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1. Digital PCR-based quantification of miR-181a in the cerebrospinal fluid aids patient stratification in pediatric acute lymphoblastic leukemia

Author

Péterffy, Borbála, Nádasi, Tamás J., Krizsán, Szilvia, Horváth, Anna, Márk, Ágnes, Barna, Gábor, Timár, Botond, Almási, Laura, Müller, Judit, Csanádi, Krisztina, Rakonczai, Anna, Nagy, Zsolt, Kállay, Krisztián, Kertész, Gabriella, Kriván, Gergely, Csóka, Monika, Sebestyén, Anna, Semsei, Ágnes F., Kovács, Gábor T., Erdélyi, Dániel J., Bödör, Csaba, Egyed, Bálint, and Alpár, Donát

Published
2024
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2. PersonALL: a genetic scoring guide for personalized risk assessment in pediatric B-cell precursor acute lymphoblastic leukemia

Author

Bedics, Gábor, Egyed, Bálint, Kotmayer, Lili, Benard-Slagter, Anne, de Groot, Karel, Bekő, Anna, Hegyi, Lajos László, Bátai, Bence, Krizsán, Szilvia, Kriván, Gergely, Erdélyi, Dániel J., Müller, Judit, Haltrich, Irén, Kajtár, Béla, Pajor, László, Vojcek, Ágnes, Ottóffy, Gábor, Ujfalusi, Anikó, Szegedi, István, Tiszlavicz, Lilla Györgyi, Bartyik, Katalin, Csanádi, Krisztina, Péter, György, Simon, Réka, Hauser, Péter, Kelemen, Ágnes, Sebestyén, Endre, Jakab, Zsuzsanna, Matolcsy, András, Kiss, Csongor, Kovács, Gábor, Savola, Suvi, Bödör, Csaba, and Alpár, Donát

Published
2023
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3. Profiling of Copy Number Alterations Using Low-Coverage Whole-Genome Sequencing Informs Differential Diagnosis and Prognosis in Primary Cutaneous Follicle Center Lymphoma

Author

Bátai, Bence, Kiss, Laura, Varga, Luca, Nagy, Ákos, Househam, Jacob, Baker, Ann-Marie, László, Tamás, Udvari, Anna, Horváth, Róbert, Nagy, Tibor, Csomor, Judit, Szakonyi, József, Schneider, Tamás, Graham, Trevor A., Alpár, Donát, Fitzgibbon, Jude, Szepesi, Ágota, and Bödör, Csaba

Published
2024
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7. Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41

Author

Homan, Claire C., Drazer, Michael W., Yu, Kai, Lawrence, David M., Feng, Jinghua, Arriola-Martinez, Luis, Pozsgai, Matthew J., McNeely, Kelsey E., Ha, Thuong, Venugopal, Parvathy, Arts, Peer, King-Smith, Sarah L., Cheah, Jesse, Armstrong, Mark, Wang, Paul, Bödör, Csaba, Cantor, Alan B., Cazzola, Mario, Degelman, Erin, DiNardo, Courtney D., Duployez, Nicolas, Favier, Remi, Fröhling, Stefan, Rio-Machin, Ana, Klco, Jeffery M., Krämer, Alwin, Kurokawa, Mineo, Lee, Joanne, Malcovati, Luca, Morgan, Neil V., Natsoulis, Georges, Owen, Carolyn, Patel, Keyur P., Preudhomme, Claude, Raslova, Hana, Rienhoff, Hugh, Ripperger, Tim, Schulte, Rachael, Tawana, Kiran, Velloso, Elvira, Yan, Benedict, Kim, Erika, Sood, Raman, Hsu, Amy P., Holland, Steven M., Phillips, Kerry, Poplawski, Nicola K., Babic, Milena, Wei, Andrew H., Forsyth, Cecily, Mar Fan, Helen, Lewis, Ian D., Cooney, Julian, Susman, Rachel, Fox, Lucy C., Blombery, Piers, Singhal, Deepak, Hiwase, Devendra, Phipson, Belinda, Schreiber, Andreas W., Hahn, Christopher N., Scott, Hamish S., Liu, Paul, Godley, Lucy A., and Brown, Anna L.

Published
2023
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8. Different prognostic impact of recurrent gene mutations in chronic lymphocytic leukemia depending on IGHV gene somatic hypermutation status: a study by ERIC in HARMONY

