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Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing.

J. Richter, M. Schlesner, S. Hoffmann, M. Kreuz, E. Leich, B. Burkhardt, M. Rosolowski, O. Ammerpohl, R. Wagener, S. Bernhart, D. Lenze, M. Szczepanowski, M. Paulsen, S. Lipinski, R. Russell, S. Adam-Klages, G. Apic, A. Claviez, D. Hasenclever, V. Hovestadt, N. Hornig, J. Korbel, D. Kube, D. Langenberger, C. Lawerenz, J. Lisfeld, K. Meyer, S. Picelli, J. Pischimarov, B. Radlwimmer, T. Rausch, M. Rohde, M. Schilhabel, R. Scholtysik, R. Spang, H. Trautmann, T. Zenz, A. Borkhardt, H. Drexler, P. Möller, R. MacLeod, C. Pott, S. Schreiber, L. Trümper, M. Loeffler, P. Stadler, P. Lichter, R. Eils, R. Küppers, M. Hummel, W. Klapper, P. Rosenstiel, A. Rosenwald, B. Brors, R. Siebert, and ICGC MMML-Seq Project. Nat Genet, 44 (12): 1316--1320 (December 2012)
DOI: 10.1038/ng.2469

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Stefan Schreiber

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Persistent symptoms and risk factors predicting prolonged time to symptom-free after SARS‑CoV‑2 infection: an analysis of the baseline examination of the German COVIDOM/NAPKON-POP cohortY. Shi, R. Strobl, C. Apfelbacher, T. Bahmer, R. Geisler, P. Heuschmann, A. Horn, H. Hoven, T. Keil, M. Krawczak and 226 other author(s). Infection, 51 (6): 1679--1694 (Dec 1, 2023)GMFilter and SXTestPlate: software tools for improving the SNPlexTM genotyping system.M. Teuber, M. Wenz, S. Schreiber, and A. Franke. BMC Bioinform., (2009)The German National Pandemic Cohort Network (NAPKON): rationale, study design and baseline characteristicsM. Schons, L. Pilgram, J. Reese, M. Stecher, G. Anton, K. Appel, T. Bahmer, A. Bartschke, C. Bellinghausen, I. Bernemann and 65 other author(s). European Journal of Epidemiology, 37 (8): 849--870 (July 2022)Genome-wide association study for colorectal cancer identifies risk polymorphisms in German familial cases and implicates MAPK signalling pathways in disease susceptibilityJ. Lascorz, A. Försti, B. Chen, S. Buch, V. Steinke, N. Rahner, E. Holinski-Feder, M. Morak, H. Schackert, H. Görgens and 24 other author(s). Carcinogenesis, 31 (9): 1612–1619 (2010)PopGen - Bevölkerungsbasierte Rekrutierung von Patienten und Kontrollen für die Untersuchung komplexer Genotyp-Phänotyp-Beziehungen (PopGen - Population-based Recruitment of Patients and Controls for the Analysis of Complex Genotype-phenotype Relationships).H. von Eller-Eberstein, M. Will, M. Krawczak, and S. Schreiber. it Inf. Technol., 49 (6): 374-380 (2007)Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing.J. Richter, M. Schlesner, S. Hoffmann, M. Kreuz, E. Leich, B. Burkhardt, M. Rosolowski, O. Ammerpohl, R. Wagener, S. Bernhart and 46 other author(s). Nat Genet, 44 (12): 1316--1320 (December 2012)Genome-wide association study of intracranial aneurysm identifies three new risk lociK. Yasuno, K. Bilguvar, P. Bijlenga, S. Low, B. Krischek, G. Auburger, M. Simon, D. Krex, Z. Arlier, N. Nayak and 59 other author(s). Nat Genet, 42 (5): 420--U69 (2010)Predictors of non-recovery from fatigue and cognitive deficits after COVID-19: a prospective, longitudinal, population-based studyT. Hartung, T. Bahmer, I. Chaplinskaya-Sobol, J. Deckert, M. Endres, K. Franzpötter, J. Geritz, K. Haeusler, G. Hein, P. Heuschmann and 20 other author(s). eClinicalMedicine, (2024)Transcriptome and genome sequencing uncovers functional variation in humansT. Lappalainen, M. Sammeth, M. Friedländer, P. Hoen, J. Monlong, M. Rivas, M. Gonzàlez-Porta, N. Kurbatova, T. Griebel, P. Ferreira and 48 other author(s). Nature, (September 2013)Reuse and integration of research data - Experiences of the NAPKON Integration CoreH. Anna-Lena, V. Jörg Janne, W. Martin, H. Wolfgang, I. Thomas, S. Stefan, H. Ralf, A. Gabriele, W. Silke, H. Johannes and 9 other author(s). (2021)

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Disambiguation of "Schreiber, Stefan"

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Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing.

Please choose a person to relate this publication to

Stefan Schreiber

Stefan Schreiber

Stefan Schreiber

Stefan Schreiber

Stefan Schreiber

Other publications of authors with the same name

Disambiguation

BibSonomy

Disambiguation of "Schreiber, Stefan"

copydeleteadd this publication to your clipboardcommunity posthistory of this postURLDOIBibTeXEndNoteAPAChicagoDIN 1505HarvardMSOffice XML Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing.

Please choose a person to relate this publication to

Stefan Schreiber

Stefan Schreiber

Stefan Schreiber

Stefan Schreiber

Stefan Schreiber

Other publications of authors with the same name

Disambiguation

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Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing.