D. Pissaloux

发表

Molecular Classification of Endometrial Stromal Sarcomas Using RNA Sequencing Defines Nosological and Prognostic Subgroups with Different Natural History

J. Blay, F. Tirode, I. Treilleux, 2020, Cancers.

Fusion partners of NTRK3 affect subcellular localization of the fusion kinase and cytomorphology of melanocytes

I. Yeh, F. Tirode, B. Bastian, 2020, Modern Pathology.

RASGRF1-rearranged Cutaneous Melanocytic Neoplasms With Spitzoid Cytomorphology

F. Tirode, D. Pissaloux, A. de la Fouchardière, 2021, The American journal of surgical pathology.

Morphologic features in a series of 352 Spitz melanocytic proliferations help predict their oncogenic drivers

F. Tirode, M. Samimi, T. Kervarrec, 2021, Virchows Archiv.

New Insights on Diagnostic Reproducibility of Biphasic Mesotheliomas: A Multi‐Institutional Evaluation by the International Mesothelioma Panel From the MESOPATH Reference Center

N. Le Stang, N. Girard, A. Nicholson, 2018, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Autocrine role for Gas6 with Tyro3 and Axl in leiomyosarcomas

J. Blay, I. Ray-Coquard, C. Caux, 2013, Targeted Oncology.

Unclassified sclerosing malignant melanomas with AKAP9-BRAF gene fusion: a report of two cases and review of BRAF fusions in melanocytic tumors

D. Hohl, L. Mortier, D. Pissaloux, 2018, Virchows Archiv.

Novel three-way complex rearrangement of TRPM1-PUM1-LCK in a case of agminated Spitz nevi arising in a giant congenital hyperpigmented macule.

F. Tirode, B. Guillot, D. Pissaloux, 2020, Pigment cell & melanoma research.

miRNA Profiling: How to Bypass the Current Difficulties in the Diagnosis and Treatment of Sarcomas

J. Blay, Angélique Gougelet, D. Ranchère‐Vince, 2011, Sarcoma.

Cutaneous Melanocytic Tumors With Concomitant NRASQ61R and IDH1R132C Mutations

F. Tirode, H. Etchevers, N. Macagno, 2020, The American journal of surgical pathology.

Combined activation of MAP kinase pathway and β-catenin signaling cause deep penetrating nevi

Robert L. Judson, Robert L Judson, I. Yeh, 2017, Nature Communications.

Activity of cabozantinib in radioresistant brain metastases from renal cell carcinoma: two case reports

C. Carrie, V. Attignon, D. Pissaloux, 2018, Journal of Medical Case Reports.

Wholistic approach: Transcriptomic analysis and beyond using archival material for molecular diagnosis

J. Blay, S. Lantuejoul, F. Tirode, 2022, Genes, chromosomes & cancer.

Clinicopathologic Features of CIC-NUTM1 Sarcomas, a New Molecular Variant of the Family of CIC-Fused Sarcomas

F. Tirode, J. Coindre, A. Italiano, 2019, The American journal of surgical pathology.

Alternative PDGFD rearrangements in dermatofibrosarcomas protuberans without PDGFB fusions

J. Blay, F. Chibon, Gaëlle Pérot, 2018, Modern Pathology.

GOPC-ROS1 mosaicism in agminated Spitz naevi: report of two cases

F. Tirode, D. Pissaloux, A. de la Fouchardière, 2021, Virchows Archiv.

Inhibition of Chondrosarcoma Growth by mTOR Inhibitor in an In Vivo Syngeneic Rat Model

J. Blay, A. Decouvelaere, D. Pissaloux, 2012, PloS one.

Mutated and amplified NRAS in a subset of cutaneous melanocytic lesions with dermal spitzoid morphology: report of two pediatric cases located on the ear

L. Thomas, F. Disant, B. Balme, 2014, Journal of cutaneous pathology.

Tumor Molecular Profiling: Pediatric Results of the ProfiLER Study.

J. Blay, D. Frappaz, P. Saintigny, 2020, JCO precision oncology.

Genetic alterations and tumor immune attack in Yo paraneoplastic cerebellar degeneration

J. Honnorat, I. Treilleux, I. Ray-Coquard, 2018, Acta Neuropathologica.

Clear Cell Tumor With Melanocytic Differentiation and ACTIN-MITF Translocation: Report of 7 Cases of a Novel Entity.

