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Cell Reports|October 13, 2015
Myeloid Dysregulation in a Human Induced Pluripotent Stem Cell Model of PTPN11-Associated Juvenile Myelomonocytic LeukemiaSonia Mulero-Navarro, Ana Sevilla, Angel C Roman, et al.Nature Genetics|October 13, 2015
Juvenile myelomonocytic leukemia displays mutations in components of the RAS pathway and the PRC2 networkAurélie Caye, Marion Strullu, Fabien Guidez, et al.Hemasphere|April 20, 2026
Biological and clinical characteristics of ETV6::RUNX1-like ALLMarketa Zaliova, Dagmar Schinnerl, Judith M Boer, et al.American Journal of Human Genetics|May 28, 2019
Activating Mutations of RRAS2 Are a Rare Cause of Noonan SyndromeYline Capri, Elisabetta Flex, Oliver H F Krumbach, et al.European Journal of Cancer (Oxford, England : 1990)|October 31, 2020
Impact of COVID-19 in paediatric early-phase cancer clinical trials in Europe: A report from the Innovative Therapies for Children with Cancer (ITCC) consortiumAlba Rubio-San-Simón, Nicolas André, Maria Giuseppina Cefalo, et al.JAMA Network Open|July 3, 2023
Measuring Safety and Outcomes for the Use of Compassionate and Off-Label Therapies for Children, Adolescents, and Young Adults With Cancer in the SACHA-France StudyPablo Berlanga, Lee Aymar Ndounga-Diakou, Isabelle Aerts, et al.Human Molecular Genetics|April 8, 2014
Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesisElisabetta Flex, Mamta Jaiswal, Francesca Pantaleoni, et al.Blood|June 25, 2024
ATM germ line pathogenic variants affect outcomes in children with ataxia-telangiectasia and hematological malignanciesSarah Elitzur, Ruth Shiloh, Jan L C Loeffen, et al.Cell Stem Cell|February 3, 2023
Clonal hematopoiesis driven by chromosome 1q/MDM4 trisomy defines a canonical route toward leukemia in Fanconi anemiaMarie Sebert, Stéphanie Gachet, Thierry Leblanc, et al.Pageof 5