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Anzahl der Publikationen: 53

Zeitschriftenartikel

Budu-Aggrey, Ashley ORCID logoORCID: https://orcid.org/0000-0002-8911-2492; Kilanowski, Anna ORCID logoORCID: https://orcid.org/0000-0001-5328-6274; Sobczyk, Maria K. ORCID logoORCID: https://orcid.org/0000-0003-0000-4100; Shringarpure, Suyash S. ORCID logoORCID: https://orcid.org/0000-0001-6464-2668; Mitchell, Ruth ORCID logoORCID: https://orcid.org/0000-0002-3506-160X; Reis, Kadri ORCID logoORCID: https://orcid.org/0000-0002-2144-5856; Reigo, Anu; Mägi, Reedik ORCID logoORCID: https://orcid.org/0000-0002-2964-6011; Nelis, Mari; Tanaka, Nao ORCID logoORCID: https://orcid.org/0000-0002-2085-4682; Brumpton, Ben M. ORCID logoORCID: https://orcid.org/0000-0002-3058-1059; Thomas, Laurent F. ORCID logoORCID: https://orcid.org/0000-0003-0548-2486; Sole-Navais, Pol ORCID logoORCID: https://orcid.org/0000-0002-3326-266X; Flatley, Christopher; Espuela-Ortiz, Antonio ORCID logoORCID: https://orcid.org/0000-0003-0572-9549; Herrera-Luis, Esther ORCID logoORCID: https://orcid.org/0000-0003-4150-5454; Lominchar, Jesus V. T.; Bork-Jensen, Jette; Marenholz, Ingo; Arnau-Soler, Aleix ORCID logoORCID: https://orcid.org/0000-0001-9768-0513; Jeong, Ayoung ORCID logoORCID: https://orcid.org/0000-0003-1542-0756; Fawcett, Katherine A. ORCID logoORCID: https://orcid.org/0000-0002-6675-2112; Baurecht, Hansjorg; Rodriguez, Elke ORCID logoORCID: https://orcid.org/0000-0003-3692-3950; Alves, Alexessander Couto ORCID logoORCID: https://orcid.org/0000-0001-8519-7356; Kumar, Ashish; Sleiman, Patrick M.; Chang, Xiao; Medina-Gomez, Carolina ORCID logoORCID: https://orcid.org/0000-0001-7999-5538; Hu, Chen; Xu, Cheng-jian ORCID logoORCID: https://orcid.org/0000-0003-1586-4672; Qi, Cancan; El-Heis, Sarah; Titcombe, Philip; Antoun, Elie; Fadista, João; Wang, Carol A. ORCID logoORCID: https://orcid.org/0000-0002-4301-3974; Thiering, Elisabeth; Wu, Baojun; Kress, Sara ORCID logoORCID: https://orcid.org/0000-0002-8007-5357; Kothalawala, Dilini M.; Kadalayil, Latha; Duan, Jiasong; Zhang, Hongmei ORCID logoORCID: https://orcid.org/0000-0003-3557-0364; Hadebe, Sabelo; Hoffmann, Thomas ORCID logoORCID: https://orcid.org/0000-0001-6893-4449; Jorgenson, Eric; Choquet, Hélène ORCID logoORCID: https://orcid.org/0000-0001-9839-8667; Risch, Neil; Njølstad, Pål ORCID logoORCID: https://orcid.org/0000-0003-0304-6728; Andreassen, Ole A. ORCID logoORCID: https://orcid.org/0000-0002-4461-3568; Johansson, Stefan ORCID logoORCID: https://orcid.org/0000-0002-2298-7008; Almqvist, Catarina ORCID logoORCID: https://orcid.org/0000-0002-1045-1898; Gong, Tong; Ullemar, Vilhelmina; Karlsson, Robert ORCID logoORCID: https://orcid.org/0000-0002-8949-2587; Magnusson, Patrik K. E. ORCID logoORCID: https://orcid.org/0000-0002-7315-7899; Szwajda, Agnieszka; Burchard, Esteban G. ORCID logoORCID: https://orcid.org/0000-0001-7475-2035; Thyssen, Jacob P.; Hansen, Torben ORCID logoORCID: https://orcid.org/0000-0001-8748-3831; Kårhus, Line L.; Dantoft, Thomas M.; Jeanrenaud, Alexander C.S.N.; Ghauri, Ahla ORCID logoORCID: https://orcid.org/0000-0003-4665-3624; Arnold, Andreas; Homuth, Georg ORCID logoORCID: https://orcid.org/0000-0001-6839-0605; Lau, Susanne; Nöthen, Markus M. ORCID logoORCID: https://orcid.org/0000-0002-8770-2464; Hübner, Norbert ORCID logoORCID: https://orcid.org/0000-0002-1218-6223; Imboden, Medea; Visconti, Alessia ORCID logoORCID: