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Olivier Delattre

This is a preview profile on BiomedExperts - the first literature-based scientific social network. It brings the right researchers together and allows them to collaborate online. Collexis and Dell provide the BiomedExperts network of +1.5 Million pre-calculated profiles free of charge to researchers worldwide.

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Bourdeaut Franck; Janoueix-Lerosey Isabelle; Lucchesi Carlo; Paris Régine; Ribeiro Agnès; de Pontual Loïc; Amiel Jeanne; Lyonnet Stanislas; Pierron Gaëlle; Michon Jean; Peuchmaur Michel; Delattre Olivier
Cholinergic switch associated with morphological differentiation in neuroblastoma.
Fattet Sarah; Haberler Christine; Legoix Patricia; Varlet Pascale; Lellouch-Tubiana Arielle; Lair Severine; Manie Elodie; Raquin Marie-Anne; Bours Danielle; Carpentier Sabrina; Barillot Emmanuel; Grill Jacques; Doz Francois; Puget Stephanie; Janoueix-Lerosey Isabelle; Delattre Olivier
Beta-catenin status in paediatric medulloblastomas: correlation of immunohistochemical expression with mutational status, genetic profiles, and clinical characteristics.
Bourdeaut Franck; de Carli Emilie; Timsit Sandra; Coze Carole; Chastagner Pascal; Sarnacki Sabine; Delattre Olivier; Peuchmaur Michel; Rubie Hervé; Michon Jean;
VIP hypersecretion as primary or secondary syndrome in neuroblastoma: A retrospective study by the Société Française des Cancers de l'Enfant (SFCE).

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All Publications

2009: Bourdeaut Franck; Janoueix-Lerosey Isabelle; Lucchesi Carlo; Paris Régine; Ribeiro Agnès; de Pontual Loïc; Amiel Jeanne; Lyonnet Stanislas; Pierron Gaëlle; Michon Jean; Peuchmaur Michel; Delattre Olivier
Cholinergic switch associated with morphological differentiation in neuroblastoma.
The Journal of pathology 2009;219(4):463-72.
2009: Fattet Sarah; Haberler Christine; Legoix Patricia; Varlet Pascale; Lellouch-Tubiana Arielle; Lair Severine; Manie Elodie; Raquin Marie-Anne; Bours Danielle; Carpentier Sabrina; Barillot Emmanuel; Grill Jacques; Doz Francois; Puget Stephanie; Janoueix-Lerosey Isabelle; Delattre Olivier
Beta-catenin status in paediatric medulloblastomas: correlation of immunohistochemical expression with mutational status, genetic profiles, and clinical characteristics.
The Journal of pathology 2009;218(1):86-94.
2009: Bourdeaut Franck; de Carli Emilie; Timsit Sandra; Coze Carole; Chastagner Pascal; Sarnacki Sabine; Delattre Olivier; Peuchmaur Michel; Rubie Hervé; Michon Jean;
VIP hypersecretion as primary or secondary syndrome in neuroblastoma: A retrospective study by the Société Française des Cancers de l'Enfant (SFCE).
Pediatric blood & cancer 2009;52(5):585-90.
2009: Janoueix-Lerosey Isabelle; Delattre Olivier
[ALK, a key gene in the pathogenesis of neuroblastoma]
Médecine sciences : M/S 2009;25(4):330-2.
2009: Janoueix-Lerosey Isabelle; Schleiermacher Gudrun; Michels Evi; Mosseri Véronique; Ribeiro Agnès; Lequin Delphine; Vermeulen Joëlle; Couturier Jérôme; Peuchmaur Michel; Valent Alexander; Plantaz Dominique; Rubie Hervé; Valteau-Couanet Dominique; Thomas Caroline; Combaret Valérie; Rousseau Raphaël; Eggert Angelika; Michon Jean; Speleman Frank; Delattre Olivier
Overall genomic pattern is a predictor of outcome in neuroblastoma.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2009;27(7):1026-33.
2009: Manié Elodie; Vincent-Salomon Anne; Lehmann-Che Jacqueline; Pierron Gaelle; Turpin Elisabeth; Warcoin Mathilde; Gruel Nadège; Lebigot Ingrid; Sastre-Garau Xavier; Lidereau Rosette; Remenieras Audrey; Feunteun Jean; Delattre Olivier; de Thé Hugues; Stoppa-Lyonnet Dominique; Stern Marc-Henri
High frequency of TP53 mutation in BRCA1 and sporadic basal-like carcinomas but not in BRCA1 luminal breast tumors.
Cancer research 2009;69(2):663-71.
2009: Rodrigues-Ferreira Sylvie; Di Tommaso Anne; Dimitrov Ariane; Cazaubon Sylvie; Gruel Nadège; Colasson Hélène; Nicolas André; Chaverot Nathalie; Molinié Vincent; Reyal Fabien; Sigal-Zafrani Brigitte; Terris Benoit; Delattre Olivier; Radvanyi François; Perez Franck; Vincent-Salomon Anne; Nahmias Clara
8p22 MTUS1 gene product ATIP3 is a novel anti-mitotic protein underexpressed in invasive breast carcinoma of poor prognosis.
PloS one 2009;4(10):e7239.
2009: Guillon Noëlle; Tirode Franck; Boeva Valentina; Zynovyev Andrei; Barillot Emmanuel; Delattre Olivier
The oncogenic EWS-FLI1 protein binds in vivo GGAA microsatellite sequences with potential transcriptional activation function.
PloS one 2009;4(3):e4932.
2009: Benetkiewicz Magdalena; Idbaih Ahmed; Cousin Pierre-Yves; Boisselier Blandine; Marie Yannick; Crinière Emmanuelle; Hoang-Xuan Khê; Delattre Jean-Yves; Sanson Marc; Delattre Olivier
NOTCH2 is neither rearranged nor mutated in t(1;19) positive oligodendrogliomas.
PloS one 2009;4(1):e4107.
2008: Tirode Franck; Delattre Olivier
[Stem cells and connective-tissue tumors: Ewing's sarcoma]
Annales de pathologie 2008;28 Spec No 1(1):S33-4.
