Catia Attanasio
Catia Attanasio
Post-Doc, UNIL
Verified email at unil.ch
TitleCited byYear
Targeted deletion of the 9p21 non-coding coronary artery disease risk interval in mice
A Visel, Y Zhu, D May, V Afzal, E Gong, C Attanasio, MJ Blow, JC Cohen, ...
Nature 464 (7287), 409, 2010
4392010
Rapid and pervasive changes in genome-wide enhancer usage during mammalian development
AS Nord, MJ Blow, C Attanasio, JA Akiyama, A Holt, R Hosseini, ...
Cell 155 (7), 1521-1531, 2013
2222013
Fine tuning of craniofacial morphology by distant-acting enhancers
C Attanasio, AS Nord, Y Zhu, MJ Blow, Z Li, DK Liberton, H Morrison, ...
Science 342 (6157), 1241006, 2013
1732013
Disease-causing 7.4 kb cis-regulatory deletion disrupting conserved non-coding sequences and their interaction with the FOXL2 promotor: implications for mutation screening
B D'haene, C Attanasio, D Beysen, J Dostie, E Lemire, P Bouchard, ...
PLoS genetics 5 (6), e1000522, 2009
922009
Tissue-specific SMARCA4 binding at active and repressed regulatory elements during embryogenesis
C Attanasio, AS Nord, Y Zhu, MJ Blow, SC Biddie, EM Mendenhall, ...
Genome research 24 (6), 920-929, 2014
542014
Outcome of donor splice site mutations accounting for congenital afibrinogenemia reflects order of intron removal in the fibrinogen alpha gene (FGA)
C Attanasio, A David, M Neerman-Arbez
Blood 101 (5), 1851-1856, 2003
542003
Identification of Novel Craniofacial Regulatory Domains Located far Upstream of SOX9 and Disrupted in Pierre Robin Sequence
CT Gordon, C Attanasio, S Bhatia, S Benko, M Ansari, TY Tan, A Munnich, ...
Human mutation 35 (8), 1011-1020, 2014
482014
An etiologic regulatory mutation in IRF6 with loss- and gain-of-function effects
WD Fakhouri, F Rahimov, C Attanasio, EN Kouwenhoven, ...
Human molecular genetics 23 (10), 2711-2720, 2014
402014
Activation of multiple cryptic donor splice sites by the common congenital afibrinogenemia mutation, FGA IVS4+ 1 G→ T
C Attanasio, P De Moerloose, SE Antonarakis, MA Morris, ...
Blood 97 (6), 1879-1881, 2001
402001
A systematic enhancer screen using lentivector transgenesis identifies conserved and non-conserved functional elements at the Olig1 and Olig2 locus
M Friedli, I Barde, M Arcangeli, S Verp, A Quazzola, J Zakany, N Lin-Marq, ...
PLoS One 5 (12), e15741, 2010
272010
Assaying the regulatory potential of mammalian conserved non-coding sequences in human cells
C Attanasio, A Reymond, R Humbert, R Lyle, MS Kuehn, S Neph, ...
Genome biology 9 (12), R168, 2008
232008
A liver enhancer in the fibrinogen gene cluster
A Fort, RJ Fish, C Attanasio, R Dosch, A Visel, M Neerman-Arbez
Blood 117 (1), 276-282, 2011
172011
Transcriptional activation by bidirectional RNA polymerase II elongation over a silent promoter
O Leupin, C Attanasio, S Marguerat, M Tapernoux, SE Antonarakis, ...
EMBO reports 6 (10), 956-960, 2005
142005
Sex-specific transcriptome analysis highlights immune and neuronal dysfunction in the developing brain cortex of 16p11. 2 deletion mouse models
P De Nittis, G Giannuzzi, E Porcu, L Dib, J Chrast, Y Herault, F Schuetz, ...
EUROPEAN JOURNAL OF HUMAN GENETICS 27, 1490-1490, 2019
2019
A Distant Regulatory 7.4 Kb Deletion Upstream of FOXL2 Causes BPES
E De Baere, B D'haene, C Attanasio, D Beysen, E Lemire, B Lorenz, ...
Investigative Ophthalmology & Visual Science 50 (13), 4119-4119, 2009
2009
Disruptions of distant regulatory elements outside FOXL2 in BPES syndrome: exploring the role of microdeletions and variants in Conserved Non-Coding sequences (CNCs)
E De Baere, B D'Haene, C Attanasio, D Beysen, M Friedli, B Lorenz, ...
Proceedings, 297-297, 2008
2008
Exploring the contribution of Conserved Non-Coding sequences (CNCs) to Blepharophimosis Syndrome (BPES)
BN D'Haene, C Attanasio, M Friedli, D Beysen, B Lorenz, P Lapunzina, ...
European Journal of Human Genetics 16, 2008
2008
Evaluation of the regulatory potential of HSA21q conserved non-coding sequences (CNCs)
C Attanasio
University of Geneva, 2007
2007
Outcome of three donor splice site mutations accounting for congenital afibrinogenemia and order of intron removal in the fibrinogen alpha gene (FGA).
M Neerman-Arbez, A David, C Attanasio
EUROPEAN JOURNAL OF HUMAN GENETICS 10, 240-240, 2002
2002
The system can't perform the operation now. Try again later.
Articles 1–19