https://orcid.org/0000-0003-4144-2019; Falchi, Mario ORCID logoORCID: https://orcid.org/0000-0002-5646-1004; Bataille, Veronique; Hysi, Pirro ORCID logoORCID: https://orcid.org/0000-0001-5752-2510; Ballardini, Natalia; Boomsma, Dorret I. ORCID logoORCID: https://orcid.org/0000-0002-7099-7972; Hottenga, Jouke J. ORCID logoORCID: https://orcid.org/0000-0002-5668-2368; Müller-Nurasyid, Martina ORCID logoORCID: https://orcid.org/0000-0003-3793-5910; Ahluwalia, Tarunveer S. ORCID logoORCID: https://orcid.org/0000-0002-7464-3354; Stokholm, Jakob ORCID logoORCID: https://orcid.org/0000-0003-4989-9769; Chawes, Bo ORCID logoORCID: https://orcid.org/0000-0001-6846-6243; Schoos, Ann-Marie M. ORCID logoORCID: https://orcid.org/0000-0002-5827-0885; Esplugues, Ana; Bustamante, Mariona ORCID logoORCID: https://orcid.org/0000-0003-0127-2860; Raby, Benjamin; Arshad, Syed; German, Chris; Esko, Tõnu; Milani, Lili A. ORCID logoORCID: https://orcid.org/0000-0002-5323-3102; Metspalu, Andres ORCID logoORCID: https://orcid.org/0000-0002-3718-796X; Terao, Chikashi ORCID logoORCID: https://orcid.org/0000-0002-6452-4095; Abuabara, Katrina; Løset, Mari ORCID logoORCID: https://orcid.org/0000-0003-3736-6551; Hveem, Kristian; Jacobsson, Bo ORCID logoORCID: https://orcid.org/0000-0001-5079-2374; Pino-Yanes, Maria ORCID logoORCID: https://orcid.org/0000-0003-0332-437X; Strachan, David P. ORCID logoORCID: https://orcid.org/0000-0001-7854-1366; Grarup, Niels ORCID logoORCID: https://orcid.org/0000-0001-5526-1070; Linneberg, Allan ORCID logoORCID: https://orcid.org/0000-0002-0994-0184; Lee, Young-Ae ORCID logoORCID: https://orcid.org/0000-0002-1817-9163; Probst-Hensch, Nicole; Weidinger, Stephan ORCID logoORCID: https://orcid.org/0000-0003-3944-252X; Jarvelin, Marjo-Riitta ORCID logoORCID: https://orcid.org/0000-0002-2149-0630; Melén, Erik ORCID logoORCID: https://orcid.org/0000-0002-8248-0663; Hakonarson, Hakon ORCID logoORCID: https://orcid.org/0000-0003-2814-7461; Irvine, Alan D. ORCID logoORCID: https://orcid.org/0000-0002-9048-2044; Jarvis, Deborah; Nijsten, Tamar ORCID logoORCID: https://orcid.org/0000-0001-9940-2875; Duijts, Liesbeth; Vonk, Judith M. ORCID logoORCID: https://orcid.org/0000-0001-7531-4547; Koppelmann, Gerard H. ORCID logoORCID: https://orcid.org/0000-0001-8567-3252; Godfrey, Keith M. ORCID logoORCID: https://orcid.org/0000-0002-4643-0618; Barton, Sheila J.; Feenstra, Bjarke ORCID logoORCID: https://orcid.org/0000-0003-1478-649X; Pennell, Craig E. ORCID logoORCID: https://orcid.org/0000-0002-0937-6165; Sly, Peter D. ORCID logoORCID: https://orcid.org/0000-0001-6305-2201; Holt, Patrick G. ORCID logoORCID: https://orcid.org/0000-0003-1193-0935; Williams, L. Keoki; Bisgaard, Hans; Bønnelykke, Klaus ORCID logoORCID: https://orcid.org/0000-0003-2003-1018; Curtin, John; Simpson, Angela; Murray, Clare ORCID logoORCID: https://orcid.org/0000-0002-8961-8055; Schikowski, Tamara; Bunyavanich, Supinda ORCID logoORCID: https://orcid.org/0000-0001-6108-439X; Weiss, Scott T.; Holloway, John W. ORCID logoORCID: https://orcid.org/0000-0001-9998-0464; Min, Josine L. ORCID logoORCID: https://orcid.org/0000-0003-4456-9824; Brown, Sara J.; Standl, Marie ORCID logoORCID: https://orcid.org/0000-0002-5345-2049 und Paternoster, Lavinia ORCID logoORCID: https://orcid.org/0000-0003-2514-0889 (2023): European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation. In: Nature Communications, Bd. 14, Nr. 1 [PDF, 3MB]

