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Segregation analysis of the Jacobsen data.
Published in:
Genetic Epidemiology, 1986, v. 3, n. S1, p. 49, doi. 10.1002/gepi.1370030708
By:
- Demenais, F.;
- Martinez, M.;
- Bonaïti-Pellié, C.;
- Clerget-Darpoux, F.;
- Feingold, N.
Publication type:
Article
Discrimination between genetic models for insulin dependent diabetes mellitus.
Published in:
Genetic Epidemiology, 1986, v. 3, n. S1, p. 313, doi. 10.1002/gepi.1370030747
By:
- Clerget-Darpoux, F.;
- Dizier, M. H.;
- Bonaïti-Pellié, C.;
- Babron, M. C.;
- Hochez, J.;
- Martinez, M.
Publication type:
Article
Multilocus linkage analysis of markers located on short arm of chromosome 11.
Published in:
Genetic Epidemiology, 1986, v. 3, n. S1, p. 129, doi. 10.1002/gepi.1370030720
By:
- Bonaïti-Pellié, C.;
- Martinez, M.;
- Clerget-Darpoux, F.
Publication type:
Article
HLA-DRB1*15 allele influences the later course of relapsing remitting multiple sclerosis.
Published in:
Genes & Immunity, 2008, v. 9, n. 6, p. 570, doi. 10.1038/gene.2008.52
By:
- Cournu-Rebeix, I.;
- Génin, E.;
- Leray, E.;
- Babron, M.-C.;
- Cohen, J.;
- Gout, C.;
- Alizadeh, M.;
- Perdry, H.;
- Semana, G.;
- Brassat, D.;
- Clerget-Darpoux, F.;
- Yaouanq, J.;
- Edan, G.;
- Rosenheim, M.;
- Fontaine, B.
Publication type:
Article
A family-based study does not confirm the association of MYO9B with celiac disease in the Italian population.
Published in:
Genes & Immunity, 2006, v. 7, n. 7, p. 606, doi. 10.1038/sj.gene.6364331
By:
- Giordano, M.;
- Marano, C.;
- Mellai, M.;
- Limongelli, M. G.;
- Bolognesi, E.;
- Clerget-Darpoux, F.;
- Momigliano-Richiardi, P.;
- Greco, L.
Publication type:
Article
Intercellular adhesion molecule-1: a protective haplotype against multiple sclerosis.
Published in:
Genes & Immunity, 2003, v. 4, n. 7, p. 518, doi. 10.1038/sj.gene.6364009
By:
- Cournu-Rebeix, I.;
- Génin, E.;
- Lesca, G.;
- Azoulay-Cayla, A.;
- Tubridy, N.;
- Noé, E.;
- Clanet, M.;
- Edan, G.;
- Clerget-Darpoux, F.;
- Sémana, C.;
- Fontaine, B.
Publication type:
Article
Chromosome 17q22–q24 and multiple sclerosis genetic susceptibility.
Published in:
Genes & Immunity, 1999, v. 1, n. 2, p. 149
By:
- Fontaine, B;
- Cournu, I;
- Arnaud, I;
- Babron, M-C;
- Eichenbaum-Voline, S;
- Oksenberg, J R;
- Pericak-Vance, M A;
- Haines, J L;
- Semama, G;
- Liblau, R;
- Lyon-Caen, O;
- Clerget-Darpoux, F;
- Clanet, M;
- Hauser, S L
Publication type:
Article
Study of two ectopeptidases in the susceptibility to celiac disease: two newly identified polymorphisms of dipeptidylpeptidase IV.
Published in:
2000
By:
- Clot, Fabienne;
- Babron, Marie-Claude;
- Percopo, Selvaggia;
- Giordano, Mara;
- Bouguerra, Faouzi;
- Clerget-Darpoux, Francoise;
- Greco, Luigi;
- Serre, Jean-Louis;
- Fulchignoni-Lataud, Marie-Claude;
- Clot, F;
- Babron, M C;
- Percopo, S;
- Giordano, M;
- Bouguerra, F;
- Clerget-Darpoux, F;
- Greco, L;
- Serre, J L;
- Fulchignoni-Lataud, M C
Publication type:
journal article
Lack of correlation between genotype and phenotype in celiac disease.
Published in:
1998
By:
- Greco, Luigi;
- Percopo, Selvaggia;
- Clot∗, Fabienne;
- Bouguerra†, Faouzi;
- Babron∗, Marie-Claude;
- Eliaou‡, Jean-François;
- Franzese, Carlo;
- Troncone, Riccardo;
- Clerget-Darpoux∗, Françoise;
- Greco, L;
- Percopo, S;
- Clot, F;
- Bouguerra, F;
- Babron, M C;
- Eliaou, J F;
- Franzese, C;
- Troncone, R;
- Clerget-Darpoux, F
Publication type:
journal article
75 HLA-DRB4 IS THE MISSING SPECIFICITY IN COELLAC DISEASE.
Published in:
Journal of Pediatric Gastroenterology & Nutrition, 1996, v. 22, n. 4, p. 428
By:
- Greco, L.;
- Eliaou, J F;
- Bouguerra, F.;
- Clot, F.;
- Barbron, M C;
- Troncone, R;
- Percopo, S;
- Clerget-Darpoux, F
Publication type:
Article
Indication of linkage and genetic heterogeneity for asthma and atopy on chromosomes 8p and 12q in 107 French EGEA families.
Published in:
European Journal of Human Genetics, 2003, v. 11, n. 8, p. 590, doi. 10.1038/sj.ejhg.5201014
By:
- Dizier, M-H;
- Quesneville, H;
- Besse-Schmittler, C;
- Guilloud-Bataille, M;
- Selinger-Leneman, H;
- Clerget-Darpoux, F;
- Demenais, F
Publication type:
Article
Comparison of family based haplotype methods using intragenic SNPs in candidate genes.
Published in:
European Journal of Human Genetics, 2002, v. 10, n. 5, p. 313, doi. 10.1038/sj.ejhg.5200808
By:
- Bourgain, C.;
- Genin, E.;
- Clerget-Darpoux, F.
Publication type:
Article
Saturation of the 5q31-q33 Candidate Region for Coeliac Disease.
Published in:
Annals of Human Genetics, 2003, v. 67, n. 3, p. 265, doi. 10.1046/j.1469-1809.2003.00026.x
By:
- Percopo, S.;
- Babron, M.-C.;
- Whalen, M.;
- De Virgiliis, S.;
- Coto, I.;
- Clerget-Darpoux, F.;
