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Number of items: 8.

Meienberg, Janine; Bruggmann, Rémy; Oexle, Konrad; Matyas, Gabor (2016). Clinical sequencing: is WGS the better WES? Human Genetics, 135(3):359-362.

Meienberg, Janine; Zerjavic, Katja; Keller, Irene; Okoniewski, Michal; Patrignani, Andrea; Ludin, Katja; Xu, Zhenyu; Steinmann, Beat; Carrel, Thierry; Röthlisberger, Benno; Schlapbach, Ralph; Bruggmann, Rémy; Matyas, Gabor (2015). New insights into the performance of human whole-exome capture platforms. Nucleic Acids Research, 43(11):e76.

Jost, Christine; Rohrbach, Marianne; Matyas, Gabor; Schoenhoff, Florian; Baumgartner, Matthias; Oxenius, Angela; Carrel, Thierry; Huebler, Michael; Min, Kan; De Pasquale, Gabriella; Landau, Klara; Kretschmar, Oliver; Odavic, Dragan; Vogt, Paul; Faletra, Francesco; Greutmann, Matthias (2015). Syndrome de Marfan. Swiss Medical Forum, 15(29-30):674-683.

Schoenhoff, Florian S; Mueller, Christoph; Czerny, Martin; Matyas, Gabor; Kadner, Alexander; Schmidli, Juerg; Carrel, Thierry (2014). Outcome of aortic surgery in patients with Loeys-Dietz syndrome primarily treated as having Marfan syndrome. European Journal of Cardio-Thoracic Surgery, 46(3):444-449.

Attenhofer Jost, Christine H; Greutmann, Matthias; Connolly, Heidi M; Weber, Roland; Rohrbach, Marianne; Oxenius, Angela; Kretschmar, Oliver; Luscher, Thomas F; Matyas, Gabor (2014). Medical treatment of aortic aneurysms in Marfan syndrome and other heritable conditions. Current Cardiology Reviews, 10(2):161-171.

Schoenhoff, Florian S; Jungi, Silvan; Czerny, Martin; Roost, Eva; Reineke, David; Matyas, Gabor; Steinmann, Beat; Schmidli, Juerg; Kadner, Alexander; Carrel, Thierry (2013). Acute aortic dissection determines the fate of initially untreated aortic segments in Marfan syndrome. Circulation, 127(15):1569-1575.

Okoniewski, Michal J; Meienberg, Janine; Patrignani, Andrea; Szabelska, Alicja; Matyas, Gabor; Schlapbach, Ralph (2013). Precise breakpoint localization of large genomic deletions using PacBio and Illumina next-generation sequencers. BioTechniques, 54(2):98-100.

Cosson, Laure; Toutain, Annick; Simard, Gilles; Kulik, Willem; Matyas, Gabor; Guichet, Agnès; Blasco, Hélène; Maakaroun-Vermesse, Zoha; Vaillant, Marie-Catherine; Le Caignec, Cédric; Chantepie, Alain; Labarthe, François (2012). Barth syndrome in a female patient. Molecular Genetics and Metabolism, 106(1):115-120.

This list was generated on Sat Jul 22 15:06:55 2017 CEST.