Zobrazeno 1 - 10
of 57
pro vyhledávání: '"J Hochez"'
Autor:
Josué Feingold, Jean Maccario, Francine Kauffmann, Francesca Sampogna, Florence Demenais, Marie Pierre Oryszczyn, J Hochez, Marie Hélène Dizier
Publikováno v:
Genetic Epidemiology. 18:128-142
The main objective of this study was to search for a major gene controlling total serum immunoglobulin E (IgE) levels, an intermediate phenotype for asthma and allergy. We studied 335 French nuclear families of the EGEA study (Epidemiological study o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f98beb5391e8af20f96258510edc98b4
https://doi.org/10.1002/(sici)1098-2272(200002)18:2<128::aid-gepi3>3.0.co
https://doi.org/10.1002/(sici)1098-2272(200002)18:2<128::aid-gepi3>3.0.co
Autor:
J Hochez, M F Tournade, Jean Lemerle, Agnès Chompret, Catherine Bonaïti-Pellié, C Moutou, C Le Bihan, J M Zucker
Publikováno v:
Journal of Medical Genetics. 31:429-434
Wilms' tumour of the kidney is known to occur in Beckwith-Wiedemann syndrome. It has also been described in four cancer prone families displaying Li-Fraumeni syndrome but it is not usually considered to be part of this syndrome. In order to detect pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4bb820a9601ca11568c3ae894ca312f
https://doi.org/10.1136/jmg.31.6.429
https://doi.org/10.1136/jmg.31.6.429
Autor:
Agnès Chompret, Marie-France Tournade, Jean Lemerle, J Hochez, Claudine Junien, C Moutou, Catherine Bonaïti-Pellié, Jean-Michel Zucker
Publikováno v:
European Journal of Human Genetics. 1:190-205
Data from 511 cases of Wilms' tumor in France (including 12 familial cases) and 8 pedigrees from the literature were analyzed to test three modifications of Knudson's classical bimutational theory, based on genomic imprinting in Wilms' tumor carcinog
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4395f44c586356bd7a71ed5d5afecd3
https://doi.org/10.1159/000472413
https://doi.org/10.1159/000472413
Autor:
Jocelyne Just, Evelyne Paty, Marie-Hélène Dizier, Jean Bousquet, Isabella Annesi-Maesano, Régis Matran, Arnaud Lemainque, Frédéric Gormand, Florence Demenais, J Hochez, Denis Charpin, Françoise Neukirch, Nicole Le Moual, Isabelle Pin, Marie-Pierre Oryszczyn, Michel Guilloud-Bataille, Emmanuelle Bouzigon, Francine Kauffmann, Mark Lathrop, Daniel Vervloet
Publikováno v:
Human Genetics
Human Genetics, Springer Verlag, 2008, 122 (6), pp.605-14. 〈10.1007/s00439-007-0439-7〉
Human Genetics, 2008, 122 (6), pp.605-14. ⟨10.1007/s00439-007-0439-7⟩
Human Genetics, Springer Verlag, 2008, 122 (6), pp.605-14. ⟨10.1007/s00439-007-0439-7⟩
Human Genetics, Springer Verlag, 2008, 122 (6), pp.605-14. 〈10.1007/s00439-007-0439-7〉
Human Genetics, 2008, 122 (6), pp.605-14. ⟨10.1007/s00439-007-0439-7⟩
Human Genetics, Springer Verlag, 2008, 122 (6), pp.605-14. ⟨10.1007/s00439-007-0439-7⟩
International audience; Asthma, allergic rhinitis (AR) and atopic dermatitis also called eczema are allergic co-morbidites, which are likely to depend on pleiotropic genetic effects as well as on specific genetic factors. After a previous genome-wide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::73f27573f9af7a4963bb353ab8c585c6
https://pubmed.ncbi.nlm.nih.gov/17943316
https://pubmed.ncbi.nlm.nih.gov/17943316
Autor:
J Hochez, Arnaud Lemainque, M H Dizier, Isabelle Pin, M Lathrop, Isabella Annesi-Maesano, Evelyne Paty, Marie-Pierre Oryszczyn, Florence Demenais, D. Charpin, N. Le Moual, Jean Bousquet, C Betard, Daniel Vervloet, Francine Kauffmann, F Gormand, R. Matran, M Guilloud-Bataille, Françoise Neukirch, Jocelyne Just, Emmanuelle Bouzigon
