Increased DNA methylation variability in rheumatoid arthritis-discordant monozygotic twins

por Webster, Amy P., Plant, Darren, Ecker, Simone, Zufferey, Flore, Bell, Jordana T., Feber, Andrew, Paul, Dirk S., Beck, Stephan, Barton, Anne, Williams, Frances M. K., Worthington, Jane
Publicado 2018

Rare Genomic Structural Variants in Complex Disease: Lessons from the Replication of Associations with Obesity

por Walters, Robin G., Coin, Lachlan J. M., Ruokonen, Aimo, de Smith, Adam J., El-Sayed Moustafa, Julia S., Jacquemont, Sebastien, Elliott, Paul, Esko, Tõnu, Hartikainen, Anna-Liisa, Laitinen, Jaana, Männik, Katrin, Martinet, Danielle, Meyre, David, Nauck, Matthias, Schurmann, Claudia, Sladek, Rob, Thorleifsson, Gudmar, Thorsteinsdóttir, Unnur, Valsesia, Armand, Waeber, Gerard, Zufferey, Flore, Balkau, Beverley, Pattou, François, Metspalu, Andres, Völzke, Henry, Vollenweider, Peter, Stefansson, Kári, Järvelin, Marjo-Riitta, Beckmann, Jacques S., Froguel, Philippe, Blakemore, Alexandra I. F.
Publicado 2013

A 600 kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders

por Zufferey, Flore, Sherr, Elliott H, Beckmann, Noam D, Hanson, Ellen, Maillard, Anne M, Hippolyte, Loyse, Macé, Aurélien, Ferrari, Carina, Kutalik, Zoltán, Andrieux, Joris, Aylward, Elizabeth, Barker, Mandy, Bernier, Raphael, Bouquillon, Sonia, Conus, Philippe, Delobel, Bruno, Faucett, W Andrew, Goin-Kochel, Robin P, Grant, Ellen, Harewood, Louise, Hunter, Jill V, Lebon, Sébastien, Ledbetter, David H, Martin, Christa Lese, Männik, Katrin, Martinet, Danielle, Mukherjee, Pratik, Ramocki, Melissa B, Spence, Sarah J, Steinman, Kyle J, Tjernagel, Jennifer, Spiro, John E, Reymond, Alexandre, Beckmann, Jacques S, Chung, Wendy K, Jacquemont, Sébastien
Publicado 2012