- Landolfo, F.;
- Greco, L.
Publication type:
Article
Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families.
Published in:
Annals of Human Genetics, 2001, v. 65, n. 1, p. 35
By:
- GRECO, L.;
- BABRON, M. C.;
- CORAZZA, G. R.;
- PERCOPO, S.;
- SICA, R.;
- CLOT, F.;
- FULCHIGNONI-LATAUD, M. C.;
- 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, J. L.;
- CLERGET-DARPOUX, F.
Publication type:
Article
Search for multifactorial disease susceptibility genes in founder populations.
Published in:
Annals of Human Genetics, 2000, v. 64, n. 3, p. 255
By:
- BOURGAIN, C.;
- GENIN, E.;
- QUESNEVILLE, H.;
- CLERGET-DARPOUX, F.
Publication type:
Article
Information provided by pairs of distantly affected relatives to search for genes involved in rare autosomal dominant diseases.
Published in:
Annals of Human Genetics, 1997, v. 61, n. 1, p. 25
By:
- GÉNIN, E.;
- BELLIS, G.;
- CLERGET-DARPOUX, F.
Publication type:
Article
Clinical methods in psychiatric genetics III. Environmental stratification may simulate a genetic effect in adoption studies.
Published in:
Acta Psychiatrica Scandinavica, 1986, v. 74, n. 4, p. 305, doi. 10.1111/j.1600-0447.1986.tb06249.x
By:
- Clerget-Darpoux, F.;
- Goldin, L. R.;
- Gershon, E. S.
Publication type:
Article
Unraveling the Genetic Component of Multifactorial Diseases: Dream or Reality.
Published in:
International Statistical Review, 2000, v. 68, n. 1, p. 45, doi. 10.1111/j.1751-5823.2000.tb00386.x
By:
- Clerget-Darpoux, F.
Publication type:
Article
Season of birth and not vitamin D receptor promoter polymorphisms is a risk factor for multiple sclerosis.
Published in:
Multiple Sclerosis (13524585), 2009, v. 15, n. 10, p. 1146, doi. 10.1177/1352458509106780
By:
- Fernandes de Abreu, D. A.;
- Babron I, M. C.;
- Rebeix, C.;
- Fontenille, J.;
- Yaouanq, D.;
- Brassat, B.;
- Fontaine, F.;
- Clerget-Darpoux, F.;
- Jehan, F.;
- Feron
Publication type:
Article
No evidence for association between the EIF2B5 gene and multiple sclerosis in French families.
Published in:
2008
By:
- Fogli, A.;
- Barbier, C.;
- Cournu-Rebeix, I.;
- Babron, M. C.;
- Clerget-Darpoux, F.;
- Fontaine, B.;
- Boespflug-Tanguy, O.
Publication type:
Letter
Improved use of SNP information to detect the role of genes.
Published in:
Genetic Epidemiology, 2003, v. 25, n. 2, p. 158, doi. 10.1002/gepi.10256
By:
- A.-S. Jannot;
- L. Essioux;
- M.G. Reese;
- F. Clerget-Darpoux
Publication type:
Article
Modelling the major histocompatibility complex susceptibility to RA using the MASC method.
Published in:
Genetic Epidemiology, 1998, v. 15, n. 4, p. 419, doi. 10.1002/(SICI)1098-2272(1998)15:4<419::AID-GEPI7>3.0.CO;2-X
By:
- Génin, E.;
- Babron, M.C.;
- McDermott, M.F.;
- Mulcahy, B.;
- Waldron-Lynch, F.;
- Adams, C.;
- Clegg, D.O.;
- Ward, R.H.;
- Shanahan, F.;
- Molloy, M.G.;
- O'Gara, F.;
- Clerget-Darpoux, F.
Publication type:
Article
Heterogeneity of marker allele frequencies hinders interpretation of linkage analysis: Illustration on chromosome 18 markers.
Published in:
Genetic Epidemiology, 1997, v. 14, n. 6, p. 669, doi. 10.1002/(SICI)1098-2272(1997)14:6<669::AID-GEPI20>3.0.CO;2-N
By:
- Margaritte-Jeannin, Patricia;
- Babron, Marie-Claude;
- Génin, Emmanuelle;
- Eichenbaum-Voline, Sophie;
- Clerget-Darpoux, F.
Publication type:
Article
Synergistic effect of two HLA heterodimers in the susceptibility to celiac disease in Tunisia.
Published in:
Genetic Epidemiology, 1997, v. 14, n. 4, p. 413, doi. 10.1002/(SICI)1098-2272(1997)14:4<413::AID-GEPI6>3.0.CO;2-3
By:
- Bouguerra, F.;
- Babron, M.C.;
- Eliaou, J.F.;
- Debbabi, A.;
- Clot, J.;
- Khaldi, F.;
- Greco, L.;
- Clerget-Darpoux, F.
Publication type:
Article
Systematic search of susceptibility loci with methods using gametic disequilibrium.
Published in:
Genetic Epidemiology, 1995, v. 12, n. 6, p. 577, doi. 10.1002/gepi.1370120609
By:
- Bickeböller, H.;
- Margaritte-Jeannin, P.;
- Babron, M.-C.;
- Clerget-Darpoux, F.
Publication type:
Article
Association in Multifactorial Traits: How to Deal with Rare Observations?
Published in:
Human Heredity, 2004, v. 58, n. 2, p. 73, doi. 10.1159/000083028
By:
- Jannot, A.-S.;
- Essioux, L.;
- Clerget-Darpoux, F.
Publication type:
Article
Alzheimer's Disease Associated with Mutations in Presenilin 2 is Rare and Variably Penetrant.
Published in:
Human Molecular Genetics, 1996, v. 5, n. 7, p. 985, doi. 10.1093/hmg/5.7.985
By:
- Sherrington, R.;
- Froelich, S.;
- Sorbi, S.;
- Campion, D.;
- Chi, H.;
- Rogaeva, E. A.;
- Levesque, G.;
- Rogaev, E. I.;
- Lin, C.;
- Liang, Y.;
- Ikeda, M.;
- Mar, L.;
- Brice, A.;
- Agid, Y.;
- Percy, M.E.;
- Clerget-Darpoux, F.;
- Piacentini, S.;
- Marcon, G.;
- Nacmias, B.;
- Amaducci, L.
Publication type:
Article

