GenomEast
Responsable : Christelle THIBAULT-CARPENTIER
Stephanie LE GRAS
Ingénieure
en bioinformatique
slegras@igbmc.fr
Plateforme(s) / Service(s)
Plateaux
Publications
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2013
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Sumoylation at chromatin governs coordinated repression of a transcriptional program essential for cell growth and proliferation
- Hélène Neyret-Kahn
- Moussa Benhamed
- Tao Ye
- Stéphanie Le Gras
- Jack-Christophe Cossec
- Pierre Lapaquette
- Oliver Bischof
- Maia Ouspenskaia
- Mary Dasso
- Jacob-Sebastian Seeler
- Irwin Davidson
- Anne Dejean
Genome Research ; Volume: 23 ; Page: 1563-1579
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Trim24-repressed VL30 retrotransposons regulate gene expression by producing noncoding RNA
- Benjamin Herquel
- Khalid Ouararhni
- Igor Martianov
- Stéphanie Le Gras
- Tao Ye
- Céline Keime
- Thierry Lerouge
- Bernard Jost
- Florence Cammas
- Régine Losson
- Irwin Davidson
Nature Structural and Molecular Biology ; Volume: 20 ; Page: 339-346
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An integrated diagnosis strategy for congenital myopathies.
- Johann Böhm
- Nasim Vasli
- Edoardo Malfatti
- Stéphanie Le Gras
- Claire Feger
- Bernard Jost
- Nicole Monnier
- Julie Brocard
- Hatice Karasoy
- Marion Gérard
- Maggie C. Walter
- Peter Reilich
- Valérie Biancalana
- Christine Kretz
- Nadia Messaddeq
- Isabelle Marty
- Joël Lunardi
- Norma B. Romero
- Jocelyn Laporte
PLoS ONE ; Volume: 8 ; Page: e67527
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Chromatin signatures and retrotransposon profiling in mouse embryos reveal regulation of LINE-1 by RNA
- Anas Fadloun
- Stéphanie Le Gras
- Bernard Jost
- Céline Ziegler-Birling
- H Takahashi
- E Gorab
- P Carninci
- Maria Elena Torres Padilla
Nature Structural and Molecular Biology ; Volume: 20 ; Page: 332-338
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2012
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Samaritan myopathy, an ultimately benign congenital myopathy, is caused by a RYR1 mutation
- Johann Böhm
- Esther Leshinsky-Silver
- Stéphane Vassilopoulos
- Stéphanie Le Gras
- Tally Lerman-Sagie
- Mira Ginzberg
- Bernard Jost
- Dorit Lev
- Jocelyn Laporte
Acta Neuropathologica ; Volume: 124 ; Page: 575-581
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Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alstrom syndromes
- Claire Redin
- Stéphanie Le Gras
- Oussema Mhamdi
- Véronique Geoffroy
- Corinne Stoetzel
- Marie-Claire Vincent
- Pietro Chiurazzi
- Didier Lacombe
- Ines Ouertani
- Florence Petit
- Marianne Till
- Alain Verloes
- Bernard Jost
- Habiba Bouhamed Chaabouni
- Helene Dollfus
- Jean-Louis Mandel
- Jean Muller
Journal of Medical Genetics ; Volume: 49 ; Page: 502-512
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Next generation sequencing for molecular diagnosis of neuromuscular diseases
- Nasim Vasli
- Johann Böhm
- Stéphanie Le Gras
- Jean Muller
- Cécile Pizot
- Bernard Jost
- Andoni Echaniz‐laguna
- Vincent Laugel
- Christine Tranchant
- Rafaelle Bernard
- Frederic Plewniak
- Serge Vicaire
- Nicolas Levy
- Jamel Chelly
- Jean-Louis Mandel
- Valerie Biancalana
- Jocelyn Laporte
Acta Neuropathologica ; Volume: 124 ; Page: 273 - 283
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Targeted high-throughput sequencing for diagnosis of genetically heterogeneous diseases: efficient mutation detection in Bardet-Biedl and Alström Syndromes
- Claire Redin
- Stéphanie Le Gras
- Oussema Mhamdi
- Véronique Geoffroy
- Corinne Stoetzel
- Marie-Claire Vincent
- Pietro Chiurazzi
- Didier Lacombe
- Ines Ouertani
- Florence Petit
- Marianne Till
- Alain Verloes
- Bernard Jost
- Habiba Bouhamed Chaabouni
- Helene Dollfus
- Jean-Louis Mandel
- Jean Muller
Journal of Medical Genetics ; Volume: 49 ; Page: 502-512
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2011
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Essential role of microphthalmia transcription factor for DNA replication, mitosis and genomic stability in melanoma
- T Strub
- S. Giuliano
- T Ye
- C Bonet
- C. Keime
- D Kobi
- S. Le Gras
- M. Cormont
- R Ballotti
- C. Bertolotto
- I Davidson
Oncogene ; Volume: 30 ; Page: 2319-2332
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2010
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A Strategy for Direct Mapping and Identification of Mutations by Whole-Genome Sequencing
- Steven Zuryn
- Stéphanie Le Gras
- Karine Jamet
- Sophie Jarriault
Genetics ; Volume: 186 ; Page: 427-430
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