Author

Mansouri, Larry, Thorvaldsdottir, Birna, Sutton, Lesley-Ann, Karakatsoulis, Georgios, Meggendorfer, Manja, Parker, Helen, Nadeu, Ferran, Brieghel, Christian, Laidou, Stamatia, Moia, Riccardo, Rossi, Davide, Catherwood, Mark, Kotaskova, Jana, Delgado, Julio, Rodríguez-Vicente, Ana E., Benito, Rocío, Rigolin, Gian Matteo, Bonfiglio, Silvia, Scarfo, Lydia, Mattsson, Mattias, Davis, Zadie, Gogia, Ajay, Rani, Lata, Baliakas, Panagiotis, Foroughi-Asl, Hassan, Jylhä, Cecilia, Skaftason, Aron, Rapado, Inmaculada, Miras, Fatima, Martinez-Lopez, Joaquín, de la Serna, Javier, Rivas, Jesús María Hernández, Thornton, Patrick, Larráyoz, María José, Calasanz, María José, Fésüs, Viktória, Mátrai, Zoltán, Bödör, Csaba, Smedby, Karin E., Espinet, Blanca, Puiggros, Anna, Gupta, Ritu, Bullinger, Lars, Bosch, Francesc, Tazón-Vega, Bárbara, Baran-Marszak, Fanny, Oscier, David, Nguyen-Khac, Florence, Zenz, Thorsten, Terol, Maria Jose, Cuneo, Antonio, Hernández-Sánchez, María, Pospisilova, Sarka, Mills, Ken, Gaidano, Gianluca, Niemann, Carsten U., Campo, Elias, Strefford, Jonathan C., Ghia, Paolo, Stamatopoulos, Kostas, and Rosenquist, Richard

Published
2023
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10. Next-Generation Sequencing–Based Genomic Profiling of Children with Acute Myeloid Leukemia

Author

Krizsán, Szilvia, Péterffy, Borbála, Egyed, Bálint, Nagy, Tibor, Sebestyén, Endre, Hegyi, Lajos László, Jakab, Zsuzsanna, Erdélyi, Dániel J., Müller, Judit, Péter, György, Csanádi, Krisztina, Kállay, Krisztián, Kriván, Gergely, Barna, Gábor, Bedics, Gábor, Haltrich, Irén, Ottóffy, Gábor, Csernus, Katalin, Vojcek, Ágnes, Tiszlavicz, Lilla Györgyi, Gábor, Krisztina Mita, Kelemen, Ágnes, Hauser, Péter, Gaál, Zsuzsanna, Szegedi, István, Ujfalusi, Anikó, Kajtár, Béla, Kiss, Csongor, Matolcsy, András, Tímár, Botond, Kovács, Gábor, Alpár, Donát, and Bödör, Csaba

Published
2023
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11. BTK and PLCG2 remain unmutated in one-third of patients with CLL relapsing on ibrutinib

Author

Bonfiglio, Silvia, Sutton, Lesley-Ann, Ljungström, Viktor, Capasso, Antonella, Pandzic, Tatjana, Weström, Simone, Foroughi-Asl, Hassan, Skaftason, Aron, Gellerbring, Anna, Lyander, Anna, Gandini, Francesca, Gaidano, Gianluca, Trentin, Livio, Bonello, Lisa, Reda, Gianluigi, Bödör, Csaba, Stavroyianni, Niki, Tam, Constantine S., Marasca, Roberto, Forconi, Francesco, Panayiotidis, Panayiotis, Ringshausen, Ingo, Jaksic, Ozren, Frustaci, Anna Maria, Iyengar, Sunil, Coscia, Marta, Mulligan, Stephen P., Ysebaert, Loïc, Strugov, Vladimir, Pavlovsky, Carolina, Walewska, Renata, Österborg, Anders, Cortese, Diego, Ranghetti, Pamela, Baliakas, Panagiotis, Stamatopoulos, Kostas, Scarfò, Lydia, Rosenquist, Richard, and Ghia, Paolo

Published
2023
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13. Electrocardiogram Features of Left Ventricular Excessive Trabeculation with Preserved Cardiac Function in Light of Cardiac Magnetic Resonance and Genetics.

Author

Farkas-Sütő, Kristóf Attila, Grebur, Kinga, Mester, Balázs, Gyulánczi, Flóra Klára, Bödör, Csaba, Vágó, Hajnalka, Merkely, Béla, and Szűcs, Andrea

Subjects
CARDIAC magnetic resonance imaging, MUSCLE mass, HEART failure, THROMBOEMBOLISM, GENETICS
Abstract

Background and Objectives: Although left ventricular excessive trabeculation (LVET) can cause heart failure, arrhythmia and thromboembolism, limited literature is available on the ECG characteristics of primary LVET with preserved left ventricular function (EF). We aimed to compare the ECG characteristics and cardiac MR (CMR) parameters of LVET individuals with preserved left ventricular EF to a control (C) group, to identify sex-specific differences, and to compare the genetic subgroups of LVET with each other and with a C population. Methods: In our study, we selected 69 LVET individuals (EF > 50%) without any comorbidities and compared them to 69 sex- and age-matched control subjects (42% females in both groups, p = 1.000; mean age LVET-vs-C: 38 ± 14 vs. 38 ± 14 years p = 0.814). We analyzed the pattern and notable parameters of the 12-lead ECG recordings. We determined the volumetric and functional parameters, as well as the muscle mass values of the left and right ventricles (LV, RV) based on the CMR recordings. Based on the genotype, three subgroups were established: pathogenic, variant of uncertain significance and benign. Results: In the LVET group, we found normal but elevated volumetric and muscle mass values and a decreased LV_EF, wider QRS, prolonged QTc, higher RV Sokolow index values and lower T wave amplitude compared to the C. When comparing MR and ECG parameters between genetic subgroups, only the QTc showed a significant difference. Over one-third of the LVET population had arrhythmic episodes and a positive family history. Conclusions: The subclinical morphological and ECG changes and the clinical background of the LVET group indicate the need for follow-up of this population, even with preserved EF. [ABSTRACT FROM AUTHOR]

