Scientific publications
Publications
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								2011- 
								Article in a journal Transcriptomic analysis of human retinal detachment reveals both inflammatory response and photoreceptor death.- Marie-Noëlle Delyfer
- Wolfgang Raffelsberger
- David Mercier
- Jean-François Korobelnik
- Alain Gaudric
- David G. Charteris
- Ramin Tadayoni
- Florence Metge
- Georges Caputo
- Pierre-Olivier Barale
- Raymond Ripp
- Jean-Denis Muller
- Olivier Poch
- José-Alain Sahel
- Thierry Léveillard
 PLoS ONE ; Volume: 6 ; Page: e28791 
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								Article in a journal A fraction of the transcription factor TAF15 participates in interactions with a subset of the spliceosomal U1 snRNP complex- Michael Leichter
- Marija Marko
- Vassiliki Ganou
- Meropi Patrinou-Georgoula
- László Tora
- Apostolia Guialis
 Biochimica et Biophysica Acta (BBA) - Proteins and Proteomics ; Volume: 1814 ; Page: 1812-1824 
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								Article in a journal Collisions between Replication and Transcription Complexes Cause Common Fragile Site Instability at the Longest Human Genes- Anne Helmrich
- Monica Ballarino
- Laszlo Tora
 Molecular Cell ; Volume: 44 ; Page: 966-977 
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								Article in a journal Identifying single copy orthologs in Metazoa.- Christopher J. Creevey
- Jean Muller
- Tobias Doerks
- Julie D. Thompson
- Detlev Arendt
- Peer Bork
 PLoS Computational Biology ; Volume: 7 ; Page: e1002269 
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								Article in a journal Identification of evolutionarily conserved exons as regulated targets for the splicing activator tra2β in development.- Sushma Grellscheid
- Caroline Dalgliesh
- Markus Storbeck
- Andrew Best
- Yilei Liu
- Miriam Jakubik
- Ylva Mende
- Ingrid Ehrmann
- Tomaz Curk
- Kristina Rossbach
- Cyril F Bourgeois
- James Stévenin
- David Grellscheid
- Michael S. Jackson
- Brunhilde Wirth
- David J. Elliott
 PLoS Genetics ; Volume: 7 ; Page: e1002390 
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								Article in a journal Homozygosity Mapping and Candidate Prioritization Identify Mutations, Missed by Whole-Exome Sequencing, in SMOC2, Causing Major Dental Developmental Defects- Agnès Bloch-Zupan
- Xavier Jamet
- Christelle Etard
- Virginie Laugel
- Jean Muller
- Véronique Geoffroy
- Jean-Pierre Strauss
- Valérie Pelletier
- Vincent Marion
- Olivier Poch
- Uwe Strahle
- Corinne Stoetzel
- Hélène Dollfus
 American Journal of Human Genetics ; Volume: 89 ; Page: 773-781 
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								Article in a journal Characterization of PTZ-Induced Seizure Susceptibility in a Down Syndrome Mouse Model That Overexpresses CSTB- Benoit Martin
- Nathalie Costet
- Jean-Charles Bizot
- Yann Hérault
- Véronique Brault
 PLoS ONE ; Volume: 6 ; Page: e27845 
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								Article in a journal The PHD Finger of Human UHRF1 Reveals a New Subgroup of Unmethylated Histone H3 Tail Readers- Nada Lallous
- Pierre Legrand
- Alastair McEwen
- Santiago Ramón-Maiques
- Jean-Pierre Samama
- Catherine Birck
 PLoS ONE ; Volume: 6 ; Page: e27599 
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								Article in a journal Preimplantation genetic diagnosis (PGD) for Huntington's disease: the experience of three European centres- Maartje van Rij
- Marjan de Rademaeker
- Céline Moutou
- Jos Cfm Dreesen
- Martine de Rycke
- Inge Liebaers
- Joep Pm Geraedts
- Christine Em de Die-Smulders
- Stéphane Viville
 European Journal of Human Genetics ; Volume: 20 ; Page: 368-375 
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								Article in a journal Profiling target genes of FGF18 in the postnatal mouse lung: possible relevance for alveolar development.- Marie-Laure Franco-Montoya
- Olivier Boucherat
- Christelle Thibault
- Bernadette Chailley-Heu
- Roberto Incitti
- Christophe Delacourt
- Jacques R. Bourbon
 Physiological Genomics ; Volume: 43 ; Page: 1226-40 
 
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