Works by Schlesner, Matthias


Results: 69
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    Recurrent mutation of the ID3 gene in Burkitt lymphoma identified by integrated genome, exome and transcriptome sequencing.

    Published in:
    Nature Genetics, 2012, v. 44, n. 12, p. 1316, doi. 10.1038/ng.2469
    By:
    • Richter, Julia;
    • Schlesner, Matthias;
    • Hoffmann, Steve;
    • Kreuz, Markus;
    • Leich, Ellen;
    • Burkhardt, Birgit;
    • Rosolowski, Maciej;
    • Ammerpohl, Ole;
    • Wagener, Rabea;
    • Bernhart, Stephan H;
    • Lenze, Dido;
    • Szczepanowski, Monika;
    • Paulsen, Maren;
    • Lipinski, Simone;
    • Russell, Robert B;
    • Adam-Klages, Sabine;
    • Apic, Gordana;
    • Claviez, Alexander;
    • Hasenclever, Dirk;
    • Hovestadt, Volker
    Publication type:
    Article
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    The genomic and transcriptional landscape of primary central nervous system lymphoma.

    Published in:
    Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-30050-y
    By:
    • Radke, Josefine;
    • Ishaque, Naveed;
    • Koll, Randi;
    • Gu, Zuguang;
    • Schumann, Elisa;
    • Sieverling, Lina;
    • Uhrig, Sebastian;
    • Hübschmann, Daniel;
    • Toprak, Umut H.;
    • López, Cristina;
    • Hostench, Xavier Pastor;
    • Borgoni, Simone;
    • Juraeva, Dilafruz;
    • Pritsch, Fabienne;
    • Paramasivam, Nagarajan;
    • Balasubramanian, Gnana Prakash;
    • Schlesner, Matthias;
    • Sahay, Shashwat;
    • Weniger, Marc;
    • Pehl, Debora
    Publication type:
    Article
    8

    The chromosomal translocation t(1;6)(p35.3;p25.2), recurrent in chronic lymphocytic leukaemia, leads to RCC1::IRF4 fusion.

    Published in:
    British Journal of Haematology, 2024, v. 205, n. 6, p. 2321, doi. 10.1111/bjh.19790
    By:
    • Jayne, Sandrine;
    • López, Cristina;
    • Put, Natalie;
    • Nagel, Inga;
    • Lierman, Els;
    • Penas, Eva Maria Murga;
    • Michaux, Lucienne;
    • Ahearne, Matthew J.;
    • Walter, Harriet S.;
    • Bens, Susanne;
    • Drewes, Cosima;
    • Szczepanowski, Monika;
    • Schlesner, Matthias;
    • Rosenstiel, Philip;
    • Wlodarska, Iwona;
    • Siebert, Reiner;
    • Dyer, Martin J. S.
    Publication type:
    Article
    9

    The chromosomal translocation t(1;6)(p35.3;p25.2), recurrent in chronic lymphocytic leukaemia, leads to RCC1::IRF4 fusion.

    Published in:
    British Journal of Haematology, 2024, v. 205, n. 6, p. 2321, doi. 10.1111/bjh.19790
    By:
    • Jayne, Sandrine;
    • López, Cristina;
    • Put, Natalie;
    • Nagel, Inga;
    • Lierman, Els;
    • Penas, Eva Maria Murga;
    • Michaux, Lucienne;
    • Ahearne, Matthew J.;
    • Walter, Harriet S.;
    • Bens, Susanne;
    • Drewes, Cosima;
    • Szczepanowski, Monika;
    • Schlesner, Matthias;
    • Rosenstiel, Philip;
    • Wlodarska, Iwona;
    • Siebert, Reiner;
    • Dyer, Martin J. S.
    Publication type:
    Article
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    Temporal multi-omics identifies LRG1 as a vascular niche instructor of metastasis.

