Gaelle Pierron
Gaelle Pierron
PhD. Responsable Adjoint Unité Génétique Somatique Institut Curie Paris
Verified email at curie.fr
Title
Cited by
Cited by
Year
Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma
I Janoueix-Lerosey, D Lequin, L Brugieres, A Ribeiro, L de Pontual, ...
Nature 455 (7215), 967-970, 2008
7802008
Fusion gene-negative alveolar rhabdomyosarcoma is clinically and molecularly indistinguishable from embryonal rhabdomyosarcoma
D Williamson, E Missiaglia, A de Reynies, G Pierron, B Thuille, ...
J Clin Oncol 28 (13), 2151-8, 2010
3332010
A new subtype of bone sarcoma defined by BCOR-CCNB3 gene fusion
G Pierron, F Tirode, C Lucchesi, S Reynaud, S Ballet, S Cohen-Gogo, ...
Nature genetics 44 (4), 461, 2012
2862012
Genomic landscape of Ewing sarcoma defines an aggressive subtype with co-association of STAG2 and TP53 mutations
F Tirode, D Surdez, X Ma, M Parker, MC Le Deley, A Bahrami, Z Zhang, ...
Cancer discovery 4 (11), 1342-1353, 2014
2572014
Identification of typical medullary breast carcinoma as a genomic sub-group of basal-like carcinomas, a heterogeneous new molecular entity
A Vincent-Salomon, N Gruel, C Lucchesi, G MacGrogan, R Dendale, ...
Breast Cancer Research 9 (2), R24, 2007
2072007
Impact of EWS-ETS fusion type on disease progression in Ewing’s sarcoma/peripheral primitive neuroectodermal tumor: prospective results from the cooperative Euro-EWING 99 trial
MC Le Deley, O Delattre, KL Schaefer, SA Burchill, G Koehler, ...
J Clin Oncol 28 (12), 1982-8, 2010
2052010
Circulating tumor DNA as a non‐invasive substitute to metastasis biopsy for tumor genotyping and personalized medicine in a prospective trial across all tumor types
R Lebofsky, C Decraene, V Bernard, M Kamal, A Blin, Q Leroy, T Rio Frio, ...
Molecular oncology 9 (4), 783-790, 2015
1972015
PAX3/FOXO1 Fusion Gene Status Is the Key Prognostic Molecular Marker in Rhabdomyosarcoma and Significantly Improves Current Risk Stratification
E Missiaglia, D Williamson, J Chisholm, P Wirapati, G Pierron, F Petel, ...
Journal of Clinical Oncology 30 (14), 1670-1677, 2012
1972012
Two types of chromosome 1p losses with opposite significance in gliomas
A Idbaih, Y Marie, G Pierron, C Brennetot, K Hoang‐Xuan, M Kujas, ...
Annals of neurology 58 (3), 483-487, 2005
1732005
High frequency of TP53 mutation in BRCA1 and sporadic basal-like carcinomas but not in BRCA1 luminal breast tumors
E Manié, A Vincent-Salomon, J Lehmann-Che, G Pierron, E Turpin, ...
Cancer research 69 (2), 663-671, 2009
1602009
Integrated genomic and transcriptomic analysis of ductal carcinoma in situ of the breast
A Vincent-Salomon, C Lucchesi, N Gruel, V Raynal, G Pierron, ...
Clinical cancer research 14 (7), 1956-1965, 2008
1472008
Frequent hSNF5/INI1 germline mutations in patients with rhabdoid tumor
F Bourdeaut, D Lequin, L Brugières, S Reynaud, C Dufour, F Doz, ...
Clinical Cancer Research 17 (1), 31-38, 2011
1412011
Accumulation of segmental alterations determines progression in neuroblastoma
G Schleiermacher, I Janoueix-Lerosey, A Ribeiro, J Klijanienko, ...
Journal of Clinical Oncology 28 (19), 3122-3130, 2010
1242010
Emergence of New ALK Mutations at Relapse of Neuroblastoma
G Schleiermacher, N Javanmardi, V Bernard, Q Leroy, J Cappo, ...
Journal of clinical oncology 32 (25), 2727-2734, 2014
1202014
hSNF5/INI1‐deficient tumours and rhabdoid tumours are convergent but not fully overlapping entities
F Bourdeaut, P Freneaux, B Thuille, A Lellouch‐Tubiana, A Nicolas, ...
The Journal of Pathology: A Journal of the Pathological Society of Great …, 2007
1202007
VAMP: visualization and analysis of array-CGH, transcriptome and other molecular profiles
PL Rosa, E Viara, P Hupé, G Pierron, S Liva, P Neuvial, I Brito, S Lair, ...
Bioinformatics 22 (17), 2066-2073, 2006
1202006
Common variants near TARDBP and EGR2 are associated with susceptibility to Ewing sarcoma
S Postel-Vinay, AS Véron, F Tirode, G Pierron, S Reynaud, H Kovar, ...
Nature genetics 44 (3), 323, 2012
1192012
BAC array CGH distinguishes mutually exclusive alterations that define clinicogenetic subtypes of gliomas
A Idbaih, Y Marie, C Lucchesi, G Pierron, E Manié, V Raynal, V Mosseri, ...
International journal of cancer 122 (8), 1778-1786, 2008
1132008
Chromosome instability accounts for reverse metastatic outcomes of pediatric and adult synovial sarcomas
P Lagarde, J Przybyl, C Brulard, G Pérot, G Pierron, O Delattre, R Sciot, ...
Journal of clinical oncology 31 (5), 608-615, 2013
1042013
High frequency of germline SUFU mutations in children with desmoplastic/nodular medulloblastoma younger than 3 years of age
L Brugières, A Remenieras, G Pierron, P Varlet, S Forget, V Byrde, ...
J Clin Oncol 30 (17), 2087-2093, 2012
1042012
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