Found: 27

Segregation analysis of the Jacobsen data.

Discrimination between genetic models for insulin dependent diabetes mellitus.

Multilocus linkage analysis of markers located on short arm of chromosome 11.

HLA-DRB1<sup>*</sup>15 allele influences the later course of relapsing remitting multiple sclerosis.

A family-based study does not confirm the association of MYO9B with celiac disease in the Italian population.

Intercellular adhesion molecule-1: a protective haplotype against multiple sclerosis.

Chromosome 17q22–q24 and multiple sclerosis genetic susceptibility.

Study of two ectopeptidases in the susceptibility to celiac disease: two newly identified polymorphisms of dipeptidylpeptidase IV.

Lack of correlation between genotype and phenotype in celiac disease.

75 HLA-DRB4 IS THE MISSING SPECIFICITY IN COELLAC DISEASE.

Indication of linkage and genetic heterogeneity for asthma and atopy on chromosomes 8p and 12q in 107 French EGEA families.

Comparison of family based haplotype methods using intragenic SNPs in candidate genes.

Saturation of the 5q31-q33 Candidate Region for Coeliac Disease.

Existence of a genetic risk factor on chromosome 5q in Italian Coeliac Disease families.

Search for multifactorial disease susceptibility genes in founder populations.

Information provided by pairs of distantly affected relatives to search for genes involved in rare autosomal dominant diseases.

Clinical methods in psychiatric genetics III. Environmental stratification may simulate a genetic effect in adoption studies.

Unraveling the Genetic Component of Multifactorial Diseases: Dream or Reality.

Season of birth and not vitamin D receptor promoter polymorphisms is a risk factor for multiple sclerosis.

No evidence for association between the EIF2B5 gene and multiple sclerosis in French families.

Improved use of SNP information to detect the role of genes.

Modelling the major histocompatibility complex susceptibility to RA using the MASC method.

Heterogeneity of marker allele frequencies hinders interpretation of linkage analysis: Illustration on chromosome 18 markers.

Synergistic effect of two HLA heterodimers in the susceptibility to celiac disease in Tunisia.

Systematic search of susceptibility loci with methods using gametic disequilibrium.

Association in Multifactorial Traits: How to Deal with Rare Observations?

Alzheimer's Disease Associated with Mutations in Presenilin 2 is Rare and Variably Penetrant.