Literature DB >> 26255151

Reply to: Familial syndromes associated with intracranial tumours: a review.

Fonnet E Bleeker1.   

Abstract

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Year:  2015        PMID: 26255151     DOI: 10.1007/s00381-015-2868-2

Source DB:  PubMed          Journal:  Childs Nerv Syst        ISSN: 0256-7040            Impact factor:   1.475


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  21 in total

1.  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
Journal:  Cell       Date:  2012-01-20       Impact factor: 41.582

2.  Biochemical and imaging surveillance in germline TP53 mutation carriers with Li-Fraumeni syndrome: a prospective observational study.

Authors:  Anita Villani; Uri Tabori; Joshua Schiffman; Adam Shlien; Joseph Beyene; Harriet Druker; Ana Novokmet; Jonathan Finlay; David Malkin
Journal:  Lancet Oncol       Date:  2011-05-19       Impact factor: 41.316

3.  TP53 alterations determine clinical subgroups and survival of patients with choroid plexus tumors.

Authors:  Uri Tabori; Adam Shlien; Berivan Baskin; Sarah Levitt; Peter Ray; Noa Alon; Cynthia Hawkins; Eric Bouffet; Malgorzata Pienkowska; Lucie Lafay-Cousin; Alexa Gozali; Nataliya Zhukova; Lisa Shane; Ignacio Gonzalez; Jonathan Finlay; David Malkin
Journal:  J Clin Oncol       Date:  2010-03-22       Impact factor: 44.544

4.  Analysis of the IDH1 codon 132 mutation in brain tumors.

Authors:  Jörg Balss; Jochen Meyer; Wolf Mueller; Andrey Korshunov; Christian Hartmann; Andreas von Deimling
Journal:  Acta Neuropathol       Date:  2008-11-05       Impact factor: 17.088

Review 5.  Constitutional mismatch repair-deficiency syndrome: have we so far seen only the tip of an iceberg?

Authors:  Katharina Wimmer; Julia Etzler
Journal:  Hum Genet       Date:  2008-08-18       Impact factor: 4.132

6.  Beyond Li Fraumeni Syndrome: clinical characteristics of families with p53 germline mutations.

Authors:  Kelly D Gonzalez; Katie A Noltner; Carolyn H Buzin; Dongqing Gu; Cindy Y Wen-Fong; Vu Q Nguyen; Jennifer H Han; Katrina Lowstuter; Jeffrey Longmate; Steve S Sommer; Jeffrey N Weitzel
Journal:  J Clin Oncol       Date:  2009-02-09       Impact factor: 44.544

Review 7.  Brain tumors and syndromes in children.

Authors:  Fonnet E Bleeker; Saskia M J Hopman; Johannes H M Merks; Cora M Aalfs; Raoul C M Hennekam
Journal:  Neuropediatrics       Date:  2014-02-17       Impact factor: 1.947

8.  Subgroup-specific prognostic implications of TP53 mutation in medulloblastoma.

Authors:  Nataliya Zhukova; Vijay Ramaswamy; Marc Remke; Elke Pfaff; David J H Shih; Dianna C Martin; Pedro Castelo-Branco; Berivan Baskin; Peter N Ray; Eric Bouffet; André O von Bueren; David T W Jones; Paul A Northcott; Marcel Kool; Dominik Sturm; Trevor J Pugh; Scott L Pomeroy; Yoon-Jae Cho; Torsten Pietsch; Marco Gessi; Stefan Rutkowski; Laszlo Bognar; Almos Klekner; Byung-Kyu Cho; Seung-Ki Kim; Kyu-Chang Wang; Charles G Eberhart; Michelle Fevre-Montange; Maryam Fouladi; Pim J French; Max Kros; Wieslawa A Grajkowska; Nalin Gupta; William A Weiss; Peter Hauser; Nada Jabado; Anne Jouvet; Shin Jung; Toshihiro Kumabe; Boleslaw Lach; Jeffrey R Leonard; Joshua B Rubin; Linda M Liau; Luca Massimi; Ian F Pollack; Young Shin Ra; Erwin G Van Meir; Karel Zitterbart; Ulrich Schüller; Rebecca M Hill; Janet C Lindsey; Ed C Schwalbe; Simon Bailey; David W Ellison; Cynthia Hawkins; David Malkin; Steven C Clifford; Andrey Korshunov; Stefan Pfister; Michael D Taylor; Uri Tabori
Journal:  J Clin Oncol       Date:  2013-07-08       Impact factor: 44.544

9.  Somatic mosaic IDH1 and IDH2 mutations are associated with enchondroma and spindle cell hemangioma in Ollier disease and Maffucci syndrome.

Authors:  Twinkal C Pansuriya; Ronald van Eijk; Pio d'Adamo; Maayke A J H van Ruler; Marieke L Kuijjer; Jan Oosting; Anne-Marie Cleton-Jansen; Jolieke G van Oosterwijk; Sofie L J Verbeke; Daniëlle Meijer; Tom van Wezel; Karolin H Nord; Luca Sangiorgi; Berkin Toker; Bernadette Liegl-Atzwanger; Mikel San-Julian; Raf Sciot; Nisha Limaye; Lars-Gunnar Kindblom; Soeren Daugaard; Catherine Godfraind; Laurence M Boon; Miikka Vikkula; Kyle C Kurek; Karoly Szuhai; Pim J French; Judith V M G Bovée
Journal:  Nat Genet       Date:  2011-11-06       Impact factor: 41.307

10.  IDH2 and TP53 mutations are correlated with gliomagenesis in a patient with Maffucci syndrome.

Authors:  Kunihiko Moriya; Mika K Kaneko; Xing Liu; Masami Hosaka; Fumiyoshi Fujishima; Jun Sakuma; Satoshi Ogasawara; Mika Watanabe; Yoji Sasahara; Shigeo Kure; Yukinari Kato
Journal:  Cancer Sci       Date:  2014-03       Impact factor: 6.518

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