F. Tirode, C. Fletcher, D. Pissaloux, 2020, The American journal of surgical pathology.

Spitz nevus with a novel TFG‐NTRK2 fusion: The first case report of NTRK2‐rearranged Spitz/Reed nevus

F. Tirode, D. Pissaloux, A. de la Fouchardière, 2021, Journal of cutaneous pathology.

Alterations in Homologous Recombination-Related Genes and Distinct Platinum Response in Metastatic Triple-Negative Breast Cancers: A Subgroup Analysis of the ProfiLER-01 Trial

J. Blay, A. Viari, I. Treilleux, 2022, Journal of personalized medicine.

148 Combined activation of MAP kinase and beta-catenin signaling define deep penetrating nevi

Robert L. Judson, Robert L Judson, L. Cerroni, 2017 .

Intracranial non-myxoid angiomatoid fibrous histiocytoma with EWSR1-CREB1 transcript fusion treated with doxorubicin: A case report

F. Ducray, J. Honnorat, D. Pissaloux, 2021, Molecular and clinical oncology.

CYSLTR2-mutant Cutaneous Melanocytic Neoplasms Frequently Simulate “Pigmented Epithelioid Melanocytoma,” Expanding the Morphologic Spectrum of Blue Tumors

F. Tirode, D. Pissaloux, A. de la Fouchardière, 2019, The American journal of surgical pathology.

SMARCA4-deficient Thoracic Sarcomas: Clinicopathologic Study of 30 Cases With an Emphasis on Their Nosology and Differential Diagnoses

J. Blay, S. Lantuejoul, F. Tirode, 2019, The American journal of surgical pathology.

Malignant melanoma with areas of rhabdomyosarcomatous differentiation arising in a giant congenital nevus with RAF1 gene fusion

F. Tirode, D. Pissaloux, M. Karanian, 2019, Pigment cell & melanoma research.

Linear variant of large plaque-type blue naevus with subcutaneous cellular nodules.

D. Pissaloux, A. de la Fouchardière, D. Michiels-Marzais, 2017, Pathology.

Primary Melanoma of the Leptomeninges with BAP1 Expression‐Loss in the Setting of a Nevus of Ota: A Clinical, Morphological and Genetic Study of 2 Cases

V. Rigau, F. Labrousse, V. Attignon, 2016, Brain pathology.

Primary leptomeningeal melanoma is part of the BAP1-related cancer syndrome

N. Janin, B. Bressac-de Paillerets, O. Cabaret, 2015, Acta Neuropathologica.

A subset of lung adenofibromas are morphological variants of solitary fibrous tumour

N. Macagno, D. Pissaloux, M. Karanian, 2022, Histopathology.

Agminated Spitz nevus arising in normal skin with redundant HRAS mutation

D. Pissaloux, A. de la Fouchardière, V. Haddad, 2017, European Journal of Dermatology.

Recurrent novel THBS1-ADGRF5 gene fusion in a new tumor subtype “Acral FibroChondroMyxoid Tumors”

F. Tirode, S. Aubert, F. Le Loarer, 2020, Modern Pathology.

Filigree-like Rete Ridges, Lobulated Nests, Rosette-like Structures, and Exaggerated Maturation Characterize Spitz Tumors With NTRK1 Fusion

I. Yeh, B. Bastian, K. Busam, 2019, The American journal of surgical pathology.

Clinical, Histopathologic, and Genomic Features of Spitz Tumors With ALK Fusions

I. Yeh, B. Bastian, K. Busam, 2015, The American journal of surgical pathology.

Melanoma arising from a long-standing pigmented trichoblastoma: clinicopathologic study with complementary aCGH/mutational analysis.