    Published in:
    Science Translational Medicine, 2021, v. 13, n. 609, p. 1, doi. 10.1126/scitranslmed.abe6805
    By:
    • Singhal, Mahak;
    • Gengenbacher, Nicolas;
    • Abdul Pari, Ashik Ahmed;
    • Kamiyama, Miki;
    • Hai, Ling;
    • Kuhn, Bianca J.;
    • Kallenberg, David M.;
    • Kulkarni, Shubhada R.;
    • Camilli, Carlotta;
    • Preuß, Stephanie F.;
    • Leuchs, Barbara;
    • Mogler, Carolin;
    • Espinet, Elisa;
    • Besemfelder, Eva;
    • Heide, Danijela;
    • Heikenwalder, Mathias;
    • Sprick, Martin R.;
    • Trumpp, Andreas;
    • Krijgsveld, Jeroen;
    • Schlesner, Matthias
    Publication type:
    Article
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    DDX3X mutations in two girls with a phenotype overlapping Toriello-Carey syndrome.

    Published in:
    American Journal of Medical Genetics. Part A, 2017, v. 173, n. 5, p. 1369, doi. 10.1002/ajmg.a.38164
    By:
    • Dikow, Nicola;
    • Granzow, Martin;
    • Graul‐Neumann, Luitgard M.;
    • Karch, Stephanie;
    • Hinderhofer, Katrin;
    • Paramasivam, Nagarajan;
    • Behl, Laura‐Jane;
    • Kaufmann, Lilian;
    • Fischer, Christine;
    • Evers, Christina;
    • Schlesner, Matthias;
    • Eils, Roland;
    • Borck, Guntram;
    • Zweier, Christiane;
    • Bartram, Claus R.;
    • Carey, John C.;
    • Moog, Ute
    Publication type:
    Article
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    Prenatal maternal stress and wheeze in children: novel insights into epigenetic regulation.

    Published in:
    Scientific Reports, 2016, p. 28616, doi. 10.1038/srep28616
    By:
    • Trump, Saskia;
    • Bieg, Matthias;
    • Gu, Zuguang;
    • Thürmann, Loreen;
    • Bauer, Tobias;
    • Bauer, Mario;
    • Ishaque, Naveed;
    • Röder, Stefan;
    • Gu, Lei;
    • Herberth, Gunda;
    • Lawerenz, Christian;
    • Borte, Michael;
    • Schlesner, Matthias;
    • Plass, Christoph;
    • Diessl, Nicolle;
    • Eszlinger, Markus;
    • Mücke, Oliver;
    • Elvers, Horst-Dietrich;
    • Wissenbach, Dirk K.;
    • von Bergen, Martin
    Publication type:
    Article
    20

    Precision oncology based on omics data: The NCT Heidelberg experience.

    Published in:
    International Journal of Cancer, 2017, v. 141, n. 5, p. 877, doi. 10.1002/ijc.30828
    By:
    • Horak, Peter;
    • Klink, Barbara;
    • Heining, Christoph;
    • Gröschel, Stefan;
    • Hutter, Barbara;
    • Fröhlich, Martina;
    • Uhrig, Sebastian;
    • Hübschmann, Daniel;
    • Schlesner, Matthias;
    • Eils, Roland;
    • Richter, Daniela;
    • Pfütze, Katrin;
    • Geörg, Christina;
    • Meißburger, Bettina;
    • Wolf, Stephan;
    • Schulz, Angela;
    • Penzel, Roland;
    • Herpel, Esther;
    • Kirchner, Martina;
    • Lier, Amelie
    Publication type:
    Article
    21

    Integrative genomic and transcriptomic analysis of leiomyosarcoma.

    Published in:
    Nature Communications, 2018, v. 9, n. 1, p. 1, doi. 10.1038/s41467-017-02602-0
    By:
    • Chudasama, Priya;
    • Mughal, Sadaf S.;
    • Sanders, Mathijs A.;
    • Hübschmann, Daniel;
    • Inn Chung;
    • Deeg, Katharina I.;
    • Siao-Han Wong;
    • Rabe, Sophie;
    • Hlevnjak, Mario;
    • Zapatka, Marc;
    • Ernst, Aurélie;
    • Kleinheinz, Kortine;
    • Schlesner, Matthias;
    • Sieverling, Lina;
    • Klink, Barbara;
    • Schröck, Evelin;
    • Hoogenboezem, Remco M.;
    • Kasper, Bernd;
    • Heilig, Christoph E.;
    • Egerer, Gerlinde
    Publication type:
    Article
    22

    A rare large duplication of MLH1 identified in Lynch syndrome.

