The complex karyotype in hematological malignancies: a comprehensive overview by the Francophone Group of Hematological Cytogenetics (GFCH)
Nguyen-Khac, F., Bidet, A., Daudignon, A., Lafage-Pochitaloff, M., Ameye, G., Bilhou-Nabéra, C., Chapiro, E., Collonge-Rame, M. A., Cuccuini, W., Douet-Guilbert, N., Eclache, V., Luquet, I., Michaux, L., Nadal, N., Penther, D., Quilichini, B., Terre, C., Lefebvre, C., Troadec, M.-B., Véronèse, L.
Published in Leukemia (01.06.2022)
Published in Leukemia (01.06.2022)
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NUP98 is rearranged in 3.8% of pediatric AML forming a clinical and molecular homogenous group with a poor prognosis
Struski, S, Lagarde, S, Bories, P, Puiseux, C, Prade, N, Cuccuini, W, Pages, M-P, Bidet, A, Gervais, C, Lafage-Pochitaloff, M, Roche-Lestienne, C, Barin, C, Penther, D, Nadal, N, Radford-Weiss, I, Collonge-Rame, M-A, Gaillard, B, Mugneret, F, Lefebvre, C, Bart-Delabesse, E, Petit, A, Leverger, G, Broccardo, C, Luquet, I, Pasquet, M, Delabesse, E
Published in Leukemia (01.03.2017)
Published in Leukemia (01.03.2017)
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XIDER: a novel X-ray detector for the next generation of high-energy synchrotron radiation sources
Williams, M, Busca, P, Collonge, M, Fajardo, P, Fischer, P, Martin, T, Ritzert, M, Ruat, M, Schimansky, D
Published in Journal of physics. Conference series (01.12.2022)
Published in Journal of physics. Conference series (01.12.2022)
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Lung function in Birt-Hogg-Dubé syndrome: a retrospective analysis of 96 patients
Daccord, C, Cottin, V, Prévot, G, Uzunhan, Y, Mornex, J F, Bonniaud, P, Borie, R, Briault, A, Collonge-Rame, M A, Crestani, B, Devouassoux, G, Freynet, O, Gondouin, A, Hauss, P A, Khouatra, C, Leroy, S, Marchand-Adam, S, Marquette, C, Montani, D, Naccache, J M, Nadeau, G, Poulalhon, N, Reynaud-Gaubert, M, Salaun, M, Wallaert, B, Cordier, J F, Faouzi, M, Lazor, R
Published in Orphanet journal of rare diseases (24.05.2020)
Published in Orphanet journal of rare diseases (24.05.2020)
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Impact of BRCA status on outcomes and survival in high-risk early breast cancers
Klajer, E., Paget-Bailly, S., Meynard, G., Meurisse, A., Bazan, F., Chaigneau, L., Dobi, E., Meneveau, N., Montcuquet, P., Villanueva, C., Thiery-Vuillemin, A., Kalbacher, E., Populaire, C., Collonge-Rame, M.-A., Gligorov, J., Curtit, E., Pivot, X., Mansi, L.
Published in Annals of oncology (01.10.2018)
Published in Annals of oncology (01.10.2018)
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Pregnancy outcomes of prenatally diagnosed Turner syndrome: a French multicenter retrospective study including a series of 975 cases
Gruchy, N., Vialard, F., Blondeel, E., Le Meur, N., Joly-Hélas, G., Chambon, P., Till, M., Herbaut-Graux, M., Vigouroux-Castera, A., Coussement, A., Lespinasse, J., Amblard, F., Jimenez, M., Lebel Roy Camille, L., Carré-Pigeon, F., Flori, E., Mugneret, F., Jaillard, S., Yardin, C., Harbuz, R., Collonge Rame, M., Vago, P., Valduga, M., Leporrier, N.
Published in Prenatal diagnosis (01.12.2014)
Published in Prenatal diagnosis (01.12.2014)
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Concepts for the data flow control on the XIDer readout ASIC
Schimansky, D., Busca, P., Collonge, M., Fajardo, P., Fischer, P., Ritzert, M., Williams, M.
Published in Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment (01.12.2023)
Published in Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment (01.12.2023)
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Incidental findings in a series of 2500 gene panel tests for a genetic predisposition to cancer: Results and impact on patients
Nambot, S., Sawka, C., Bertolone, G., Cosset, E., Goussot, V., Derangère, V., Boidot, R., Baurand, A., Robert, M., Coutant, C., Loustalot, C., Thauvin-Robinet, C., Ghiringhelli, F., Lançon, A., Populaire, C., Damette, A., Collonge-Rame, M.A., Meunier-Beillard, N., Lejeune, C., Albuisson, J., Faivre, L.
Published in European journal of medical genetics (01.05.2021)
Published in European journal of medical genetics (01.05.2021)
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XIDER: First Prototypes and Results with the Digital Integration Readout Scheme
Williams, M., Busca, P., Collonge, M., Fajardo, P., Fischer, P., Martin, T., Ritzert, M., Ruat, M., Schimansky, D.
Published in 2021 IEEE Nuclear Science Symposium and Medical Imaging Conference (NSS/MIC) (16.10.2021)
Published in 2021 IEEE Nuclear Science Symposium and Medical Imaging Conference (NSS/MIC) (16.10.2021)
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Conference Proceeding
Exploring the time-resolving capabilities of XIDer assemblies
Williams, M., Busca, P., Collonge, M., Fajardo, P., Fischer, P., Martin, T., Ritzert, M., Ruat, M., Schimansky, D.
