O
Olivier Bernard
Researcher at French Institute for Research in Computer Science and Automation
Publications - 830
Citations - 42407
Olivier Bernard is an academic researcher from French Institute for Research in Computer Science and Automation. The author has contributed to research in topics: Liver transplantation & Segmentation. The author has an hindex of 96, co-authored 790 publications receiving 37878 citations. Previous affiliations of Olivier Bernard include Intelligence and National Security Alliance & Institut national des sciences appliquées.
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Chromosomal abnormalities in transformed Ph-negative myeloproliferative neoplasms are associated to the transformation subtype and independent of JAK2 and the TET2 mutations.
Florence Nguyen-Khac,Claude Lesty,Virginie Eclache,Lucile Couronné,Olivier Kosmider,Joris Andrieux,Marie-Agnès Collonge-Rame,Dominique Penther,Marina Lafage,Chrystele Bilhou-Nabera,Elise Chapiro,Marie-Joelle Mozziconacci,Francine Mugneret,Nathalie Gachard,Nathalie Nadal,Eric Lippert,Stéphanie Struski,Nicole Dastugue,Christine Cabrol,Olivier Bernard +19 more
TL;DR: There was no evidence that JAK2 or TET2 mutations were associated with the type of MPN transformation, whereas thetype of cytogenetic abnormalities were strongly linked, perhaps indicating that they play a specific role in the transformation process.
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Mechanical and microstructural characterisation of oxide films damage
TL;DR: In this paper, three point-bending tests with simultaneous observations by scanning electron microscopy were performed on NiO films developed at 800°C in air for various times (i.e. oxide thicknesses) on industrial nickel.
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Mutations in the novel gene FOPV are associated with familial autosomal dominant and non-familial obliterative portal venopathy.
Claude Besmond,Dominique Valla,Laurence Hubert,Karine Poirier,Brigitte Grosse,Catherine Guettier,Olivier Bernard,Emmanuel Gonzales,Emmanuel Jacquemin +8 more
TL;DR: The aim was to identify a candidate gene of OPV, a disease thought to be responsible for many cases of portal hypertension in the absence of cirrhosis or obstruction of large portal or hepatic veins.
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AG-221, an Oral, Selective, First-in-Class, Potent IDH2-R140Q Mutant Inhibitor, Induces Differentiation in a Xenotransplant Model
Cyril Quivoron,Cyril Quivoron,Cyril Quivoron,Muriel D. David,Muriel D. David,Muriel D. David,Kim Straley,Jeremy Travins,Hyeryun Kim,Yue Chen,Dongwei Zhu,Véronique Saada,Véronique Saada,Véronique Saada,Olivia Bawa,Paule Opolon,Mélanie Polrot,Jean-Baptiste Micol,Christophe Willekens,Olivier Bernard,Olivier Bernard,Olivier Bernard,Hua Yang,Sam Agresta,Stéphane de Botton,Stéphane de Botton,Stéphane de Botton,Katharine E. Yen,Virginie Penard-Lacronique +28 more
TL;DR: Test of the biological activity of AG-221, an oral, reversible and selective inhibitor of mutated IDH2 currently in phase I trials, developed primary human AML xenograft models and induced a burst of proliferation of human blasts followed by myeloid differentiation starting at day 20 in peripheral blood.
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Enhancing PUFA-rich polar lipids in Tisochrysis lutea using adaptive laboratory evolution (ALE) with oscillating thermal stress
Manon Gachelin,M. Boutoute,Gregory Carrier,Amélie Talec,Eric Pruvost,Freddy Guihéneuf,Olivier Bernard,Antoine Sciandra +7 more
TL;DR: Thermal stress impacted cell size, total lipid cell content, and all lipid classes, and DHA cell content partitioned to polar lipids tripled throughout the experiment, suggesting their potential role in adjusting membrane fluidity to temperature shifts.