    Published in:
    Hereditary Cancer in Clinical Practice, 2021, v. 19, n. 1, p. 1, doi. 10.1186/s13053-021-00167-0
    By:
    • Kumar, Abhishek;
    • Paramasivam, Nagarajan;
    • Bandapalli, Obul Reddy;
    • Schlesner, Matthias;
    • Chen, Tianhui;
    • Sijmons, Rolf;
    • Dymerska, Dagmara;
    • Golebiewska, Katarzyna;
    • Kuswik, Magdalena;
    • Lubinski, Jan;
    • Hemminki, Kari;
    • Försti, Asta
    Publication type:
    Article
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    Putative second hit rare genetic variants in families with seemingly GBA-associated Parkinson's disease.

    Published in:
    NPJ Genomic Medicine, 2021, v. 6, n. 1, p. 1, doi. 10.1038/s41525-020-00163-8
    By:
    • Aslam, Muhammad;
    • Kandasamy, Nirosiya;
    • Ullah, Anwar;
    • Paramasivam, Nagarajan;
    • Öztürk, Mehmet Ali;
    • Naureen, Saima;
    • Arshad, Abida;
    • Badshah, Mazhar;
    • Khan, Kafaitullah;
    • Wajid, Muhammad;
    • Abbasi, Rashda;
    • Ilyas, Muhammad;
    • Eils, Roland;
    • Schlesner, Matthias;
    • Wade, Rebecca C.;
    • Ahmad, Nafees;
    • von Engelhardt, Jakob
    Publication type:
    Article
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    Cell segmentation-free inference of cell types from in situ transcriptomics data.

    Published in:
    Nature Communications, 2021, v. 12, p. 1, doi. 10.1038/s41467-021-23807-4
    By:
    • Park, Jeongbin;
    • Choi, Wonyl;
    • Tiesmeyer, Sebastian;
    • Long, Brian;
    • Borm, Lars E.;
    • Garren, Emma;
    • Nguyen, Thuc Nghi;
    • Tasic, Bosiljka;
    • Codeluppi, Simone;
    • Graf, Tobias;
    • Schlesner, Matthias;
    • Stegle, Oliver;
    • Eils, Roland;
    • Ishaque, Naveed
    Publication type:
    Article
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    Cell segmentation-free inference of cell types from in situ transcriptomics data.

    Published in:
    Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-23807-4
    By:
    • Park, Jeongbin;
    • Choi, Wonyl;
    • Tiesmeyer, Sebastian;
    • Long, Brian;
    • Borm, Lars E.;
    • Garren, Emma;
    • Nguyen, Thuc Nghi;
    • Tasic, Bosiljka;
    • Codeluppi, Simone;
    • Graf, Tobias;
    • Schlesner, Matthias;
    • Stegle, Oliver;
    • Eils, Roland;
    • Ishaque, Naveed
    Publication type:
    Article
    29

    Cell segmentation-free inference of cell types from in situ transcriptomics data.

    Published in:
    Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-23807-4
    By:
    • Park, Jeongbin;
    • Choi, Wonyl;
    • Tiesmeyer, Sebastian;
    • Long, Brian;
    • Borm, Lars E.;
    • Garren, Emma;
    • Nguyen, Thuc Nghi;
    • Tasic, Bosiljka;
    • Codeluppi, Simone;
    • Graf, Tobias;
    • Schlesner, Matthias;
    • Stegle, Oliver;
    • Eils, Roland;
    • Ishaque, Naveed
    Publication type:
    Article
    30

    Framework for quality assessment of whole genome cancer sequences.

    Published in:
    Nature Communications, 2020, v. 11, n. 1, p. N.PAG, doi. 10.1038/s41467-020-18688-y
    By:
    • Whalley, Justin P.;
    • Buchhalter, Ivo;
    • Rheinbay, Esther;
    • Raine, Keiran M.;
    • Stobbe, Miranda D.;
    • Kleinheinz, Kortine;
    • Werner, Johannes;
    • Beltran, Sergi;
    • Gut, Marta;
    • Hübschmann, Daniel;
    • Hutter, Barbara;
    • Livitz, Dimitri;
    • Perry, Marc D.;
    • Rosenberg, Mara;
    • Saksena, Gordon;
    • Trotta, Jean-Rémi;
    • Eils, Roland;
    • Gerhard, Daniela S.;
    • Campbell, Peter J.;
    • Schlesner, Matthias
    Publication type:
    Article
    31

    Cancer Predisposition Genes in Cancer-Free Families.