Published
2024
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16. Author Correction: Genome-wide association study identifies susceptibility loci for acute myeloid leukemia

Author

Lin, Wei-Yu, Fordham, Sarah E., Hungate, Eric, Sunter, Nicola J., Elstob, Claire, Xu, Yaobo, Park, Catherine, Quante, Anne, Strauch, Konstantin, Gieger, Christian, Skol, Andrew, Rahman, Thahira, Sucheston-Campbell, Lara, Wang, Junke, Hahn, Theresa, Clay-Gilmour, Alyssa I., Jones, Gail L., Marr, Helen J., Jackson, Graham H., Menne, Tobias, Collin, Mathew, Ivey, Adam, Hills, Robert K., Burnett, Alan K., Russell, Nigel H., Fitzgibbon, Jude, Larson, Richard A., Le Beau, Michelle M., Stock, Wendy, Heidenreich, Olaf, Alharbi, Abrar, Allsup, David J., Houlston, Richard S., Norden, Jean, Dickinson, Anne M., Douglas, Elisabeth, Lendrem, Clare, Daly, Ann K., Palm, Louise, Piechocki, Kim, Jeffries, Sally, Bornhäuser, Martin, Röllig, Christoph, Altmann, Heidi, Ruhnke, Leo, Kunadt, Desiree, Wagenführ, Lisa, Cordell, Heather J., Darlay, Rebecca, Andersen, Mette K., Fontana, Maria C., Martinelli, Giovanni, Marconi, Giovanni, Sanz, Miguel A., Cervera, José, Gómez-Seguí, Inés, Cluzeau, Thomas, Moreilhon, Chimène, Raynaud, Sophie, Sill, Heinz, Voso, Maria Teresa, Lo-Coco, Francesco, Dombret, Hervé, Cheok, Meyling, Preudhomme, Claude, Gale, Rosemary E., Linch, David, Gaal-Wesinger, Julia, Masszi, Andras, Nowak, Daniel, Hofmann, Wolf-Karsten, Gilkes, Amanda, Porkka, Kimmo, Milosevic Feenstra, Jelena D., Kralovics, Robert, Grimwade, David, Meggendorfer, Manja, Haferlach, Torsten, Krizsán, Szilvia, Bödör, Csaba, Stölzel, Friedrich, Onel, Kenan, and Allan, James M.

Published
2022
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20. Higher-order connections between stereotyped subsets: implications for improved patient classification in CLL

Author

Agathangelidis, Andreas, Chatzidimitriou, Anastasia, Gemenetzi, Katerina, Giudicelli, Veronique, Karypidou, Maria, Plevova, Karla, Davis, Zadie, Yan, Xiao-Jie, Jeromin, Sabine, Schneider, Christof, Pedersen, Lone Bredo, Tschumper, Renee C., Sutton, Lesley-Ann, Baliakas, Panagiotis, Scarfò, Lydia, van Gastel, Ellen J., Armand, Marine, Tausch, Eugen, Biderman, Bella, Baer, Constance, Bagnara, Davide, Navarro, Alba, Langlois de Septenville, Anne, Guido, Valentina, Mitterbauer-Hohendanner, Gerlinde, Dimovski, Aleksandar, Brieghel, Christian, Lawless, Sarah, Meggendorfer, Manja, Brazdilova, Kamila, Ritgen, Matthias, Facco, Monica, Tresoldi, Cristina, Visentin, Andrea, Patriarca, Andrea, Catherwood, Mark, Bonello, Lisa, Sudarikov, Andrey, Vanura, Katrina, Roumelioti, Maria, Skuhrova Francova, Hana, Moysiadis, Theodoros, Veronese, Silvio, Giannopoulos, Krzysztof, Mansouri, Larry, Karan-Djurasevic, Teodora, Sandaltzopoulos, Raphael, Bödör, Csaba, Fais, Franco, Kater, Arnon, Panovska, Irina, Rossi, Davide, Alshemmari, Salem, Panagiotidis, Panagiotis, Costeas, Paul, Espinet, Blanca, Antic, Darko, Foroni, Letizia, Montillo, Marco, Trentin, Livio, Stavroyianni, Niki, Gaidano, Gianluca, Francia di Celle, Paola, Niemann, Carsten, Campo, Elias, Anagnostopoulos, Achilles, Pott, Christiane, Fischer, Kirsten, Hallek, Michael, Oscier, David, Stilgenbauer, Stephan, Haferlach, Claudia, Jelinek, Diane, Chiorazzi, Nicholas, Pospisilova, Sarka, Lefranc, Marie-Paule, Kossida, Sofia, Langerak, Anton W., Belessi, Chrysoula, Davi, Frederic, Rosenquist, Richard, Ghia, Paolo, and Stamatopoulos, Kostas

Published
2021
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21. Genetic Characterization of Primary Mediastinal B-Cell Lymphoma : Pathogenesis and Patient Outcomes

Author

Noerenberg, Daniel, Briest, Franziska, Hennch, Cornelius, Yoshida, Kenichi, Hablesreiter, Raphael, Takeuchi, Yasuhide, Ueno, Hiroo, Staiger, Annette M., Ziepert, Marita, Asmar, Fazila, Locher, Benjamin N., Toth, Erika, Weber, Thomas, Amini, Rose-Marie, Klapper, Wolfram, Bouzani, Maria, Poeschel, Viola, Rosenwald, Andreas, Held, Gerhard, Campo, Elias, Ishaque, Naveed, Stamatopoulos, Kostas, Kanellis, George, Anagnostopoulos, Ioannis, Bullinger, Lars, Goldschmidt, Neta, Zinzani, Pier Luigi, Bödör, Csaba, Rosenquist, Richard, Vassilakopoulos, Theodoros P., Ott, German, Ogawa, Seishi, Damm, Frederik, Noerenberg, Daniel, Briest, Franziska, Hennch, Cornelius, Yoshida, Kenichi, Hablesreiter, Raphael, Takeuchi, Yasuhide, Ueno, Hiroo, Staiger, Annette M., Ziepert, Marita, Asmar, Fazila, Locher, Benjamin N., Toth, Erika, Weber, Thomas, Amini, Rose-Marie, Klapper, Wolfram, Bouzani, Maria, Poeschel, Viola, Rosenwald, Andreas, Held, Gerhard, Campo, Elias, Ishaque, Naveed, Stamatopoulos, Kostas, Kanellis, George, Anagnostopoulos, Ioannis, Bullinger, Lars, Goldschmidt, Neta, Zinzani, Pier Luigi, Bödör, Csaba, Rosenquist, Richard, Vassilakopoulos, Theodoros P., Ott, German, Ogawa, Seishi, and Damm, Frederik

Abstract

Purpose Primary mediastinal large B-cell lymphoma (PMBCL) is a rare aggressive lymphoma predominantly affecting young female patients. Large-scale genomic investigations and genetic markers for risk stratification are lacking. Patients and Methods To elucidate the full spectrum of genomic alterations, samples from 340 patients with previously untreated PMBCL were investigated by whole-genome (n = 20), whole-exome (n = 78), and targeted (n = 308) sequencing. Statistically significant prognostic variables were identified using a multivariable Cox regression model and confirmed by L1/L2 regularized regressions. Results Whole-genome sequencing revealed a commonly disrupted p53 pathway with nonredundant somatic structural variations (SVs) in TP53-related genes (TP63, TP73, and WWOX) and identified novel SVs facilitating immune evasion (DOCK8 and CD83). Integration of mutation and copy-number data expanded the repertoire of known PMBCL alterations (eg, ARID1A, P2RY8, and PLXNC1) with a previously unrecognized role for epigenetic/chromatin modifiers. Multivariable analysis identified six genetic lesions with significant prognostic impact. CD58 mutations (31%) showed the strongest association with worse PFS (hazard ratio [HR], 2.52 [95% CI, 1.50 to 4.21]; P < .001) and overall survival (HR, 2.33 [95% CI, 1.14 to 4.76]; P = .02). IPI high-risk patients with mutated CD58 demonstrated a particularly poor prognosis, with 5-year PFS and OS rates of 41% and 58%, respectively. The adverse prognostic significance of the CD58 mutation status was predominantly observed in patients treated with nonintensified regimens, indicating that dose intensification may, to some extent, mitigate the impact of this high-risk marker. By contrast, DUSP2-mutated patients (24%) displayed durable responses (PFS: HR, 0.2 [95% CI, 0.07 to 0.55]; P = .002) and prolonged OS (HR, 0.11 [95% CI, 0.01 to 0.78]; P = .028). Upon CHOP-like treatment, these patients had very favorable outcome, with 5-year PFS

Published
2024
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22. The effect of excessive trabeculation on cardiac rotation—A multimodal imaging study.

