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Centre national de génotypage (CNG)  - 2007


  1. Bouslam, N., Bouhouche, A., Benomar, A., Hanein, S., Klebe, S., Azzedine, H., Giandomenico, S.D., Boland-Auge, A., Santorelli, F.M., Durr, A., Brice, A., Yahyaoui, M. and Stevanin, G., A novel locus for autosomal recessive spastic ataxia on chromosome 17p. Hum Genet, 2007, 121(3-4): p. 413-20.
  2. Bouzigon, E., Siroux, V., Dizier, M.H., Lemainque, A., Pison, C., Lathrop, M., Kauffmann, F., Demenais, F. and Pin, I., Scores of asthma and asthma severity reveal new regions of linkage in EGEA families. Eur Respir J, 2007.


  3. Bouzigon, E., Ulgen, A., Dizier, M.H., Siroux, V., Lathrop, M., Kauffmann, F., Pin, I. and Demenais, F., Evidence for a pleiotropic QTL on chromosome 5q13 influencing both time to asthma onset and asthma score in French EGEA families. Hum Genet, 2007.


  4. Chelbi, S.T., Mondon, F., Jammes, H., Buffat, C., Mignot, T.M., Tost, J., Busato, F., Gut, I., Rebourcet, R., Laissue, P., Tsatsaris, V., Goffinet, F., Rigourd, V., Carbonne, B., Ferre, F. and Vaiman, D., Expressional and Epigenetic Alterations of Placental Serine Protease Inhibitors. SERPINA3 Is a Potential Marker of Preeclampsia. Hypertension, 2007, 49(1): p. 76-83


  5. Danoy, P., Sonoda, E., Lathrop, M., Takeda, S. and Matsuda, F., A naturally occurring genetic variant of human XRCC2 (R188H) confers increased resistance to cisplatin-induced DNA damage. Biochem Biophys Res Commun, 2007, 352(3): p. 763-8.


  6. Dizier, M.H., Bouzigon, E., Guilloud-Bataille, M., Siroux, V., Lemainque, A., Boland, A., Lathrop, M. and Demenais, F., Evidence for gene x smoking exposure interactions in a genome-wide linkage screen of asthma and bronchial hyper-responsiveness in EGEA families. Eur J Hum Genet, 2007.


  7. Fischer, J., Lefèvre, C., Morava, E., Mussini, J.M., Laforet, P., Negre-Salvayre, A., Lathrop, M. and Salvayre, R., The gene encoding adipose triglyceride lipase (PNPLA2) is mutated in neutral lipid storage disease with myopathy. Nat Genet, 2007, 39(1): p. 28-30.


  8. Fradin, D., Heath, S., Lathrop, M. and Bougneres, P., QTLs for fasting glucose in young Europeans replicate previous findings for type 2 diabetes in 2q23-24 and other locations. Diabetes, 2007.


  9. Hadjadj, S., Tarnow, L., Forsblom, C., Kazeem, G., Marre, M., Groop, P.H., Parving, H.H., Cambien, F., Tregouet, D.A., Gut, I.G., Theva, A., Gauguier, D., Farrall, M., Cox, R., Matsuda, F., Lathrop, M. and Hager-Vionnet, N., Association between angiotensin-converting enzyme gene polymorphisms and diabetic nephropathy: case-control, haplotype, and family-based study in three European populations. J Am Soc Nephrol, 2007, 18(4): p. 1284-91.


  10. Lesueur, F., Bouadjar, B., Lefèvre, C., Jobard, F., Audebert, S., Lakhdar, H., Martin, L., Tadini, G., Karaduman, A., Emre, S., Saker, S., Lathrop, M. and Fischer, J., Novel mutations in ALOX12B in patients with autosomal recessive congenital ichthyosis and evidence for genetic heterogeneity on chromosome 17p13. J Invest Dermatol, 2007, 127(4): p. 829-34.


  11. Lesueur, F., Lefèvre, C., Has, C., Guilloud-Bataille, M., Oudot, T., Mahe, E., Lahfa, M., Mansouri, S., Mosharraf-Olmolk, H., Sobel, E., Heath, S., Lathrop, M., Dizier, M-H., Prud'homme J-F., Fischer, J., Confirmation of Psoriasis Susceptibility Loci on Chromosome 6p21 and 20p13 in French Families. Journal of Investigative Dermatology, 2007.


  12. Libioulle, C., Louis, E., Hansoul, S., Sandor, C., Farnir, F., Franchimont, D., Vermeire, S., Dewit, O., de Vos, M., Dixon, A., Demarche, B., Gut, I., Heath, S., Foglio, M., Liang, L., Laukens, D., Mni, M., Zelenika, D., Gossum, A.V., Rutgeerts, P., Belaiche, J., Lathrop, M. and Georges, M., Novel Crohn Disease Locus Identified by Genome-Wide Association Maps to a Gene Desert on 5p13.1 and Modulates Expression of PTGER4. PLoS Genet, 2007, 3(4): p. e58.


  13. Mauger, F., Bauer, K., Calloway, C.D., Semhoun, J., Nishimoto, T., Myers, T.W., Gelfand, D.H. and Gut, I.G., DNA sequencing by MALDI-TOF MS using alkali cleavage of RNA/DNA chimeras. Nucleic Acids Res, 2007, 35(8): p. e62.


  14. Partonen, T., Treutlein, J., Alpman, A., Frank, J., Johansson, C., Depner, M., Aron, L., Rietschel, M., Wellek, S., Soronen, P., Paunio, T., Koch, A., Chen, P., Lathrop, M., Adolfsson, R., Persson, M.L., Kasper, S., Schalling, M., Peltonen, L. and Schumann, G., Three circadian clock genes Per2, Arntl, and Npas2 contribute to winter depression. Ann Med, 2007, 39(3): p. 229-38.


  15. Thiery, G., Shchepinov, M.S., Southern, E.M., Audebourg, A., Audard, V., Terris, B. and Gut, I.G., Multiplex target protein imaging in tissue sections by mass spectrometry--TAMSIM. Rapid Commun Mass Spectrom, 2007, 21(6): p. 823-9.


  16. Vasilescu, A., Terashima, Y., Enomoto, M., Heath, S., Poonpiriya, V., Gatanaga, H., Do, H., Diop, G., Hirtzig, T., Auewarakul, P., Lauhakirti, D., Sura, T., Charneau, P., Marullo, S., Therwath, A., Oka, S., Kanegasaki, S., Lathrop, M., Matsushima, K., Zagury, J.F. and Matsuda, F., A haplotype of the human CXCR1 gene protective against rapid disease progression in HIV-1+ patients. Proc Natl Acad Sci U S A, 2007, 104(9): p. 3354-9.
Archives : 2007