    Published in:
    Cancers, 2020, v. 12, n. 10, p. 2770, doi. 10.3390/cancers12102770
    By:
    • Zheng, Guoqiao;
    • Catalano, Calogerina;
    • Bandapalli, Obul Reddy;
    • Paramasivam, Nagarajan;
    • Chattopadhyay, Subhayan;
    • Schlesner, Matthias;
    • Sijmons, Rolf;
    • Hemminki, Akseli;
    • Dymerska, Dagmara;
    • Lubinski, Jan;
    • Hemminki, Kari;
    • Försti, Asta
    Publication type:
    Article
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    T‐cell prolymphocytic leukemia is associated with deregulation of oncogenic microRNAs on transcriptional and epigenetic level.

    Published in:
    Genes, Chromosomes & Cancer, 2022, v. 61, n. 7, p. 432, doi. 10.1002/gcc.23034
    By:
    • Patil, Paurnima;
    • Hillebrecht, Sina;
    • Chteinberg, Emil;
    • López, Cristina;
    • Toprak, Umut H.;
    • Seufert, Julian;
    • Bernhart, Stephan H.;
    • Kretzmer, Helene;
    • Bergmann, Anke K.;
    • Bens, Susanne;
    • Högel, Josef;
    • Müller, Annika;
    • Jebaraj, Billy Michael;
    • Schrader, Alexandra;
    • Johansson, Patricia;
    • Costa, Dolors;
    • Schlesner, Matthias;
    • Dürig, Jan;
    • Herling, Marco;
    • Campo, Elias
    Publication type:
    Article
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    The PCBP1 gene encoding poly(rc) binding protein i is recurrently mutated in Burkitt lymphoma.

    Published in:
    Genes, Chromosomes & Cancer, 2015, v. 54, n. 9, p. 555, doi. 10.1002/gcc.22268
    By:
    • Wagener, Rabea;
    • Aukema, Sietse M.;
    • Schlesner, Matthias;
    • Haake, Andrea;
    • Burkhardt, Birgit;
    • Claviez, Alexander;
    • Drexler, Hans G.;
    • Hummel, Michael;
    • Kreuz, Markus;
    • Loeffler, Markus;
    • Rosolowski, Maciej;
    • López, Cristina;
    • Möller, Peter;
    • Richter, Julia;
    • Rohde, Marius;
    • Betts, Matthew J.;
    • Russell, Robert B.;
    • Bernhart, Stephan H.;
    • Hoffmann, Steve;
    • Rosenstiel, Philip
    Publication type:
    Article
    36

    Recurrent RHOA mutations in pediatric Burkitt lymphoma treated according to the NHL-BFM protocols.

    Published in:
    Genes, Chromosomes & Cancer, 2014, v. 53, n. 11, p. 911, doi. 10.1002/gcc.22202
    By:
    • Rohde, Marius;
    • Richter, Julia;
    • Schlesner, Matthias;
    • Betts, Matthew J.;
    • Claviez, Alexander;
    • Bonn, Bettina R.;
    • Zimmermann, Martin;
    • Damm‐Welk, Christine;
    • Russell, Robert B.;
    • Borkhardt, Arndt;
    • Eils, Roland;
    • Hoell, Jessica I.;
    • Szczepanowski, Monika;
    • Oschlies, Ilske;
    • Klapper, Wolfram;
    • Burkhardt, Birgit;
    • Siebert, Reiner
    Publication type:
    Article
    37

    Genetic lesions of the TRAF3 and MAP3K14 genes in classical Hodgkin lymphoma.

    Published in:
    British Journal of Haematology, 2012, v. 157, n. 6, p. 702, doi. 10.1111/j.1365-2141.2012.09113.x
    By:
    • Otto, Claudia;
    • Giefing, Maciej;
    • Massow, Anne;
    • Vater, Inga;
    • Gesk, Stefan;
    • Schlesner, Matthias;
    • Richter, Julia;
    • Klapper, Wolfram;
    • Hansmann, Martin-Leo;
    • Siebert, Reiner;
    • Küppers, Ralf
    Publication type:
    Article
    38

    PerSurge (NOA-30) phase II trial of perampanel treatment around surgery in patients with progressive glioblastoma.