Author

Grebur, Kinga, Mester, Balázs, Horváth, Márton, Farkas-Sütő, Kristóf, Gregor, Zsófia, Kiss, Anna Réka, Tóth, Attila, Kovács, Attila, Fábián, Alexandra, Lakatos, Bálint Károly, Fekete, Bálint András, Csonka, Katalin, Bödör, Csaba, Merkely, Béla, Vágó, Hajnalka, and Szűcs, Andrea

Subjects
SPECKLE tracking echocardiography, CARDIAC magnetic resonance imaging, VENTRICULAR ejection fraction, NUCLEOTIDE sequencing, RIGID bodies, SPECKLE interference
Abstract

Background: Cardiac rotational parameters in primary symptomatic left ventricular noncompaction (LVNC) with preserved left ventricular ejection fraction (LVEF) are not well understood. We aimed to analyze cardiac rotation measured with cardiac magnetic resonance feature-tracking (CMR-FT) and speckle-tracking echocardiography (Echo-ST) in LVNC morphology subjects with preserved LVEF and different genotypes and healthy controls. Methods: Our retrospective study included 54 LVNC subjects with preserved LVEF and 54 control individuals. We evaluated functional and rotational parameters with CMR in the total study population and with echocardiography in 39 LVNC and 40 C individuals. All LVNC subjects were genotyped with a 174-gene next-generation sequencing panel and grouped into the subgroups: benign (B), variant of uncertain significance (VUS), and pathogenic (P). Results: In comparison with controls, LVNC subjects had reduced apical rotational degree (p = 0.004) and one-third had negative apical rotation. While the degree of apical rotation was comparable between the three genetic subgroups, they differed significantly in the direction of apical rotation (p<0.001). In contrast to control and B groups, all four studied cardiac rotational patterns were identified in the P and VUS subgroups, namely normal rotation, positive and negative rigid body rotation, and reverse rotation. When the CMR-FT and Echo-ST methods were compared, the direction and pattern of cardiac rotation had moderate to good association (p<0.001) whereas the rotational degrees showed no reasonable correlation or agreement. Conclusion: While measuring cardiac rotation using both CMR-FT and Echo-ST methods, subclinical mechanical differences were identified in subjects with LVNC phenotype and preserved LVEF, especially in cases with genetic involvement. [ABSTRACT FROM AUTHOR]

Published
2024
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23. Noninvazív rejekció utánkövetése szolid szervek átültetését követően: a donoreredetű sejtmentes DNS vizsgálata.

Author

Teszák, Tímea, Bödör, Csaba, Hegyi, Lajos, Lévay, Luca, Nagy, Beáta, Fintha, Attila, Merkely, Béla, and Sax, Balázs

Abstract

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Published
2024
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24. Correction: Different prognostic impact of recurrent gene mutations in chronic lymphocytic leukemia depending on IGHV gene somatic hypermutation status: a study by ERIC in HARMONY

Author

Mansouri, Larry, Thorvaldsdottir, Birna, Sutton, Lesley-Ann, Karakatsoulis, Georgios, Meggendorfer, Manja, Parker, Helen, Nadeu, Ferran, Brieghel, Christian, Laidou, Stamatia, Moia, Riccardo, Rossi, Davide, Catherwood, Mark, Kotaskova, Jana, Delgado, Julio, Rodríguez-Vicente, Ana E., Benito, Rocío, Rigolin, Gian Matteo, Bonfiglio, Silvia, Scarfo, Lydia, Mattsson, Mattias, Davis, Zadie, Gogia, Ajay, Rani, Lata, Baliakas, Panagiotis, Foroughi-Asl, Hassan, Jylhä, Cecilia, Skaftason, Aron, Rapado, Inmaculada, Miras, Fatima, Martinez-Lopez, Joaquín, de la Serna, Javier, Rivas, Jesús María Hernández, Thornton, Patrick, Larráyoz, María José, Calasanz, María José, Fésüs, Viktória, Mátrai, Zoltán, Bödör, Csaba, Smedby, Karin E., Espinet, Blanca, Puiggros, Anna, Gupta, Ritu, Bullinger, Lars, Bosch, Francesc, Tazón-Vega, Bárbara, Baran-Marszak, Fanny, Oscier, David, Nguyen-Khac, Florence, Zenz, Thorsten, Terol, Maria Jose, Cuneo, Antonio, Hernández-Sánchez, María, Pospisilova, Sarka, Mills, Ken, Gaidano, Gianluca, Niemann, Carsten U., Campo, Elias, Strefford, Jonathan C., Ghia, Paolo, Stamatopoulos, Kostas, and Rosenquist, Richard

Published
2023
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25. Comprehensive profiling of disease-relevant copy number aberrations for advanced clinical diagnostics of pediatric acute lymphoblastic leukemia

Author

Kiss, Richárd, Gángó, Ambrus, Benard-Slagter, Anne, Egyed, Bálint, Haltrich, Irén, Hegyi, Lajos, de Groot, Karel, Király, Péter Attila, Krizsán, Szilvia, Kajtár, Béla, Pikó, Henriett, Pajor, László, Vojcek, Ágnes, Matolcsy, András, Kovács, Gábor, Szuhai, Károly, Savola, Suvi, Bödör, Csaba, and Alpár, Donát