Kohshour, Mojtaba Oraki; Kannaiyan, Nirmal R.; Falk, August Jernbom; Papiol, Sergi; Heilbronner, Urs; Budde, Monika; Kalman, Janos L.; Schulte, Eva C.; Rietschel, Marcella; Witt, Stephanie; Forstner, Andreas J.; Heilmann-Heimbach, Stefanie; Nöthen, Markus M.; Spitzer, Carsten; Malchow, Berend; Müller, Thorsten; Wiltfang, Jens; Falkai, Peter; Schmitt, Andrea; Rossner, Moritz J.; Nilsson, Peter und Schulze, Thomas G. (2022): Comparative serum proteomic analysis of a selected protein panel in individuals with schizophrenia and bipolar disorder and the impact of genetic risk burden on serum proteomic profiles. In: Translational Psychiatry, Bd. 12, Nr. 1, 471

Price, Kaitlyn M.; Wigg, Karen G.; Eising, Else; Feng, Yu; Blokland, Kirsten; Wilkinson, Margaret; Kerr, Elizabeth N.; Guger, Sharon L.; Abbondanza, Filippo; Allegrini, Andrea G.; Andlauer, Till F. M.; Bates, Timothy C.; Bernard, Manon; Bonte, Milene; Boomsma, Dorret I.; Bourgeron, Thomas; Brandeis, Daniel; Carreiras, Manuel; Ceroni, Fabiola; Csepe, Valeria; Dale, Philip S.; DeFries, John C.; Jong, Peter F. de; Demonet, Jean Francois; Zeeuw, Eveline L. de; Franken, Marie-Christine J.; Francks, Clyde; Gerritse, Margot; Gialluisi, Alessandro; Gordon, Scott D.; Gruen, Jeffrey R.; Hayiou-Thomas, Marianna E.; Hernandez-Cabrera, Juan; Hottenga, Jouke-Jan; Hulme, Charles; Jansen, Philip R.; Kere, Juha; Koomar, Tanner; Landerl, Karin; Leonard, Gabriel T.; Liao, Zhijie; Luciano, Michelle; Lyytinen, Heikki; Martin, Nicholas G.; Martinelli, Angela; Maurer, Urs; Michaelson, Jacob J.; Mirza-Schreiber, Nazanin; Moll, Kristina; Monaco, Anthony P.; Morgan, Angela T.; Müller-Myhsok, Bertram; Newbury, Dianne F.; Nöthen, Markus M.; Olson, Richard K.; Paracchini, Silvia; Paus, Tomas; Pausova, Zdenka; Pennell, Craig E.; Pennington, Bruce F.; Plomin, Robert J.; Ramus, Franck; Reilly, Sheena; Richer, Louis; Rimfeld, Kaili; Schulte-Korne, Gerd; Shapland, Chin Yang; Simpson, Nuala H.; Smith, Shelley D.; Snowling, Margaret J.; St Pourcain, Beate; Stein, John F.; Talcott, Joel B.; Tiemeier, Henning; Tomblin, J. Bruce; Truong, Dongnhu T.; Bergen, Elsje van; Schröff, Marc P. van der; Donkelaar, Marjolein van; Verhoef, Ellen; Wang, Carol A.; Watkins, Kate E.; Whitehouse, Andrew J. O.; Willcutt, Erik G.; Wright, Margaret J.; Zhu, Gu; Fisher, Simon E.; Lovett, Maureen W.; Strug, Lisa J. und Barr, Cathy L. (2022): Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities. In: Translational Psychiatry, Bd. 12, Nr. 1, 495