2008: Janoueix-Lerosey Isabelle; Lequin Delphine; Brugières Laurence; Ribeiro Agnès; de Pontual Loïc; Combaret Valérie; Raynal Virginie; Puisieux Alain; Schleiermacher Gudrun; Pierron Gaëlle; Valteau-Couanet Dominique; Frebourg Thierry; Michon Jean; Lyonnet Stanislas; Amiel Jeanne; Delattre Olivier
Somatic and germline activating mutations of the ALK kinase receptor in neuroblastoma.
Nature 2008;455(7215):967-70.
2008: Fix Anne; Lucchesi Carlo; Ribeiro Agnès; Lequin Delphine; Pierron Gaëlle; Schleiermacher Gudrun; Delattre Olivier; Janoueix-Lerosey Isabelle
Characterization of amplicons in neuroblastoma: high-resolution mapping using DNA microarrays, relationship with outcome, and identification of overexpressed genes.
Genes, chromosomes & cancer 2008;47(10):819-34.
2008: Bernard-Pierrot Isabelle; Gruel Nadège; Stransky Nicolas; Vincent-Salomon Anne; Reyal Fabien; Raynal Virginie; Vallot Céline; Pierron Gaëlle; Radvanyi François; Delattre Olivier
Characterization of the recurrent 8p11-12 amplicon identifies PPAPDC1B, a phosphatase protein, as a new therapeutic target in breast cancer.
Cancer research 2008;68(17):7165-75.
2008: Bourdeaut Franck; Fréneaux Paul; Thuille Bénédicte; Bergeron Christophe; Laurence Valérie; Brugières Laurence; Vérité Cécile; Michon Jean; Delattre Olivier; Orbach Daniel
Extra-renal non-cerebral rhabdoid tumours.
Pediatric blood & cancer 2008;51(3):363-8.
2008: Caramel Julie; Quignon Frédérique; Delattre Olivier
RhoA-dependent regulation of cell migration by the tumor suppressor hSNF5/INI1.
Cancer research 2008;68(15):6154-61.
2008: Idbaih Ahmed; Kouwenhoven Mathilde; Jeuken Judith; Carpentier Catherine; Gorlia Thierry; Kros Johan M; French Pim; Teepen Johannes L; Delattre Olivier; Delattre Jean-Yves; van den Bent Martin; Hoang-Xuan Khê
Chromosome 1p loss evaluation in anaplastic oligodendrogliomas.
Neuropathology : official journal of the Japanese Society of Neuropathology 2008;28(4):440-3.
2008: Bourdeaut F; Ribeiro A; Paris R; Pierron G; Couturier J; Peuchmaur M; Delattre O
In neuroblastic tumours, Schwann cells do not harbour the genetic alterations of neuroblasts but may nevertheless share the same clonal origin.
Oncogene 2008;27(21):3066-71.
2008: Vincent-Salomon Anne; Lucchesi Carlo; Gruel Nadège; Raynal Virginie; Pierron Gaëlle; Goudefroye Rémi; Reyal Fabien; Radvanyi François; Salmon Rémy; Thiery Jean-Paul; Sastre-Garau Xavier; Sigal-Zafrani Brigitte; Fourquet Alain; Delattre Olivier;
Integrated genomic and transcriptomic analysis of ductal carcinoma in situ of the breast.
Clinical cancer research : an official journal of the American Association for Cancer Research 2008;14(7):1956-65.
2008: Idbaih Ahmed; Marie Yannick; Lucchesi Carlo; Pierron Gaëlle; Manié Elodie; Raynal Virginie; Mosseri Véronique; Hoang-Xuan Khê; Kujas Michèle; Brito Isabel; Mokhtari Karima; Sanson Marc; Barillot Emmanuel; Aurias Alain; Delattre Jean-Yves; Delattre Olivier
BAC array CGH distinguishes mutually exclusive alterations that define clinicogenetic subtypes of gliomas.
International journal of cancer. Journal international du cancer 2008;122(8):1778-86.
2008: Bourdeaut Franck; Guiochon-Mantel Anne; Fabre Monique; Martelli Hélène; Patte Catherine; Porta Gilda; Bernard Olivier; Delattre Olivier; Jacquemin Emmanuel
Alagille syndrome and nephroblastoma: Unusual coincidence of two rare disorders.
Pediatric blood & cancer 2008;50(4):908-11.
2008: Tirode Franck; Laud-Duval Karine; Delattre Olivier
[Cellular origin of Ewing's tumor. A corner of the veil is lifted]
Médecine sciences : M/S 2008;24(3):248-50.
2008: Caramel J; Medjkane S; Quignon F; Delattre O
The requirement for SNF5/INI1 in adipocyte differentiation highlights new features of malignant rhabdoid tumors.
Oncogene 2008;27(14):2035-44.
2008: Ducray François; Idbaih Ahmed; de Reyniès Aurélien; Bièche Ivan; Thillet Joëlle; Mokhtari Karima; Lair Séverine; Marie Yannick; Paris Sophie; Vidaud Michel; Hoang-Xuan Khê; Delattre Olivier; Delattre Jean-Yves; Sanson Marc
Anaplastic oligodendrogliomas with 1p19q codeletion have a proneural gene expression profile.
Molecular cancer 2008;7():41.
2007: de Pontual Loïc; Trochet Delphine; Bourdeaut Franck; Thomas Sophie; Etchevers Heather; Chompret Agnes; Minard Véronique; Valteau Dominique; Brugieres Laurence; Munnich Arnold; Delattre Olivier; Lyonnet Stanislas; Janoueix-Lerosey Isabelle; Amiel Jeanne
Methylation-associated PHOX2B gene silencing is a rare event in human neuroblastoma.
European journal of cancer (Oxford, England : 1990) 2007;43(16):2366-72.
2007: Idbaih Ahmed; Boisselier Blandine; Sanson Marc; Crinière Emmanuelle; Liva Stéphane; Marie Yannick; Carpentier Catherine; Paris Sophie; Laigle-Donadey Florence; Mokhtari Karima; Kujas Michèle; Hoang-Xuan Khê; Delattre Olivier; Delattre Jean-Yves
Tumor genomic profiling and TP53 germline mutation analysis of first-degree relative familial gliomas.
