User profiles for Olivier Kosmider

olivier kosmider

Verified email at cch.aphp.fr
Cited by 11511

[HTML][HTML] Mutation in TET2 in Myeloid Cancers

…, S Trannoy, A Massé, O Kosmider… - … England Journal of …, 2009 - Mass Medical Soc
Background The myelodysplastic syndromes and myeloproliferative disorders are associated
with deregulated production of myeloid cells. The mechanisms underlying these disorders …

[PDF][PDF] Elevated calprotectin and abnormal myeloid cell subsets discriminate severe from mild COVID-19

…, L Derosa, C Almire, C Hénon, O Kosmider… - Cell, 2020 - cell.com
Blood myeloid cells are known to be dysregulated in coronavirus disease 2019 (COVID-19),
caused by SARS-CoV-2. It is unknown whether the innate myeloid response differs with …

Molecular international prognostic scoring system for myelodysplastic syndromes

…, G Sanz, AA van de Loosdrecht, O Kosmider… - NEJM …, 2022 - evidence.nejm.org
Background Risk stratification and therapeutic decision-making for myelodysplastic
syndromes (MDS) are based on the International Prognostic Scoring System–Revised (IPSS-R), …

[PDF][PDF] Prognostic score including gene mutations in chronic myelomonocytic leukemia

R Itzykson, O Kosmider, A Renneville… - Journal of clinical …, 2013 - researchgate.net
Purpose Several prognostic scoring systems have been proposed for chronic myelomonocytic
leukemia (CMML), a disease in which some gene mutations—including ASXL1—have …

Implications of TP53 allelic state for genome stability, clinical presentation and outcomes in myelodysplastic syndromes

…, M Jädersten, M Tobiasson, O Kosmider… - Nature medicine, 2020 - nature.com
Tumor protein p53 (TP53) is the most frequently mutated gene in cancer 1 , 2 . In patients with
myelodysplastic syndromes (MDS), TP53 mutations are associated with high-risk disease …

TET2 mutation is an independent favorable prognostic factor in myelodysplastic syndromes (MDSs)

O Kosmider, V Gelsi-Boyer, M Cheok… - Blood, The Journal …, 2009 - ashpublications.org
Oncogenic pathways underlying in the development of myelodysplastic syndromes (MDS)
remain poorly characterized, but mutations of the ten-eleven translocation 2 (TET2) gene are …

Clonal architecture of chronic myelomonocytic leukemias

R Itzykson, O Kosmider, A Renneville… - Blood, The Journal …, 2013 - ashpublications.org
Genomic studies in chronic myeloid malignancies, including myeloproliferative neoplasms (MPN),
myelodysplastic syndromes (MDS), and MPN/MDS, have identified common …

Mutations affecting mRNA splicing define distinct clinical phenotypes and correlate with patient outcome in myelodysplastic syndromes

F Damm, O Kosmider, V Gelsi-Boyer… - Blood, The Journal …, 2012 - ashpublications.org
A cohort of MDS patients was examined for mutations affecting 4 splice genes (SF3B1,
SRSF2, ZRSR2, and U2AF35) and evaluated in the context of clinical and molecular markers. …

Inhibiting glutamine uptake represents an attractive new strategy for treating acute myeloid leukemia

…, AS Green, M Uzunov, O Kosmider… - Blood, The Journal …, 2013 - ashpublications.org
Cancer cells require nutrients and energy to adapt to increased biosynthetic activity, and
protein synthesis inhibition downstream of mammalian target of rapamycin complex 1 (mTORC1…

[HTML][HTML] TET2 gene mutation is a frequent and adverse event in chronic myelomonocytic leukemia

O Kosmider, V Gelsi-Boyer, M Ciudad, C Racoeur… - …, 2009 - ncbi.nlm.nih.gov
Background Acquired somatic deletions and loss-of-function mutations in one or several
codons of the TET2 (Ten-Eleven Translocation-2) gene were recently identified in …