Confirmation of mutation landscape of NF1‐associated malignant peripheral nerve sheath tumors
Sohier, Pierre, Luscan, Armelle, Lloyd, Angharad, Ashelford, Kevin, Laurendeau, Ingrid, Briand‐Suleau, Audrey, Vidaud, Dominique, Ortonne, Nicolas, Pasmant, Eric, Upadhyaya, Meena
Published in Genes chromosomes & cancer (01.05.2017)
Published in Genes chromosomes & cancer (01.05.2017)
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EZH2 mutations in follicular lymphoma distort H3K27me3 profiles and alter transcriptional responses to PRC2 inhibition
Romero, Pierre, Richart, Laia, Aflaki, Setareh, Petitalot, Ambre, Burton, Megan, Michaud, Audrey, Masliah-Planchon, Julien, Kuhnowski, Frédérique, Le Cam, Samuel, Baliñas-Gavira, Carlos, Méaudre, Céline, Luscan, Armelle, Hamza, Abderaouf, Legoix, Patricia, Vincent-Salomon, Anne, Wassef, Michel, Holoch, Daniel, Margueron, Raphaël
Published in Nature communications (24.04.2024)
Published in Nature communications (24.04.2024)
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Could Digital PCR Be an Alternative as a Non-Invasive Prenatal Test for Trisomy 21: A Proof of Concept Study
El Khattabi, Laïla Allach, Rouillac-Le Sciellour, Christelle, Le Tessier, Dominique, Luscan, Armelle, Coustier, Audrey, Porcher, Raphael, Bhouri, Rakia, Nectoux, Juliette, Sérazin, Valérie, Quibel, Thibaut, Mandelbrot, Laurent, Tsatsaris, Vassilis, Vialard, François, Dupont, Jean-Michel
Published in PloS one (11.05.2016)
Published in PloS one (11.05.2016)
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Competitive allele specific TaqMan PCR for KRAS, BRAF and EGFR mutation detection in clinical formalin fixed paraffin embedded samples
Didelot, Audrey, Le Corre, Delphine, Luscan, Armelle, Cazes, Aurélie, Pallier, Karine, Emile, Jean-François, Laurent-Puig, Pierre, Blons, Hélène
Published in Experimental and molecular pathology (01.06.2012)
Published in Experimental and molecular pathology (01.06.2012)
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Case Report: How whole-genome sequencing-based cell-free DNA prenatal testing can help identify a marker mhromosome
Kleinfinger, Pascale, Brechard, Marie, Luscan, Armelle, Trost, Detlef, Boughalem, Aicha, Mylene Valduga, Serero DR, Stéphane, Costa, Jean-Marc, Lohmann, Laurence
Published in Frontiers in genetics (26.09.2022)
Published in Frontiers in genetics (26.09.2022)
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The Activation of the WNT Signaling Pathway Is a Hallmark in Neurofibromatosis Type 1 Tumorigenesis
LUSCAN, Armelle, SHACKLEFORD, Ghjuvan'ghjacumu, BORDERIE, Didier, DE RAEDT, Thomas, VALEYRIE-ALLANORE, Laurence, LAROUSSERIE, Frédérique, TERRIS, Benoît, LANTIERI, Laurent, VIDAUD, Michel, VIDAUD, Dominique, WOLKENSTEIN, Pierre, PARFAIT, Béatrice, MASLIAH-PLANCHON, Julien, BIECHE, Ivan, MASSAAD, Charbel, PASMANT, Eric, LAURENDEAU, Ingrid, ORTONNE, Nicolas, VARIN, Jennifer, LALLEMAND, François, LEROY, Karen, DUMAINE, Valérie, HIVELIN, Mikael
Published in Clinical cancer research (15.01.2014)
Published in Clinical cancer research (15.01.2014)
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MicroRNAome profiling in benign and malignant neurofibromatosis type 1-associated nerve sheath tumors: evidences of PTEN pathway alterations in early NF1 tumorigenesis
Masliah-Planchon, Julien, Pasmant, Eric, Luscan, Armelle, Laurendeau, Ingrid, Ortonne, Nicolas, Hivelin, Mikael, Varin, Jennifer, Valeyrie-Allanore, Laurence, Dumaine, Valérie, Lantieri, Laurent, Leroy, Karen, Parfait, Béatrice, Wolkenstein, Pierre, Vidaud, Michel, Vidaud, Dominique, Bièche, Ivan
Published in BMC genomics (13.07.2013)
Published in BMC genomics (13.07.2013)
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NF1 mutations identify molecular and clinical subtypes of lung adenocarcinomas
Tlemsani, Camille, Pécuchet, Nicolas, Gruber, Aurelia, Laurendeau, Ingrid, Danel, Claire, Riquet, Marc, Le Pimpec‐Barthes, Françoise, Fabre, Elizabeth, Mansuet‐Lupo, Audrey, Damotte, Diane, Alifano, Marco, Luscan, Armelle, Rousseau, Benoit, Vidaud, Dominique, Varin, Jennifer, Parfait, Beatrice, Bieche, Ivan, Leroy, Karen, Laurent‐Puig, Pierre, Terris, Benoit, Blons, Helene, Vidaud, Michel, Pasmant, Eric
Published in Cancer medicine (Malden, MA) (01.08.2019)
Published in Cancer medicine (Malden, MA) (01.08.2019)
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Journal Article
NF1 single and multi-exons copy number variations in neurofibromatosis type 1
Imbard, Apolline, Pasmant, Eric, Sabbagh, Audrey, Luscan, Armelle, Soares, Magali, Goussard, Philippe, Blanché, Hélène, Laurendeau, Ingrid, Ferkal, Salah, Vidaud, Michel, Pinson, Stéphane, Bellanne-Chantelot, Christine, Vidaud, Dominique, Wolkenstein, Pierre, Parfait, Béatrice
Published in Journal of human genetics (01.04.2015)
Published in Journal of human genetics (01.04.2015)
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Journal Article
PRC2 loss amplifies Ras-driven transcription and confers sensitivity to BRD4-based therapies
De Raedt, Thomas, Beert, Eline, Pasmant, Eric, Luscan, Armelle, Brems, Hilde, Ortonne, Nicolas, Helin, Kristian, Hornick, Jason L., Mautner, Victor, Kehrer-Sawatzki, Hildegard, Clapp, Wade, Bradner, James, Vidaud, Michel, Upadhyaya, Meena, Legius, Eric, Cichowski, Karen
Published in Nature (London) (09.10.2014)
Published in Nature (London) (09.10.2014)
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Journal Article
Neurofibromatosis type 1 molecular diagnosis: what can NGS do for you when you have a large gene with loss of function mutations?