C. Mateus, G. Tomasic, D. Pissaloux, 2014, The American Journal of dermatopathology.

β-Catenin nuclear expression discriminates deep penetrating nevi from other cutaneous melanocytic tumors

D. Pissaloux, A. de la Fouchardière, J. Jacquemus, 2019, Virchows Archiv.

Melanomas Associated With Blue Nevi or Mimicking Cellular Blue Nevi: Clinical, Pathologic, and Molecular Study of 11 Cases Displaying a High Frequency of GNA11 Mutations, BAP1 Expression Loss, and a Predilection for the Scalp

L. Thomas, B. Dréno, F. Grange, 2016, The American journal of surgical pathology.

Attempting to Solve the Pigmented Epithelioid Melanocytoma (PEM) Conundrum

F. Tirode, N. Macagno, D. Pissaloux, 2022, The American journal of surgical pathology.

Cutaneous Melanocytoma With CRTC1-TRIM11 Fusion: Report of 5 Cases Resembling Clear Cell Sarcoma

D. Pissaloux, M. Karanian, A. de la Fouchardière, 2017, The American journal of surgical pathology.

Compound Clear Cell Sarcoma of the Skin—A Potential Diagnostic Pitfall

S. Billings, E. Calonje, D. Pissaloux, 2019, The American journal of surgical pathology.

Solid papillary mesothelial tumor

N. Le Stang, F. Galateau-Sallé, S. Dacic, 2021, Modern Pathology.

Recent Advances on Immunohistochemistry and Molecular Biology for the Diagnosis of Adnexal Sweat Gland Tumors

M. Battistella, N. Macagno, T. Kervarrec, 2022, Cancers.

SMARCA4 inactivation defines a group of undifferentiated thoracic malignancies transcriptionally related to BAF-deficient sarcomas

N. Girard, J. Blay, F. Galateau-Sallé, 2015, Nature Genetics.

Pleomorphic Sarcomas: The State of the Art.

J. Coindre, A. Crombé, F. Le Loarer, 2019, Surgical pathology clinics.

MDM4 amplification in a case of de‐differentiated liposarcoma and in‐silico data supporting an oncogenic event alternative to MDM2 amplification in a subset of cases

J. Blay, J. Coindre, D. Ranchère‐Vince, 2017, Histopathology.

Genomic Instability Is Defined by Specific Tumor Microenvironment in Ovarian Cancer: A Subgroup Analysis of AGO OVAR 12 Trial

R. Kimmig, D. Spaeth, I. Treilleux, 2022, Cancers.

Impact of Molecular Analysis on the Final Sarcoma Diagnosis: A Study on 763 Cases Collected During a European Epidemiological Study

J. Blay, F. Chibon, J. Coindre, 2013, The American journal of surgical pathology.

Immune and Genetic Signatures of Breast Carcinomas Triggering Anti-Yo–Associated Paraneoplastic Cerebellar Degeneration

J. Honnorat, A. Viari, I. Treilleux, 2022, Neurology: Neuroimmunology & Neuroinflammation.

Genomic alterations and radioresistance in breast cancer: an analysis of the ProfiLER protocol

N. Magné, J. Blay, I. Ray-Coquard, 2017, Annals of oncology : official journal of the European Society for Medical Oncology.

Advances in the classification of round cell sarcomas

F. Le Loarer, D. Pissaloux, M. Karanian, 2021, Histopathology.

Therapeutic relevance of molecular screening program in patients with metastatic sarcoma: Analysis from the ProfiLER 01 trial

J. Blay, O. Trédan, H. Vanacker, 2020, Translational oncology.

A subset of epithelioid and spindle cell rhabdomyosarcomas is associated with TFCP2 fusions and common ALK upregulation

S. Salas, F. Tirode, J. Coindre, 2019, Modern Pathology.

Germline CDKN2A/P16INK4A mutations contribute to genetic determinism of sarcoma

J. Barrett, G. Mann, P. Terrier, 2017, Journal of Medical Genetics.

Actionable molecular alterations in advanced gynaecologic malignancies: updated results from the ProfiLER programme.

J. Blay, A. Viari, I. Ray-Coquard, 2019, European journal of cancer.

Update on Families of Round Cell Sarcomas Other than Classical Ewing Sarcomas.

F. Tirode, J. Coindre, F. Le Loarer, 2017, Surgical pathology clinics.

Comprehensive molecular and pathological evaluation of transitional mesothelioma assisted by deep learning approach: a multi institutional study of the International Mesothelioma Panel from MESOPATH Reference Center.

