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Results: 1-25 | 26-26
Results: 1-25/26
Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population
Authors: Verpillat, P Bouley, S Campion, D Hannequin, D Dubois, B Belliard, S Puel, M Thomas-Anterion, C Agid, Y Brice, A Clerget-Darpoux, F
Citation: P. Verpillat et al., Use of haplotype information to test involvement of the LRP gene in Alzheimer's disease in the French population, EUR J HUM G, 9(6), 2001, pp. 464-468
Modeling of HLA class II susceptibility to type I diabetes reveals an effect associated with DPB1
Authors: Valdes, AM Noble, JA Genin, E Clerget-Darpoux, F Erlich, HA Thomson, G
Citation: Am. Valdes et al., Modeling of HLA class II susceptibility to type I diabetes reveals an effect associated with DPB1, GENET EPID, 21(3), 2001, pp. 212-223
Homogeneity of asthma genome scan results
Authors: Babron, MC Selinger-Leneman, H Dizier, MH Clerget-Darpoux, F
Citation: Mc. Babron et al., Homogeneity of asthma genome scan results, GENET EPID, 21, 2001, pp. S44-S48
Maximum identity length contrast: A powerful method for susceptibility gene detection in isolated populations
Authors: Bourgain, C Genin, E Margaritte-Jeannin, P Clerget-Darpoux, F
Citation: C. Bourgain et al., Maximum identity length contrast: A powerful method for susceptibility gene detection in isolated populations, GENET EPID, 21, 2001, pp. S560-S564
Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families
Authors: Greco, L Babron, MC Corazza, GR Percopo, S Sica, R Clot, F Fulchignoni-Lataud, MC Zavattari, P Momigliano-Richiardi, P Casari, G Gasparini, P Tosi, R Mantovani, V De Virgiliis, S Iacono, G D'Alfonso, A Selinger-Leneman, H Lemainque, A Serre, JL Clerget-Darpoux, F
Citation: L. Greco et al., Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families, ANN HUM GEN, 65, 2001, pp. 35-41
Use of closely related affected individuals for the genetic study of complex diseases in founder populations
Authors: Bourgain, C Genin, E Holopainen, P Mustalahti, K Maki, M Partanen, J Clerget-Darpoux, F
Citation: C. Bourgain et al., Use of closely related affected individuals for the genetic study of complex diseases in founder populations, AM J HU GEN, 68(1), 2001, pp. 154-159
APOE promoter polymorphisms do not confer independent risk for Alzheimer'sdisease in a French population
Authors: Zurutuza, L Verpillat, P Raux, G Hannequin, D Puel, M Belliard, S Michon, A Pothin, Y Camuzat, A Penet, C Martin, C Brice, A Campion, D Clerget-Darpoux, F Frebourg, T
Citation: L. Zurutuza et al., APOE promoter polymorphisms do not confer independent risk for Alzheimer'sdisease in a French population, EUR J HUM G, 8(9), 2000, pp. 713-716
Modeling the HLA component in rheumatoid arthritis: Sensitivity to DRB1 allele frequencies
Authors: du Montcel, ST Reviron, D Genin, E Roudier, J Mercier, P Clerget-Darpoux, F
Citation: St. Du Montcel et al., Modeling the HLA component in rheumatoid arthritis: Sensitivity to DRB1 allele frequencies, GENET EPID, 19(4), 2000, pp. 422-428
Genetic susceptibility to multiple sclerosis
Authors: Fontaine, B Clerget-Darpoux, F
Citation: B. Fontaine et F. Clerget-darpoux, Genetic susceptibility to multiple sclerosis, PATH BIOL, 48(1), 2000, pp. 87-92
alpha 2-macroglobulin gene and Alzheimer's disease: Confirmation of association by haplotypes analyses
Authors: Verpillat, P Bouley, S Hannequin, D Belliard, S Puel, M Thomas-Anterion, C Dubois, B Agid, Y Campion, D Clerget-Darpoux, F Brice, A
Citation: P. Verpillat et al., alpha 2-macroglobulin gene and Alzheimer's disease: Confirmation of association by haplotypes analyses, ANN NEUROL, 48(3), 2000, pp. 400-402
Mutations in the neuroserpin gene are rare in familial dementia
Authors: Camuzat, A Verpillat, P Dubois, B Penet, C Agid, CPY Brice, A Clerget-Darpoux, F Moreaud, O Puel, M Kinter, J Kozlov, S Berger, P Sonderegger, P Raux, G Campion, D Hannequin, D Frebourg, T
Citation: A. Camuzat et al., Mutations in the neuroserpin gene are rare in familial dementia, ANN NEUROL, 47(5), 2000, pp. 688-688
Unraveling the genetic component of multifactorial diseases: Dream or reality
Authors: Clerget-Darpoux, F
Citation: F. Clerget-darpoux, Unraveling the genetic component of multifactorial diseases: Dream or reality, INT STAT R, 68(1), 2000, pp. 45-51
Study of two ectopeptidases in the susceptibility to celiac disease: Two newly identified polymorphisms of dipeptidylpeptidase IV
Authors: Clot, F Babron, MC Percopo, S Giordano, M Bouguerra, F Clerget-Darpoux, F Greco, L Serre, JL Fulchignoni-Lataud, MC
