Skip to Main content
Number of documents

11

Karim LABRECHE CV


Journal articles10 documents

  • Bouzidi Amira, Labreche Karim, Baron Marine, Veyri Marianne, Denis Jérôme Alexandre, et al.. Low-Coverage Whole Genome Sequencing of Cell-Free DNA From Immunosuppressed Cancer Patients Enables Tumor Fraction Determination and Reveals Relevant Copy Number Alterations. Frontiers in Cell and Developmental Biology, Frontiers media, 2021. ⟨hal-03363081⟩
  • Isaias Hernández-Verdin, Karim Labreche, Marion Benazra, Karima Mokhtari, Khe Hoang-Xuan, et al.. Tracking the Genetic Susceptibility Background of B-Cell Non-Hodgkin's Lymphomas from Genome-Wide Association Studies. International Journal of Molecular Sciences, MDPI, 2020, 22 (1), pp.122. ⟨10.3390/ijms22010122⟩. ⟨hal-03146385⟩
  • Karim Labreche, Mailys Daniau, Amit Sud, Philip Law, Louis Royer-Perron, et al.. A genome-wide association study identifies susceptibility loci for primary central nervous system lymphoma at 6p25.3 and 3p22.1: a LOC Network study. Neuro-Oncology, Oxford University Press (OUP), 2019, 21 (8), pp.1039-1048. ⟨10.1093/neuonc/noz088⟩. ⟨hal-02328989⟩
  • Linden Disney-Hogg, Amit Sud, Philip Law, Alex Cornish, Ben Kinnersley, et al.. Influence of obesity-related risk factors in the aetiology of glioma. British Journal of Cancer, Cancer Research UK, 2018, 118 (7), pp.1020-1027. ⟨10.1038/s41416-018-0009-x⟩. ⟨hal-02149333⟩
  • Hannah Takahashi, Alex Cornish, Amit Sud, Philip Law, Ben Kinnersley, et al.. Mendelian randomisation study of the relationship between vitamin D and risk of glioma. Scientific Reports, Nature Publishing Group, 2018, 8 (1), pp.2339. ⟨10.1038/s41598-018-20844-w⟩. ⟨hal-01960114⟩
  • Aurélie Bruno, Karim Labreche, Mailys Daniau, Blandine Boisselier, Guillaume Gauchotte, et al.. Identification of novel recurrent ETV6-IgH fusions in primary central nervous system lymphoma. Neuro-Oncology, Oxford University Press (OUP), 2018, 20 (8), pp.1092-1100. ⟨10.1093/neuonc/noy019⟩. ⟨pasteur-02862388⟩
  • Karim Labreche, Ben Kinnersley, Giulia Berzero, Anna Luisa Di Stefano, Amithys Rahimian, et al.. Diffuse gliomas classified by 1p/19q co-deletion, TERT promoter and IDH mutation status are associated with specific genetic risk loci. Acta Neuropathologica, Springer Verlag, 2018, 135 (5), pp.743-755. ⟨10.1007/s00401-018-1825-z⟩. ⟨hal-01974524⟩
  • Beatrice S. Melin, Jill S. Barnholtz-Sloan, Margaret R. Wrensch, Christoffer Johansen, Dora Il'Yasova, et al.. Genome-wide association study of glioma subtypes identifies specific differences in genetic susceptibility to glioblastoma and non-glioblastoma tumors. Nature Genetics, Nature Publishing Group, 2017, 49 (5), pp.789-794. ⟨10.1038/ng.3823⟩. ⟨hal-01602681⟩
  • Karim Labreche, Iva Simeonova, Aurélie Kamoun, Vincent Gleize, Daniel Chubb, et al.. TCF12 is mutated in anaplastic oligodendroglioma. Nature Communications, Nature Publishing Group, 2015, 6, pp.7207. ⟨10.1038/ncomms8207⟩. ⟨hal-01295222⟩
  • Kevin Litchfield, Brenda Summersgill, Shawn Yost, Razvan Sultana, Karim Labreche, et al.. Whole-exome sequencing reveals the mutational spectrum of testicular germ cell tumours. Nature Communications, Nature Publishing Group, 2015, 6, pp.5973. ⟨10.1038/ncomms6973⟩. ⟨hal-01116429⟩

Theses1 document