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	Title	Authors / Editors	Date
unige:102014	KIAA1109 Variants Are Associated with a Severe Disorder of Brain Development and Arthrogryposis	Gueneau, Lucie; Fish, Richard; Shamseldin, Hanan E.; Voisin, Norine; ... Reymond, Alexandre	2018
unige:103594	Inactivation of AMMECR1 is associated with growth, bone, and heart alterations	Moysés-Oliveira, Mariana; Giannuzzi, Giuliana; Fish, Richard; Rosenfeld, Jill A; ... Reymond, Alexandre	2018
unige:89657	Population Variation and Genetic Control of Modular Chromatin Architecture in Humans	Waszak, Sebastian M; Delaneau, Olivier; Gschwind, Andreas R; Kilpinen, Leena Helena; ... Dermitzakis, Emmanouil	2015
unige:90277	Identification and removal of low-complexity sites in allele-specific analysis of ChIP-seq data	Waszak, Sebastian M; Kilpinen, Leena Helena; Gschwind, Andreas R; Orioli, Andrea; ... Deplancke, Bart	2014
unige:90278	Coordinated effects of sequence variation on DNA binding, chromatin structure, and transcription	Kilpinen, Leena Helena; Waszak, Sebastian M; Gschwind, Andreas R; Raghav, Sunil K; ... Dermitzakis, Emmanouil	2013
unige:9198	Identifying protein-coding genes in genomic sequences	Harrow, Jennifer; Nagy, Alinda; Reymond, Alexandre; Alioto, Tyler; ... Guigo, Roderic	2009
unige:8879	Variation in novel exons (RACEfrags) of the MECP2 gene in Rett syndrome patients and controls	Makrythanasis, Periklis; Kapranov, Philipp; Bartoloni, Lucia; Reymond, Alexandre; ... Antonarakis, Stylianos	2009
unige:19091	Williams-Beuren syndrome TRIM50 encodes an E3 ubiquitin ligase	Micale, Lucia; Fusco, Carmela; Augello, Bartolomeo; Napolitano, Luisa M. R.; ... Reymond, Alexandre	2008
unige:1281	Assaying the regulatory potential of mammalian conserved non-coding sequences in human cells	Attanasio, Catia; Reymond, Alexandre; Humbert, Richard; Lyle, Robert; ... Stamatoyannopoulos, John A.	2008
unige:9167	Efficient targeted transcript discovery via array-based normalization of RACE libraries	Djebali, Sarah; Kapranov, Philipp; Foissac, Sylvain; Lagarde, Julien; ... Guigo, Roderic	2008
unige:8715	Prominent use of distal 5' transcription start sites and discovery of a large number of additional exons in ENCODE regions	Denoeud, France; Kapranov, Philipp; Ucla, Catherine; Frankish, Adam; ... Reymond, Alexandre	2007
unige:9089	Structured RNAs in the ENCODE selected regions of the human genome	Washietl, Stefan; Pedersen, J. S.; Korbel, J. O.; Stocsits, Claudia; ... Stadler, P. F.	2007
unige:8871	Islands of euchromatin-like sequence and expressed polymorphic sequences within the short arm of human chromosome 21	Lyle, Robert; Prandini, Paola; Osoegawa, Kazutoyo; ten Hallers, Boudewijn; ... Antonarakis, Stylianos	2007
unige:9112	Pseudogenes in the ENCODE regions: consensus annotation, analysis of transcription, and evolution	Zheng, Deyou; Frankish, Adam; Baertsch, Robert; Kapranov, Philipp; ... Gerstein, M. B.	2007
unige:9059	The implications of alternative splicing in the ENCODE protein complement	Antonarakis, Stylianos; Reymond, Alexandre	2007
unige:8730	Conserved noncoding sequences are selectively constrained and not mutation cold spots	Drake, J. A.; Bird, Christine; Nemesh, James; Thomas, D. J.; ... Hirschhorn, J. N.	2006
unige:8815	Two high throughput technologies to detect segmental aneuploidies identify new Williams-Beuren syndrome patients with atypical deletions	Howald, C.; Merla, Giuseppe; Digilio, M. C.; Amenta, S.; ... Reymond, Alexandre	2006
unige:9177	EGASP: the human ENCODE Genome Annotation Assessment Project	Guigo, Roderic; Flicek, Paul; Abril, J. F.; Reymond, Alexandre; ... Reese, M. G.	2006
unige:9197	GENCODE: producing a reference annotation for ENCODE	Harrow, Jennifer; Denoeud, France; Frankish, Adam; Reymond, Alexandre; ... Guigo, Roderic	2006
unige:8897	Submicroscopic deletion in patients with Williams-Beuren syndrome influences expression levels of the nonhemizygous flanking genes	Merla, Giuseppe; Howald, Cedric; Henrichsen, C. N.; Lyle, Robert; ... Reymond, Alexandre	2006

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