Pesquisa | Biblioteca Virtual em Saúde

1.

Mesenchymal Hamartoma of the Liver and DICER1 Syndrome.

Apellaniz-Ruiz, Maria; Segni, Maria; Kettwig, Matthias; Glüer, Sylvia; Pelletier, Dylan; Nguyen, Van-Hung; Wagener, Rabea; López, Cristina; Muchantef, Karl; Bouron-Dal Soglio, Dorothée; Sabbaghian, Nelly; Wu, Mona K; Zannella, Stefano; Fabian, Marc R; Siebert, Reiner; Menke, Jan; Priest, John R; Foulkes, William D.

N Engl J Med; 380(19): 1834-1842, 2019 05 09.

Artigo em Inglês | MEDLINE | ID: mdl-31067372

2.

The mutational landscape of Burkitt-like lymphoma with 11q aberration is distinct from that of Burkitt lymphoma.

Wagener, Rabea; Seufert, Julian; Raimondi, Francesco; Bens, Susanne; Kleinheinz, Kortine; Nagel, Inga; Altmüller, Janine; Thiele, Holger; Hübschmann, Daniel; Kohler, Christian W; Nürnberg, Peter; Au-Yeung, Rex; Burkhardt, Birgit; Horn, Heike; Leoncini, Lorenzo; Jaffe, Elaine S; Ott, German; Rymkiewicz, Grzegorz; Schlesner, Matthias; Russell, Robert B; Klapper, Wolfram; Siebert, Reiner.

Blood; 133(9): 962-966, 2019 02 28.

Artigo em Inglês | MEDLINE | ID: mdl-30567752

3.

IG-MYC ⁺ neoplasms with precursor B-cell phenotype are molecularly distinct from Burkitt lymphomas.

Wagener, Rabea; López, Cristina; Kleinheinz, Kortine; Bausinger, Julia; Aukema, Sietse M; Nagel, Inga; Toprak, Umut H; Seufert, Julian; Altmüller, Janine; Thiele, Holger; Schneider, Christof; Kolarova, Julia; Park, Jeongbin; Hübschmann, Daniel; Murga Penas, Eva M; Drexler, Hans G; Attarbaschi, Andishe; Hovland, Randi; Kjeldsen, Eigil; Kneba, Michael; Kontny, Udo; de Leval, Laurence; Nürnberg, Peter; Oschlies, Ilske; Oscier, David; Schlegelberger, Brigitte; Stilgenbauer, Stephan; Wössmann, Wilhelm; Schlesner, Matthias; Burkhardt, Birgit; Klapper, Wolfram; Jaffe, Elaine S; Küppers, Ralf; Siebert, Reiner.

Blood; 132(21): 2280-2285, 2018 Nov 22.

Artigo em Inglês | MEDLINE | ID: mdl-30282799

4.

Reconstruction of rearranged T-cell receptor loci by whole genome and transcriptome sequencing gives insights into the initial steps of T-cell prolymphocytic leukemia.

Patil, Paurnima; Cieslak, Agata; Bernhart, Stephan H; Toprak, Umut H; Wagener, Rabea; López, Cristina; Wiehle, Laura; Bens, Susanne; Altmüller, Janine; Franitza, Marek; Scholz, Ingrid; Jayne, Sandrine; Ahearne, Matthew J; Scheffold, Annika; Jebaraj, Billy M C; Schneider, Christof; Costa, Dolors; Braun, Till; Schrader, Alexandra; Campo, Elias; Dyer, Martin J S; Nürnberg, Peter; Dürig, Jan; Johansson, Patricia; Böttcher, Sebastian; Schlesner, Matthias; Herling, Marco; Stilgenbauer, Stephan; Macintyre, Elizabeth; Siebert, Reiner.

Genes Chromosomes Cancer; 2019 Nov 02.

Artigo em Inglês | MEDLINE | ID: mdl-31677197

5.

DIEGO: detection of differential alternative splicing using Aitchison's geometry.

Doose, Gero; Bernhart, Stephan H; Wagener, Rabea; Hoffmann, Steve.

Bioinformatics; 34(6): 1066-1068, 2018 03 15.

Artigo em Inglês | MEDLINE | ID: mdl-29088309

6.

