| Biallelic loss of CDKN2A is associated with poor response to treatment in pediatric acute lymphoblastic leukemia M Braun, A Pastorczak, W Fendler, J Madzio, B Tomasik, J Taha, ... Leukemia & lymphoma 58 (5), 1162-1171, 2017 | 51 | 2017 |
| Neutrophil elastase defects in congenital neutropenia Z Rydzynska, B Pawlik, D Krzyzanowski, W Mlynarski, J Madzio Frontiers in Immunology 12, 653932, 2021 | 31 | 2021 |
| Targeting the thioredoxin system as a novel strategy against B‐cell acute lymphoblastic leukemia K Fidyt, A Pastorczak, A Goral, K Szczygiel, W Fendler, A Muchowicz, ... Molecular Oncology 13 (5), 1180-1195, 2019 | 31 | 2019 |
| Differential regulation of serum microRNA expression by HNF1β and HNF1α transcription factors W Fendler, J Madzio, K Kozinski, K Patel, J Janikiewicz, M Szopa, A Tracz, ... Diabetologia 59 (7), 1463-1473, 2016 | 23 | 2016 |
| Surface expression of cytokine receptor-like factor 2 increases risk of relapse in pediatric acute lymphoblastic leukemia patients harboring IKZF1 deletions A Pastorczak, L Sedek, M Braun, J Madzio, A Sonsala, M Twardoch, ... Oncotarget 9 (40), 25971, 2018 | 17 | 2018 |
| Prognostic significance of IKZF1 deletions and IKZF1plus profile in children with B‐cell precursor acute lymphoblastic leukemia treated according to the ALL‐IC … M Braun, A Pastorczak, Ł Sędek, J Taha, J Madzio, I Jatczak‐Pawlik, ... Hematological Oncology 40 (3), 430-441, 2022 | 13 | 2022 |
| GATA3 germline variant is associated with CRLF2 expression and predicts outcome in pediatric B‐cell precursor acute lymphoblastic leukemia J Madzio, A Pastorczak, L Sedek, M Braun, J Taha, K Wypyszczak, ... Genes, Chromosomes and Cancer 58 (9), 619-626, 2019 | 12 | 2019 |
| Selected miRNA levels are associated with IKZF1 microdeletions in pediatric acute lymphoblastic leukemia J Krzanowski, J Madzio, A Pastorczak, A Tracz, M Braun, J Tabarkiewicz, ... Oncology Letters 14 (3), 3853-3861, 2017 | 11 | 2017 |
| Potent, p53-independent induction of NOXA sensitizes MLL-rearranged B-cell acute lymphoblastic leukemia cells to venetoclax K Fidyt, A Pastorczak, J Cyran, NT Crump, A Goral, J Madzio, ... Oncogene 41 (11), 1600-1609, 2022 | 10 | 2022 |
| Genetic variability of GCKR alters lipid profiles in children with monogenic and autoimmune diabetes A Tracz, J Madzio, P Gnys, B Malachowska, M Borowiec, K Wyka, ... Experimental and Clinical Endocrinology & Diabetes, 503-509, 2014 | 6 | 2014 |
| Heterozygous carriers of germline c. 657_661del5 founder mutation in NBN gene are at risk of central nervous system relapse of B-cell precursor acute lymphoblastic leukemia B Tomasik, A Pastorczak, W Fendler, M Bartłomiejczyk, M Braun, M Mycko, ... haematologica 103 (5), e200, 2018 | 5 | 2018 |
| A high prevalence of neutrophil‐specific antibodies in ELANE‐mutated severe congenital neutropenia W Dobrewa, J Madzio, K Babol‐Pokora, P Lopacz, A Gierszon, K Guz, ... Pediatric Blood & Cancer 70 (4), e30247, 2023 | 4 | 2023 |
| The kinetics of blast clearance are associated with copy number alterations in childhood B-cell acute lymphoblastic leukemia Z Urbańska, M Lejman, J Taha, J Madzio, K Ostrowska, K Miarka-Walczyk, ... Neoplasia 35, 100840, 2023 | 4 | 2023 |
| Gene expression of ASNS, LGMN and CTSB is elevated in a subgroup of childhood BCP‑ALL with PAX5 deletion E Wrona, J Jakubowska, B Pawlik, A Pastorczak, J Madzio, M Lejman, ... Oncology letters 18 (6), 6926-6932, 2019 | 4 | 2019 |
| The paradox of autoimmunity and autoinflammation in inherited neutrophil disorders–in search of common patterns D Krzyzanowski, A Oszer, J Madzio, M Zdunek, J Kolodrubiec, B Urbanski, ... Frontiers in Immunology 14, 1128581, 2023 | 2 | 2023 |
| Molecular background and therapeutic perspectives of acute lymphoblastic leukemia BCR-ABL1-like J Madzio, A Pastorczak, W Młynarski Hematologia 5 (2), 154-161, 2014 | 2 | 2014 |
| Elevated level of lysophosphatidic acid among patients with HNF1B mutations and its role in RCAD syndrome: a multiomic study B Małachowska, J Janikiewicz, K Pietrowska, K Wyka, J Madzio, ... Metabolomics 18 (3), 15, 2022 | 1 | 2022 |
| Neutrophil functions in patients with neutropenia due to glycogen storage disease type 1b treated with empagliflozin M Kaczor, S Malicki, J Folkert, E Dobosz, D Bryzek, B Chru¶cicka-Smaga, ... Blood Advances, bloodadvances. 2023012403, 2024 | | 2024 |
| Concomitant inhibition of the thioredoxin system and nonhomologous DNA repair potently sensitizes Philadelphia‐positive lymphoid leukemia to tyrosine kinase inhibitors L Komorowski, A Dabkowska, J Madzio, A Pastorczak, K Szczygiel, ... HemaSphere 8 (3), e56, 2024 | | 2024 |
| CRISPR/Cas9 Strategy for Correcting ELANE Mutations and Restoring Neutrophil Differentiation in Severe Congenital Neutropenia: Insights from Patient-Derived iPSCs Z Rydzynska, D Grzela, MI Linder, W Dobrewa, Z Urbanska, B Pawlik, ... Blood 142, 4100, 2023 | | 2023 |
Marcin BraunMedical University of LodzVerified email at umed.lodz.pl