Published in Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment (01.12.2023)
Published in Nuclear instruments & methods in physics research. Section A, Accelerators, spectrometers, detectors and associated equipment (01.12.2023)
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Corticosurrénalome et syndrome de Lynch
Arbey, A.-S, Schillo, F, Mohn, A, Penfornis, A, Collonge Rame, M.-A, Vienet, G
Published in Annales d'endocrinologie (01.09.2012)
Published in Annales d'endocrinologie (01.09.2012)
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Bilan des examens chromosomiques de 277 couples candidats à l'injection intracytoplasmique de spermatozoïde
HOCQUET, D, ROUX, C, COLLONGE-RAME, M.-A, FELLMANN, F, BRESSON, J. L
Published in Andrologie (Lille, France) (01.12.1999)
Published in Andrologie (Lille, France) (01.12.1999)
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212PImpact of BRCA status on outcomes and survival in high-risk early breast cancers
Klajer, E, Paget-Bailly, S, Meynard, G, Meurisse, A, Bazan, F, Chaigneau, L, Dobi, E, Meneveau, N, Montcuquet, P, Villanueva, C, Thiery-Vuillemin, A, Kalbacher, E, Populaire, C, Collonge-Rame, M -A, Gligorov, J, Curtit, E, Pivot, X, Mansi, L
Published in Annals of oncology (01.10.2018)
Published in Annals of oncology (01.10.2018)
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Pattern of chromosomal imbalances in non-B virus related hepatocellular carcinoma detected by comparative genomic hybridization
Collonge-Rame, M.A, Bresson-Hadni, S, Koch, S, Carbillet, J.P, Blagosklonova, O, Mantion, G, Miguet, J.P, Heyd, B, Bresson, J.L
Published in Cancer genetics and cytogenetics (01.05.2001)
Published in Cancer genetics and cytogenetics (01.05.2001)
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Molecular basis of the Li–Fraumeni syndrome: an update from the French LFS families
Bougeard, G, Sesboüé, R, Baert-Desurmont, S, Vasseur, S, Martin, C, Tinat, J, Brugières, L, Chompret, A, Paillerets, B Bressac-de, Stoppa-Lyonnet, D, Bonaïti-Pellié, C, Frébourg, T
Published in Journal of medical genetics (01.08.2008)
Published in Journal of medical genetics (01.08.2008)
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Real-life study of BRCA genetic screening in metastatic breast cancer
Meynard, G., Villanueva, C., Thiery-Vuillemin, A., Mansi, L., Montcuquet, P., Meneveau, N., Chaigneau, L., Bazan, F., Almotlak, H., Dobi, E., Nguyen Tan Hon, T., Klajer, E., Fagnoni-Legat, C., Paget-Bailly, S., Meurisse, A., Collonge-Rame, M-A., Populaire-Ventron, C., Pivot, X., Curtit, E.
Published in Annals of oncology (01.09.2017)
Published in Annals of oncology (01.09.2017)
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Mutation screening of MIR146A/B and BRCA1/2 3'-UTRs in the GENESIS study
Garcia, Amandine I, Buisson, Monique, Damiola, Francesca, Tessereau, Chloé, Barjhoux, Laure, Verny-Pierre, Carole, Sornin, Valérie, Dondon, Marie-Gabrielle, Eon-Marchais, Séverine, Caron, Olivier, Gautier-Villars, Marion, Coupier, Isabelle, Buecher, Bruno, Vennin, Philippe, Belotti, Muriel, Lortholary, Alain, Gesta, Paul, Dugast, Catherine, Noguès, Catherine, Fricker, Jean-Pierre, Faivre, Laurence, Stoppa-Lyonnet, Dominique, Andrieu, Nadine, Sinilnikova, Olga M, Mazoyer, Sylvie
Published in European journal of human genetics : EJHG (01.08.2016)
Published in European journal of human genetics : EJHG (01.08.2016)
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PB1868 B‐CELL PROLYMPHOCYTIC LEUKEMIA (B‐PLL) AND PROLYMPHOCYTOID MANTLE CELL LYMPHOMA (PMCL) (MORE THAN 55% OF PROLYMPHOCYTES) ARE CLOSED BUT DISTINCT ENTITIES. ON BEHALF GFCH AND FILO GROUPS
Chapiro, E., Diop, K., Dessen, P., Roos‐Weil, D., Gabillaud, C., Pramil, E., Maloum, K., Settegrana, C., Baseggio, L., Davi, F., Le Garff‐Tavernier, M., Droin, N., Algrin, C., Leblond, V., Eclache, V., Gaillard, B., Callet‐Bauchu, E., Muller, M., Lefebvre, C., Nadal, N., Ittel, A., Struski, S., Collonge‐Rame, M.‐A., Quilichini, B., Fert‐Ferrer, S., Auger, N., Radford‐Weiss, I., Susin, S., Bernard, O., Nguyen‐Khac, F.
Published in HemaSphere (01.06.2019)
Published in HemaSphere (01.06.2019)
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Chromosomal factors of infertility in candidate couples for ICSI: an equal risk of constitutional aberrations in women and men
Gekas, J., Thepot, F., Turleau, C., Siffroi, J.P., Dadoune, J.P., Briault, S., Rio, M., Bourouillou, G., Carré-Pigeon, F., Wasels, R., Benzacken, B., Association des Cytogeneticiensde Langue Francaise, The
Published in Human reproduction (Oxford) (01.01.2001)
Published in Human reproduction (Oxford) (01.01.2001)
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