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Gelot C, Guirouilh-Barbat J, Le Guen T, Dardillac E, Chailleux C, Canitrot Y, Lopez BS. The Cohesin Complex Prevents the End Joining of Distant DNA Double-Strand Ends. Mol Cell. 2015 Dec 10. (WES, SureSelect Agilent) pii: S1097-2765(15)00862-X. doi: 10.1016/j.molcel.2015.11.002. [Epub ahead of print] http://www.ncbi.nlm.nih.gov/pubmed/26687679 http://www.ncbi.nlm.nih.gov/pubmed/26687679

Cattoir V, Isnard C, Cosquer T, Odhiambo A, Bucquet F, Guérin F, Giard JC
Genomic analysis of reduced susceptibility to tigecycline in Enterococcus faecium.
Antimicrob Agents Chemother. 2015 Jan;59(1):239-44. (WGS)  doi: 10.1128/AAC.04174-14. Epub 2014 Oct 27. PMID: 25348531 http://www.ncbi.nlm.nih.gov/pubmed/25348531

Pertesi M, Galia P, Nazaret N, Vallée M, Garderet L, Leleu X, Avet-Loiseau H, Foll M, Byrnes G, Lachuer J, McKay JD, Dumontet C.
Rare Circulating Cells in Familial Waldenström Macroglobulinemia Displaying the MYD88 L265P Mutation Are Enriched by Epstein-Barr Virus Immortalization.
PLoS One. 2015 Sep 9;10(9):e0136505. doi: 10.1371/journal.pone.0136505. eCollection 2015 (Technologie Haloplex, Agilent) http://www.ncbi.nlm.nih.gov/pubmed/26352266

Lars P. Jordheim, Vincent Ribrag, Hervé Ghesquieres, Sophie Pallardy, Richard Delarue, Hervé Tilly, Corinne Haioun, Fabrice Jardin, Delphine Demangel, Gilles A. Salles, and Charles Dumontet
Single nucleotide polymorphisms in ABCB1 and CBR1 can predict toxicity to R- CHOP type regimens in patients with diffuse non Hodgkin lymphoma
Haematologica 2015 May;100(5):e204-6. doi: 10.3324/haematol.2014.120113. Epub 2015 Jan 30 (Taqman SNP assay)  http://www.ncbi.nlm.nih.gov/pubmed/25637052

Ohta T, Kim YH, Oh JE, Satomi K, Nonoguchi N, Keyvani K, Pierscianek D, Sure U, Mittelbronn M, Paulus W, Vital A, Yokoo H, McDonald K, Kleihues P, Nazaret N, Barbet F, Lachuer J, Ohgaki H.
Alterations of the RRAS and ERCC1 Genes at 19q13 in Gemistocytic Astrocytomas.
J Neuropathol Exp Neurol. 2014 Sep 4 (WEShttp://www.ncbi.nlm.nih.gov/pubmed/25192052

André F, Bachelot T, Commo F, Campone M, Arnedos M, Dieras V, Lacroix-Triki M, Lacroix L, Cohen P, Gentien D, Adélaide J, Dalenc F, Goncalves A, Levy C, Ferrero JM, Bonneterre J, Lefeuvre C, Jimenez M, Filleron T, Bonnefoi H.
Comparative genomic hybridisation array and DNA sequencing to direct treatment of metastatic breast cancer: a multicentre prospective trial.
(SAFIR01/UNICANCER)  Lancet Oncol. 2014 Mar;15(3):267-74  (Microarray Affymetrix SNP 6.0).http://www.ncbi.nlm.nih.gov/pubmed/24508104

Nagaishi M. Kim YH., Mittelbronn M.,  Giangaspero F., Paulus W., Brokinkel B., Vital A., Tanaka Y., Nakazato Y., Legras-Lachuer C., Lachuer J., Ohgaki H.
Amplification of the STOML3, FREM2, and LHFP genes is associated with mesenchymal differentiation in gliosarcoma.
Am J Pathology. 2012 May;180(5):1816-23.

Kim YH, Lachuer J, Mittelbronn M, Paulus W, Brokinkel B, Keyvani K, Sure U, Wrede K, Nobusawa S, Nakazato Y, Tanaka Y, Vital A, Mariani L, Ohgaki H
Alterations in the RB1 pathway in low-grade diffuse gliomas lacking common genetic alterations.
Brain Pathol. 2011 Nov;21(6):645-51.

A. Wierinckx, M. Roche, G. Raverot, C. Legras-Lachuer, S. Croze, N. Nazaret, C. Rey, C. Auger, E. Jouanneau, P. Chanson, J. Trouillas, J. Lachuer
Integrated genomic profiling identifies loss of chromosome 11p impacting transcriptomic activity in aggressive pituitary PRL tumours.
Brain Pathol. 2011 Sep;21(5):533-543.

Nobusawa S, Lachuer J, Wierinckx A, Kim YH, Huang J, Legras-Lachuer C, Kleihues P, Ohgaki H.
Intratumoral patterns of genomic imbalance in glioblastomas.
Brain Pathol. 2010 Sep;20(5):936-44.

Dumontet C, Landi S, Reiman T, Perry T, Plesa A, Bellini I, Barale R, Pilarski LM, Troncy J, Tavtigian S, Gemignani F.
Genetic polymorphisms associated with outcome in multiple myeloma patients receiving high-dose melphalan
Bone Marrow Transplant. 2010 Aug;45(8):1316-24

Schluth-Bolard C., M. Till, A. Labalme, C. Rey , E. Banquart, A. Fautrelle, T.  Martin-Denavit, M. Le Lorc’h, S. P. Romana, V. Lazar , P. Edery, D. Sanlaville.
TWIST microdeletion identified by array CGH in a patient presenting Saethre-Chotzen phenotype and a complex rearrangement involving chromosomes 2 and 7.
Eur J Med Genet. 2008 Mar-Apr;51(2):156-64. Epub 2007 Dec 24.