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Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity. by Robin G Walters, Lachlan J M Coin, Aimo Ruokonen, Adam J de Smith, Julia S El-Sayed Moustafa, Sebastien Jacquemont, Paul Elliott, Tõnu Esko, Anna-Liisa Hartikainen, Jaana Laitinen, Katrin Männik, Danielle Martinet, David Meyre, Matthias Nauck, Claudia Schurmann, Rob Sladek, Gudmar Thorleifsson, Unnur Thorsteinsdóttir, Armand Valsesia, Gerard Waeber, Flore Zufferey, Beverley Balkau, François Pattou, Andres Metspalu, Henry Völzke, Peter Vollenweider, Kári Stefansson, Marjo-Riitta Järvelin, Jacques S Beckmann, Philippe Froguel, Alexandra I F Blakemore
Published 2013-01-01Get full text
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Paediatric Personalized Research Network Switzerland (SwissPedHealth): a joint paediatric national data stream by Julia A Bielicki, Luregn J Schlapbach, Klara Posfay-Barbe, Sven Schulzke, Martin Stocker, Anita Rauch, Christopher B Forrest, Effy Vayena, Claudia E Kuehni, Jacques Fellay, Philipp Latzin, Christian Kahlert, Seraina Prader, Ben D Spycher, Katrin Männik, Jana Pachlopnik Schmid, Klara M Posfay-Barbe, Roger Lauener, Keith Harshman, Kelly Ormond, Manon Jaboyedoff, Eric Giannoni, Tatjana Welzel, Dylan Lawless, Rebeca Mozun, Fabiën N Belle, Andrea Agostini, Matthias R Baumgartner, D Sean Froese, Sandra Goetze, Kathrin Hofmann, Aurélie Martin Necker, Patrick G A Pedrioli, Sven M Schulzke, Nicola Zamboni, Julia E Vogt, Audrey van Drogen, Aurélie Martin Necker, Cornelia Hagman, D Sean Froese, Daphné Chopard, Eirini I Petrou, Emanuele Palumbo, Ioannis Xenarios, Jana Pachlopnik Schmid, Léa Ho Dac, Lorenz M Leuenberger, Mariam Ait Oumelloul, Nicole Goebel, Simon Boutry, Thomas M Sutter, Varvara Dimopoulou, Vito RT Zanotelli, Xeni Deligianni, Xenia Bovermann, Yara Shoman, Anna Hartung
Published 2024-12-01Get full text
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