Nature Communications (Feb 2020)

The complex genetic landscape of familial MDS and AML reveals pathogenic germline variants

  • Ana Rio-Machin,
  • Tom Vulliamy,
  • Nele Hug,
  • Amanda Walne,
  • Kiran Tawana,
  • Shirleny Cardoso,
  • Alicia Ellison,
  • Nikolas Pontikos,
  • Jun Wang,
  • Hemanth Tummala,
  • Ahad Fahad H. Al Seraihi,
  • Jenna Alnajar,
  • Findlay Bewicke-Copley,
  • Hannah Armes,
  • Michael Barnett,
  • Adrian Bloor,
  • Csaba Bödör,
  • David Bowen,
  • Pierre Fenaux,
  • Andrew Green,
  • Andrew Hallahan,
  • Henrik Hjorth-Hansen,
  • Upal Hossain,
  • Sally Killick,
  • Sarah Lawson,
  • Mark Layton,
  • Alison M. Male,
  • Judith Marsh,
  • Priyanka Mehta,
  • Rogier Mous,
  • Josep F. Nomdedéu,
  • Carolyn Owen,
  • Jiri Pavlu,
  • Elspeth M. Payne,
  • Rachel E. Protheroe,
  • Claude Preudhomme,
  • Nuria Pujol-Moix,
  • Aline Renneville,
  • Nigel Russell,
  • Anand Saggar,
  • Gabriela Sciuccati,
  • David Taussig,
  • Cynthia L. Toze,
  • Anne Uyttebroeck,
  • Peter Vandenberghe,
  • Brigitte Schlegelberger,
  • Tim Ripperger,
  • Doris Steinemann,
  • John Wu,
  • Joanne Mason,
  • Paula Page,
  • Susanna Akiki,
  • Kim Reay,
  • Jamie D. Cavenagh,
  • Vincent Plagnol,
  • Javier F. Caceres,
  • Jude Fitzgibbon,
  • Inderjeet Dokal

DOI
https://doi.org/10.1038/s41467-020-14829-5
Journal volume & issue
Vol. 11, no. 1
pp. 1 – 12

Abstract

Read online

Familial myeloid malignancies have recently been classified as separate disease entities. Here, using whole-exome sequencing of affected pedigrees - the authors highlight genetic variants associated with these conditions.