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Becker, Jessica, Czamara, Darina, Scerri, Tom S, Ramus, Franck, Csepe, Valeria, Talcott, Joel B, Stein, John, Morris, Andrew, Ludwig, Kerstin U, Hoffmann, Per et al (show 31 more authors) , Honbolygo, Ferenc, Toth, Denes, Fauchereau, Fabien, Bogliotti, Caroline, Iannuzzi, Stephanie, Chaix, Yves, Valdois, Sylviane, Billard, Catherine, George, Florence, Soares-Boucaud, Isabelle, Gerard, Christophe-Loic, van der Mark, Sanne, Schulz, Enrico, Vaessen, Anniek, Maurer, Urs, Lohvansuu, Kaisa, Lyytinen, Heikki, Zucchelli, Marco, Brandeis, Daniel, Blomertw, Leo, Leppanen, Paavo HT, Bruder, Jennifer, Monaco, Anthony P, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Kere, Juha, Landerl, Karin, Noethen, Markus M, Schulte-Koerne, Gerd, Paracchini, Silvia, Peyrard-Janvid, Myriam and Schumacher, Johannes (2014) Genetic analysis of dyslexia candidate genes in the European cross-linguistic NeuroDys cohort. EUROPEAN JOURNAL OF HUMAN GENETICS, 22 (5). pp. 675-680.

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Kim-Hellmuth, Sarah, Bechheim, Matthias, Puetz, Benno, Mohammadi, Pejman, Nedelec, Yohann, Giangreco, Nicholas, Becker, Jessica, Kaiser, Vera, Fricker, Nadine, Beier, Esther et al (show 9 more authors) , Boor, Peter, Castel, Stephane E, Noethen, Markus M, Barreiro, Luis B, Pickrell, Joseph K, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Lappalainen, Tuuli, Schumacher, Johannes and Hornung, Veit (2017) Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations. NATURE COMMUNICATIONS, 8 (1). 266-.

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Gialluisi, Alessandro, Andlauer, Till FM, Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U, Czamara, Darina, St Pourcain, Beate, Brandler, William et al (show 35 more authors) , Honbolygo, Ferenc, Toth, Denes, Csepe, Valeria, Huguet, Guillaume, Morris, Andrew P, Hulslander, Jacqueline, Willcutt, Erik G, DeFries, John C, Olson, Richard K, Smith, Shelley D, Pennington, Bruce F, Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppanen, Paavo HT, Brandeis, Daniel, Bonte, Milene, Stein, John F, Talcott, Joel B, Fauchereau, Fabien, Wilcke, Arndt, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P, Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S, Paracchini, Silvia, Fisher, Simon E, Schumacher, Johannes, Noethen, Markus M, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X and Schulte-Koerne, Gerd (2019) Genome-wide association scan identifies new variants associated with a cognitive predictor of dyslexia. TRANSLATIONAL PSYCHIATRY, 9 (1). 77-.

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Forstner, Andreas J, Awasthi, Swapnil, Wolf, Christiane, Maron, Eduard, Erhardt, Angelika, Czamara, Darina, Eriksson, Elias, Lavebratt, Catharina, Allgulander, Christer, Friedrich, Nina et al (show 65 more authors) , Becker, Jessica, Hecker, Julian, Rambau, Stefanie, Conrad, Rupert, Geiser, Franziska, McMahon, Francis J, Moebus, Susanne, Hess, Timo, Buerfent, Benedikt C, Hoffmann, Per, Herms, Stefan, Heilmann-Heimbach, Stefanie, Kockum, Ingrid, Olsson, Tomas, Alfredsson, Lars, Weber, Heike, Alpers, Georg W, Arolt, Volker, Fehm, Lydia, Fydrich, Thomas, Gerlach, Alexander L, Hamm, Alfons, Kircher, Tilo, Pane-Farre, Christiane A, Pauli, Paul, Rief, Winfried, Strohle, Andreas, Plag, Jens, Lang, Thomas, Wittchen, Hans-Ulrich, Mattheisen, Manuel, Meier, Sandra, Metspalu, Andres, Domschke, Katharina, Reif, Andreas, Hovatta, Iiris, Lindefors, Nils, Andersson, Evelyn, Schalling, Martin, Mbarek, Hamdi, Milaneschi, Yuri, de Geus, Eco JC, Boomsma, Dorret I, Penninx, Brenda WJH, Thorgeirsson, Thorgeir E, Steinberg, Stacy, Stefansson, Kari, Stefansson, Hreinn, Muller-Myhsok, Bertram ORCID: 0000-0002-0719-101X, Hansen, Thomas Folkmann, Borglum, Anders D, Werge, Thomas, Mortensen, Preben Bo, Nordentoft, Merete, Hougaard, David M, Hultman, Christina M, Sullivan, Patrick F, Nothen, Markus M, Woldbye, David PD, Mors, Ole, Binder, Elisabeth B, Rueck, Christian, Ripke, Stephan, Deckert, Juergen and Schumacher, Johannes (2021) Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression. MOLECULAR PSYCHIATRY, 26 (8). pp. 4179-4190.

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Gialluisi, Alessandro, Andlauer, Till FM, Mirza-Schreiber, Nazanin, Moll, Kristina, Becker, Jessica, Hoffmann, Per, Ludwig, Kerstin U, Czamara, Darina, St Pourcain, Beate, Honbolygo, Ferenc et al (show 39 more authors) , Toth, Denes, Csepe, Valeria, Huguet, Guillaume, Chaix, Yves, Iannuzzi, Stephanie, Demonet, Jean-Francois, Morris, Andrew P, Hulslander, Jacqueline, Willcutt, Erik G, DeFries, John C, Olson, Richard K, Smith, Shelley D, Pennington, Bruce F, Vaessen, Anniek, Maurer, Urs, Lyytinen, Heikki, Peyrard-Janvid, Myriam, Leppanen, Paavo HT, Brandeis, Daniel, Bonte, Milene, Stein, John F, Talcott, Joel B, Fauchereau, Fabien, Wilcke, Arndt, Kirsten, Holger, Mueller, Bent, Francks, Clyde, Bourgeron, Thomas, Monaco, Anthony P, Ramus, Franck, Landerl, Karin, Kere, Juha, Scerri, Thomas S, Paracchini, Silvia, Fisher, Simon E, Schumacher, Johannes, Noethen, Markus M, Mueller-Myhsok, Bertram ORCID: 0000-0002-0719-101X and Schulte-Koerne, Gerd (2021) Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. MOLECULAR PSYCHIATRY, 26 (7). pp. 3004-3017.