Cancer genetics and cytogenetics 2007;176(2):121-6.
2007: Marangoni Elisabetta; Vincent-Salomon Anne; Auger Nathalie; Degeorges Armelle; Assayag Franck; de Cremoux Patricia; de Plater Ludmilla; Guyader Charlotte; De Pinieux Gonzague; Judde Jean-Gabriel; Rebucci Magali; Tran-Perennou Carine; Sastre-Garau Xavier; Sigal-Zafrani Brigitte; Delattre Olivier; Diéras Véronique; Poupon Marie-France
A new model of patient tumor-derived breast cancer xenografts for preclinical assays.
Clinical cancer research : an official journal of the American Association for Cancer Research 2007;13(13):3989-98.
2007: Schleiermacher G; Michon J; Huon I; d'Enghien C Dubois; Klijanienko J; Brisse H; Ribeiro A; Mosseri V; Rubie H; Munzer C; Thomas C; Valteau-Couanet D; Auvrignon A; Plantaz D; Delattre O; Couturier J;
Chromosomal CGH identifies patients with a higher risk of relapse in neuroblastoma without MYCN amplification.
British journal of cancer 2007;97(2):238-46.
2007: Tirode Franck; Laud-Duval Karine; Prieur Alexandre; Delorme Bruno; Charbord Pierre; Delattre Olivier
Mesenchymal stem cell features of Ewing tumors.
Cancer cell 2007;11(5):421-9.
2007: Mariani Odette; Brennetot Caroline; Coindre Jean-Michel; Gruel Nadège; Ganem Carine; Delattre Olivier; Stern Marc-Henri; Aurias Alain
JUN oncogene amplification and overexpression block adipocytic differentiation in highly aggressive sarcomas.
Cancer cell 2007;11(4):361-74.
2007: de Cremoux Patricia; Jourdan-Da-Silva Nathalie; Couturier Jérôme; Tran-Perennou Carine; Schleiermacher Gudrun; Fehlbaum Pascale; Doz François; Mosseri Véronique; Delattre Olivier; Klijanienko Jerzy; Vielh Philippe; Michon Jean
Role of chemotherapy resistance genes in outcome of neuroblastoma.
Pediatric blood & cancer 2007;48(3):311-7.
2007: Berrebi Dominique; Benkirane Amal; Ferkdadji Latifa; de Lagausie Pascal; Delattre Olivier; Chomette Pascale; Schleiermacher Gudrun; Michon Jean; Peuchmaur Michel
[Atypical desmoplastic small round cell tumor in a very young child]
Annales de pathologie 2007;27(1):53-5.
2007: Bourdeaut F; Fréneaux P; Thuille B; Lellouch-Tubiana A; Nicolas A; Couturier J; Pierron G; Sainte-Rose C; Bergeron C; Bouvier R; Rialland X; Laurence V; Michon J; Sastre-Garau X; Delattre O
hSNF5/INI1-deficient tumours and rhabdoid tumours are convergent but not fully overlapping entities.
The Journal of pathology 2007;211(3):323-30.
2007: Vincent-Salomon Anne; Gruel Nadège; Lucchesi Carlo; MacGrogan Gaëtan; Dendale Remi; Sigal-Zafrani Brigitte; Longy Michel; Raynal Virginie; Pierron Gaëlle; de Mascarel Isabelle; Taris Corinne; Stoppa-Lyonnet Dominique; Pierga Jean-Yves; Salmon Rémy; Sastre-Garau Xavier; Fourquet Alain; Delattre Olivier; de Cremoux Patricia; Aurias Alain
Identification of typical medullary breast carcinoma as a genomic sub-group of basal-like carcinomas, a heterogeneous new molecular entity.
Breast cancer research : BCR 2007;9(2):R24.
2006: Vermeulen J; Ballet S; Oberlin O; Peter M; Pierron G; Longavenne E; Laurence V; Kanold J; Chastagner P; Lejars O; Blay J-Y; Marec-Berard P; Michon J; Delattre O; Schleiermacher G
Incidence and prognostic value of tumour cells detected by RT-PCR in peripheral blood stem cell collections from patients with Ewing tumour.
British journal of cancer 2006;95(10):1326-33.
2006: Albanese Patricia; Belin Marie-France; Delattre Olivier
The tumour suppressor hSNF5/INI1 controls the differentiation potential of malignant rhabdoid cells.
European journal of cancer (Oxford, England : 1990) 2006;42(14):2326-34.
2006: La Rosa Philippe; Viara Eric; Hupé Philippe; Pierron Gaëlle; Liva Stéphane; Neuvial Pierre; Brito Isabel; Lair Séverine; Servant Nicolas; Robine Nicolas; Manié Elodie; Brennetot Caroline; Janoueix-Lerosey Isabelle; Raynal Virginie; Gruel Nadège; Rouveirol Céline; Stransky Nicolas; Stern Marc-Henri; Delattre Olivier; Aurias Alain; Radvanyi François; Barillot Emmanuel
VAMP: visualization and analysis of array-CGH, transcriptome and other molecular profiles.
Bioinformatics (Oxford, England) 2006;22(17):2066-73.
2006: Mendiola Marta; Carrillo Jaime; García Eva; Lalli Enzo; Hernández Teresa; de Alava Enrique; Tirode Franck; Delattre Olivier; García-Miguel Purificación; López-Barea Fernando; Pestaña Angel; Alonso Javier
The orphan nuclear receptor DAX1 is up-regulated by the EWS/FLI1 oncoprotein and is highly expressed in Ewing tumors.
International journal of cancer. Journal international du cancer 2006;118(6):1381-9.
2005: Janoueix-Lerosey Isabelle; Hupé Philippe; Maciorowski Zofia; La Rosa Philippe; Schleiermacher Gudrun; Pierron Gaëlle; Liva Stéphane; Barillot Emmanuel; Delattre Olivier
Preferential occurrence of chromosome breakpoints within early replicating regions in neuroblastoma.
Cell cycle (Georgetown, Tex.) 2005;4(12):1842-6.
2005: Bonazzi Vanessa; Medjkane Souhila; Quignon Frédérique; Delattre Olivier
Complementation analyses suggest species-specific functions of the SNF5 homology domain.
