Accumulation of Segmental Alterations Determines Progression in Neuroblastoma

Gudrun Schleiermacher , Isabelle Janoueix-Lerosey , Agnès Ribeiro , Jerzy Klijanienko
Journal of Clinical Oncology 28 ( 19) 3122 -3130

108
2010
Genome-wide association study identifies multiple new loci associated with Ewing sarcoma susceptibility

Mitchell J. Machiela , Thomas G. P. Grünewald , Didier Surdez , Stephanie Reynaud
Nature Communications 9 ( 1) 3184 -3184

20
2018
Balanced Translocations Disrupting SMARCB1 Are Hallmark Recurrent Genetic Alterations in Renal Medullary Carcinomas

Julien Calderaro , Julien Masliah-Planchon , Wilfrid Richer , Laetitia Maillot
European Urology 69 ( 6) 1055 -1061

87
2016
Locoregionally administered B7-H3-targeted CAR T cells for treatment of atypical teratoid/rhabdoid tumors.

Daniel Williamson , Pascal D. Johann , Marcel Kool , Stefan Pfister
Nature Medicine 26 ( 5) 712 -719

142
2020
The orphan nuclear receptor DAX1 is up-regulated by the EWS/FLI1 oncoprotein and is highly expressed in Ewing tumors.

Marta Mendiola , Jaime Carrillo , Eva García , Enzo Lalli
International Journal of Cancer 118 ( 6) 1381 -1389

63
2006
Complementation analyses suggest species-specific functions of the SNF5 homology domain.

Vanessa Bonazzi , Souhila Medjkane , Frédérique Quignon , Olivier Delattre
Biochemical and Biophysical Research Communications 336 ( 2) 634 -638

1
2005
51
2016
Extraosseous localized ewing tumors: improved outcome with anthracyclines--the French society of pediatric oncology and international society of pediatric oncology.

Jérôme Sales de Gauzy , Anne Gomez-Brouchet , Annie Rey , Olivier Delattre
Journal of Clinical Oncology 25 ( 10) 1176 -1182

40
2007
Dinucleotide repeat polymorphism at the D22S268 locus

Claude Marineau , Chantal Baron , Olivier Delattre , Jessica Zucman
Human Molecular Genetics 2 ( 3) 336 -336

28
1993
Isolation of cosmids and fetal brain cDNAs from the proximal long arm of human chromosome 22

Valérie Lamour , Nicolas Lévy , Chantal Desmaze , Véronique Baude
Human Molecular Genetics 2 ( 5) 535 -540

4
1993
Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus

Marc Sanson , Claude Marineau , Chantale Desmaze , Mohini Lutchman
Human Molecular Genetics 2 ( 8) 1215 -1220

45
1993
Oncogenic conversion of a novel orphan nuclear receptor by chromosome translocation

Yves Labelle , Jessica Zucman , Göran Stenman , Lars-Gunnar Kindblom
Human Molecular Genetics 4 ( 12) 2219 -2226

189
1995
131
1995
Variation in cadherins and catenins expression is linked to both proliferation and transformation of Rhabdomyosarcoma

Sophie Charrasse , Franck Comunale , Elisabeth Gilbert , Olivier Delattre
Oncogene 23 ( 13) 2420 -2430

42
2004
Gene expression profiling of 1p35-36 genes in neuroblastoma.

Isabelle Janoueix-Lerosey , Eugene Novikov , Marta Monteiro , Nadège Gruel
Oncogene 23 ( 35) 5912 -5922

52
2004
Stepwise occurrence of a complex unbalanced translocation in neuroblastoma leading to insertion of a telomere sequence and late chromosome 17q gain

Gudrun Schleiermacher , Franck Bourdeaut , Valérie Combaret , Gaelle Picrron
Oncogene 24 ( 20) 3377 -3384

23
2005
SMARCB1/INI1 inactivation in renal medullary carcinoma.

Julien Calderaro , Julien Moroch , Gaelle Pierron , Florence Pedeutour
Histopathology 61 ( 3) 428 -435

76
2012
Association of Partial Chromosome 3 Deletion in Uveal Melanomas With Metastasis-Free Survival.

Manuel Rodrigues , Khadija Ait Rais , Flore Salviat , Nathalie Algret
JAMA Ophthalmology 138 ( 2) 182 -188

6
2020