Julien Vibert
Overview
Explore the profile of Julien Vibert including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
15
Citations
120
Followers
0
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Assi T, Moussa T, Ngo C, Faron M, Verret B, Levy A, et al.
Cancer Treat Rev
. 2025 Feb;
134:102904.
PMID: 40020639
Tenosynovial giant cell tumor is a non-malignant primary locally aggressive articular disease that affects the synovium of joints, tendon sheaths, and bursae. It is characterized by a translocation t (1;2),...
2.
Unger M, Loeffler C, Zigutyte L, Sainath S, Lenz T, Vibert J, et al.
bioRxiv
. 2025 Jan;
PMID: 39829845
Background: Genomic data is essential for clinical decision-making in precision oncology. Bioinformatic algorithms are widely used to analyze next-generation sequencing (NGS) data, but they face two major challenges. First, these...
3.
Guegan J, El Ghazzi N, Vibert J, Rey C, Vanhersecke L, Coindre J, et al.
J Hematol Oncol
. 2024 Oct;
17(1):100.
PMID: 39444039
Undifferentiated pleomorphic sarcomas (UPS) represent a prevalent and aggressive subtype of soft tissue sarcomas (STS) in adults. Despite advancements in loco regional treatments, many patients with high grade STS, including...
4.
Kawai-Kawachi A, Lenormand M, Astier C, Herbel N, Cutrona M, Ngo C, et al.
Cancer Res
. 2024 Oct;
85(1):154-170.
PMID: 39412947
Desmoplastic small round cell tumor (DSRCT) is an aggressive sarcoma subtype that is driven by the EWS-WT1 chimeric transcription factor. The prognosis for DSRCT is poor, and major advances in...
5.
Benani A, Vibert J, Demuth S
Med Sci (Paris)
. 2024 Sep;
40(8-9):661-664.
PMID: 39303119
Recent technological advances in data science hold great promise in medicine. Large-sized high-quality datasets are essential but often difficult to obtain due to privacy, cost, and practical challenges. Here, we...
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.
Henon C, Vibert J, Eychenne T, Gruel N, Colmet-Daage L, Ngo C, et al.
Cell Rep Med
. 2024 May;
5(6):101582.
PMID: 38781959
Desmoplastic small round cell tumor (DSRCT) is a rare, aggressive sarcoma driven by the EWSR1::WT1 chimeric transcription factor. Despite this unique oncogenic driver, DSRCT displays a polyphenotypic differentiation of unknown...
8.
Ngo C, Cotteret S, Deneche I, Kfoury M, Chehab R, Tran-Dien A, et al.
Hum Pathol
. 2024 Apr;
148:14-22.
PMID: 38688412
Mullerian adenosarcoma is a rare malignant biphasic tumor. The mesenchymal component may be low or high grade, with or without sarcomatous overgrowth (SO). Little is known about the molecular heterogeneity...
9.
Belkouchi Y, Talbot H, Lassau N, Lawrance L, Farhane S, Feki-Mkaouar R, et al.
Clin Cancer Res
. 2023 Jan;
29(8):1528-1534.
PMID: 36719966
Purpose: The objective of the study is to propose the immunotherapy progression decision (iPD) score, a practical tool based on patient features that are available at the first evaluation of...
10.
Ngo C, Verret B, Vibert J, Cotteret S, Levy A, Le Pechoux C, et al.
Genes Chromosomes Cancer
. 2022 Aug;
62(1):52-56.
PMID: 35932215
Extraskeletal myxoid chondrosarcoma (EMC) is a rare soft tissue neoplasm of uncertain lineage characterized by the pathognomonic rearrangement of the NR4A3 gene, which in most cases is fused with EWSR1....