Biochemical and biophysical research communications 2005;336(2):634-8.
2005: Bourdeaut Franck; Trochet Delphine; Janoueix-Lerosey Isabelle; Ribeiro Agnès; Deville Anne; Coz Carole; Michiels Jean-François; Lyonnet Stanislas; Amiel Jeanne; Delattre Olivier
Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma.
Cancer letters 2005;228(1-2):51-8.
2005: Idbaih Ahmed; Marie Yannick; Pierron Gaëlle; Brennetot Caroline; Hoang-Xuan Khê; Kujas Michèle; Mokhtari Karima; Sanson Marc; Lejeune Julie; Aurias Alain; Delattre Olivier; Delattre Jean-Yves
Two types of chromosome 1p losses with opposite significance in gliomas.
Annals of neurology 2005;58(3):483-7.
2005: Schleiermacher Gudrun; Bourdeaut Franck; Combaret Valérie; Picrron Gaelle; Raynal Virginie; Aurias Alain; Ribeiro Agnes; Janoueix-Lerosey Isabelle; Delattre Olivier
Stepwise occurrence of a complex unbalanced translocation in neuroblastoma leading to insertion of a telomere sequence and late chromosome 17q gain.
Oncogene 2005;24(20):3377-84.
2005: Rousseau-Merck Marie-Françoise; Fiette Laurence; Klochendler-Yeivin Agnès; Delattre Olivier; Aurias Alain
Chromosome mechanisms and INI1 inactivation in human and mouse rhabdoid tumors.
Cancer genetics and cytogenetics 2005;157(2):127-33.
2005: Reyal Fabien; Stransky Nicolas; Bernard-Pierrot Isabelle; Vincent-Salomon Anne; de Rycke Yann; Elvin Paul; Cassidy Andrew; Graham Alexander; Spraggon Carolyn; Désille Yoann; Fourquet Alain; Nos Claude; Pouillart Pierre; Magdelénat Henri; Stoppa-Lyonnet Dominique; Couturier Jérôme; Sigal-Zafrani Brigitte; Asselain Bernard; Sastre-Garau Xavier; Delattre Olivier; Thiery Jean Paul; Radvanyi François
Visualizing chromosomes as transcriptome correlation maps: evidence of chromosomal domains containing co-expressed genes--a study of 130 invasive ductal breast carcinomas.
Cancer research 2005;65(4):1376-83.
2004: Hostein Isabelle; Andraud-Fregeville Marie; Guillou Louis; Terrier-Lacombe Marie-José; Deminière Colette; Ranchère Dominique; Lussan Catherine; Longavenne Elisabeth; Bui Nguyen Binh; Delattre Olivier; Coindre Jean-Michel
Rhabdomyosarcoma: value of myogenin expression analysis and molecular testing in diagnosing the alveolar subtype: an analysis of 109 paraffin-embedded specimens.
Cancer 2004;101(12):2817-24.
2004: Laprie Anne; Michon Jean; Hartmann Olivier; Munzer Caroline; Leclair Marc-David; Coze Carole; Valteau-Couanet Dominique; Plantaz Dominique; Carrie Christian; Habrand Jean-Louis; Bergeron Christophe; Chastagner Pascal; Défachelles Anne-Sophie; Delattre Olivier; Combaret Valérie; Bénard Jean; Pérel Yves; Gandemer Virginie; Rubie Hervé;
High-dose chemotherapy followed by locoregional irradiation improves the outcome of patients with international neuroblastoma staging system Stage II and III neuroblastoma with MYCN amplification.
Cancer 2004;101(5):1081-9.
2004: Prieur Alexandre; Tirode Franck; Cohen Pinchas; Delattre Olivier
EWS/FLI-1 silencing and gene profiling of Ewing cells reveal downstream oncogenic pathways and a crucial role for repression of insulin-like growth factor binding protein 3.
Molecular and cellular biology 2004;24(16):7275-83.
2004: Janoueix-Lerosey Isabelle; Novikov Eugene; Monteiro Marta; Gruel Nadège; Schleiermacher Gudrun; Loriod Béatrice; Nguyen Catherine; Delattre Olivier
Gene expression profiling of 1p35-36 genes in neuroblastoma.
Oncogene 2004;23(35):5912-22.
2004: Fix Anne; Peter Martine; Pierron Gaëlle; Aurias Alain; Delattre Olivier; Janoueix-Lerosey Isabelle
High-resolution mapping of amplicons of the short arm of chromosome 1 in two neuroblastoma tumors by microarray-based comparative genomic hybridization.
Genes, chromosomes & cancer 2004;40(3):266-70.
2004: Medjkane Souhila; Novikov Eugene; Versteege Isabella; Delattre Olivier
The tumor suppressor hSNF5/INI1 modulates cell growth and actin cytoskeleton organization.
Cancer research 2004;64(10):3406-13.
2004: Trochet Delphine; Bourdeaut Franck; Janoueix-Lerosey Isabelle; Deville Anne; de Pontual Loïc; Schleiermacher Gudrun; Coze Carole; Philip Nicole; Frébourg Thierry; Munnich Arnold; Lyonnet Stanislas; Delattre Olivier; Amiel Jeanne
Germline mutations of the paired-like homeobox 2B (PHOX2B) gene in neuroblastoma.
American journal of human genetics 2004;74(4):761-4.
2004: Schleiermacher Gudrun; Raynal Virginie; Janoueix-Lerosey Isabelle; Combaret Valérie; Aurias Alain; Delattre Olivier
Variety and complexity of chromosome 17 translocations in neuroblastoma.
Genes, chromosomes & cancer 2004;39(2):143-50.
2003: Schleiermacher Gudrun; Janoueix-Lerosey Isabelle; Combaret Valérie; Derré Josette; Couturier Jérome; Aurias Alain; Delattre Olivier
Combined 24-color karyotyping and comparative genomic hybridization analysis indicates predominant rearrangements of early replicating chromosome regions in neuroblastoma.
Cancer genetics and cytogenetics 2003;141(1):32-42.