Citation: F. Clot et al., Study of two ectopeptidases in the susceptibility to celiac disease: Two newly identified polymorphisms of dipeptidylpeptidase IV, J PED GASTR, 30(4), 2000, pp. 464-466
Cytokines in genetic susceptibility to multiple sclerosis: a candidate gene approach
Authors: Reboul, J Mertens, C Levillayer, F Eichenbaum-Voline, S Vilkoren, T Cournu, I Babron, MC Lyon-Caen, O Clerget-Darpoux, F Edan, G Clanet, M Brahic, M Bureau, JF Fontaine, B Liblau, R
Citation: J. Reboul et al., Cytokines in genetic susceptibility to multiple sclerosis: a candidate gene approach, J NEUROIMM, 102(1), 2000, pp. 107-112
The HLA-DRB4 gene does not explain genetic susceptibility in HLA-DQ2-negative celiac disease - Response
Authors: Clot, F Gianfrani, C Babron, MC Bouguerra, F Southwood, S Kagnoff, MF Troncone, R Percopo, S Eliaou, JF Clerget-Darpoux, F Sette, A Greco, L
Citation: F. Clot et al., The HLA-DRB4 gene does not explain genetic susceptibility in HLA-DQ2-negative celiac disease - Response, IMMUNOGENET, 51(3), 2000, pp. 251-251
The triangle test statistic (TTS): a test of genetic homogeneity using departure from the triangle constraints in IBD distribution among affected sib-pairs
Authors: Dizier, MH Quesneville, H Prum, B Selinger-Leneman, H Clerget-Darpoux, F
Citation: Mh. Dizier et al., The triangle test statistic (TTS): a test of genetic homogeneity using departure from the triangle constraints in IBD distribution among affected sib-pairs, ANN HUM GEN, 64, 2000, pp. 433-442
Search for multifactorial disease susceptibility genes in founder populations
Authors: Bourgain, C Genin, E Quesneville, H Clerget-Darpoux, F
Citation: C. Bourgain et al., Search for multifactorial disease susceptibility genes in founder populations, ANN HUM GEN, 64, 2000, pp. 255-265
The HLA component of type I diabetes
Authors: Clerget-Darpoux, F
Citation: F. Clerget-darpoux, The HLA component of type I diabetes, AM J HU GEN, 66(4), 2000, pp. 1468-1468
Susceptibility to coeliac disease in Tunisian children and GM immunoglobulin allotypes
Authors: Bouguerra, F Dugoujon, JM Babron, MC Greco, L Khaldi, F Debbabi, A Bennaceur, B Clerget-Darpoux, F
Citation: F. Bouguerra et al., Susceptibility to coeliac disease in Tunisian children and GM immunoglobulin allotypes, EUR J IMM, 26(4), 1999, pp. 293-297
Strategies for detecting susceptibility genes in a complex disease
Authors: Babron, MC Barillot, E Margaritte-Jeannin, P Clerget-Darpoux, F
Citation: Mc. Babron et al., Strategies for detecting susceptibility genes in a complex disease, GENET EPID, 17, 1999, pp. S479-S483
Detection and modeling of disease susceptibility locus effects: How much can be learned from contrast of populations?
Authors: Genin, E Guyon, F Margaritte-Jeannin, P Quesneville, H Clerget-Darpoux, F
Citation: E. Genin et al., Detection and modeling of disease susceptibility locus effects: How much can be learned from contrast of populations?, GENET EPID, 17, 1999, pp. S569-S574
Departure from the triangle constraints in discordant sib pairs: A test for genetic heterogeneity
Authors: Quesneville, H Dizier, MH Clerget-Darpoux, F
Citation: H. Quesneville et al., Departure from the triangle constraints in discordant sib pairs: A test for genetic heterogeneity, GENET EPID, 17, 1999, pp. S685-S689
HLA-DR53 molecules are associated with susceptibility to celiac disease and selectively bind gliadin-derived peptides
Authors: Clot, F Gianfrani, C Babron, MC Bouguerra, F Southwood, S Kagnoff, MF Troncone, R Percopo, S Eliaou, JF Clerget-Darpoux, F Sette, A Greco, L
Citation: F. Clot et al., HLA-DR53 molecules are associated with susceptibility to celiac disease and selectively bind gliadin-derived peptides, IMMUNOGENET, 49(9), 1999, pp. 800-807
Early-onset autosomal dominant Alzheimer disease: Prevalence, genetic heterogeneity, and mutation spectrum
Authors: Campion, D Dumanchin, C Hannequin, D Dubois, B Belliard, S Puel, M Thomas-Anterion, C Michon, A Martin, C Charbonnier, F Raux, G Camuzat, A Penet, C Mesnage, V Martinez, M Clerget-Darpoux, F Brice, A Frebourg, T
Citation: D. Campion et al., Early-onset autosomal dominant Alzheimer disease: Prevalence, genetic heterogeneity, and mutation spectrum, AM J HU GEN, 65(3), 1999, pp. 664-670
Linkage and association study of the CTLA-4 region in coeliac disease for Italian and Tunisian populations
Authors: Clot, F Fulchignoni-Lataud, MC Renoux, C Percopo, S Bouguerra, F Babron, MC Djilai-Saiah, I Caillat-Zucman, S Clerget-Darpoux, F Greco, L Serre, JL
Citation: F. Clot et al., Linkage and association study of the CTLA-4 region in coeliac disease for Italian and Tunisian populations, TISSUE ANTI, 54(5), 1999, pp. 527-530
Risultati: 1-25 | 26-26