• Issue

    Genes, Chromosomes and Cancer: Volume 58, Issue 8

    507-604
    August 2019
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ISSUE INFORMATION - TOC

Free Access

Table of Content Volume 58, Number 8, August 2019

  • Pages: 507-508
  • First Published: 01 June 2019

RESEARCH ARTICLES

5q21 deletion is often heterogeneous in prostate cancer

Martina Kluth,  Zaid Al Kilani,  Cansu Özden,  Khakan Hussein,  Sohall Frogh,  Christina Möller-Koop,  Eike Burandt,  Stefan Steurer,  Franziska Büscheck,  Frank Jacobsen,  Andreas M. Luebke,  Sarah Minner,  Maria Christina Tsourlakis,  Doris Hoeflmayer,  Corinna Wittmer,  Thorsten Schlomm,  Guido Sauter,  Ronald Simon,  Waldemar Wilczak, 
  • Pages: 509-515
  • First Published: 09 January 2019

Newly diagnosed multiple myeloma patients carrying monoallelic deletion of the whole locus of immunoglobulin heavy chain gene have a better prognosis compared to those with t(4;14) and t(14;16)

Adrian Duek,  Luba Trakhtenbrot,  Ninette Amariglio,  Noam Benyamini,  Itay Zilbershats,  Chezi Ganzel,  Olga Shevetz,  Ronit Leiba,  Gabriela Rozic,  Arnon Nagler,  Merav Leiba, 
  • Pages: 516-520
  • First Published: 24 January 2019

Early detection of the PAX3-FOXO1 fusion gene in circulating tumor-derived DNA in a case of alveolar rhabdomyosarcoma

Minenori Eguchi-Ishimae,  Mari Tezuka,  Tomoki Kokeguchi,  Kozo Nagai,  Kyoko Moritani,  Sachiko Yonezawa,  Hisamichi Tauchi,  Kiriko Tokuda,  Yasushi Ishida,  Eiichi Ishii,  Mariko Eguchi, 
  • Pages: 521-529
  • First Published: 10 February 2019

Characterization of human telomerase reverse transcriptase promoter methylation and transcription factor binding in differentiated thyroid cancer cell lines

Brittany A. Avin,  Yongchun Wang,  Timothy Gilpatrick,  Rachael E. Workman,  Isac Lee,  Winston Timp,  Christopher B. Umbricht,  Martha A. Zeiger, 
  • Pages: 530-540
  • First Published: 21 January 2019
Open Access

Comprehensive molecular and clinicopathological analysis of vascular malformations: A study of 319 cases

Roel W. Ten Broek,  Astrid Eijkelenboom,  Carine J. M. van der Vleuten,  Eveline J. Kamping,  Marleen Kets,  Bas H. Verhoeven,  Katrien Grünberg,  Leo J. Schultze Kool,  Bastiaan B. J. Tops,  Marjolijn J. L. Ligtenberg,  Uta Flucke, 
  • Pages: 541-550
  • First Published: 24 January 2019

Pediatric acute myeloid leukemia with t(7;21)(p22;q22)

Prabakaran Paulraj,  Steven Diamond,  Faisal Razzaqi,  J. Daniel Ozeran,  Maria Longhurst,  Erica F. Andersen,  Reha M. Toydemir,  Bo Hong, 
  • Pages: 551-557
  • First Published: 31 January 2019
Open Access

Novel TG-FGFR1 and TRIM33-NTRK1 transcript fusions in papillary thyroid carcinoma

Aleksandra Pfeifer,  Dagmara Rusinek,  Jadwiga Żebracka-Gala,  Agnieszka Czarniecka,  Ewa Chmielik,  Ewa Zembala-Nożyńska,  Bartosz Wojtaś,  Bartłomiej Gielniewski,  Sylwia Szpak-Ulczok,  Małgorzata Oczko-Wojciechowska,  Jolanta Krajewska,  Joanna Polańska,  Barbara Jarząb, 
  • Pages: 558-566
  • First Published: 21 January 2019

Acute leukemias harboring KMT2A/MLLT10 fusion: a 10-year experience from a single genomics laboratory

Jess F. Peterson,  William R. Sukov,  Beth A. Pitel,  Stephanie A. Smoley,  Kathryn E. Pearce,  Reid G. Meyer,  Cynthia M. Williamson,  James B. Smadbeck,  George Vasmatzis,  Nicole L. Hoppman,  Patricia T. Greipp,  Linda B. Baughn,  Rhett P. Ketterling, 
  • Pages: 567-577
  • First Published: 01 February 2019
Open Access

Tumor mutational burden standardization initiatives: Recommendations for consistent tumor mutational burden assessment in clinical samples to guide immunotherapy treatment decisions

Albrecht Stenzinger,  Jeffrey D. Allen,  Jörg Maas,  Mark D. Stewart,  Diana M. Merino,  Madison M. Wempe,  Manfred Dietel, 
  • Pages: 578-588
  • First Published: 21 January 2019

BRIEF REPORTS

RNA sequencing identifies a novel USP9X-USP6 promoter swap gene fusion in a primary aneurysmal bone cyst

Patrick R. Blackburn,  Jaime I. Davila,  Rory A. Jackson,  Numrah Fadra,  Mazen A. Atiq,  Beth A. Pitel,  Asha A. Nair,  Todd J. VanDeWalker,  Mark G. Hessler,  Sara K. Hovel,  Rebecca N. Wehrs,  Karen J. Fritchie,  Robert B. Jenkins,  Kevin C. Halling,  Katherine B. Geiersbach, 
  • Pages: 589-594
  • First Published: 14 February 2019
Open Access

A recurrent clonally distinct Burkitt lymphoma case highlights genetic key events contributing to oncogenesis

Dominique Penther,  Pierre-Julien Viailly,  Sylvain Latour,  Pascaline Etancelin,  Elodie Bohers,  Hélène Vellemans,  Vincent Camus,  Anne Lise Menard,  Sophie Coutant,  Hélène Lanic,  Emilie Lemasle,  Fanny Drieux,  Liana Veresezan,  Philippe Ruminy,  Anna Raimbault,  Jean Soulier,  Thierry Frebourg,  Hervé Tilly,  Fabrice Jardin, 
  • Pages: 595-601
  • First Published: 18 February 2019

LETTER TO THE EDITOR

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

Leanne de Kock,  Morten Hillmer,  Rabea Wagener,  Dorothée Bouron-Dal Soglio,  Nelly Sabbaghian,  Reiner Siebert,  John R. Priest,  Michal Miller,  William D. Foulkes, 
  • Pages: 602-604
  • First Published: 30 December 2018