    Published in:
    BMC Cancer, 2024, v. 24, n. 1, p. 1, doi. 10.1186/s12885-024-11846-1
    By:
    • Heuer, Sophie;
    • Burghaus, Ina;
    • Gose, Maria;
    • Kessler, Tobias;
    • Sahm, Felix;
    • Vollmuth, Philipp;
    • Venkataramani, Varun;
    • Hoffmann, Dirk;
    • Schlesner, Matthias;
    • Ratliff, Miriam;
    • Hopf, Carsten;
    • Herrlinger, Ulrich;
    • Ricklefs, Franz;
    • Bendszus, Martin;
    • Krieg, Sandro M.;
    • Wick, Antje;
    • Wick, Wolfgang;
    • Winkler, Frank
    Publication type:
    Article
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    Characterization of rare germline variants in familial multiple myeloma.

    Published in:
    2021
    By:
    • Catalano, Calogerina;
    • Paramasivam, Nagarajan;
    • Blocka, Joanna;
    • Giangiobbe, Sara;
    • Huhn, Stefanie;
    • Schlesner, Matthias;
    • Weinhold, Niels;
    • Sijmons, Rolf;
    • de Jong, Mirjam;
    • Langer, Christian;
    • Preuss, Klaus-Dieter;
    • Nilsson, Björn;
    • Durie, Brian;
    • Goldschmidt, Hartmut;
    • Bandapalli, Obul Reddy;
    • Hemminki, Kari;
    • Försti, Asta
    Publication type:
    Correction Notice
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    Pheno-seq – linking visual features and gene expression in 3D cell culture systems.

    Published in:
    Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-48771-4
    By:
    • Tirier, Stephan M.;
    • Park, Jeongbin;
    • Preußer, Friedrich;
    • Amrhein, Lisa;
    • Gu, Zuguang;
    • Steiger, Simon;
    • Mallm, Jan-Philipp;
    • Krieger, Teresa;
    • Waschow, Marcel;
    • Eismann, Björn;
    • Gut, Marta;
    • Gut, Ivo G.;
    • Rippe, Karsten;
    • Schlesner, Matthias;
    • Theis, Fabian;
    • Fuchs, Christiane;
    • Ball, Claudia R.;
    • Glimm, Hanno;
    • Eils, Roland;
    • Conrad, Christian
    Publication type:
    Article
    49

    Investigation of Rare Non-Coding Variants in Familial Multiple Myeloma.

    Published in:
    Cells (2073-4409), 2023, v. 12, n. 1, p. 96, doi. 10.3390/cells12010096
    By:
    • Niazi, Yasmeen;
    • Paramasivam, Nagarajan;
    • Blocka, Joanna;
    • Kumar, Abhishek;
    • Huhn, Stefanie;
    • Schlesner, Matthias;
    • Weinhold, Niels;
    • Sijmons, Rolf;
    • De Jong, Mirjam;
    • Durie, Brian;
    • Goldschmidt, Hartmut;
    • Hemminki, Kari;
    • Försti, Asta
    Publication type:
    Article
    50

    Genomic footprints of activated telomere maintenance mechanisms in cancer.

    Published in:
    Nature Communications, 2020, v. 11, n. 1, p. 1, doi. 10.1038/s41467-019-13824-9
    By:
    • Sieverling, Lina;
    • Hong, Chen;
    • Koser, Sandra D.;
    • Ginsbach, Philip;
    • Kleinheinz, Kortine;
    • Hutter, Barbara;
    • Braun, Delia M.;
    • Cortés-Ciriano, Isidro;
    • Xi, Ruibin;
    • Kabbe, Rolf;
    • Park, Peter J.;
    • Eils, Roland;
    • Schlesner, Matthias;
    • PCAWG-Structural Variation Working Group;
    • Akdemir, Kadir C.;
    • Alvarez, Eva G.;
    • Baez-Ortega, Adrian;
    • Beroukhim, Rameen;
    • Boutros, Paul C.;
    • Bowtell, David D. L.
    Publication type:
    Article