Pasmant, Eric, Parfait, Béatrice, Luscan, Armelle, Goussard, Philippe, Briand-Suleau, Audrey, Laurendeau, Ingrid, Fouveaut, Corinne, Leroy, Chrystel, Montadert, Annelore, Wolkenstein, Pierre, Vidaud, Michel, Vidaud, Dominique
Published in European journal of human genetics : EJHG (01.05.2015)
Published in European journal of human genetics : EJHG (01.05.2015)
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Journal Article
Mutations in SETD2 cause a novel overgrowth condition
Luscan, Armelle, Laurendeau, Ingrid, Malan, Valérie, Francannet, Christine, Odent, Sylvie, Giuliano, Fabienne, Lacombe, Didier, Touraine, Renaud, Vidaud, Michel, Pasmant, Eric, Cormier-Daire, Valérie
Published in Journal of medical genetics (01.08.2014)
Published in Journal of medical genetics (01.08.2014)
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Journal Article
NF1 Molecular Characterization and Neurofibromatosis Type I Genotype-Phenotype Correlation: The French Experience
Sabbagh, Audrey, Pasmant, Eric, Imbard, Apolline, Luscan, Armelle, Soares, Magali, Blanché, Hélène, Laurendeau, Ingrid, Ferkal, Salah, Vidaud, Michel, Pinson, Stéphane, Bellanné-Chantelot, Christine, Vidaud, Dominique, Parfait, Béatrice, Wolkenstein, Pierre
Published in Human mutation (01.11.2013)
Published in Human mutation (01.11.2013)
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Journal Article
EZH1/2 function mostly within canonical PRC2 and exhibit proliferation-dependent redundancy that shapes mutational signatures in cancer
Wassef, Michel, Luscan, Armelle, Aflaki, Setareh, Zielinski, Dina, Jansen, Pascal W. T. C., Baymaz, H. Irem, Battistella, Aude, Kersouani, Carole, Servant, Nicolas, Wallace, Margaret R., Romero, Pierre, Kosmider, Olivier, Just, Pierre-Alexandre, Hivelin, Mikaël, Jacques, Sébastien, Vincent-Salomon, Anne, Vermeulen, Michiel, Vidaud, Michel, Pasmant, Eric, Margueron, Raphaël
Published in Proceedings of the National Academy of Sciences - PNAS (26.03.2019)
Published in Proceedings of the National Academy of Sciences - PNAS (26.03.2019)
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Journal Article
SETD2 and DNMT3A screen in the Sotos-like syndrome French cohort
Tlemsani, Camille, Luscan, Armelle, Leulliot, Nicolas, Bieth, Eric, Afenjar, Alexandra, Baujat, Geneviève, Doco-Fenzy, Martine, Goldenberg, Alice, Lacombe, Didier, Lambert, Laetitia, Odent, Sylvie, Pasche, Jérôme, Sigaudy, Sabine, Buffet, Alexandre, Violle-Poirsier, Céline, Briand-Suleau, Audrey, Laurendeau, Ingrid, Chin, Magali, Saugier-Veber, Pascale, Vidaud, Dominique, Cormier-Daire, Valérie, Vidaud, Michel, Pasmant, Eric, Burglen, Lydie
Published in Journal of medical genetics (01.11.2016)
Published in Journal of medical genetics (01.11.2016)
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Genome Alert!: A standardized procedure for genomic variant reinterpretation and automated gene–phenotype reassessment in clinical routine
Yauy, Kevin, Lecoquierre, François, Baert-Desurmont, Stéphanie, Trost, Detlef, Boughalem, Aicha, Luscan, Armelle, Costa, Jean-Marc, Geromel, Vanna, Raymond, Laure, Richard, Pascale, Coutant, Sophie, Broutin, Mélanie, Lanos, Raphael, Fort, Quentin, Cackowski, Stenzel, Testard, Quentin, Diallo, Abdoulaye, Soirat, Nicolas, Holder, Jean-Marc, Duforet-Frebourg, Nicolas, Bouge, Anne-Laure, Beaumeunier, Sacha, Bertrand, Denis, Audoux, Jerome, Genevieve, David, Mesnard, Laurent, Nicolas, Gael, Thevenon, Julien, Philippe, Nicolas
Published in Genetics in medicine (01.06.2022)
Published in Genetics in medicine (01.06.2022)
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Journal Article
Noninvasive Prenatal Screening for Trisomy 21 in Patients with a Vanishing Twin
Kleinfinger, Pascale, Luscan, Armelle, Descourvieres, Léa, Buzas, Daniela, Boughalem, Aicha, Serero, Stéphane, Valduga, Mylène, Trost, Detlef, Costa, Jean-Marc, Vivanti, Alexandre J, Lohmann, Laurence
Published in Genes (03.11.2022)
Published in Genes (03.11.2022)
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