Zobrazeno 1 - 10
of 432
pro vyhledávání: '"F. Clerget-Darpoux"'
Autor:
D A, Fernandes de Abreu, M C, Babron, M C I, Babron, I, Rebeix, C, Rebeix, C, Fontenille, J, Fontenille, J, Yaouanq, D, Yaouanq, D, Brassat, B, Brassat, B, Fontaine, F, Fontaine, F, Clerget-Darpoux, F, Jehan, F, Feron
Publikováno v:
Multiple Sclerosis Journal. 15:1146-1152
Both genetic and environmental factors contribute to multiple sclerosis, the most common neurodegenerative disorder with onset in young adults. The objective of the current study is, based on the hypothesis that environmentally predisposed individual
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7494f1d5fa357abca098e5bc1ca288e
https://doi.org/10.1177/1352458509106780
https://doi.org/10.1177/1352458509106780
Autor:
F. Clerget-Darpoux
Publikováno v:
International Statistical Review. 68:45-51
La majorite des maladies humaines ont une etiologie complexe et resultent de l'interaction de facteurs genetiques et d'environnement. Une strategie populaire pour detecter des facteurs de risque genetique est la recherche systematique de liaison sur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::326f79d00cbf160da2b8e6e2728bbdb5
https://doi.org/10.1111/j.1751-5823.2000.tb00386.x
https://doi.org/10.1111/j.1751-5823.2000.tb00386.x
Publikováno v:
Annals of Human Genetics. 62:419-429
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ae1b7b4e2f0e672f1e53fd561ddedfb5
https://doi.org/10.1017/s000348009800712x
https://doi.org/10.1017/s000348009800712x
Akademický článek
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Publikováno v:
Annals of Human Genetics. 61:25-36
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3c067b4652554893d1d4bc427ed439c0
https://doi.org/10.1017/s0003480096005970
https://doi.org/10.1017/s0003480096005970
Autor:
F Clerget-Darpoux
Publikováno v:
Atlas of Genetics and Cytogenetics in Oncology and Haematology.
IIIStatistical properties of the method of lod scores III1. The test procedure III1.1. Impact of non-sequentiality III1.2. Maximization of the lod score over the [0, 1/2] interval III1.3 References III-2. Genotype information III-2.1. Ambiguity in ph
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3f9d24361dbfeec6e458c055888f2766
https://doi.org/10.4267/2042/37914
https://doi.org/10.4267/2042/37914
Autor:
T. D'Amato, D. Campion, Ph. Gorwood, M. Jay, O. Sabate, C. Petit, M. Abbar, A. Malafosse, M. Leboyer, D. Hillaire, F. Clerget-Darpoux, J. Feingold, G. Waksman, J. Mallet
Publikováno v:
Scopus-Elsevier
Because of an association between sexual aneuploidies and schizophrenia, and because schizophrenic siblings have been found to be more often of the same than of the opposite sex, the susceptibility locus for schizophrenia is thought to lie within the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::288ea1f15a5c1ac45e62206b35aac021
https://doi.org/10.1192/bjp.161.1.59
https://doi.org/10.1192/bjp.161.1.59
Publikováno v:
Revue neurologique. 163(6-7)
Multiple Sclerosis (MS) is a multifactorial disorder caused by the interaction of environmental factors with a genetic predisposition.The chromosomal region comprising MHC contains one or several genes which contributes from 20 to 50 p. 100 to MS gen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::15f202a44717f200977308d131f26f90
https://pubmed.ncbi.nlm.nih.gov/17607189
https://pubmed.ncbi.nlm.nih.gov/17607189
Autor:
M. G. Limongelli, M. Bourgey, G. Calcagno, N. Tinto, D. Gennarelli, P. Margaritte Jeannin, O. Esposito, C. Marano, R. Troncone, A. Spampanato, C. Natale, F. Clerget Darpoux, L. Sacchetti, L. Greco
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______3730::5fb44da1a627d4b2c93f8b2b5b4cb633
http://hdl.handle.net/11588/495910
http://hdl.handle.net/11588/495910
Autor:
Gérard Said, A. Ferreira, Jérôme Carayol, Micheline Misrahi, V Planté-Bordeneuve, Catherine Bonaïti-Pellié, F Clerget-Darpoux, D Adams
Publikováno v:
Journal of medical genetics. 40(11)
Among the hereditary systemic amyloidosis, transthyretin (TTR) neuropathies (OMIM #176300) are devastating disorders with an autosomal dominant transmission, expressed mainly as a progressive fibre length dependent sensorimotor polyneuropathy and lif
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00097988f187f5238c60315477045a58
https://pubmed.ncbi.nlm.nih.gov/14627687
https://pubmed.ncbi.nlm.nih.gov/14627687