Publications by authors named "Huriye Cin"

6Publications

Dissecting the genomic complexity underlying medulloblastoma.

Authors:
David T W Jones Natalie Jäger Marcel Kool Thomas Zichner Barbara Hutter Marc Sultan Yoon-Jae Cho Trevor J Pugh Volker Hovestadt Adrian M Stütz Tobias Rausch Hans-Jörg Warnatz Marina Ryzhova Sebastian Bender Dominik Sturm Sabrina Pleier Huriye Cin Elke Pfaff Laura Sieber Andrea Wittmann Marc Remke Hendrik Witt Sonja Hutter Theophilos Tzaridis Joachim Weischenfeldt Benjamin Raeder Meryem Avci Vyacheslav Amstislavskiy Marc Zapatka Ursula D Weber Qi Wang Bärbel Lasitschka Cynthia C Bartholomae Manfred Schmidt Christof von Kalle Volker Ast Chris Lawerenz Jürgen Eils Rolf Kabbe Vladimir Benes Peter van Sluis Jan Koster Richard Volckmann David Shih Matthew J Betts Robert B Russell Simona Coco Gian Paolo Tonini Ulrich Schüller Volkmar Hans Norbert Graf Yoo-Jin Kim Camelia Monoranu Wolfgang Roggendorf Andreas Unterberg Christel Herold-Mende Till Milde Andreas E Kulozik Andreas von Deimling Olaf Witt Eberhard Maass Jochen Rössler Martin Ebinger Martin U Schuhmann Michael C Frühwald Martin Hasselblatt Nada Jabado Stefan Rutkowski André O von Bueren Dan Williamson Steven C Clifford Martin G McCabe V Peter Collins Stephan Wolf Stefan Wiemann Hans Lehrach Benedikt Brors Wolfram Scheurlen Jörg Felsberg Guido Reifenberger Paul A Northcott Michael D Taylor Matthew Meyerson Scott L Pomeroy Marie-Laure Yaspo Jan O Korbel Andrey Korshunov Roland Eils Stefan M Pfister Peter Lichter

Nature 2012 Aug;488(7409):100-5

Division of Pediatric Neurooncology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, Heidelberg 69120, Germany.

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August 2012

Genome sequencing of pediatric medulloblastoma links catastrophic DNA rearrangements with TP53 mutations.

Authors:
Tobias Rausch David T W Jones Marc Zapatka Adrian M Stütz Thomas Zichner Joachim Weischenfeldt Natalie Jäger Marc Remke David Shih Paul A Northcott Elke Pfaff Jelena Tica Qi Wang Luca Massimi Hendrik Witt Sebastian Bender Sabrina Pleier Huriye Cin Cynthia Hawkins Christian Beck Andreas von Deimling Volkmar Hans Benedikt Brors Roland Eils Wolfram Scheurlen Jonathon Blake Vladimir Benes Andreas E Kulozik Olaf Witt Dianna Martin Cindy Zhang Rinnat Porat Diana M Merino Jonathan Wasserman Nada Jabado Adam Fontebasso Lars Bullinger Frank G Rücker Konstanze Döhner Hartmut Döhner Jan Koster Jan J Molenaar Rogier Versteeg Marcel Kool Uri Tabori David Malkin Andrey Korshunov Michael D Taylor Peter Lichter Stefan M Pfister Jan O Korbel

Cell 2012 Jan;148(1-2):59-71

European Molecular Biology Laboratory, Meyerhofstr. 1, 69117 Heidelberg, Germany.

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January 2012

FSTL5 is a marker of poor prognosis in non-WNT/non-SHH medulloblastoma.

Authors:
Marc Remke Thomas Hielscher Andrey Korshunov Paul A Northcott Sebastian Bender Marcel Kool Frank Westermann Axel Benner Huriye Cin Marina Ryzhova Dominik Sturm Hendrik Witt Daniel Haag Grischa Toedt Andrea Wittmann Anna Schöttler André O von Bueren Andreas von Deimling Stefan Rutkowski Wolfram Scheurlen Andreas E Kulozik Michael D Taylor Peter Lichter Stefan M Pfister

J Clin Oncol 2011 Oct 12;29(29):3852-61. Epub 2011 Sep 12.

German Cancer Research Center, Im Neuenheimer Feld 280, D-69120 Heidelberg, Germany.

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October 2011

Oncogenic FAM131B-BRAF fusion resulting from 7q34 deletion comprises an alternative mechanism of MAPK pathway activation in pilocytic astrocytoma.

Authors:
Huriye Cin Claus Meyer Ricarda Herr Wibke G Janzarik Sally Lambert David T W Jones Karine Jacob Axel Benner Hendrik Witt Marc Remke Sebastian Bender Fabian Falkenstein Ton Nu Van Anh Heike Olbrich Andreas von Deimling Arnulf Pekrun Andreas E Kulozik Astrid Gnekow Wolfram Scheurlen Olaf Witt Heymut Omran Nada Jabado V Peter Collins Tilman Brummer Rolf Marschalek Peter Lichter Andrey Korshunov Stefan M Pfister

Acta Neuropathol 2011 Jun 20;121(6):763-74. Epub 2011 Mar 20.

Division of Molecular Genetics, German Cancer Research Center, Heidelberg, Germany.

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June 2011

Functional characterization of a BRAF insertion mutant associated with pilocytic astrocytoma.

Authors:
Anja E Eisenhardt Heike Olbrich Michael Röring Wibke Janzarik Ton Nu Van Anh Huriye Cin Marc Remke Hendrik Witt Andrey Korshunov Stefan M Pfister Heymut Omran Tilman Brummer

Int J Cancer 2011 Nov 25;129(9):2297-303. Epub 2011 Jul 25.

Centre for Biological Systems Analysis (ZBSA), Albert-Ludwigs-University, Freiburg, Germany.

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November 2011

Identification and characterisation of a large senataxin (SETX) gene duplication in ataxia with ocular apraxia type 2 (AOA2).

Authors:
Larissa Arning Ludger Schöls Huriye Cin Manfred Souquet Jörg T Epplen Dagmar Timmann

Neurogenetics 2008 Oct 29;9(4):295-9. Epub 2008 Jul 29.

Department of Human Genetics, Ruhr University, Bochum, Germany.

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October 2008