2003: Schleiermacher Gudrun; Peter Martine; Oberlin Odile; Philip Thierry; Rubie Hervé; Mechinaud Françoise; Sommelet-Olive Danièle; Landman-Parker Judith; Bours Danièle; Michon Jean; Delattre Olivier;
Increased risk of systemic relapses associated with bone marrow micrometastasis and circulating tumor cells in localized ewing tumor.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 2003;21(1):85-91.
2002: Sancéau Josiane; Poupon Marie-France; Delattre Olivier; Sastre-Garau Xavier; Wietzerbin Juana
Strong inhibition of Ewing tumor xenograft growth by combination of human interferon-alpha or interferon-beta with ifosfamide.
Oncogene 2002;21(50):7700-9.
2002: Versteege Isabella; Medjkane Souhila; Rouillard Danny; Delattre Olivier
A key role of the hSNF5/INI1 tumour suppressor in the control of the G1-S transition of the cell cycle.
Oncogene 2002;21(42):6403-12.
2002: Mérel Philippe; Prieur Alexandre; Pfeiffer Petra; Delattre Olivier
Absence of major defects in non-homologous DNA end joining in human breast cancer cell lines.
Oncogene 2002;21(36):5654-9.
2002: Lee Hwei-Yee; Yoon Chui-Shuen; Sevenet Nicolas; Rajalingam Vasanthi; Delattre Olivier; Walford Norman Q
Rhabdoid tumor of the kidney is a component of the rhabdoid predisposition syndrome.
Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society 2002;5(4):395-9.
2002: Hostein Isabelle; Menard Armelle; Bui Bin Nguyen; Lussan Cathy; Wafflart Jean; Delattre Olivier; Peter Martine; Benhattar Jean; Guillou Louis; Coindre Jean-Michel
Molecular detection of the synovial sarcoma translocation t(X;18) by real-time polymerase chain reaction in paraffin-embedded material.
Diagnostic molecular pathology : the American journal of surgical pathology, part B 2002;11(1):16-21.
2001: Brisset S; Schleiermacher G; Peter M; Mairal A; Oberlin O; Delattre O; Aurias A
CGH analysis of secondary genetic changes in Ewing tumors: correlation with metastatic disease in a series of 43 cases.
Cancer genetics and cytogenetics 2001;130(1):57-61.
2001: Ferlicot S; Coué O; Gilbert E; Beuzeboc P; Servois V; Klijanienko J; Delattre O; Vielh P
Intraabdominal desmoplastic small round cell tumor: report of a case with fine needle aspiration, cytologic diagnosis and molecular confirmation.
Acta cytologica 2001;45(4):617-21.
2001: Schleiermacher G; Delattre O
[Detection of micrometastases and circulating tumour cells using molecular biology technics in solid tumours]
Bulletin du cancer 2001;88(6):561-70.
2001: Melot T; Dauphinot L; Sévenet N; Radvanyi F; Delattre O
Characterization of a new brain-specific isoform of the EWS oncoprotein.
European journal of biochemistry / FEBS 2001;268(12):3483-9.
2001: Peter M; Gilbert E; Delattre O
A multiplex real-time pcr assay for the detection of gene fusions observed in solid tumors.
Laboratory investigation; a journal of technical methods and pathology 2001;81(6):905-12.
2001: Dauphinot L; De Oliveira C; Melot T; Sevenet N; Thomas V; Weissman B E; Delattre O
Analysis of the expression of cell cycle regulators in Ewing cell lines: EWS-FLI-1 modulates p57KIP2and c-Myc expression.
Oncogene 2001;20(25):3258-65.
2001: Schmitz U; Mueller W; Weber M; Sévenet N; Delattre O; von Deimling A
INI1 mutations in meningiomas at a potential hotspot in exon 9.
British journal of cancer 2001;84(2):199-201.
2000: Sancéau J; Hiscott J; Delattre O; Wietzerbin J
IFN-beta induces serine phosphorylation of Stat-1 in Ewing's sarcoma cells and mediates apoptosis via induction of IRF-1 and activation of caspase-7.
Oncogene 2000;19(30):3372-83.
2000: Janoueix-Lerosey I; Penther D; Thioux M; de Crémoux P; Derré J; Ambros P; Vielh P; Bénard J; Aurias A; Delattre O
Molecular analysis of chromosome arm 17q gain in neuroblastoma.
Genes, chromosomes & cancer 2000;28(3):276-84.
2000: Javelaud D; Wietzerbin J; Delattre O; Besançon F
Induction of p21Waf1/Cip1 by TNFalpha requires NF-kappaB activity and antagonizes apoptosis in Ewing tumor cells.
Oncogene 2000;19(1):61-8.
1999: Melot T; Delattre O
E1A and the Ewing tumor translocation.
Nature medicine 1999;5(12):1331.
1999: Sévenet N; Lellouch-Tubiana A; Schofield D; Hoang-Xuan K; Gessler M; Birnbaum D; Jeanpierre C; Jouvet A; Delattre O
Spectrum of hSNF5/INI1 somatic mutations in human cancer and genotype-phenotype correlations.
Human molecular genetics 1999;8(13):2359-68.
1999: Sévenet N; Sheridan E; Amram D; Schneider P; Handgretinger R; Delattre O
Constitutional mutations of the hSNF5/INI1 gene predispose to a variety of cancers.
American journal of human genetics 1999;65(5):1342-8.
1999: Rousseau-Merck M F; Versteege I; Legrand I; Couturier J; Mairal A; Delattre O; Aurias A
hSNF5/INI1 inactivation is mainly associated with homozygous deletions and mitotic recombinations in rhabdoid tumors.
Cancer research 1999;59(13):3152-6.
1999: Janoueix-Lerosey I; Delattre O
[Update on genetic markers of cancer]
Bulletin du cancer 1999;86(1):15-21.
1998: Versteege I; Sévenet N; Lange J; Rousseau-Merck M F; Ambros P; Handgretinger R; Aurias A; Delattre O
Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer.
Nature 1998;394(6689):203-6.
1998: Fagnou C; Michon J; Peter M; Bernoux A; Oberlin O; Zucker J M; Magdelenat H; Delattre O
Presence of tumor cells in bone marrow but not in blood is associated with adverse prognosis in patients with Ewing's tumor. Société Française d'Oncologie Pédiatrique.
