Quantifying the role of transcript levels in mediating DNA methylation effects on complex traits and diseases von Sadler, Marie C., Auwerx, Chiara, Lepik, Kaido, Porcu, Eleonora, Kutalik, Zoltán

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Breaking down causes, consequences, and mediating effects of telomere length variation on human health von Moix, Samuel, Sadler, Marie C, Kutalik, Zoltán, Auwerx, Chiara

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Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome von Porcu, Eleonora, Sadler, Marie C., Lepik, Kaido, Auwerx, Chiara, Wood, Andrew R., Weihs, Antoine, Sleiman, Maroun S. Bou, Ribeiro, Diogo M., Bandinelli, Stefania, Tanaka, Toshiko, Nauck, Matthias, Völker, Uwe, Delaneau, Olivier, Metspalu, Andres, Teumer, Alexander, Frayling, Timothy, Santoni, Federico A., Reymond, Alexandre, Kutalik, Zoltán

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Exploiting the mediating role of the metabolome to unravel transcript-to-phenotype associations von Auwerx, Chiara, Sadler, Marie C, Woh, Tristan, Reymond, Alexandre, Kutalik, Zoltán, Porcu, Eleonora

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From pharmacogenetics to pharmaco-omics: Milestones and future directions von Auwerx, Chiara, Sadler, Marie C., Reymond, Alexandre, Kutalik, Zoltán

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Rare copy-number variants as modulators of common disease susceptibility von Auwerx, Chiara, Jõeloo, Maarja, Sadler, Marie C, Tesio, Nicolò, Ojavee, Sven, Clark, Charlie J, Mägi, Reedik, Reymond, Alexandre, Kutalik, Zoltán

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Promises and challenges in pharmacoepigenetics von Smith, Delaney A, Sadler, Marie C, Altman, Russ B

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Mendelian randomization to assess causality between uromodulin, blood pressure and chronic kidney disease von Ponte, Belen, Sadler, Marie C., Olinger, Eric, Vollenweider, Peter, Bochud, Murielle, Padmanabhan, Sandosh, Hayward, Caroline, Kutalik, Zoltán, Devuyst, Olivier

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The individual and global impact of copy-number variants on complex human traits von Auwerx, Chiara, Lepamets, Maarja, Sadler, Marie C., Patxot, Marion, Stojanov, Miloš, Baud, David, Mägi, Reedik, Esko, Tõnu, Metspalu, Andres, Milani, Lili, Mägi, Reedik, Nelis, Mari, Porcu, Eleonora, Reymond, Alexandre, Kutalik, Zoltán

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Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts von Giannuzzi, Giuliana, Chatron, Nicolas, Mannik, Katrin, Auwerx, Chiara, Pradervand, Sylvain, Willemin, Gilles, Hoekzema, Kendra, Nuttle, Xander, Chrast, Jacqueline, Sadler, Marie C., Porcu, Eleonora, Herault, Yann, Isidor, Bertrand, Gilbert-Dussardier, Brigitte, Eichler, Evan E., Kutalik, Zoltan, Reymond, Alexandre

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Author Correction: Possible association of 16p11.2 copy number variation with altered lymphocyte and neutrophil counts von Giannuzzi, Giuliana, Chatron, Nicolas, Mannik, Katrin, Auwerx, Chiara, Pradervand, Sylvain, Willemin, Gilles, Hoekzema, Kendra, Nuttle, Xander, Chrast, Jacqueline, Sadler, Marie C., Porcu, Eleonora, Herault, Yann, Isidor, Bertrand, Gilbert-Dussardier, Brigitte, Eichler, Evan E., Kutalik, Zoltan, Reymond, Alexandre

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Sex- and age-dependent genetics of longevity in a heterogeneous mouse population von Bou Sleiman, Maroun, Roy, Suheeta, Gao, Arwen W, Sadler, Marie C, von Alvensleben, Giacomo V G, Li, Hao, Sen, Saunak, Harrison, David E, Nelson, James F, Strong, Randy, Miller, Richard A, Kutalik, Zoltán, Williams, Robert W, Auwerx, Johan

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Multi-layered genetic approaches to identify approved drug targets von Sadler, Marie C., Auwerx, Chiara, Deelen, Patrick, Kutalik, Zoltán

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The impact of 22q11.2 copy-number variants on human traits in the general population von Zamariolli, Malú, Auwerx, Chiara, Sadler, Marie C., van der Graaf, Adriaan, Lepik, Kaido, Schoeler, Tabea, Moysés-Oliveira, Mariana, Dantas, Anelisa G., Melaragno, Maria Isabel, Kutalik, Zoltán

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Response to Bassett et al von Zamariolli, Malú, Auwerx, Chiara, Sadler, Marie C, van der Graaf, Adriaan, Lepik, Kaido, Schoeler, Tabea, Moysés-Oliveira, Mariana, Dantas, Anelisa G, Melaragno, Maria Isabel, Kutalik, Zoltán

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Causality-enriched epigenetic age uncouples damage and adaptation von Ying, Kejun, Liu, Hanna, Tarkhov, Andrei E, Sadler, Marie C, Lu, Ake T, Moqri, Mahdi, Horvath, Steve, Kutalik, Zoltán, Shen, Xia, Gladyshev, Vadim N

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Chromosomal deletions on 16p11.2 encompassing SH2B1 are associated with accelerated metabolic disease von Hanssen, Ruth, Auwerx, Chiara, Jõeloo, Maarja, Sadler, Marie C, Henning, Elana, Keogh, Julia, Bounds, Rebecca, Smith, Miriam, Firth, Helen V, Kutalik, Zoltán, Farooqi, I Sadaf, Reymond, Alexandre, Lawler, Katherine

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Computational Surveillance of Microbial Water Quality With Online Flow Cytometry von Sadler, Marie C., Senouillet, Jérémy, Kuenzi, Simon, Grasso, Luigino, Watson, Douglas C.

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Mendelian randomization to assess causality between uromodulin, blood pressure and chronic kidney disease von Ponte, Belen, Sadler, Marie C, Olinger, Eric, Vollenweider, Peter, Bochud, Murielle, Padmanabhan, Sandosh, Hayward, Caroline, Kutalik, Zoltán, Devuyst, Olivier

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Additional file 2 of Breaking down causes, consequences, and mediating effects of telomere length variation on human health von Moix, Samuel, Sadler, Marie C, Kutalik, Zoltán, Auwerx, Chiara

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