Publikováno v:
Genes and Immunity
Genes and Immunity, 2005, 6 (2), pp.95-102. ⟨10.1038/sj.gene.6364163⟩
Genes and Immunity, Nature Publishing Group: Open Access Hybrid Model Option B, 2005, 6 (2), pp.95-102. ⟨10.1038/sj.gene.6364163⟩
Genes and Immunity, 2005, 6 (2), pp.95-102. ⟨10.1038/sj.gene.6364163⟩
Genes and Immunity, Nature Publishing Group: Open Access Hybrid Model Option B, 2005, 6 (2), pp.95-102. ⟨10.1038/sj.gene.6364163⟩
International audience; In the sample of 295 French EGEA families with at least one asthmatic subject, a genome screen was conducted to identify potential linkage regions specific either to allergic rhinitis (AR) or to asthma as well as those shared
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b87f1ea984f8f7bae225590ee0f06ebe
https://hal.sorbonne-universite.fr/hal-00595641
https://hal.sorbonne-universite.fr/hal-00595641
Publikováno v:
Annals of human biology. 22(3)
The distribution of surnames in 90 distinct regions in France during two successive periods, 1889-1915 and 1916-1940, is analysed from the civil birth registers of the 36,500 administrative units in France. A new approach, called 'Mobile Site Method'
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::970486e305b5fd04d30355dd500e6599
https://pubmed.ncbi.nlm.nih.gov/7574444
https://pubmed.ncbi.nlm.nih.gov/7574444
Autor:
Henri Roché, Agnès Chompret, Jean Lemerle, Philippe Tron, J Hochez, D. Frappaz, M. Brunat-Mentigny, Dominique Steschenko, Jean-Michel Zucker, Francois Dusol, Catherine Bonaïti-Pellié, Martine Munzer, Marie-France Tournade, Colette Bachelot, Danielle Sommelet‐Olive, C Moutou
Publikováno v:
Medical and pediatric oncology. 20(4)
A complete family history was obtained for 501 patients with Wilms' tumor, treated in departments of pediatric oncology in whole France. The information was collected by self-questionnaire and/or by interview of parents. The proportion of bilateral c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fb620f93b03eedd3b353292a6ebae388
https://pubmed.ncbi.nlm.nih.gov/1318995
https://pubmed.ncbi.nlm.nih.gov/1318995
Publikováno v:
Tissue antigens. 36(1)
In the present paper, an extension of segregation analysis is proposed using information on the joint segregation of two unlinked markers conditional on the disease status in nuclear families, in order to consider two-locus models with one locus link
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e1cf4e87f13f340bc4847d3d646f13fc
https://pubmed.ncbi.nlm.nih.gov/2247883
https://pubmed.ncbi.nlm.nih.gov/2247883
Autor:
M H Dizier, Catherine Bonaïti-Pellié, J Hochez, Marie-Claude Babron, Françoise Clerget-Darpoux, Maria Martinez
Publikováno v:
Europe PubMed Central
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ea1f125385a546fe51e30962201d0d7
https://doi.org/10.1002/gepi.1370030747
https://doi.org/10.1002/gepi.1370030747
Publikováno v:
Genetic Epidemiology. 6:71-75
The purpose of our study was to examine evidence for the role of a second genetic factor in the susceptibility to IDDM, in addition to that located in the HLA region. To do this, we have studied the joint segregation of HLA and another marker conditi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90346f26cc6e2f209d8839749cbdde18
https://doi.org/10.1002/gepi.1370060114
https://doi.org/10.1002/gepi.1370060114