Zobrazeno 1 - 10
of 78
pro vyhledávání: '"C. Lonjou"'
Autor:
J.-C. Roujeau, Martin Schumacher, C Lonjou, Nicolas Borot, Hervé Le-Louët, Maja Mockenhaupt, Alain Hovnanian, L Thomas, N Ledger, Erika Graf, C de Toma
Publikováno v:
The Pharmacogenomics Journal. 6:265-268
Stevens-Johnson syndrome (SJS) and toxic epidermal necrolysis (TEN) are rare but severe cutaneous adverse drug reactions, which can be caused by a certain number of specific drugs among which is carbamazepine, an antiepileptic agent. A very strong as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d28700bab9702c46f89316e720d752ec
https://doi.org/10.1038/sj.tpj.6500356
https://doi.org/10.1038/sj.tpj.6500356
Autor:
James P. Kushner, C. Lonjou, Newton E. Morton, Lynn B. Jorde, Andrew Collins, Richard S. Ajioka
Publikováno v:
ResearcherID
Recombination acts on the genetic map, not on the physical map. On the other hand, the physical map is usually more accurate. Choice of the genetic or physical map for positional cloning by allelic association depends on the goodness of fit of data t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b37613eb00ce85b99401f2d4f95930a6
https://doi.org/10.1073/pnas.95.19.11366
https://doi.org/10.1073/pnas.95.19.11366
Publikováno v:
ResearcherID
Recently a graphical study of linkage disequilibrium around the CAPN3 locus failed to refine the 1.3-Mb interval suggested by haplotype sharing. On the contrary, the Malecot model as implemented in the ALLASS program maps CAPN3 within 3 kb of its tru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d78b2a5cfddb25c171fc53f9491eeda
https://doi.org/10.1159/000022825
https://doi.org/10.1159/000022825
Autor:
E. D. Albert, C. Lonjou, Jacques Hors, Elie Ohayon, Anne Cambon-Thomsen, P. Bourret, John Clayton
Publikováno v:
European Journal of Immunogenetics. 19:311-322
A likelihood approach to HLA serology has been developed in which the aim is not to define a recognition set for a serum but to describe the serum's ability to react with each and every antigen in the test cells, this ability being quantified in term
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b3b9b95f127d1d184a954ece6c1d637
https://doi.org/10.1111/j.1744-313x.1992.tb00074.x
https://doi.org/10.1111/j.1744-313x.1992.tb00074.x
Autor:
M. Eliaszewicz, J.-C. Roujeau, C. Lonjou, X. Sicard, Pierre Wolkenstein, Zulma G. Vitezica, Alain Hovnanian
Publikováno v:
British Journal of Dermatology
British Journal of Dermatology, Wiley, 2008, 159 (2), pp.501-503. ⟨10.1111/j.1365-2133.2008.08660.x⟩
British Journal of Dermatology, Wiley, 2008, 159 (2), pp.501-503. ⟨10.1111/j.1365-2133.2008.08660.x⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::769a37e1f410b918a01631afa93d8aa7
https://hal.inrae.fr/hal-02666743
https://hal.inrae.fr/hal-02666743
Autor:
William J. Tapper, C. Lonjou, Nikolas Maniatis, Eiram Elahi, Newton E. Morton, Andrew Collins, W. Zhang
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 100(10)
Whereas the human linkage map appears on limited evidence to be constant over populations, maps of linkage disequilibrium (LD) vary among populations that differ in gene history. The greatest difference is between populations of sub-Saharan origin an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7877fa516518bd6e18243b6256959ee1
https://pubmed.ncbi.nlm.nih.gov/12721363
https://pubmed.ncbi.nlm.nih.gov/12721363
Publikováno v:
Annals of human genetics. 66(Pt 1)
Linkage tests to localize oligogenes have been extended during the past year. Using simulated data and multiplex selection we find that several tests on affected sib pairs have comparable power and type I error. Three variants of SIBPAL2 are favoured
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8713b0349beecf55a0c704890c6eb119
https://pubmed.ncbi.nlm.nih.gov/12015003
https://pubmed.ncbi.nlm.nih.gov/12015003
Autor:
N S Thomas, Jane Dewar, C. Lonjou, Q. Peng, Newton E. Morton, John W. Holloway, Stephen T. Holgate, Tom R. Gaunt, I Gomes, J Wilkinson, Bianca Beghe, Ian P. Hall
Publikováno v:
Scopus-Elsevier
Atopy and asthma are complex genetic diseases resulting from the interactions of a number of genetic and environmental factors. We had previously reported allelic association between the IL9 marker on chromosome 5q31-33 and atopy. In order to further
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5891602ce56fb05abfc9d8f0922b6085
https://pubmed.ncbi.nlm.nih.gov/11294563
https://pubmed.ncbi.nlm.nih.gov/11294563
Autor:
John W. Holloway, Ian P. Hall, Newton E. Morton, Klaus A. Deichmann, William O.C.M. Cookson, Lyle J. Palmer, Tarja Laitinen, Matthias Wjst, H. Chen, C. Lonjou, Kathleen C. Barnes
Publikováno v:
Proceedings of the National Academy of Sciences of the United States of America. 97(20)
The central problem of complex inheritance is to map oligogenes for disease susceptibility, integrating linkage and association over samples that differ in several ways. Combination of evidence over multiple samples with 1,037 families supports loci
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8f93637619a2d71d54ac71821618b4b8
https://pubmed.ncbi.nlm.nih.gov/11005866
https://pubmed.ncbi.nlm.nih.gov/11005866
Publikováno v:
Clinical and experimental allergy : journal of the British Society for Allergy and Clinical Immunology. 29
Combination of evidence over samples, each of which is too small to be conclusive, is the central problem in complex inheritance. There are three approaches: meta-analysis, prospective collaboration, and retrospective collaboration. Our experience wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::417c36c4dcc46f90a65fc7691d7b3aa0
https://pubmed.ncbi.nlm.nih.gov/10641569
https://pubmed.ncbi.nlm.nih.gov/10641569