Journal of clinical oncology : official journal of the American Society of Clinical Oncology 1998;16(5):1707-11.
1998: Bertolotti A; Melot T; Acker J; Vigneron M; Delattre O; Tora L
EWS, but not EWS-FLI-1, is associated with both TFIID and RNA polymerase II: interactions between two members of the TET family, EWS and hTAFII68, and subunits of TFIID and RNA polymerase II complexes.
Molecular and cellular biology 1998;18(3):1489-97.
1998: Rosty C; Peter M; Zucman J; Validire P; Delattre O; Aurias A
Cytogenetic and molecular analysis of a t(1;22)(p36;q11.2) in a rhabdoid tumor with a putative homozygous deletion of chromosome 22.
Genes, chromosomes & cancer 1998;21(2):82-9.
1998: Delattre O
[Contribution of cytogenetic and molecular biologic techniques to the diagnosis of round cell tumors in children]
Annales de pathologie 1998;18(5 Suppl):91-2.
1997: Melot T; Gruel N; Doubeikovski A; Sevenet N; Teillaud J L; Delattre O
Production and characterization of mouse monoclonal antibodies to wild-type and oncogenic FLI-1 proteins.
Hybridoma 1997;16(5):457-64.
1997: Desmaze C; Brizard F; Turc-Carel C; Melot T; Delattre O; Thomas G; Aurias A
Multiple chromosomal mechanisms generate an EWS/FLI1 or an EWS/ERG fusion gene in Ewing tumors.
Cancer genetics and cytogenetics 1997;97(1):12-9.
1997: de Cremoux P; Thioux M; Peter M; Vielh P; Michon J; Delattre O; Magdelenat H
Polymerase chain reaction compared with dot blotting for the determination of N-myc gene amplification in neuroblastoma.
International journal of cancer. Journal international du cancer 1997;72(3):518-21.
1997: Peter M; Couturier J; Pacquement H; Michon J; Thomas G; Magdelenat H; Delattre O
A new member of the ETS family fused to EWS in Ewing tumors.
Oncogene 1997;14(10):1159-64.
1997: Zucman-Rossi J; Batzer M A; Stoneking M; Delattre O; Thomas G
Interethnic polymorphism of EWS intron 6: genome plasticity mediated by Alu retroposition and recombination.
Human genetics 1997;99(3):357-63.
1996: Peter M; Mugneret F; Aurias A; Thomas G; Magdelenat H; Delattre O
An EWS/ERG fusion with a truncated N-terminal domain of EWS in a Ewing's tumor.
International journal of cancer. Journal international du cancer 1996;67(3):339-42.
1996: Doz F; Peter M; Schleiermacher G; Vielh P; Validire P; Putterman M; Blanquet V; Desjardins L; Dufier J L; Zucker J M; Mosseri V; Thomas G; Magdelénat H; Delattre O
N-MYC amplification, loss of heterozygosity on the short arm of chromosome 1 and DNA ploidy in retinoblastoma.
European journal of cancer (Oxford, England : 1990) 1996;32A(4):645-9.
1996: Schleiermacher G; Delattre O; Peter M; Mosseri V; Delonlay P; Vielh P; Thomas G; Zucker J M; Magdelénat H; Michon J
Clinical relevance of loss heterozygosity of the short arm of chromosome 1 in neuroblastoma: a single-institution study.
International journal of cancer. Journal international du cancer 1996;69(2):73-8.
1996: Kleinfinger P; Labelle Y; Melot T; Thomas G; Delattre O; Aurias A
Localization of TEC to 9q22.3-q31 by fluorescence in situ hybridization.
Annales de génétique 1996;39(4):233-5.
1995: Peter M; Magdelenat H; Michon J; Melot T; Oberlin O; Zucker J M; Thomas G; Delattre O
Sensitive detection of occult Ewing's cells by the reverse transcriptase-polymerase chain reaction.
British journal of cancer 1995;72(1):96-100.
1995: Demczuk S; Delattre O; Vignal A; Weissenbach J; Thomas G; Aurias A
Physical mapping of 30 CA repeats on human chromosome 22.
Genomics 1995;27(2):345-7.
1995: Demczuk S; Aledo R; Zucman J; Delattre O; Desmaze C; Dauphinot L; Jalbert P; Rouleau G A; Thomas G; Aurias A
Cloning of a balanced translocation breakpoint in the DiGeorge syndrome critical region and isolation of a novel potential adhesion receptor gene in its vicinity.
Human molecular genetics 1995;4(4):551-8.
1995: Hoang-Xuan K; Merel P; Vega F; Hugot J P; Cornu P; Delattre J Y; Poisson M; Thomas G; Delattre O
Analysis of the NF2 tumor-suppressor gene and of chromosome 22 deletions in gliomas.
International journal of cancer. Journal international du cancer 1995;60(4):478-81.
1995: Schleiermacher G; Peter M; Michon J; Zucker J M; Thomas G; Magdelénat H; Delattre O
A multiplex PCR assay for routine evaluation of deletion of the short arm of chromosome 1 in neuroblastoma.
European journal of cancer (Oxford, England : 1990) 1995;31A(4):535-8.
1994: Plougastel B; Mattei M G; Thomas G; Delattre O
Cloning and chromosome localization of the mouse Ews gene.
Genomics 1994;23(1):278-81.
1994: Delattre O; Zucman J; Melot T; Garau X S; Zucker J M; Lenoir G M; Ambros P F; Sheer D; Turc-Carel C; Triche T J
The Ewing family of tumors--a subgroup of small-round-cell tumors defined by specific chimeric transcripts.
The New England journal of medicine 1994;331(5):294-9.
1994: Schleiermacher G; Peter M; Michon J; Hugot J P; Vielh P; Zucker J M; Magdelénat H; Thomas G; Delattre O
Two distinct deleted regions on the short arm of chromosome 1 in neuroblastoma.
Genes, chromosomes & cancer 1994;10(4):275-81.
1994: Desmaze C; Zucman J; Delattre O; Melot T; Thomas G; Aurias A
Interphase molecular cytogenetics of Ewing's sarcoma and peripheral neuroepithelioma t(11;22) with flanking and overlapping cosmid probes.