G. Wainrib, P. Courtiol, C. Maussion, 2020, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

SRF Fusions Other Than With RELA Expand the Molecular Definition of SRF-fused Perivascular Tumors

J. Blay, F. Tirode, A. Kelsey, 2020, The American journal of surgical pathology.

Superficial CD34‐positive fibroblastic tumor and PRDM10‐rearranged soft tissue tumor are overlapping entities: a comprehensive study of 20 cases

F. Tirode, J. Coindre, I. Soubeyran, 2021, Histopathology.

Melanocytic tumors with MAP3K8 fusions: report of 33 cases with morphological-genetic correlations

I. Yeh, F. Tirode, I. Masse, 2019, Modern Pathology.

Spectrum of Melanocytic Tumors Harboring BRAF Gene Fusions: 58 Cases with Histomorphologic and Genetic Correlations.

I. Yeh, F. Tirode, B. Bastian, 2023, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

Clear cell tumor with melanocytic differentiation and MITF-CREM translocation: a novel entity similar to clear cell sarcoma

F. Tirode, D. Pissaloux, A. de la Fouchardière, 2021, Virchows Archiv.

Regorafenib or Tamoxifen for platinum-sensitive recurrent ovarian cancer with rising CA125 and no evidence of clinical or RECIST progression: A GINECO randomized phase II trial (REGOVAR).

I. Treilleux, I. Ray-Coquard, O. Trédan, 2021, Gynecologic oncology.

Very long‐term survivors among patients with metastatic soft tissue sarcoma

J. Blay, F. Tirode, I. Ray-Coquard, 2019, Cancer medicine.

Aldehyde Dehydrogenase, a Therapeutic Target in Chordoma: Analysis in 3D Cellular Models

J. Blay, F. Tirode, D. Pissaloux, 2021, Cells.

Fusion partners of NTRK3 affect subcellular localization of the fusion kinase and cytomorphology of melanocytes

I. Yeh, F. Tirode, B. Bastian, 2020, Modern Pathology.

Intra‐ and extra‐cranial BCOR‐ITD tumours are separate entities within the BCOR ‐rearranged family

O. Delattre, F. Tirode, D. Orbach, 2022, The journal of pathology. Clinical research.

Specific and Sensitive Diagnosis of BCOR-ITD in Various Cancers by Digital PCR

P. Varlet, D. Figarella-Branger, R. Appay, 2021, Frontiers in Oncology.

Non-rhabdoid pediatric SMARCB1-deficient tumors: overlap between chordomas and malignant rhabdoid tumors?

F. Bourdeaut, A. Decouvelaere, D. Pissaloux, 2014, Cancer genetics.

Predicting everolimus treatment efficacy in patients with advanced endometrial carcinoma: a GINECO group study

T. Petit, I. Treilleux, I. Ray-Coquard, 2013, Targeted Oncology.

CRTC1‐TRIM11 fusion defined melanocytic tumors: A series of four cases

F. Tirode, S. Billings, J. Ko, 2019, Journal of cutaneous pathology.

Genetic analyses of undifferentiated small round cell sarcoma identifies a novel sarcoma subtype with a recurrent CRTC1‐SS18 gene fusion

C. Antonescu, F. Tirode, D. Ranchère‐Vince, 2018, The Journal of pathology.

Molecular profile to guide personalized medicine in adult patients with primary brain tumors: results from the ProfiLER trial

J. Blay, F. Ducray, S. Lantuejoul, 2021, Medical Oncology.

Genomic complexity in pediatric synovial sarcomas (Synobio study): the European pediatric soft tissue sarcoma group (EpSSG) experience

F. Chibon, A. Ferrari, A. Kelsey, 2018, Cancer medicine.

Radioresistance and genomic alterations in head and neck squamous cell cancer: Sub‐analysis of the ProfiLER protocol

N. Magné, J. Blay, O. Trédan, 2021, Head & neck.

Complete response to CSF1R inhibitor in a translocation variant of teno-synovial giant cell tumor without genomic alteration of the CSF1 gene.