Schmidt, Andreas W. ORCID logoORCID: https://orcid.org/0000-0001-5609-290X; Kühnapfel, Andreas ORCID logoORCID: https://orcid.org/0000-0003-3668-0784; Kirsten, Holger ORCID logoORCID: https://orcid.org/0000-0002-3126-7950; Grallert, Harald ORCID logoORCID: https://orcid.org/0000-0002-6876-9655; Hellerbrand, Claus; Kiefer, Falk; Mann, Karl; Mueller, Sebastian; Nöthen, Markus M.; Peters, Annette ORCID logoORCID: https://orcid.org/0000-0001-6645-0985; Ridinger, Monika; Frank, Josef; Rietschel, Marcella; Soranzo, Nicole; Soyka, Michael; Wodarz, Norbert ORCID logoORCID: https://orcid.org/0000-0001-9070-8448; Malerba, Giovanni; Gambaro, Giovanni ORCID logoORCID: https://orcid.org/0000-0001-5733-2370; Gieger, Christian; Scholz, Markus; Krug, Sebastian; Michl, Patrick ORCID logoORCID: https://orcid.org/0000-0002-0401-5600; Ewers, Maren ORCID logoORCID: https://orcid.org/0000-0002-9029-2240; Witt, Heiko ORCID logoORCID: https://orcid.org/0000-0001-7791-7341; Laumen, Helmut ORCID logoORCID: https://orcid.org/0000-0002-5885-5242 und Rosendahl, Jonas ORCID logoORCID: https://orcid.org/0000-0003-4513-0506 (2022): Colocalization analysis of pancreas eQTLs with risk loci from alcoholic and novel non-alcoholic chronic pancreatitis GWAS suggests potential disease causing mechanisms. In: Pancreatology, Bd. 22, Nr. 4: S. 449-456

Tilch, Erik; Schormair, Barbara ORCID logoORCID: https://orcid.org/0000-0003-0942-5243; Zhao, Chen; Högl, Birgit; Stefani, Ambra; Berger, Klaus; Trenkwalder, Claudia; Bachmann, Cornelius G.; Hornyak, Magdolna; Fietze, Ingo; Müller-Nurasyid, Martina ORCID logoORCID: https://orcid.org/0000-0003-3793-5910; Peters, Annette; Herms, Stefan; Nöthen, Markus M.; Müller-Myhsok, Bertram; Oexle, Konrad und Winkelmann, Juliane (2022): ExomeChip-based rare variant association study in restless legs syndrome. In: Sleep Medicine, Bd. 94: S. 26-30

Forstner, Andreas J.; Awasthi, Swapnil; Wolf, Christiane; Maron, Eduard; Erhardt, Angelika; Czamara, Darina; Eriksson, Elias; Lavebratt, Catharina; Allgulander, Christer; Friedrich, Nina; 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; Ströhle, 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; Geus, Eco J. C. de; Boomsma, Dorret I.; Penninx, Brenda W. J. H.; Thorgeirsson, Thorgeir E.; Steinberg, Stacy; Stefansson, Kari; Stefansson, Hreinn; Müller-Myhsok, Bertram; Hansen, Thomas Folkmann; Borglum, Anders D.; Werge, Thomas; Mortensen, Preben Bo; Nordentoft, Merete; Hougaard, David M.; Hultman, Christina M.; Sullivan, Patrick F.; Nöthen, Markus M.; Woldbye, David P. D.; Mors, Ole; Binder, Elisabeth B.; Rueck, Christian; Ripke, Stephan; Deckert, Jürgen und Schumacher, Johannes (2021): Genome-wide association study of panic disorder reveals genetic overlap with neuroticism and depression. In: Molecular Psychiatry, Bd. 26, Nr. 8: S. 4179-4190

