Browsing by Author Riess, Olaf

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Showing results 1 to 3 of 3
Issue DateTitleAuthor(s)
1-Sep-2020Improved diagnosis of rare disease patients through systematic detection of runs of homozygosityMatalonga Borrel, Lesley; Laurie, Steven; Papakonstantinou, Anastasios; Piscia, Davide; Mereu, Elisabetta; Bullich, Gemma; Thompson, Rachel; Horvath, Rita; Pérez Jurado, Luis; Riess, Olaf; Gut, Ivo; van Ommen, Gert Jan; Lochmüller, Hanns; Beltrán, Sergi; RD-Connect Genome-Phenome Analysis Platform and UR; Cormand Rifà, Bru; Balcells Comas, Susana; Grinberg Vaisman, Daniel Raúl; Urreizti, Roser; Garrabou Tornos, Glòria
19-Feb-2020Towards a European health research and innovation cloud (HRIC)Aarestrup, Frank M.; Albeyatti, Abdullah; Armitage, W. John; Auffray, Charles; Augello, Luca; Balling, Rudi; Benhabiles, Nora; Bertolini, Guido; Bjaalie, Jan G.; Black, Michaela; Blomberg, Niklas; Bogaert, Petronille; Bubak, Marian; Claerhout, Barbara; Clarke, Laura; De Meulder, Bertrand; D'Errico, Gianni; Di Meglio, Alberto; Forgo, Nikolaus; Gans-Combe, Caroline; Gray, Alexander Edward; Gut, Ivo; Gyllenberg, Alexandra; Hemmrich-Stanisak, Georg; Hjorth, Lars; Ioannidis, Yannis; Jarmalaite, Sonata; Kel, Alexander; Kherif, Ferath; Korbel, Jan O.; Larue, Catherine; Laszlo, M.; Maas, Andrew; Magalhaes, Luis; Manneh-Vangramberen, Isabelle; Morley-Fletcher, Edwin; Ohmann, Christian; Oksvold, Per; Oxtoby, Neil P.; Perseil, Isabelle; Pezoulas, Vasileios; Riess, Olaf; Riper, Heleen; Roca Torrent, Josep; Rosenstiel, Philip; Sabatier, Philippe; Sanz, Ferran; Tayeb, Monir; Thomassen, Gard; Van Bussel, Johann C.H.; Van den Bulcke, Marc; Van Oyen, Herman
12-Jul-2016Uniparental disomy of chromosome 16 unmasks recessive mutations of FA2H/SPG35 in 4 familiesSoehn, Anne S.; Rattay, Tim W.; Beck-Wödl, Stefanie; Schäferhoff, Karin; Monk, Dave Nicholas; Döbler-Neumann, Marion; Hörtnagel, Konstanze; Schlüter, Agatha; Ruiz, Montserrat; Pujol Onofre, Aurora; Züchner, Stephan; Riess, Olaf; Schüle, Rebecca; Bauer, Peter; Schöls, Ludger