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Author Details
Full Name
Franck Bourdeaut
Affiliation
SIREDO Oncology Center, Institut Curie Hospital, and Universite de Paris
ORCID
Career Start Year
2001
Papers
161
H Index
40
Expertise
CM4AI Collaborator
Antoine Forget (CM4AI)
PMID
Paper Title
Journal Title
Published Year
36413100
NTRK-rearranged spindle cell neoplasms are ubiquitous tumours of myofibroblastic lineage with a distinct methylation class.
Histopathology
2023
37863903
Imaging and multi-omics datasets converge to define different neural progenitor origins for ATRT-SHH subgroups.
Nat Commun
2023
37524406
First report of medulloblastoma in a patient with MUTYH-associated polyposis.
Neuropathol Appl Neurobiol
2023
37605249
Diagnostic accuracy of a minimal immunohistochemical panel in at/rt molecular subtyping, correlated to dna-methylation profiling.
Acta Neuropathol Commun
2023
37349135
A comprehensive analysis of infantile central nervous system tumors to improve distinctive criteria for infant-type hemispheric glioma versus desmoplastic infantile ganglioglioma/astrocytoma.
Brain Pathol
2023
37014508
Molecular characterisation defines clinically-actionable heterogeneity within Group 4 medulloblastoma and improves disease risk-stratification.
Acta Neuropathol
2023
37444642
Cell-Free DNA Extracted from CSF for the Molecular Diagnosis of Pediatric Embryonal Brain Tumors.
Cancers (Basel)
2023
37379234
Clinical outcome of pediatric medulloblastoma patients with Li-Fraumeni syndrome.
Neuro Oncol
2023
37236926
SMARCB1 regulates a TFCP2L1-MYC transcriptional switch promoting renal medullary carcinoma transformation and ferroptosis resistance.
Nat Commun
2023
37169337
Pediatric Tumors and Developmental Anomalies: A French Nationwide Cohort Study.
J Pediatr
2023
36810692
Assessment of Puberty and Hypothalamic-Pituitary-Gonadal Axis Function After Childhood Brain Tumor Treatment.
J Clin Endocrinol Metab
2023
36609284
Pediatric high-grade glioma MYCN is frequently associated with Li-Fraumeni syndrome.
Acta Neuropathol Commun
2023
36835950
Retrospective National "Real Life" Experience of the SFCE with the Metronomic MEMMAT and MEMMAT-like Protocol.
J Clin Med
2023
36794424
GH and Childhood-onset Craniopharyngioma: When to Initiate GH Replacement Therapy?
J Clin Endocrinol Metab
2023
33283872
Corrigendum to: Molecular subgrouping of atypical teratoid/rhabdoid tumors-a reinvestigation and current consensus.
Neuro Oncol
2022
35768194
Cancer risk and tumour spectrum in 172 patients with a germline <i>SUFU</i> pathogenic variation: a collaborative study of the SIOPE Host Genome Working Group.
J Med Genet
2022
35580293
Checkpoint Immunotherapy in Pediatrics: Here, Gone, and Back Again.
Am Soc Clin Oncol Educ Book
2022
36446943
Author Correction: Failure of human rhombic lip differentiation underlies medulloblastoma formation.
Nature
2022
36131014
Failure of human rhombic lip differentiation underlies medulloblastoma formation.
Nature
2022
34918112
High Prevalence of Early Endocrine Disorders After Childhood Brain Tumors in a Large Cohort.
J Clin Endocrinol Metab
2022
34887247
Imaging Features with Histopathologic Correlation of CNS High-Grade Neuroepithelial Tumors with a <i>BCOR</i> Internal Tandem Duplication.
AJNR Am J Neuroradiol
2022
35239111
The role of irinotecan-bevacizumab as rescue regimen in children with low-grade gliomas: a retrospective nationwide study in 72 patients.
J Neurooncol
2022
35174661
Intra- and extra-cranial BCOR-ITD tumours are separate entities within the BCOR-rearranged family.
J Pathol Clin Res
2022
35326637
Dramatic In Vivo Efficacy of the EZH2-Inhibitor Tazemetostat in <i>PBRM1</i>-Mutated Human Chordoma Xenograft.
Cancers (Basel)
2022
35199222
Immunohistochemistry as a tool to identify ELP1-associated medulloblastoma.
Acta Neuropathol
2022
35051358
Rare germline heterozygous missense variants in BRCA1-associated protein 1, BAP1, cause a syndromic neurodevelopmental disorder.
Am J Hum Genet
2022
35164878
High-grade childhood intra-parenchymal brain tumor clustering with ATRT and expanding the cancer spectrum related to inherited SMARCE1 truncating variations.
Acta Neuropathol Commun
2022
34460114
A malignant choroid plexus tumour with prevailing immature blastematous elements.