Published
2020
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26. Genetic, clinical and imaging implications of a noncompaction phenotype population with preserved ejection fraction

Author

Grebur, Kinga, primary, Mester, Balázs, additional, Fekete, Bálint András, additional, Kiss, Anna Réka, additional, Gregor, Zsófia, additional, Horváth, Márton, additional, Farkas-Sütő, Kristóf, additional, Csonka, Katalin, additional, Bödör, Csaba, additional, Merkely, Béla, additional, Vágó, Hajnalka, additional, and Szűcs, Andrea, additional

Published
2024
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28. Genome-wide association study identifies susceptibility loci for acute myeloid leukemia

Author

Lin, Wei-Yu, Fordham, Sarah E., Hungate, Eric, Sunter, Nicola J., Elstob, Claire, Xu, Yaobo, Park, Catherine, Quante, Anne, Strauch, Konstantin, Gieger, Christian, Skol, Andrew, Rahman, Thahira, Sucheston-Campbell, Lara, Wang, Junke, Hahn, Theresa, Clay-Gilmour, Alyssa I., Jones, Gail L., Marr, Helen J., Jackson, Graham H., Menne, Tobias, Collin, Mathew, Ivey, Adam, Hills, Robert K., Burnett, Alan K., Russell, Nigel H., Fitzgibbon, Jude, Larson, Richard A., Le Beau, Michelle M., Stock, Wendy, Heidenreich, Olaf, Alharbi, Abrar, Allsup, David J., Houlston, Richard S., Norden, Jean, Dickinson, Anne M., Douglas, Elisabeth, Lendrem, Clare, Daly, Ann K., Palm, Louise, Piechocki, Kim, Jeffries, Sally, Bornhäuser, Martin, Röllig, Christoph, Altmann, Heidi, Ruhnke, Leo, Kunadt, Desiree, Wagenführ, Lisa, Cordell, Heather J., Darlay, Rebecca, Andersen, Mette K., Fontana, Maria C., Martinelli, Giovanni, Marconi, Giovanni, Sanz, Miguel A., Cervera, José, Gómez-Seguí, Inés, Cluzeau, Thomas, Moreilhon, Chimène, Raynaud, Sophie, Sill, Heinz, Voso, Maria Teresa, Lo-Coco, Francesco, Dombret, Hervé, Cheok, Meyling, Preudhomme, Claude, Gale, Rosemary E., Linch, David, Gaal-Wesinger, Julia, Masszi, Andras, Nowak, Daniel, Hofmann, Wolf-Karsten, Gilkes, Amanda, Porkka, Kimmo, Milosevic Feenstra, Jelena D., Kralovics, Robert, Grimwade, David, Meggendorfer, Manja, Haferlach, Torsten, Krizsán, Szilvia, Bödör, Csaba, Stölzel, Friedrich, Onel, Kenan, and Allan, James M.

Published
2021
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31. Genetic Characterization of Primary Mediastinal B-Cell Lymphoma: Pathogenesis and Patient Outcomes

Author

Noerenberg, Daniel, primary, Briest, Franziska, additional, Hennch, Cornelius, additional, Yoshida, Kenichi, additional, Hablesreiter, Raphael, additional, Takeuchi, Yasuhide, additional, Ueno, Hiroo, additional, Staiger, Annette M., additional, Ziepert, Marita, additional, Asmar, Fazila, additional, Locher, Benjamin N., additional, Toth, Erika, additional, Weber, Thomas, additional, Amini, Rose-Marie, additional, Klapper, Wolfram, additional, Bouzani, Maria, additional, Poeschel, Viola, additional, Rosenwald, Andreas, additional, Held, Gerhard, additional, Campo, Elías, additional, Ishaque, Naveed, additional, Stamatopoulos, Kostas, additional, Kanellis, George, additional, Anagnostopoulos, Ioannis, additional, Bullinger, Lars, additional, Goldschmidt, Neta, additional, Zinzani, Pier Luigi, additional, Bödör, Csaba, additional, Rosenquist, Richard, additional, Vassilakopoulos, Theodoros P., additional, Ott, German, additional, Ogawa, Seishi, additional, and Damm, Frederik, additional

Published
2023
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32. GENOTYPE/PHENOTYPE ASSOCIATIONS IN 174 INDIVIDUALS WITH GERMLINE GATA2 MUTATIONS

Author

Kotmayer, Lili, primary, Kozyra, Emilia, additional, Kaiser, Maximilian, additional, Dworzak, Michael, additional, Moerloose, Barbara De, additional, Starý, Jan, additional, Hasle, Henrik, additional, Jahnukainen, Kirsi, additional, Polychronopoulou, Sophia, additional, Kállay, Krisztián, additional, Smith, Owen, additional, Barzilai, Shlomit, additional, Masetti, Riccardo, additional, Buechner, Jochen, additional, Ussowicz, Marek, additional, Kjollerstrom, Paula, additional, Boďová, Ivana, additional, Kavcic, Marko, additional, Catala, Albert, additional, Turkiewicz, Dominik, additional, Schmugge, Markus, additional, Haas, Valérie De, additional, Voss, Rebecca, additional, Bigas, Anna, additional, Romero, Damia, additional, Bödör, Csaba, additional, Erlacher, Miriam, additional, Giorgetti, Alessandra, additional, Niemeyer, Charlotte, additional, and Wlodarski, Marcin, additional

