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| Ultrasensitive Detection of NOTCH1 c.7544_7545delCT Mutations in Chronic Lymphocytic Leukemia by Droplet Digital PCR Reveals High Frequency of Subclonal Mutations and Predicts Clinical Outcome in Cases with Trisomy 12. The Journal of molecular diagnostics : JMD 2020 Feb . Hoofd Catherine, Huang Steven J, Gusscott Samuel, Lam Sonya, Wong Rachel, Johnston Alexa, Ben-Neriah Susana, Steidl Christian, Scott David W, Bruyere Helene, Gillan Tanya L, Toze Cynthia L, Gerrie Alina S, Weng Andrew |
| Impact of gene mutations and chromosomal aberrations on progression-free survival in chronic lymphocytic leukemia patients treated with front-line chemoimmunotherapy: Clinical practice experience. Leukemia research 2019 Apr 81 75-81. Spunarova Michaela, Tom Nikola, Pavlova Sarka, Mraz Marek, Brychtova Yvona, Doubek Michael, Panovska Anna, Skuhrova Francova Hana, Brzobohata Anna, Pospisilova Sarka, Mayer Jiri, Trbusek Mart |
| Mutational and cytogenetic analyses of 188 CLL patients with trisomy 12: A retrospective study from the French Innovative Leukemia Organization (FILO) working group. Genes, chromosomes & cancer 2018 Sep . Roos-Weil Damien, Nguyen-Khac Florence, Chevret Sylvie, Touzeau Cyrille, Roux Clémence, Lejeune Julie, Cosson Adrien, Mathis Stéphanie, Feugier Pierre, Leprêtre Stéphane, Béné Marie-Christine, Baron Marine, Raynaud Sophie, Struski Stéphanie, Eclache Virginie, Sutton Laurent, Lesty Claude, Merle-Béral Hélène, Cymbalista Florence, Ysebaert Loïc, Davi Frédéric, Leblond Véronique, |
| NOTCH1 mutation and its prognostic significance in Chinese chronic lymphocytic leukemia: a retrospective study of 317 cases. Cancer medicine 2018 Mar . Zou Yixin, Fan Lei, Xia Yi, Miao Yi, Wu Wei, Cao Lei, Wu Jiazhu, Zhu Huayuan, Qiao Chun, Wang Li, Xu Wei, Li Jianyo |
| NOTCH1 mutations are associated with high CD49d expression in chronic lymphocytic leukemia: link between the NOTCH1 and the NF-?B pathways. Leukemia 2017 Sep . Benedetti D, Tissino E, Pozzo F, Bittolo T, Caldana C, Perini C, Martorelli D, Bravin V, D'Agaro T, Rossi F M, Bomben R, Santinelli E, Zaja F, Pozzato G, Chiarenza A, Di Raimondo F, Del Poeta G, Rossi D, Gaidano G, Dal Bo M, Gattei V, Zucchetto |
| The morphology of CLL revisited: the clinical significance of prolymphocytes and correlations with prognostic/molecular markers in the LRF CLL4 trial. British journal of haematology 2016 May . Oscier David, Else Monica, Matutes Estella, Morilla Ricardo, Strefford Jonathan C, Catovsky Dani |
| Recurrent mutations refine prognosis in chronic lymphocytic leukemia. Leukemia 2015 Feb 29 (2): 329-36. Baliakas P, Hadzidimitriou A, Sutton L-A, Rossi D, Minga E, Villamor N, Larrayoz M, Kminkova J, Agathangelidis A, Davis Z, Tausch E, Stalika E, Kantorova B, Mansouri L, Scarfò L, Cortese D, Navrkalova V, Rose-Zerilli M J J, Smedby K E, Juliusson G, Anagnostopoulos A, Makris A M, Navarro A, Delgado J, Oscier D, Belessi C, Stilgenbauer S, Ghia P, Pospisilova S, Gaidano G, Campo E, Strefford J C, Stamatopoulos K, Rosenquist R, |
| Insulin growth factor 1 receptor expression is associated with NOTCH1 mutation, trisomy 12 and aggressive clinical course in chronic lymphocytic leukaemia. PloS one 2015 10 (3): e0118801. Maura Francesco, Mosca Laura, Fabris Sonia, Cutrona Giovanna, Matis Serena, Lionetti Marta, Agnelli Luca, Barbieri Marzia, D'Anca Marianna, Manzoni Martina, Colombo Monica, Massucco Carlotta, Reverberi Daniele, Gentile Massimo, Recchia Anna Grazia, Bossio Sabrina, Ilariucci Fiorella, Musolino Caterina, Di Raimondo Francesco, Cortelezzi Agostino, Morabito Fortunato, Ferrarini Manlio, Neri Antoni |
| NOTCH1, SF3B1, BIRC3 and TP53 mutations in patients with chronic lymphocytic leukemia undergoing first-line treatment: correlation with biological parameters and response to treatment. Leukemia & lymphoma 2014 Dec 55 (12): 2785-92. Chiaretti Sabina, Marinelli Marilisa, Del Giudice Ilaria, Bonina Silvia, Piciocchi Alfonso, Messina Monica, Vignetti Marco, Rossi Davide, Di Maio Valeria, Mauro Francesca Romana, Guarini Anna, Gaidano Gianluca, Foà Rob |