Array-based profiling of the lymphoma cell DNA methylome does not unequivocally distinguish primary lymphomas of the central nervous system from non-CNS diffuse large B-cell lymphomas.

Vogt, Julia; Wagener, Rabea; Montesinos-Rongen, Manuel; Ammerpohl, Ole; Paulus, Werner; Deckert, Martina; Siebert, Reiner.

Genes Chromosomes Cancer; 2018 Oct 03.

Artigo em Inglês | MEDLINE | ID: mdl-30284345

7.

Multiple DICER1-related tumors in a child with a large interstitial 14q32 deletion.

de Kock, Leanne; Geoffrion, Dominique; Rivera, Barbara; Wagener, Rabea; Sabbaghian, Nelly; Bens, Susanne; Ellezam, Benjamin; Bouron-Dal Soglio, Dorothée; Ordóñez, Jessica; Sacharow, Stephanie; Polo Nieto, Jose Fernando; Guillerman, R Paul; Vujanic, Gordan M; Priest, John R; Siebert, Reiner; Foulkes, William D.

Genes Chromosomes Cancer; 57(5): 223-230, 2018 05.

Artigo em Inglês | MEDLINE | ID: mdl-29315962

8.

A recurrent 11q aberration pattern characterizes a subset of MYC-negative high-grade B-cell lymphomas resembling Burkitt lymphoma.

Salaverria, Itziar; Martin-Guerrero, Idoia; Wagener, Rabea; Kreuz, Markus; Kohler, Christian W; Richter, Julia; Pienkowska-Grela, Barbara; Adam, Patrick; Burkhardt, Birgit; Claviez, Alexander; Damm-Welk, Christine; Drexler, Hans G; Hummel, Michael; Jaffe, Elaine S; Küppers, Ralf; Lefebvre, Christine; Lisfeld, Jasmin; Löffler, Markus; Macleod, Roderick A F; Nagel, Inga; Oschlies, Ilske; Rosolowski, Maciej; Russell, Robert B; Rymkiewicz, Grzegorz; Schindler, Detlev; Schlesner, Matthias; Scholtysik, René; Schwaenen, Carsten; Spang, Rainer; Szczepanowski, Monika; Trümper, Lorenz; Vater, Inga; Wessendorf, Swen; Klapper, Wolfram; Siebert, Reiner.

Blood; 123(8): 1187-98, 2014 Feb 20.

Artigo em Inglês | MEDLINE | ID: mdl-24398325

9.

The PCBP1 gene encoding poly(rC) binding protein I is recurrently mutated in Burkitt lymphoma.

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; Schilhabel, Markus; Szczepanowski, Monika; Trümper, Lorenz; Klapper, Wolfram; Siebert, Reiner.

Genes Chromosomes Cancer; 54(9): 555-64, 2015 Sep.

Artigo em Inglês | MEDLINE | ID: mdl-26173642

10.

Further evidence that full gene deletions of DICER1 predispose to DICER1 syndrome.

de Kock, Leanne; Hillmer, Morten; Wagener, Rabea; Soglio, Dorothée Bouron-Dal; Sabbaghian, Nelly; Siebert, Reiner; Priest, John R; Miller, Michal; Foulkes, William D.

Genes Chromosomes Cancer; 58(8): 602-604, 2019 08.

Artigo em Inglês | MEDLINE | ID: mdl-30597651

11.

Cryptic insertion of MYC exons 2 and 3 into the IGH locus detected by whole genome sequencing in a case of MYC-negative Burkitt lymphoma.

Wagener, Rabea; Bens, Susanne; Toprak, Umut H; Seufert, Julian; López, Cristina; Scholz, Ingrid; Herbrueggen, Heidi; Oschlies, Ilske; Stilgenbauer, Stephan; Schlesner, Matthias; Klapper, Wolfram; Burkhardt, Birgit; Siebert, Reiner.

Haematologica; 2019 May 09.

Artigo em Inglês | MEDLINE | ID: mdl-31073073

12.

Immunohistochemical detection of inhibitor of DNA binding 3 mutational variants in mature aggressive B-cell lymphoma.

Szczepanowski, Monika; Masqué-Soler, Neus; Schlesner, Matthias; Haake, Andrea; Richter, Julia; Wagener, Rabea; Burkhardt, Birgit; Kreuz, Markus; Siebert, Reiner; Klapper, Wolfram.

