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Bouillon Anne-Sophie

Département de médecine interne > Service d'hématologie clinique

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Main Referenced Co-authors
Beier, Fabian (6)
Brummendorf, Tim H. (4)
Begemann, Matthias (3)
Koschmieder, Steffen (3)
Schemionek, Mirle (3)
Main Referenced Keywords
Male (3); Middle Aged (3); Female (2); Humans (2); Adult (1);
Main Referenced Disciplines
Hematology (7)

Publications (total 7)

The most downloaded
246 downloads
Kirschner, M., Maurer, A., Wlodarski, M. W., Ventura Ferreira, M. S., Bouillon, A.-S., Halfmeyer, I., Blau, W., Kreuter, M., Rosewich, M., Corbacioglu, S., Beck, J., Schwarz, M., Bittenbring, J., Radsak, M. P., Wilk, C. M., Koschmieder, S., Begemann, M., Kurth, I., Schemionek, M., ... Beier, F. (2018). Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita. Leukemia, 32 (8), 1762-1767. doi:10.1038/s41375-018-0125-x https://hdl.handle.net/2268/246788

The most cited

30 citations (Scopus®)

Ferreira, M. S. V., Kirschner, M., Halfmeyer, I., Estrada, N., Xicoy, B., Isfort, S., Vieri, M., Zamora, L., Abels, A., Bouillon, A.-S., Begemann, M., Schemionek, M., Maurer, A., Koschmieder, S., Wilop, S., Panse, J., Brummendorf, T. H., & Beier, F. (2019). Comparison of flow-FISH and MM-qPCR telomere length assessment techniques for the screening of telomeropathies. Annals of the New York Academy of Sciences, 1-11. doi:10.1111/nyas.14248 https://hdl.handle.net/2268/246786

Fiegle, E., Crysandt, M., Bouillon, A.-S., Silling, G., Elbracht, M., Begemann, M., Brümmendorf, T. H., Beier, F., & Jost, E. (2021). Successful allogeneic stem cell transplantation of a patient with Werner syndrome and acute myeloid leukemia. Leukemia Research, 108, 106609. doi:10.1016/j.leukres.2021.106609
Peer Reviewed verified by ORBi

Ferreira, M. S. V., Sorensen, M. D., Pusch, S., Beier, D., Bouillon, A.-S., Kristensen, B. W., Brummendorf, T. H., Beier, C. P., & Beier, F. (2020). Alternative lengthening of telomeres is the major telomere maintenance mechanism in astrocytoma with isocitrate dehydrogenase 1 mutation. Journal of Neuro-Oncology, 147 (1), 1-14. doi:10.1007/s11060-020-03394-y
Peer Reviewed verified by ORBi

Azerad, M.-A., BAYOUDH, F., Weber, T., Minon, J.-M., Ketelsleggers, O., HOYOUX, M., Ren, X., Kaye, O., De Marneffe, N., Fraipont, V., Masset, C., Bouillon, A.-S., JASPERS, A., Tebache, M., D'Hoen, G., Habibi, A., Efira, A., Thachil, J., Deckmyn, H., & BEGUIN, Y. (2020). Sickle cell disease and COVID-19: Atypical presentations and favorable outcomes. EJHaem, 1 (jha 2.74), 338-341. doi:10.1002/jha2.74
Peer Reviewed verified by ORBi

Ferreira, M. S. V., Kirschner, M., Halfmeyer, I., Estrada, N., Xicoy, B., Isfort, S., Vieri, M., Zamora, L., Abels, A., Bouillon, A.-S., Begemann, M., Schemionek, M., Maurer, A., Koschmieder, S., Wilop, S., Panse, J., Brummendorf, T. H., & Beier, F. (2019). Comparison of flow-FISH and MM-qPCR telomere length assessment techniques for the screening of telomeropathies. Annals of the New York Academy of Sciences, 1-11. doi:10.1111/nyas.14248
Peer Reviewed verified by ORBi

Ferreira, M. S. V., Crysandt, M., Braunschweig, T., Jost, E., Voss, B., Bouillon, A.-S., Knuechel, R., Brummendorf, T. H., & Beier, F. (2018). Presence of TERT Promoter Mutations is a Secondary Event and Associates with Elongated Telomere Length in Myxoid Liposarcomas. International Journal of Molecular Sciences, 19 (2). doi:10.3390/ijms19020608
Peer Reviewed verified by ORBi

Bouillon, A.-S., Ventura Ferreira, M. S., Awad, S. A., Richter, J., Hochhaus, A., Kunzmann, V., Dengler, J., Janssen, J., Ossenkoppele, G., Westerweel, P. E., Te Boekhorst, P. A. W., Mahon, F.-X., Hjorth-Hansen, H., Isfort, S., Fioretos, T., Hummel, S., Schemionek, M., Wilop, S., Koschmieder, S., ... Brummendorf, T. H. (2018). Telomere shortening correlates with leukemic stem cell burden at diagnosis of chronic myeloid leukemia. Blood Advances, 2 (13), 1572-1579. doi:10.1182/bloodadvances.2018017772
Peer Reviewed verified by ORBi

Kirschner, M., Maurer, A., Wlodarski, M. W., Ventura Ferreira, M. S., Bouillon, A.-S., Halfmeyer, I., Blau, W., Kreuter, M., Rosewich, M., Corbacioglu, S., Beck, J., Schwarz, M., Bittenbring, J., Radsak, M. P., Wilk, C. M., Koschmieder, S., Begemann, M., Kurth, I., Schemionek, M., ... Beier, F. (2018). Recurrent somatic mutations are rare in patients with cryptic dyskeratosis congenita. Leukemia, 32 (8), 1762-1767. doi:10.1038/s41375-018-0125-x
Peer Reviewed verified by ORBi

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