Maroulio Pertesi

Research Engineer
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  1. 2020
  2. Genetic predisposition for multiple myeloma

    Maroulio Pertesi, Went, M., Markus Hansson, Kari Hemminki, Houlston, R. S. & Björn Nilsson, 2020 Jan 8, In : Leukemia.

    Research output: Contribution to journalReview article

  3. 2019
  4. Exome sequencing identifies germline variants in DIS3 in familial multiple myeloma

    Maroulio Pertesi, Björn Nilsson, McKay, J. D., Dumontet, C. & et al., 2019, In : Leukemia. 33, 9, p. 2324-2330

    Research output: Contribution to journalLetter

  5. 2017
  6. Haplotype analysis reveals that the recurrent BRCA1 deletion of exons 23 and 24 is a Greek founder mutation

    Apostolou, P., M. Pertesi, Aleporou-Marinou, V., Dimitrakakis, C., Papadimitriou, C., Razis, E., Christodoulou, C., Fountzilas, G., Yannoukakos, D., Konstantopoulou, I. & Fostira, F., 2017, In : Clinical Genetics. 91, 3, p. 482-487

    Research output: Contribution to journalArticle