Neuropathol Appl Neurobiol
2022
32888134
Genetic testing and surveillance in infantile myofibromatosis: a report from the SIOPE Host Genome Working Group.
Fam Cancer
2021
33601323
Bromodomain and extra-terminal inhibitors-A consensus prioritisation after the Paediatric Strategy Forum for medicinal product development of epigenetic modifiers in children-ACCELERATE.
Eur J Cancer
2021
33741928
The transcriptional landscape of Shh medulloblastoma.
Nat Commun
2021
33484663
Predisposition to cancer in children and adolescents.
Lancet Child Adolesc Health
2021
33755151
Are B7-H3 CAR-T cells the future universal treatment for pediatric brain tumors?
Neuro Oncol
2021
33532948
Current recommendations for clinical surveillance and genetic testing in rhabdoid tumor predisposition: a report from the SIOPE Host Genome Working Group.
Fam Cancer
2021
34717763
CNS tumors with YWHAE:NUTM2 and KDM2B-fusions present molecular similarities to extra-CNS tumors having BCOR internal tandem duplication or alternative fusions.
Acta Neuropathol Commun
2021
34389065
Supratentorial non-RELA, ZFTA-fused ependymomas: a comprehensive phenotype genotype correlation highlighting the number of zinc fingers in ZFTA-NCOA1/2 fusions.
Acta Neuropathol Commun
2021
34076831
What does a non-response to induction chemotherapy imply in high-risk medulloblastomas?
J Neurooncol
2021
34176585
[Intellectual disability and cancer in children: An analysis of the decision-making process].
Bull Cancer
2021
34151521
A novel case of cribriform neuroepithelial tumor: A potential diagnostic pitfall in the ventricular system.
Pediatr Blood Cancer
2021
34340841
[Cancer in children with intellectual disabilities: Questioning and ethical issues].
Bull Cancer
2021
34259072
A CBF decrease in the left supplementary motor areas: New insight into postoperative pediatric cerebellar mutism syndrome using arterial spin labeling perfusion MRI.
J Cereb Blood Flow Metab
2021
33999421
SMARCA4-deficient rhabdoid tumours show intermediate molecular features between SMARCB1-deficient rhabdoid tumours and small cell carcinomas of the ovary, hypercalcaemic type.
J Pathol
2021
34134020
Wilms tumour surveillance in at-risk children: Literature review and recommendations from the SIOP-Europe Host Genome Working Group and SIOP Renal Tumour Study Group.
Eur J Cancer
2021
33377141
Prognostic relevance of clinical and molecular risk factors in children with high-risk medulloblastoma treated in the phase II trial PNET HR+5.
Neuro Oncol
2021
33079397
Immune responses in genomically simple SWI/SNF-deficient cancers.
Cancer
2021
33331994
Atypical teratoid/rhabdoid tumors (ATRTs) with SMARCA4 mutation are molecularly distinct from SMARCB1-deficient cases.
Acta Neuropathol
2021
31504825
Medulloblastomas associated with an APC germline pathogenic variant share the good prognosis of CTNNB1-mutated medulloblastomas.
Neuro Oncol
2020
32025728
High-grade gliomas in adolescents and young adults highlight histomolecular differences from their adult and pediatric counterparts.
Neuro Oncol
2020
31889194
Molecular subgrouping of atypical teratoid/rhabdoid tumors-a reinvestigation and current consensus.
Neuro Oncol
2020
31677015
The histomolecular criteria established for adult anaplastic pilocytic astrocytoma are not applicable to the pediatric population.
Acta Neuropathol
2020
1 - 50 of 161
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Julien Masliah-Planchon
Curie Institute Hospital Group
Co-authored papers
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Institut Curie Hospital
Co-authored papers
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Fran??ois Doz
Institut Curie and University Paris Cite
Co-authored papers
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Christelle Dufour
Universite Paris-Saclay
Co-authored papers
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Pascale Varlet
Institut de Psychiatrie et Neurosciences de Paris (IPNP), INSERM, University of Paris
Co-authored papers
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St??phanie Puget
Necker Hospital, Assistance Publique-Hopitaux de Paris
Co-authored papers
24
Jacques Grill
Co-authored papers
22
Laurence Brugi??res
Universite Paris-Saclay
Co-authored papers
21
Kevin Beccaria
Hopital Universitaire Necker-Enfants Malades
Co-authored papers
18
Paul Fr??neaux
Institut Curie
Co-authored papers
16
Gudrun Schleiermacher
Institut Curie
Co-authored papers
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Marcel Kool
Hopp Children's Cancer Center (KiTZ)
Co-authored papers
14
Stefan M Pfister
Hopp Children's Cancer Center Heidelberg (KiTZ)
Co-authored papers
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Olivier Ayrault
Institut Curie, PSL Research University, CNRS UMR, INSERM
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13
Jean Michon
Institut Curie
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13
Dominique Figarella-Branger
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Michael D Taylor
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