Cancer genetics and cytogenetics 1994;74(1):13-8.
1994: Hamelin R; Zucman J; Melot T; Delattre O; Thomas G
p53 mutations in human tumors with chimeric EWS/FLI-1 genes.
International journal of cancer. Journal international du cancer 1994;57(3):336-40.
1994: Ruttledge M H; Sarrazin J; Rangaratnam S; Phelan C M; Twist E; Merel P; Delattre O; Thomas G; Nordenskjöld M; Collins V P
Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas.
Nature genetics 1994;6(2):180-4.
1994: Desmaze C; Zucman J; Delattre O; Melot T; Thomas G; Aurias A
Precise localization on chromosome 12 of the ATF-1 gene by fluorescence in situ hybridization.
Human genetics 1994;93(2):207-8.
1994: Ruttledge M H; Xie Y G; Han F Y; Giovannini M; Janson M; Fransson I; Werelius B; Delattre O; Thomas G; Evans G
Physical mapping of the NF2/meningioma region on human chromosome 22q12.
Genomics 1994;19(1):52-9.
1994: Twist E C; Ruttledge M H; Rousseau M; Sanson M; Papi L; Merel P; Delattre O; Thomas G; Rouleau G A
The neurofibromatosis type 2 gene is inactivated in schwannomas.
Human molecular genetics 1994;3(1):147-51.
1994: Michon J; Delattre O; Zucker J M; Peter M; Delonlay P; Luciani S; Mosseri V; Vielh P; Neuenschwander S; Thomas G
Prospective evaluation of Nmyc amplification and deletion of the short arm of chromosome 1 in neuroblastoma tumours: a single institution study.
Progress in clinical and biological research 1994;385():11-7.
1994: Thomas G; Mérel P; Sanson M; Hoang-Xuan K; Zucman J; Desmaze C; Melot T; Aurias A; Delattre O
Neurofibromatosis type 2.
European journal of cancer (Oxford, England : 1990) 1994;30A(13):1981-7.
1994: Thomas G; Delattre O; Zucman J; Merel P; Desmaze C; Melot T; Sanson M; Hoang-Xuan K; Plougastel B; Dejong P
Genetic alterations in the chromosome 22q12 region associated with development of neuroectodermal tumors.
Cold Spring Harbor symposia on quantitative biology 1994;59():555-64.
1993: Plougastel B; Zucman J; Peter M; Thomas G; Delattre O
Genomic structure of the EWS gene and its relationship to EWSR1, a site of tumor-associated chromosome translocation.
Genomics 1993;18(3):609-15.
1993: Desmaze C; Prieur M; Amblard F; Aikem M; LeDeist F; Demczuk S; Zucman J; Plougastel B; Delattre O; Croquette M F
Physical mapping by FISH of the DiGeorge critical region (DGCR): involvement of the region in familial cases.
American journal of human genetics 1993;53(6):1239-49.
1993: Sanson M; Zhang F; Demczuk S; Delattre O; DeJong P; Aurias A; Thomas G; Rouleau G A
Isolation and mapping of 45 NotI linking clones to chromosome 22.
Genomics 1993;17(3):776-9.
1993: Zucman J; Delattre O; Desmaze C; Epstein A L; Stenman G; Speleman F; Fletchers C D; Aurias A; Thomas G
EWS and ATF-1 gene fusion induced by t(12;22) translocation in malignant melanoma of soft parts.
Nature genetics 1993;4(4):341-5.
1993: Sanson M; Marineau C; Desmaze C; Lutchman M; Ruttledge M; Baron C; Narod S; Delattre O; Lenoir G; Thomas G
Germline deletion in a neurofibromatosis type 2 kindred inactivates the NF2 gene and a candidate meningioma locus.
Human molecular genetics 1993;2(8):1215-20.
1993: Rose T M; Lagrou M J; Fransson I; Werelius B; Delattre O; Thomas G; de Jong P J; Todaro G J; Dumanski J P
The genes for oncostatin M (OSM) and leukemia inhibitory factor (LIF) are tightly linked on human chromosome 22.
Genomics 1993;17(1):136-40.
1993: Marineau C; Baron C; Delattre O; Zucman J; Thomas G; Rouleau G A
Dinucleotide repeat polymorphism at the D22S268 locus.
Human molecular genetics 1993;2(3):336.
1993: Fon E A; Demczuk S; Delattre O; Thomas G; Rouleau G A
Mapping of the human adenylosuccinate lyase (ADSL) gene to chromosome 22q13.1-->q13.2.
Cytogenetics and cell genetics 1993;64(3-4):201-3.
1992: Zucman J; Delattre O; Desmaze C; Plougastel B; Joubert I; Melot T; Peter M; De Jong P; Rouleau G; Aurias A
Cloning and characterization of the Ewing's sarcoma and peripheral neuroepithelioma t(11;22) translocation breakpoints.
Genes, chromosomes & cancer 1992;5(4):271-7.
1992: Peter M; Michon J; Vielh P; Neuenschwander S; Nakamura Y; Sonsino E; Zucker J M; Vergnaud G; Thomas G; Delattre O
PCR assay for chromosome 1p deletion in small neuroblastoma samples.
International journal of cancer. Journal international du cancer 1992;52(4):544-8.
1992: Delattre O; Zucman J; Plougastel B; Desmaze C; Melot T; Peter M; Kovar H; Joubert I; de Jong P; Rouleau G
Gene fusion with an ETS DNA-binding domain caused by chromosome translocation in human tumours.
Nature 1992;359(6391):162-5.
1992: Aubry M; Marineau C; Zhang F R; Zahed L; Figlewicz D; Delattre O; Thomas G; de Jong P J; Julien J P; Rouleau G A
Cloning of six new genes with zinc finger motifs mapping to short and long arms of human acrocentric chromosome 22 (p and q11.2).
Genomics 1992;13(3):641-8.
1992: Desmaze C; Zucman J; Delattre O; Thomas G; Aurias A
Unicolor and bicolor in situ hybridization in the diagnosis of peripheral neuroepithelioma and related tumors.
Genes, chromosomes & cancer 1992;5(1):30-4.