J. Blay, F. Tirode, L. Eberst, 2018, Annals of oncology : official journal of the European Society for Medical Oncology.

Expanding the molecular spectrum of tenosynovial giant cell tumors

J. Blay, F. Tirode, I. Ray-Coquard, 2022, Frontiers in Oncology.

Cutaneous Melanocytic Tumor With CRTC1::TRIM11 Translocation

F. Tirode, C. Fletcher, S. Billings, 2022, The American journal of surgical pathology.

Molecular screening program to select molecular-based recommended therapies for metastatic cancer patients: analysis from the ProfiLER trial.

J. Blay, S. Boyault, S. Lantuejoul, 2019, Annals of oncology : official journal of the European Society for Medical Oncology.

FNBP1-BRAF fusion in a primary melanoma of the lung.

F. Tirode, T. Kervarrec, D. Pissaloux, 2021, Pathology.

RASGRF2 gene fusions identified in a variety of melanocytic lesions with distinct morphological features

F. Tirode, I. Masse, J. Caramel, 2021, Pigment cell & melanoma research.

Melanocytic Myxoid Spindle Cell Tumor With ALK Rearrangement (MMySTAR): Report of 4 Cases of a Nevus Variant With Potential Diagnostic Challenge

D. Pissaloux, M. Karanian, A. de la Fouchardière, 2017, The American journal of surgical pathology.

Single Time Frame Overview of the Genetic Changes in Conjunctival Melanoma from Intraepithelial Disease to Invasive Melanoma: A Study of 4 Exenteration Specimens Illustrating the Potential Role of Cyclin D1

D. Pissaloux, A. de la Fouchardière, H. Mudhar, 2021, Ocular Oncology and Pathology.

Agminated Spitz naevus with an activating HRAS Q61R mutation.

F. Tirode, T. Kervarrec, D. Pissaloux, 2021, Pathology.

Response to chemotherapy is not related to chromosome instability in synovial sarcoma.

J. Blay, F. Chibon, P. Lagarde, 2014, Annals of oncology : official journal of the European Society for Medical Oncology.

Unpigmented nodule with loss of BAP1 expression in a medium-sized congenital nevus

D. Pissaloux, Christine Castillo, S. Paindavoine, 2015, EJD. European journal of dermatology.

Atypical cutaneous melanocytic tumours arising in two patients with Li-Fraumeni syndrome.

D. Pissaloux, A. de la Fouchardière, J. Jacquemus, 2017, Pathology (Sydney).

Recurrent FOXK1::GRHL and GPS2::GRHL fusions in trichogerminoma

F. Tirode, T. Jouary, D. Schrama, 2022, The Journal of pathology.

SRF-FOXO1 and SRF-NCOA1 Fusion Genes Delineate a Distinctive Subset of Well-differentiated Rhabdomyosarcoma

J. Blay, F. Tirode, F. Le Loarer, 2020, The American journal of surgical pathology.

Routine molecular screening of advanced refractory cancer patients: An analysis of the first 2490 patients of the ProfiLER study.

J. Blay, A. Viari, O. Trédan, 2017 .

Micro‐RNA profiles in osteosarcoma as a predictive tool for ifosfamide response

J. Blay, Angélique Gougelet, D. Pissaloux, 2011, International journal of cancer.

Distinct regulations driving YAP1 expression loss in poroma, porocarcinoma and RB1‐deficient skin carcinoma

F. Tirode, D. Schrama, R. Houben, 2023, Histopathology.

Clinical characteristics and outcomes for children, adolescents and young adults with “CIC‐fused” or “BCOR‐rearranged” soft tissue sarcomas: A multi‐institutional European retrospective analysis

F. Tirode, A. Ferrari, D. Orbach, 2023, Cancer medicine.

A Combination of MTAP and p16 Immunohistochemistry Can Substitute for CDKN2A Fluorescence In Situ Hybridization in Diagnosis and Prognosis of Pleural Mesotheliomas.

N. Le Stang, S. Dacic, F. Tirode, 2022, Archives of pathology & laboratory medicine.

Genetics of adnexal tumors: An update.

