| Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease DB Beck, MA Ferrada, KA Sikora, AK Ombrello, JC Collins, W Pei, ... New England Journal of Medicine 383 (27), 2628-2638, 2020 | 679 | 2020 |
| Asymmetrically modified nucleosomes P Voigt, G LeRoy, WJ Drury, BM Zee, J Son, DB Beck, NL Young, ... Cell 151 (1), 181-193, 2012 | 454 | 2012 |
| Specific peptide interference reveals BCL6 transcriptional and oncogenic mechanisms in B-cell lymphoma cells JM Polo, T Dell'Oso, SM Ranuncolo, L Cerchietti, D Beck, GF Da Silva, ... Nature medicine 10 (12), 1329-1335, 2004 | 353 | 2004 |
| PR-Set7 and H4K20me1: at the crossroads of genome integrity, cell cycle, chromosome condensation, and transcription DB Beck, H Oda, SS Shen, D Reinberg Genes & development 26 (4), 325-337, 2012 | 324 | 2012 |
| The tumor suppressor SirT2 regulates cell cycle progression and genome stability by modulating the mitotic deposition of H4K20 methylation L Serrano, P Martínez-Redondo, A Marazuela-Duque, BN Vazquez, ... Genes & development 27 (6), 639-653, 2013 | 285 | 2013 |
| The C-terminal domain of RNA polymerase II is modified by site-specific methylation RJ Sims III, LA Rojas, D Beck, R Bonasio, R Schüller, WJ Drury III, D Eick, ... Science 332 (6025), 99-103, 2011 | 261 | 2011 |
| Regulation of the histone H4 monomethylase PR-Set7 by CRL4Cdt2-mediated PCNA-dependent degradation during DNA damage H Oda, MR Hübner, DB Beck, M Vermeulen, J Hurwitz, DL Spector, ... Molecular cell 40 (3), 364-376, 2010 | 250 | 2010 |
| Mutations that prevent caspase cleavage of RIPK1 cause autoinflammatory disease N Lalaoui, SE Boyden, H Oda, GM Wood, DL Stone, D Chau, L Liu, ... Nature 577 (7788), 103-108, 2020 | 224 | 2020 |
| Somatic Mutations in UBA1 Define a Distinct Subset of Relapsing Polychondritis Patients With VEXAS MA Ferrada, KA Sikora, Y Luo, KV Wells, B Patel, EM Groarke, ... Arthritis & Rheumatology 73 (10), 1886-1895, 2021 | 152 | 2021 |
| Benign and malignant hematologic manifestations in patients with VEXAS syndrome due to somatic mutations in UBA1 IE Obiorah, BA Patel, EM Groarke, W Wang, M Trick, AK Ombrello, ... Blood advances 5 (16), 3203-3215, 2021 | 152* | 2021 |
| Novel somatic mutations in UBA1 as a cause of VEXAS syndrome JA Poulter, JC Collins, C Cargo, RM De Tute, P Evans, D Ospina Cardona, ... Blood, The Journal of the American Society of Hematology 137 (26), 3676-3681, 2021 | 145 | 2021 |
| The role of PR-Set7 in replication licensing depends on Suv4-20h DB Beck, A Burton, H Oda, C Ziegler-Birling, ME Torres-Padilla, ... Genes & development 26 (23), 2580-2589, 2012 | 139 | 2012 |
| Adult-onset autoinflammation caused by somatic mutations in UBA1: a Dutch case series of patients with VEXAS CI van der Made, J Potjewijd, A Hoogstins, HPJ Willems, AJ Kwakernaak, ... Journal of Allergy and Clinical Immunology 149 (1), 432-439. e4, 2022 | 128 | 2022 |
| Ruxolitinib is more effective than other JAK inhibitors to treat VEXAS syndrome: a retrospective multicenter study M Heiblig, MA Ferrada, MT Koster, T Barba, M Gerfaud-Valentin, ... Blood, The Journal of the American Society of Hematology 140 (8), 927-931, 2022 | 112 | 2022 |
| Estimated prevalence and clinical manifestations of UBA1 variants associated with VEXAS syndrome in a clinical population DB Beck, DL Bodian, V Shah, UL Mirshahi, J Kim, Y Ding, SJ Magaziner, ... Jama 329 (4), 318-324, 2023 | 81 | 2023 |
| Clinical heterogeneity of the VEXAS syndrome: a case series MJ Koster, T Kourelis, KK Reichard, TA Kermani, DB Beck, DO Cardona, ... Mayo Clinic Proceedings 96 (10), 2653-2659, 2021 | 75 | 2021 |
| The Role of Host Genetic Factors in Coronavirus Susceptibility: Review of Animal and Systematic Review of Human Literature M LoPresti, DB Beck, P Duggal, DAT Cummings, BD Solomon medRxiv, 2020 | 73 | 2020 |
| Second case of HOIP deficiency expands clinical features and defines inflammatory transcriptome regulated by LUBAC H Oda, DB Beck, HS Kuehn, N Sampaio Moura, P Hoffmann, M Ibarra, ... Frontiers in immunology 10, 479, 2019 | 71 | 2019 |
| Translation of cytoplasmic UBA1 contributes to VEXAS syndrome pathogenesis MA Ferrada, S Savic, DO Cardona, JC Collins, H Alessi, ... Blood, The Journal of the American Society of Hematology 140 (13), 1496-1506, 2022 | 66 | 2022 |
| Delineation of a human Mendelian disorder of the DNA demethylation machinery: TET3 deficiency DB Beck, A Petracovici, C He, HW Moore, RJ Louie, M Ansar, S Douzgou, ... The American Journal of Human Genetics 106 (2), 234-245, 2020 | 65 | 2020 |