Published
2023
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34. Low‐burden TP53 mutations represent frequent genetic events in CLL with an increased risk for treatment initiation

Author

László, Tamás, primary, Kotmayer, Lili, additional, Fésüs, Viktória, additional, Hegyi, Lajos, additional, Gróf, Stefánia, additional, Nagy, Ákos, additional, Kajtár, Béla, additional, Balogh, Alexandra, additional, Weisinger, Júlia, additional, Masszi, Tamás, additional, Nagy, Zsolt, additional, Farkas, Péter, additional, Demeter, Judit, additional, Istenes, Ildikó, additional, Szász, Róbert, additional, Gergely, Lajos, additional, Sulák, Adrienn, additional, Borbényi, Zita, additional, Lévai, Dóra, additional, Schneider, Tamás, additional, Pettendi, Piroska, additional, Bodai, Emese, additional, Szerafin, László, additional, Rejtő, László, additional, Bátai, Árpád, additional, Dömötör, Mária Á, additional, Sánta, Hermina, additional, Plander, Márk, additional, Szendrei, Tamás, additional, Hamed, Aryan, additional, Lázár, Zsolt, additional, Pauker, Zsolt, additional, Radványi, Gáspár, additional, Kiss, Adrienn, additional, Körösmezey, Gábor, additional, Jakucs, János, additional, Dombi, Péter J, additional, Simon, Zsófia, additional, Klucsik, Zsolt, additional, Gurzó, Mihály, additional, Tiboly, Márta, additional, Vidra, Tímea, additional, Ilonczai, Péter, additional, Bors, András, additional, Andrikovics, Hajnalka, additional, Egyed, Miklós, additional, Székely, Tamás, additional, Masszi, András, additional, Alpár, Donát, additional, Matolcsy, András, additional, and Bödör, Csaba, additional

Published
2023
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35. Truncated titin is structurally integrated into the human dilated cardiomyopathic sarcomere

Author

Kellermayer, Dalma, primary, Tordai, Hedvig, additional, Kiss, Balázs, additional, Török, György, additional, Péter, Dániel M., additional, Sayour, Alex Ali, additional, Pólos, Miklós, additional, Hartyánszky, István, additional, Szilveszter, Bálint, additional, Labeit, Siegfried, additional, Gángó, Ambrus, additional, Bedics, Gábor, additional, Bödör, Csaba, additional, Radovits, Tamás, additional, Merkely, Bela, additional, and Kellermayer, Miklós S.Z., additional

Published
2023
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36. Hogyan változott az akut myeloid leukaemiás betegek túlélése a terápiás lehetőségek bővülésével az elmúlt 10 évben klinikánkon?

Author

Gaál, Lilla, primary, Ruff, Eszter, additional, Wiedemann, Ádám, additional, Svorenj, Szabolcs, additional, Szita, Virág Réka, additional, Tóth, András Dávid, additional, Masszi, András, additional, Horváth, Laura, additional, Szombath, Gergely, additional, Nagy, Zsolt, additional, Várkonyi, Judit, additional, Benedek†, Szabolcs, additional, Farkas, Péter, additional, Bödör, Csaba, additional, Masszi, Tamás, additional, and Varga, Gergely, additional

Published
2023
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43. Quantitative assessment of JAK2 V617F and CALR mutations in Philadelphia negative myeloproliferative neoplasms

Author

Gángó, Ambrus, Mózes, Réka, Boha, Zsófia, Kajtár, Béla, Timár, Botond, Király, Péter Attila, Kiss, Richárd, Fésüs, Viktória, Nagy, Noémi, Demeter, Judit, Körösmezey, Gábor, Borbényi, Zita, Marton, Imelda, Szőke, Anita, Masszi, Tamás, Farkas, Péter, Várkonyi, Judit, Plander, Márk, Pósfai, Éva, Egyed, Miklós, Pál, Katalin, Radványi, Gáspár, Hamed, Aryan, Csomor, Judit, Matolcsy, András, Alpár, Donát, and Bödör, Csaba

Published
2018
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44. Droplet Digital PCR Is a Novel Screening Method Identifying Potential Cardiac G-Protein-Coupled Receptors as Candidate Pharmacological Targets in a Rat Model of Pressure-Overload-Induced Cardiac Dysfunction