M. Battistella, N. Macagno, T. Kervarrec, 2023, Annales de dermatologie et de venereologie.

NTRK2 gene fusion and resistance mutation: Seventeen‐year course of a paediatric glioma

C. Mottolese, D. Poncet, A. Vasiljevic, 2021, Pediatric blood & cancer.

Natural history and treatment efficacy in an ambispective case series of NTRK-rearranged mesenchymal tumors

F. Tirode, A. Le Cesne, H. Vanacker, 2023, ESMO open.

Genomic alterations and radioresistance in breast cancer: an analysis of the ProfiLER protocol.

I. Ray-Coquard, O. Trédan, N. Chopin, 2017, Annals of Oncology.

Identification of a novel translocation producing an in-frame fusion of TAF15 and ETV4 in a case of extraosseous Ewing sarcoma revealed in the prenatal period

F. Chotel, C. Picard, F. Dijoud, 2022, Virchows Archiv.

GRM1 gene fusions as an alternative molecular driver in blue nevi and related melanomas.

F. Tirode, N. Poulalhon, M. Samimi, 2023, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

Small-Cell Lung Cancer Transformation as a Mechanism of Resistance to Pralsetinib in RET-Rearranged Lung Adenocarcinoma: A Case Report.

S. Lantuejoul, A. Bouhamama, T. Franceschi, 2022, Clinical lung cancer.

Rhabdoid component emerging as a subclonal evolution of paediatric glioneuronal tumours

P. Varlet, D. Frappaz, A. Jouvet, 2018, Neuropathology and applied neurobiology.

Molecular screening program to select molecular-based recommended therapies for metastatic cancer patients: analysis from the ProfiLER trial.

J. Blay, S. Boyault, S. Lantuejoul, 2019 .

Histological and genetic features of 51 Melanocytic Neoplasms with Protein Kinase C fusion genes.

I. Yeh, F. Tirode, B. Bastian, 2023, Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc.

Recurrent PAK2 rearrangements in poroma with folliculo‐sebaceous differentiation

F. Tirode, M. Battistella, S. Mourah, 2023, Histopathology.

About BRAF Mutations and p16 Expression in Melanomas Associated With Blue Nevi or Mimicking Cellular Blue Nevi: Author's Reply.

D. Pissaloux, A. de la Fouchardière, V. Haddad, 2016, The American journal of surgical pathology.

A comprehensive analysis of infantile central nervous system tumors to improve distinctive criteria for infant‐type hemispheric glioma versus desmoplastic infantile ganglioglioma/astrocytoma

P. Varlet, N. Boddaert, S. Puget, 2023, Brain pathology.

Sweat Gland Tumors Arising on Acral Sites: A Molecular Survey.

A. Nicolas, F. Tirode, T. Jouary, 2023, The American journal of surgical pathology.

Expanding the Spectrum of Primary Cutaneous Carcinoma With BRD3-NUTM1 Fusion.

J. Lehmann-Che, M. Battistella, N. Macagno, 2021, The American journal of surgical pathology.

Thoracic NUT carcinoma: Common pathological features despite diversity of clinical presentations.

G. Ferretti, S. Lantuejoul, S. Khochbin, 2021, Lung cancer.

Gene fusions in poroma, porocarcinoma and related adnexal skin tumours: An update.

F. Tirode, A. Barlier, D. Schrama, 2023, Histopathology.

Identifying actionable targets in advanced cancer patients: Preliminary results from the Profiler program.

J. Blay, D. Frappaz, P. Biron, 2014 .

The histone deacetylase inhibitor panobinostat is active in patients with advanced pretreated ovarian sex-cord tumors.

J. Blay, I. Treilleux, I. Ray-Coquard, 2014, Annals of oncology : official journal of the European Society for Medical Oncology.

Combined activation of MAP kinase pathway and β-catenin signaling cause deep penetrating nevi

Robert L. Judson, I. Yeh, L. Cerroni, 2017, Nature Communications.

[Molecular biology of sarcoma and therapeutic choices].

J. Blay, I. Ray-Coquard, P. Cassier, 2015, Bulletin du Cancer.

A subset of epithelioid and spindle cell rhabdomyosarcomas is associated with TFCP2 fusions and common ALK upregulation

S. Salas, F. Tirode, J. Coindre, 2019, Modern Pathology.