1. Ewing sarcoma family of tumors in children younger than 10 years of age
Pediatr Blood Cancer, 2017, 64(4) p. e26275
DOI: 10.1002/pbc.26275
2. Histological and immunohistochemical characteristics of undifferentiated small round cell sarcomas associated with CIC-DUX4 and BCOR-CCNB3 fusion genes
Virchows Arch, 2017, 470(4) p. 373
DOI: 10.1007/s00428-017-2072-8
3. Practical use and utility of fluorescence in situ hybridization in the pathological diagnosis of soft tissue and bone tumors.
J Orthop Sci, 2017, 22 p. 6
DOI: S0949-2658(17)30035-0
4. Primary CIC-DUX4 round cell sarcoma of the kidney: A treatment-refractory tumor with poor outcome
Pathology - Research and Practice, 2017, 213(2) p. 154
DOI: 10.1016/j.prp.2016.11.015
5. Primary undifferentiated small round cell sarcoma of the deep abdominal wall with a novel variant of t(10;19) CIC-DUX4 gene fusion
Pathology - Research and Practice, 2017, 213(10) p. 1315
DOI: 10.1016/j.prp.2017.06.008
6. The Utility of ETV1, ETV4, and ETV5 RNA In Situ Hybridization in the Diagnosis of CIC‐DUX4 Sarcomas
Year: 2017
7. Sarcomas with CIC-rearrangements are a distinct pathologic entity with aggressive outcome: a clinicopathologic and molecular study of 115 cases
Year: 2017
8. ETV transcriptional upregulation is more reliable than RNA sequencing algorithms and FISH in diagnosing round cell sarcomas with CIC gene rearrangements
Year: 2017
9. A case of CIC‐rearranged undifferentiated round‐cell sarcoma with exclusive spindled morphology and diffuse CD99 positivity: a potential pitfall
Year: 2017
10. Novel exon–exon breakpoint in CIC-DUX4 fusion sarcoma identified by anchored multiplex PCR (Archer FusionPlex Sarcoma Panel)
Year: 2017
11. Primary undifferentiated small round cell sarcoma of the deep abdominal wall with a novel variant of t (10; 19) CIC-DUX4 gene fusion
Year: 2017
12. A new mode of DNA binding distinguishes Capicua from other HMG-box factors and explains its mutation patterns in cancer
Year: 2017
13. Recently Discovered Fusion Genes and Their Implications in Cancer
Year: 2017
14. Sarcoma With CIC-DUX4 Gene Fusion: Case Report of Kidney Tumor Location in a 12-year-old Boy
Year: 2017
15. A t (4; 19) pediatric undifferentiated sarcoma with a novel variant of the CIC-DUX4 fusion transcript
Year: 2017
16. Update on Families of Round Cell Sarcomas Other than Classical Ewing Sarcomas
Year: 2017
17. Undifferentiated “round” cell (“Ewing-like”) sarcoma: not always so-round nor Ewing-like
Year: 2017
18. Head and Neck Round Cell Sarcomas: A Comparative Clinicopathologic Analysis of 2 Molecular Subsets: Ewing and CIC-Rearranged Sarcomas
Year: 2017
21. Dermal primitive non-neural granular cell tumour: a case report
Year: 2017
24. CIC-DUX4fusion-positive round-cell sarcomas of soft tissue and bone: a single-institution morphological and molecular analysis of seven cases
Histopathology, 2016, 69(4) p. 624
DOI: 10.1111/his.12985
25. Targeted next-generation sequencing of CIC-DUX4 soft tissue sarcomas demonstrates low mutational burden and recurrent chromosome 1p loss.
Hum. Pathol., 2016, 58 p. 1
DOI: S0046-8177(16)30212-X
26. Ewing sarcoma: a chronicle of molecular pathogenesis
Human Pathology, 2016, 55 p. 91
DOI: 10.1016/j.humpath.2016.05.008
27. CIC-rearranged Sarcomas
The American Journal of Surgical Pathology, 2016, 40(3) p. 313
DOI: 10.1097/PAS.0000000000000570
28. Refinements in Sarcoma Classification in the Current 2013 World Health Organization Classification of Tumours of Soft Tissue and Bone.
