How to combine multiple tools for the genetic diagnosis work-up of pediatric B-cell acute lymphoblastic leukemia

Related articles

1. Integrated Whole Genome and Transcriptome Sequencing as a Framework for Pediatric and Adolescent AML Diagnosis and Risk Assessment

   This article has 29 authors:

   1. Lu Wang
   2. Rebecca Voss
   3. Victor Pastor
   4. Maria Cardenas
   5. Priyadarshini Kumar
   6. Jamie Maciaszek
   7. Maria Namwanje
   8. Jing Ma
   9. Jennifer Neary
   10. Meiling Jin
   11. Masayuki Umeda
   12. Mark Wilkinson
   13. Debbie Payne-Turner
   14. Mohammad Eldomery
   15. Jingqun Ma
   16. Jiali Gu
   17. James Dalton
   18. Samantha Melton
   19. Yen-Chun Liu
   20. Scott Foy
   21. Michael Rusch
   22. David Wheeler
   23. Jinghui Zhang
   24. Kim Nichols
   25. Seth Karol
   26. Hiroto Inaba
   27. Raul Ribeiro
   28. Jeffrey Rubnitz
   29. Jeffery Klco

2. Gain of chromosome 17 is an early genetic abnormality in neuroblastoma with PPM1D emerging as a strong candidate oncogene driving tumor progression

   This article has 25 authors:

   1. Jelena Milosevic
   2. Susanne Fransson
   3. Johanna Svensson
   4. Jörg Otte
   5. Thale K. Olsen
   6. Baldur Sveinbjornsson
   7. Falk Hertwig
   8. Christoph Bartenhagen
   9. Frida Abel
   10. Susanne E. Reinsbach
   11. Anna Djos
   12. Niloufar Javanmardi
   13. Yao Shi
   14. Jane Y Hehir-Kwa
   15. Arjen Mensenkamp
   16. Godelieve AM Tytgat
   17. Johan Holmberg
   18. Jan J Molenaar
   19. Marjolijn Jongmans
   20. Matthias Fischer
   21. Ninib Baryawno
   22. David Gisselsson
   23. Tommy Martinsson
   24. Per Kogner
   25. John Inge Johnsen

3. Whole genome sequencing-based analysis of genetic predisposition to adult glioblastoma

   This article has 7 authors:

   1. Mark P. van Opijnen
   2. Devin R. van Valkengoed
   3. Joep de Ligt
   4. Filip Y.F. de Vos
   5. Marike L.D. Broekman
   6. Edwin Cuppen
   7. Roelof Koster