Author

Sayour, Nabil V., primary, Tóth, Viktória É., additional, Nagy, Regina N., additional, Vörös, Imre, additional, Gergely, Tamás G., additional, Onódi, Zsófia, additional, Nagy, Noémi, additional, Bödör, Csaba, additional, Váradi, Barnabás, additional, Ruppert, Mihály, additional, Radovits, Tamás, additional, Bleckwedel, Federico, additional, Zelarayán, Laura C., additional, Pacher, Pal, additional, Ágg, Bence, additional, Görbe, Anikó, additional, Ferdinandy, Péter, additional, and Varga, Zoltán V., additional

Published
2023
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47. POSTER: AML-588 Advancements in the Diagnosis of Acute Myeloid Leukemia Through the Application of Optical Genome Mapping

Author

Svorenj, Szabolcs, primary, Farkas, Péter, additional, Horváth, Laura, additional, Tárkányi, Ilona, additional, Szombath, Gergely, additional, Demeter, Judit, additional, Csonka, Katalin, additional, Hegyi, Lajos, additional, Barta, Aranka Bettina Bohusné, additional, Bödör, Csaba, additional, and Bekő, Anna, additional

Published
2023
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48. SERCA2a Protein Levels Are Unaltered in Human Heart Failure

Author

Ragone, Isabella, primary, Barallobre-Barreiro, Javier, additional, Takov, Kaloyan, additional, Theofilatos, Konstantinos, additional, Yin, Xiaoke, additional, Schmidt, Lukas Emanuel, additional, Domenech, Nieves, additional, Crespo-Leiro, Maria Generosa, additional, van der Voorn, Stephanie M., additional, Vink, Aryan, additional, van Veen, Toon A.B., additional, Bödör, Csaba, additional, Merkely, Béla, additional, Radovits, Tamás, additional, and Mayr, Manuel, additional

Published
2023
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49. PB1909: LOW-BURDEN TP53 MUTATIONS REPRESENT FREQUENT GENETIC EVENTS IN CLL WITH AN INCREASED RISK FOR TREATMENT INITIATION

Author

László, Tamás, primary, Kotmayer, Lili, additional, Hegyi, Lajos, additional, Gróf, Stefánia, additional, Kajtár, Béla, additional, Balogh, Alexandra, additional, Weisinger, Júlia, additional, Masszi, Tamás, additional, Nagy, Zsolt, additional, Demeter, Judit, additional, Farkas, Péter, additional, Istenes, Ildikó, additional, Szász, Róbert, additional, Gergely, Lajos, additional, Sulák, Adrienn, additional, Borbényi, Zita, additional, Lévai, Dóra, additional, Schneider, Tamás, additional, Szaleczky, Erika, additional, Pettendi, Piroska, additional, Bodai, Emese, additional, Szerafin, László, additional, Rejtő, László, additional, Bátai, Árpád, additional, Dömötör, Mária Ágnes, additional, Sánta, Hermina, additional, Plander, Márk, additional, Szendrei, Tamás, additional, Ilonczai, Péter, additional, Hamed, Aryan, additional, Lázár, Zsolt, additional, Pauker, Zsolt, additional, Radványi, Gáspár, additional, Kiss, Adrienn, additional, Körösmezey, Gábor, additional, Jakucs, János, additional, Dombi, Péter János, additional, Simon, Zsófia, additional, Klucsik, Zsolt, additional, Gurzó, Mihály, additional, Tiboly, Márta, additional, Vidra, Tímea, additional, Bors, András, additional, Andrikovics, Hajnalka, additional, Egyed, Miklós, additional, Székely, Tamás, additional, Masszi, András, additional, Matolcsy, András, additional, Alpár, Donát, additional, and Bödör, Csaba, additional

Published
2023
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50. P718: EPIGENOME PROFILING REVEALS ABERRANT DNA METHYLATION SIGNATURE IN GATA2 DEFICIENCY

Author

Marin-Bejar, Oskar, primary, Romero-Moya, Damia, additional, Rodriguez-Ubreva, Javier, additional, Distefano, Maximiliano, additional, Lessi, Francesca, additional, Aretini, Paolo, additional, Liquori, Alessandro, additional, Castaño, Julio, additional, Kozyra, Emilia, additional, Kotmayer, Lili, additional, Bueno, Clara, additional, Cervera, José, additional, Carlos Rodriguez-Gallego, José, additional, F Nomdedeu, Josep, additional, Murillo-Sanjuán, Laura, additional, Díaz de Heredia, Cristina, additional, Pérez-Martinez, Antonio, additional, López-Cardenas, Félix, additional, Martínez-Laperche, Carolina, additional, Dorado-Herrero, Nieves, additional, M Marco, Francisco, additional, Prósper, Felipe, additional, Menendez, Pablo, additional, Valcárcel, David, additional, Ballestar, Esteban, additional, Bödör, Csaba, additional, Bigas, Anna, additional, Catalá, Albert, additional, W Wlodarski, Marcin, additional, and Giorgetti, Alessandra, additional

Published
2023
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