1992: Zucman J; Delattre O; Desmaze C; Azambuja C; Rouleau G; De Jong P; Aurias A; Thomas G
Rapid isolation of cosmids from defined subregions by differential Alu-PCR hybridization on chromosome 22-specific library.
Genomics 1992;13(2):395-401.
1992: Laurent-Puig P; Olschwang S; Delattre O; Remvikos Y; Asselain B; Melot T; Validire P; Muleris M; Girodet J; Salmon R J
Survival and acquired genetic alterations in colorectal cancer.
Gastroenterology 1992;102(4 Pt 1):1136-41.
1992: Desmaze C; Zucman J; Delattre O; Thomas G; Aurias A
In situ hybridization of PCR amplified inter-Alu sequences from a hybrid cell line.
Human genetics 1992;88(5):541-4.
1992: Sanson M; Richard S; Delattre O; Poliwka M; Mikol J; Philippon J; Thomas G
Allelic loss on chromosome 22 correlates with histopathological predictors of recurrence of meningiomas.
International journal of cancer. Journal international du cancer 1992;50(3):391-4.
1991: Laurent-Puig P; Olschwang S; Delattre O; Validire P; Melot T; Mosseri V; Salmon R J; Thomas G
Association of Ki-ras mutation with differentiation and tumor-formation pathways in colorectal carcinoma.
International journal of cancer. Journal international du cancer 1991;49(2):220-3.
1991: Delattre O; Azambuja C J; Aurias A; Zucman J; Peter M; Zhang F; Hors-Cayla M C; Rouleau G; Thomas G
Mapping of human chromosome 22 with a panel of somatic cell hybrids.
Genomics 1991;9(4):721-7.
1990: Sanson M; Delattre O; Couturier J; Philippon J; Cophignon J; Derome P; Rouleau G A; Thomas G
Parental origin of chromosome 22 alleles lost in meningioma.
American journal of human genetics 1990;47(5):877-80.
1990: Zhang F R; Aurias A; Delattre O; Stern M H; Benitez J; Rouleau G; Thomas G
Mapping of human chromosome 22 by in situ hybridization.
Genomics 1990;7(3):319-24.
1990: Couturier J; Delattre O; Kujas M; Philippon J; Peter M; Rouleau G; Aurias A; Thomas G
Assessment of chromosome 22 anomalies in neurinomas by combined karyotype and RFLP analyses.
Cancer genetics and cytogenetics 1990;45(1):55-62.
1990: Zhang F R; Delattre O; Rouleau G; Couturier J; Lefrançois; Thomas G; Aurias A
The neuroepithelioma breakpoint on chromosome 22 is proximal to the meningioma locus.
Genomics 1990;6(1):174-7.
1990: Muleris M; Delattre O; Olschwang S; Dutrillaux A M; Remvikos Y; Salmon R J; Thomas G; Dutrillaux B
Cytogenetic and molecular approaches of polyploidization in colorectal adenocarcinomas.
Cancer genetics and cytogenetics 1990;44(1):107-18.
1990: Laurent-Puig P; Delattre O; Olschwang S; Remvikos Y; Melot T; Salmon R J; Frelat G; Thomas G
[A joint study of mutation of the Ki-ras oncogene and overexpression of the Tp53 oncogene in colorectal cancer]
Gastroentérologie clinique et biologique 1990;14(4):347-51.
1989: Lefrançois D; Olschwang S; Delattre O; Muleris M; Dutrillaux A M; Thomas G; Dutrillaux B
Preservation of chromosome and DNA characteristics of human colorectal adenocarcinomas after passage in nude mice.
International journal of cancer. Journal international du cancer 1989;44(5):871-8.
1989: Delattre O; Olschwang S; Law D J; Melot T; Remvikos Y; Salmon R J; Sastre X; Validire P; Feinberg A P; Thomas G
Multiple genetic alterations in distal and proximal colorectal cancer.
Lancet 1989;2(8659):353-6.
1989: Delattre O; Zhang F R; Gross M S; N'guyen V C; Thomas G
RFLP identified by the anonymous DNA segment OLVIIF5 at 21q22.1-22.3 [HGM9 no.D21S143]
Nucleic acids research 1989;17(4):1790.
1989: Delattre O; Gross M S; de Taud M F; N'guyen V C; Thomas G
RFLP identified by the anonymous DNA segment OLVIID1 on chromosome 6 [HGM9 no.D6S47]
Nucleic acids research 1989;17(4):1789.
1989: Zhang F R; Aurias A; Delattre O; Thomas G
RFLP identified by the anonymous DNA segment FZ V D11 at 22q13 [HGM9 no.D22S80]
Nucleic acids research 1989;17(4):1791.
1988: Monpezat J P; Delattre O; Bernard A; Grunwald D; Remvikos Y; Muleris M; Salmon R J; Frelat G; Dutrillaux B; Thomas G
Loss of alleles on chromosome 18 and on the short arm of chromosome 17 in polyploid colorectal carcinomas.
International journal of cancer. Journal international du cancer 1988;41(3):404-8.
1988: Zhang F R; Monpezat J P; Delattre O; Aurias A; Thomas G
RFLP identified by the anonymous DNA segment FZ VI A2 at 22q11.2 [HGM no. D22S20]
Nucleic acids research 1988;16(6):2739.
1988: Delattre O; Grunwald M; Bernard A; Grunwald D; Thomas G; Frelat G; Aurias A
Recurrent t(11;22) breakpoint mapping by chromosome flow sorting and spot-blot hybridization.
Human genetics 1988;78(2):140-3.
1988: Delattre O; Bernard A; Malfoy B; Marlhens F; Viegas-Pequignot E; Brossard C; Haguenauer O; Creau-Goldberg N; N'guyen V C; Dutrillaux B
Studies on the human chromosome 3 centromere with a newly cloned alphoid DNA probe.
Human heredity 1988;38(3):156-67.
1987: Delattre O; Bernard A; Malfoy B; Marlhens F; Viegas-Pequignot E; Brossard C; Haguenauer O; Creau-Goldberg N; Van Cong N; Dutrillaux B
Isolation and characterization of an alphoid DNA sequence recently amplified on human chromosome 3.
Nucleic acids research 1987;15(20):8561.

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