Surg. Oncol. Clin. N. Am., 2016, 25 p. 6
DOI: 10.1016/j.soc.2016.05.001
29. Defining Ewing and Ewing-like small round cell tumors (SRCT): The need for molecular techniques in their categorization and differential diagnosis. A study of 200 cases
Annals of Diagnostic Pathology, 2016, 22 p. 25
DOI: 10.1016/j.anndiagpath.2016.03.002
30. New Brain Tumor Entities Emerge from Molecular Classification of CNS-PNETs
Cell, 2016, 164(5) p. 1060
DOI: 10.1016/j.cell.2016.01.015
31. CIC-rearranged sarcomas: a study of 20 cases and comparisons with Ewing sarcomas
Year: 2016
32. CIC–DUX4 fusion‐positive round‐cell sarcomas of soft tissue and bone: a single‐institution morphological and molecular analysis of seven cases
Year: 2016
33. Evaluation of NKX2-2 expression in round cell sarcomas and other tumors with EWSR1 rearrangement: imperfect specificity for Ewing sarcoma
Year: 2016
34. Recurrent BCOR internal tandem duplication and YWHAE-NUTM2B fusions in soft tissue undifferentiated round cell sarcoma of infancy: overlapping genetic features …
Year: 2016
35. ETV4 is a useful marker for the diagnosis of CIC-rearranged undifferentiated round-cell sarcomas: a study of 127 cases including mimicking lesions
Year: 2016
36. Round cell sarcoma with CIC‐DUX4 gene fusion: Discussion of the distinctive cytomorphologic, immunohistochemical, and molecular features in the …
Year: 2016
37. Defining Ewing and Ewing-like small round cell tumors (SRCT): The need for molecular techniques in their categorization and differential diagnosis. A study of 200 …
Year: 2016
38. Activity and mechanism of action of histone deacetylase inhibitors in synovial sarcoma
Year: 2016
39. Clinical outcomes of undifferentiated sarcomas are similar with that of other spindle cell sarcomas of specific histologic types: an institutional experience
Year: 2016
40. Fluorescence in situ hybridization in surgical pathology: principles and applications
Year: 2016
41. Pediatric soft tissue tumor pathology: A happy morpho-molecular union
Year: 2016
42. Atypical Ewing sarcoma breakpoint region 1 fluorescence in‐situ hybridization signal patterns in bone and soft tissue tumours: diagnostic experience with 135 cases
Year: 2016
43. Novel peptides and combination of peptides for use in immunotherapy against ovarian cancer and other cancers
Year: 2016
44. Non-mesenchymal Mimics of Sarcoma.
Surg Pathol Clin, 2015, 8 p. 4
DOI: 10.1016/j.path.2015.05.010
45. A case of mediastinum undifferentiated high grade pleomorphic sarcoma.
Int J Clin Exp Med, 2015, 8 p. 1
46. BCOR-CCNB3 fusions are frequent in undifferentiated sarcomas of male children.
Mod. Pathol., 2015, 28 p. 5
DOI: 1
47. Ewing-like sarcoma with CIC-DUX4 gene fusion in a patient with neurofibromatosis type 1. A hitherto unreported association
Pathology - Research and Practice, 2015, 211(11) p. 877
DOI: 10.1016/j.prp.2015.08.003
48. Ifosfamide
Reactions Weekly, 2015, 1566(1) p. 124
DOI: 10.1007/s40278-015-4741-1
49. SMARCA4 (BRG1) loss of expression is a useful marker for the diagnosis of ovarian small cell carcinoma of the hypercalcemic type (ovarian rhabdoid tumor): a …
Year: 2015
50. Immunohistochemistry as potential diagnostic pitfall in the most common solid tumors of children and adolescents
Year: 2015
51. High-grade undifferentiated small round cell sarcoma with t (4; 19)(q35; q13. 1) CIC-DUX4 fusion: emerging entities of soft tissue tumors with unique …
Year: 2015
52. The new kids on the block: recently characterized soft tissue tumors
Year: 2015
53. Quatrième édition de la classification OMS des tumeurs des tissus mous
Year: 2015