Haematologica; 101(6): e259-61, 2016 06.

Artigo em Inglês | MEDLINE | ID: mdl-26992947

13.

MDM4 Is Targeted by 1q Gain and Drives Disease in Burkitt Lymphoma.

Hüllein, Jennifer; Slabicki, Mikolaj; Rosolowski, Maciej; Jethwa, Alexander; Habringer, Stefan; Tomska, Katarzyna; Kurilov, Roma; Lu, Junyan; Scheinost, Sebastian; Wagener, Rabea; Huang, Zhiqin; Lukas, Marina; Yavorska, Olena; Helfrich, Hanne; Scholtysik, René; Bonneau, Kyle; Tedesco, Donato; Küppers, Ralf; Klapper, Wolfram; Pott, Christiane; Stilgenbauer, Stephan; Burkhardt, Birgit; Löffler, Markus; Trümper, Lorenz H; Hummel, Michael; Brors, Benedikt; Zapatka, Marc; Siebert, Reiner; Kreuz, Markus; Keller, Ulrich; Huber, Wolfgang; Zenz, Thorsten.

Cancer Res; 79(12): 3125-3138, 2019 Jun 15.

Artigo em Inglês | MEDLINE | ID: mdl-31000522

14.

Genomic and transcriptomic changes complement each other in the pathogenesis of sporadic Burkitt lymphoma.

López, Cristina; Kleinheinz, Kortine; Aukema, Sietse M; Rohde, Marius; Bernhart, Stephan H; Hübschmann, Daniel; Wagener, Rabea; Toprak, Umut H; Raimondi, Francesco; Kreuz, Markus; Waszak, Sebastian M; Huang, Zhiqin; Sieverling, Lina; Paramasivam, Nagarajan; Seufert, Julian; Sungalee, Stephanie; Russell, Robert B; Bausinger, Julia; Kretzmer, Helene; Ammerpohl, Ole; Bergmann, Anke K; Binder, Hans; Borkhardt, Arndt; Brors, Benedikt; Claviez, Alexander; Doose, Gero; Feuerbach, Lars; Haake, Andrea; Hansmann, Martin-Leo; Hoell, Jessica; Hummel, Michael; Korbel, Jan O; Lawerenz, Chris; Lenze, Dido; Radlwimmer, Bernhard; Richter, Julia; Rosenstiel, Philip; Rosenwald, Andreas; Schilhabel, Markus B; Stein, Harald; Stilgenbauer, Stephan; Stadler, Peter F; Szczepanowski, Monika; Weniger, Marc A; Zapatka, Marc; Eils, Roland; Lichter, Peter; Loeffler, Markus; Möller, Peter; Trümper, Lorenz.

Nat Commun; 10(1): 1459, 2019 03 29.

Artigo em Inglês | MEDLINE | ID: mdl-30926794

15.

Sellar Region Atypical Teratoid/Rhabdoid Tumors (ATRT) in Adults Display DNA Methylation Profiles of the ATRT-MYC Subgroup.

Johann, Pascal D; Bens, Susanne; Oyen, Florian; Wagener, Rabea; Giannini, Caterina; Perry, Arie; Raisanen, Jack M; Reis, Gerald F; Nobusawa, Sumihito; Arita, Kazunori; Felsberg, Jörg; Reifenberger, Guido; Agaimy, Abbas; Buslei, Rolf; Capper, David; Pfister, Stefan M; Schneppenheim, Reinhard; Siebert, Reiner; Frühwald, Michael C; Paulus, Werner; Kool, Marcel; Hasselblatt, Martin.

Am J Surg Pathol; 42(4): 506-511, 2018 Apr.

Artigo em Inglês | MEDLINE | ID: mdl-29324471

16.

Opposing Effects of CREBBP Mutations Govern the Phenotype of Rubinstein-Taybi Syndrome and Adult SHH Medulloblastoma.

