet. 2001;42:287-97.
23. Curtis D, North BV, Sham PC. Use of an artificial neural network to detect association between a disease and multiple marker genotypes. Ann Hum Genet. 2001;65:95-107.
24. Bonney GE, Lathrop GM, Lalouel JM. Combined linkage and segregation analysis using regressive models. Am J Hum Genet. 1988;43:29-37.
25. O'Connell JR, Weeks DE. The VITESSE algorithm for rapid exact multilocus linkage analysis via genotype set-recoding and fuzzy inheritance. Nat Genet. 1995;11:402-8.
26. O'Connell JR, Weeks DE. An optimal algorithm for automatic genotype elimination. Am J Hum Genet. 1999;65:1733-40.
27. Demenais F, Lathrop M. REGRESS: a computer program including the regressive approach into LINKAGE programs. Genet Epidemiol. 1994;11:291.
28. Martinez M, Abel L, Demenais F. How can maximum likelihood methods reveal candidate gene effects on a quantitative trait? Genet Epidemiol. 1995;12:789-94.
29. Brand E, Chatelain N, Paillard F, Tiret L, Visvikis S, Lathrop M, Soubrier F, Demenais F. Detection of putative functional angiotensinogen (AGT) gene variants controlling plasma AGT levels by combined segregation-linkage analysis. Eur J Hum Genet. 2002;10:715-23.
30. Goldstein AM, Martinez M, Tucker MA, Demenais F. Gene-covariate interaction between dysplastic nevi and the CDKN2A gene in American melanoma-prone families. Cancer Epidemiol Biomarkers Prev. 2000;9:889-94.
31. Chaudru V, Laing A, Dunston GM, Adams-Campbell LL, Williams R, Lynch JJ, Leffall LD, DeWitty RL, Gause BL, Bonney GE, Demenais F. Interactions between genetic and reproductive factors in breast cancer risk in a population-based sample of African-American families. Genet Epidemiol. 2002;22:285-97.