Olivier Delattre
Overview
Explore the profile of Olivier Delattre including associated specialties, affiliations and a list of published articles.
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Articles
316
Citations
16522
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Recent Articles
1.
Geyer F, Ritter A, Kinn-Gurzo S, Faehling T, Li J, Jarosch A, et al.
Cancer Commun (Lond)
. 2025 Mar;
PMID: 40088092
No abstract available.
2.
Kasan M, Geyer F, Siebenlist J, Sill M, Ollinger R, Faehling T, et al.
Nat Commun
. 2025 Jan;
16(1):380.
PMID: 39753532
Human cancer cell lines are the mainstay of cancer research. Recent reports showed that highly mutated adult carcinoma cell lines (mainly HeLa and MCF-7) present striking diversity across laboratories and...
3.
Filser M, Torrejon J, Merchadou K, Dufour C, Girard E, Bourneix C, et al.
Neuro Oncol
. 2024 Dec;
PMID: 39731757
Background: Medulloblastoma (MB) is one of the most prevalent embryonal malignant brain tumors. Current classification organizes these tumors into four molecular subgroups (WNT, SHH, Group 3, and Group 4 MB)....
4.
Dupuy M, Gueguinou M, Postec A, Brion R, Tesfaye R, Mullard M, et al.
Oncogene
. 2024 Nov;
44(2):79-91.
PMID: 39487324
Ewing sarcoma (ES) is characterized by EWS::FLI1 or EWS::ERG fusion proteins. Knowing that ion channels are involved in tumorigenesis, this work aimed to study the involvement of the KCNN1 gene,...
5.
Cyrta J, Dermawan J, Tauziede-Espariat A, Liu T, Rosenblum M, Shroff S, et al.
J Pathol
. 2024 Sep;
264(3):305-317.
PMID: 39344423
CREB gene family (ATF1, CREB1, CREM) fusions with either EWSR1 or FUS gene partners drive the pathogenesis of a wide range of neoplasms, including various soft tissue tumors, intracranial myxoid...
6.
Gruel N, Quignot C, Lesage L, El Zein S, Bonvalot S, Tzanis D, et al.
Nat Commun
. 2024 Sep;
15(1):7941.
PMID: 39266532
Dedifferentiated liposarcoma (DDLPS) is the most frequent high-grade soft tissue sarcoma subtype. It is characterized by a component of undifferentiated tumor cells coexisting with a component of well-differentiated adipocytic tumor...
7.
Thomson G, Filser M, Guerrini-Rousseau L, Tauziede-Espariat A, Bourneix C, Gauthier-Villars M, et al.
Neuro Oncol
. 2024 Aug;
26(11):2102-2112.
PMID: 39093628
Background: Rhabdoid tumors (RT) are aggressive, rare tumors predominantly affecting young children, characterized by biallelic SMARCB1 gene inactivation. While most SMARCB1 alterations are acquired de novo, a third of cases...
8.
Jacquin N, Flippot R, Masliah-Planchon J, Grisay G, Brillet R, Dupain C, et al.
NPJ Precis Oncol
. 2024 Jul;
8(1):147.
PMID: 39025947
Metastatic carcinoma of presumed renal origin (rCUP) has recently emerged as a new entity within the heterogeneous entity of Cancers of Unknown Primary (CUP) but their biological features and optimal...
9.
Guerrini-Rousseau L, Masliah-Planchon J, Filser M, Tauziede-Espariat A, Entz-Werle N, Maugard C, et al.
Neurooncol Adv
. 2024 Jul;
6(1):vdae075.
PMID: 38962751
Background: pathogenic variants (PV) have been recently identified as the most frequent variants predisposing to Sonic Hedgehog (SHH) medulloblastomas (MB); however, guidelines are still lacking for genetic counseling in this...
10.
Bobin C, Iddir Y, Butterworth C, Masliah-Planchon J, Saint-Charles A, Bellini A, et al.
Clin Cancer Res
. 2024 May;
30(15):3316-3328.
PMID: 38787533
Purpose: The study of cell-free DNA (cfDNA) enables sequential analysis of tumor cell-specific genetic alterations in patients with neuroblastoma. Experimental Design: Eighteen patients with relapsing neuroblastoma having received lorlatinib, a...