| 14q deletions are associated with trisomy 12, NOTCH1 mutations and unmutated IGHV genes in chronic lymphocytic leukemia and small lymphocytic lymphoma. Genes, chromosomes & cancer 2014 Aug 53 (8): 657-66. Cosson Adrien, Chapiro Elise, Belhouachi Nabila, Cung Hong-Anh, Keren Boris, Damm Frederik, Algrin Caroline, Lefebvre Christine, Fert-Ferrer Sandra, Luquet Isabelle, Gachard Nathalie, Mugneret Francine, Terre Christine, Collonge-Rame Marie-Agnes, Michaux Lucienne, Rafdord-Weiss Isabelle, Talmant Pascaline, Veronese Lauren, Nadal Nathalie, Struski Stephanie, Barin Carole, Helias Catherine, Lafage Marina, Lippert Eric, Auger Nathalie, Eclache Virginie, Roos-Weil Damien, Leblond Veronique, Settegrana Catherine, Maloum Karim, Davi Frederic, Merle-Beral Helene, Lesty Claude, Nguyen-Khac Florence, |
| B-cell receptor configuration and mutational analysis of patients with chronic lymphocytic leukaemia and trisomy 12 reveal recurrent molecular abnormalities. Hematological oncology 2014 Mar 32 (1): 22-30. Falisi Erika, Novella Elisabetta, Visco Carlo, Guercini Nicola, Maura Francesco, Giaretta Ilaria, Pomponi Fabrizio, Nichele Ilaria, Finotto Silvia, Montaldi Annamaria, Neri Antonino, Rodeghiero Frances |
| SF3B1 mutations correlated to cytogenetics and mutations in NOTCH1, FBXW7, MYD88, XPO1 and TP53 in 1160 untreated CLL patients. Leukemia 2014 Jan 28 (1): 108-17. Jeromin S, Weissmann S, Haferlach C, Dicker F, Bayer K, Grossmann V, Alpermann T, Roller A, Kohlmann A, Haferlach T, Kern W, Schnittger |
| Clonal evolution in chronic lymphocytic leukemia: analysis of correlations with IGHV mutational status, NOTCH1 mutations and clinical significance. Genes, chromosomes & cancer 2013 Oct 52 (10): 920-7. López Cristina, Delgado Julio, Costa Dolors, Villamor Neus, Navarro Alba, Cazorla Maite, Gómez Cándida, Arias Amparo, Muñoz Concha, Cabezas Sandra, Baumann Tycho, Rozman María, Aymerich Marta, Colomer Dolors, Pereira Arturo, Cobo Francesc, López-Guillermo Armando, Campo Elías, Carrió A |
| Association between molecular lesions and specific B-cell receptor subsets in chronic lymphocytic leukemia. Blood 2013 Jun 121 (24): 4902-5. Rossi Davide, Spina Valeria, Bomben Riccardo, Rasi Silvia, Dal-Bo Michele, Bruscaggin Alessio, Rossi Francesca Maria, Monti Sara, Degan Massimo, Ciardullo Carmela, Serra Roberto, Zucchetto Antonella, Nomdedeu Josep, Bulian Pietro, Grossi Alberto, Zaja Francesco, Pozzato Gabriele, Laurenti Luca, Efremov Dimitar G, Di-Raimondo Francesco, Marasca Roberto, Forconi Francesco, Del Poeta Giovanni, Gaidano Gianluca, Gattei Valt |
| The clinical significance of NOTCH1 and SF3B1 mutations in the UK LRF CLL4 trial. Blood 2013 Jan 121 (3): 468-75. Oscier David G, Rose-Zerilli Matthew J J, Winkelmann Nils, Gonzalez de Castro David, Gomez Belen, Forster Jade, Parker Helen, Parker Anton, Gardiner Anne, Collins Andrew, Else Monica, Cross Nicholas C P, Catovsky Daniel, Strefford Jonathan |
| NOTCH1 mutations identify a genetic subgroup of chronic lymphocytic leukemia patients with high risk of transformation and poor outcome. Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K 2012 Dec . Villamor N, Conde L, Martínez-Trillos A, Cazorla M, Navarro A, Beà S, López C, Colomer D, Pinyol M, Aymerich M, Rozman M, Abrisqueta P, Baumann T, Delgado J, Giné E, González-Díaz M, Hernández JM, Colado E, Payer AR, Rayon C, Navarro B, José Terol M, Bosch F, Quesada V, Puente XS, López-Otín C, Jares P, Pereira A, Campo E, López-Guillermo A |
| NOTCH1 mutations in +12 chronic lymphocytic leukemia (CLL) confer an unfavorable prognosis, induce a distinctive transcriptional profiling and refine the intermediate prognosis of +12 CLL. Haematologica 2012 Mar 97 (3): 437-41. Del Giudice Ilaria, Rossi Davide, Chiaretti Sabina, Marinelli Marilisa, Tavolaro Simona, Gabrielli Sara, Laurenti Luca, Marasca Roberto, Rasi Silvia, Fangazio Marco, Guarini Anna, Gaidano Gianluca, Foà Rob |
| NOTCH1 mutations in CLL associated with trisomy 12. Blood 2012 Jan 119 (2): 329-31. Balatti Veronica, Bottoni Arianna, Palamarchuk Alexey, Alder Hansjuerg, Rassenti Laura Z, Kipps Thomas J, Pekarsky Yuri, Croce Carlo |
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- Page last updated:Jan 20, 2022
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