Marion Strullu

Juvenile myelomonocytic leukemia displays mutations in components of the RAS pathway and the PRC2 network

Aurélie Caye, Marion Strullu, Fabien Guidez et al. · Nature Genetics · 2015 · 191 citations

Medicine, Genetics, Oncology +16

Activating mutations in RRAS underlie a phenotype within the RASopathy spectrum and contribute to leukaemogenesis

Elisabetta Flex, Mamta Jaiswal, Francesca Pantaleoni et al. · Human Molecular Genetics · 2014 · 142 citations · Full text

Medicine, Genetics, Molecular Genetics +17

Juvenile myelomonocytic leukaemia and Noonan syndrome

Marion Strullu, Aurélie Caye, Julie Lachenaud et al. · Journal of Medical Genetics · 2014 · 135 citations · Full text

Medicine, Hematology, Pediatrics +17

Activating Mutations of RRAS2 Are a Rare Cause of Noonan Syndrome

Yline Capri, Elisabetta Flex, Oliver H.F. Krumbach et al. · The American Journal of Human Genetics · 2019 · 81 citations · Full text

Life Sciences, Genetics, Molecular Genetics +4

Myeloid Dysregulation in a Human Induced Pluripotent Stem Cell Model of PTPN11-Associated Juvenile Myelomonocytic Leukemia

Sonia Mulero‐Navarro, Ana Sevilla, Ángel Román et al. · Cell Reports · 2015 · 77 citations · Full text

Life Sciences, Genetics, Oncology +17