Merk, Daniel J; Ohli, Jasmin; Merk, Natalie D; Thatikonda, Venu; Morrissy, Sorana; Schoof, Melanie; Schmid, Susanne N; Harrison, Luke; Filser, Severin; Ahlfeld, Julia; Erkek, Serap; Raithatha, Kaamini; Andreska, Thomas; Weißhaar, Marc; Launspach, Michael; Neumann, Julia E; Shakarami, Mehdi; Plenker, Dennis; Marra, Marco A; Li, Yisu; Mungall, Andrew J; Moore, Richard A; Ma, Yussanne; Jones, Steven J M; Lutz, Beat; Ertl-Wagner, Birgit; Rossi, Andrea; Wagener, Rabea; Siebert, Reiner; Jung, Andreas; Eberhart, Charles G; Lach, Boleslaw; Sendtner, Michael; Pfister, Stefan M; Taylor, Michael D; Chavez, Lukas; Kool, Marcel; Schüller, Ulrich.

Dev Cell; 44(6): 709-724.e6, 2018 03 26.

Artigo em Inglês | MEDLINE | ID: mdl-29551561

17.

Functionally Null RAD51D Missense Mutation Associates Strongly with Ovarian Carcinoma.

Rivera, Barbara; Di Iorio, Massimo; Frankum, Jessica; Nadaf, Javad; Fahiminiya, Somayyeh; Arcand, Suzanna L; Burk, David L; Grapton, Damien; Tomiak, Eva; Hastings, Valerie; Hamel, Nancy; Wagener, Rabea; Aleynikova, Olga; Giroux, Sylvie; Hamdan, Fadi F; Dionne-Laporte, Alexandre; Zogopoulos, George; Rousseau, Francois; Berghuis, Albert M; Provencher, Diane; Rouleau, Guy A; Michaud, Jacques L; Mes-Masson, Anne-Marie; Majewski, Jacek; Bens, Susanne; Siebert, Reiner; Narod, Steven A; Akbari, Mohammad R; Lord, Christopher J; Tonin, Patricia N; Orthwein, Alexandre; Foulkes, William D.

Cancer Res; 77(16): 4517-4529, 2017 08 15.

Artigo em Inglês | MEDLINE | ID: mdl-28646019

18.

DNA methylome analysis in Burkitt and follicular lymphomas identifies differentially methylated regions linked to somatic mutation and transcriptional control.

Kretzmer, Helene; Bernhart, Stephan H; Wang, Wei; Haake, Andrea; Weniger, Marc A; Bergmann, Anke K; Betts, Matthew J; Carrillo-de-Santa-Pau, Enrique; Doose, Gero; Gutwein, Jana; Richter, Julia; Hovestadt, Volker; Huang, Bingding; Rico, Daniel; Jühling, Frank; Kolarova, Julia; Lu, Qianhao; Otto, Christian; Wagener, Rabea; Arnolds, Judith; Burkhardt, Birgit; Claviez, Alexander; Drexler, Hans G; Eberth, Sonja; Eils, Roland; Flicek, Paul; Haas, Siegfried; Humme, Michael; Karsch, Dennis; Kerstens, Hinrik H D; Klapper, Wolfram; Kreuz, Markus; Lawerenz, Chris; Lenzek, Dido; Loeffler, Markus; López, Cristina; MacLeod, Roderick A F; Martens, Joost H A; Kulis, Marta; Martín-Subero, José Ignacio; Möller, Peter; Nage, Inga; Picelli, Simone; Vater, Inga; Rohde, Marius; Rosenstiel, Philip; Rosolowski, Maciej; Russell, Robert B; Schilhabel, Markus; Schlesner, Matthias.

Nat Genet; 47(11): 1316-1325, 2015 Nov.

Artigo em Inglês | MEDLINE | ID: mdl-26437030

19.

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

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; Hornig, Nadine; Korbel, Jan O; Kube, Dieter; Langenberger, David; Lawerenz, Chris; Lisfeld, Jasmin; Meyer, Katharina; Picelli, Simone; Pischimarov, Jordan; Radlwimmer, Bernhard; Rausch, Tobias; Rohde, Marius; Schilhabel, Markus; Scholtysik, René; Spang, Rainer; Trautmann, Heiko; Zenz, Thorsten; Borkhardt, Arndt; Drexler, Hans G; Möller, Peter; MacLeod, Roderick A F; Pott, Christiane; Schreiber, Stefan; Trümper, Lorenz; Loeffler, Markus; Stadler, Peter F; Lichter, Peter; Eils, Roland; Küppers, Ralf; Hummel, Michael.

Nat Genet; 44(12): 1316-20, 2012 Dec.

Artigo em Inglês | MEDLINE | ID: mdl-23143595

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