Heilbronner, Urs; Streit, Fabian; Vogl, Thomas; Senner, Fanny; Schaupp, Sabrina K.; Reich-Erkelenz, Daniela; Papiol, Sergi; Oraki Kohshour, Mojtaba; Klöhn-Saghatolislam, Farahnaz; Kalman, Janos L.; Heilbronner, Maria; Gade, Katrin; Comes, Ashley L.; Budde, Monika; Andlauer, Till F. M.; Anderson-Schmidt, Heike; Adorjan, Kristina; Stürmer, Til; Loerbroks, Adrian; Amelang, Manfred; Poisel, Eric; Foo, Jerome; Heilmann-Heimbach, Stefanie; Forstner, Andreas J.; Degenhardt, Franziska; Zimmermann, Jörg; Wiltfang, Jens; von Hagen, Martin; Spitzer, Carsten; Schmauss, Max; Reininghaus, Eva; Reimer, Jens; Konrad, Carsten; Juckel, Georg; Lang, Fabian U.; Jäger, Markus; Figge, Christian; Fallgatter, Andreas J.; Dietrich, Detlef E.; Dannlowski, Udo; Baune, Bernhardt T.; Arolt, Volker; Anghelescu, Ion-George; Nöthen, Markus M.; Witt, Stephanie H.; Andreassen, Ole A.; Chen, Chi-Hua; Falkai, Peter ORCID logoORCID: https://orcid.org/0000-0003-2873-8667; Rietschel, Marcella; Schulze, Thomas G. und Schulte, Eva C. (2021): Interplay between the genetics of personality traits, severe psychiatric disorders and COVID-19 host genetics in the susceptibility to SARS-CoV-2 infection. In: BJPsych open, Bd. 7, Nr. 6, e188 [PDF, 453kB]

Shadrin, Alexey A.; Mucha, Sören; Ellinghaus, David; Makarious, Mary B.; Blauwendraat, Cornelis; Sreelatha, Ashwin A. K.; Heras-Garvin, Antonio; Ding, Jinhui; Hammer, Monia; Foubert-Samier, Alexandra; Meissner, Wassilios G.; Rascol, Olivier; Pavy-Le Traon, Anne; Frei, Oleksandr; O'Connell, Kevin S.; Bahrami, Shahram; Schreiber, Stefan; Lieb, Wolfgang; Müller-Nurasyid, Martina; Schminke, Ulf; Homuth, Georg; Schmidt, Carsten O.; Nöthen, Markus M.; Hoffmann, Per; Gieger, Christian; Wenning, Gregor; Gibbs, J. Raphael; Franke, Andre; Hardy, John; Stefanova, Nadia; Gasser, Thomas; Singleton, Andrew; Houlden, Henry; Scholz, Sonja W.; Andreassen, Ole A. und Sharma, Manu (2020): Shared Genetics of Multiple System Atrophy and Inflammatory Bowel Disease. In: Movement Disorders, Bd. 36, Nr. 2: S. 449-459

Gialluisi, Alessandro; Andlauer, Till F. M.; Mirza-Schreiber, Nazanin; Moll, Kristina; Becker, Jessica; Hoffmann, Per; Ludwig, Kerstin U.; Czamara, Darina; Pourcain, Beate St; Honbolygó, Ferenc; Tóth, Dénes; Csépe, Valéria; 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; Leppänen, Paavo H. T.; Brandeis, Daniel; Bonte, Milene; Stein, John F.; Talcott, Joel B.; Fauchereau, Fabien; Wilcke, Arndt; Kirsten, Holger; Müller, Bent; Francks, Clyde; Bourgeron, Thomas; Monaco, Anthony P.; Ramus, Franck; Landerl, Karin; Kere, Juha; Scerri, Thomas S.; Paracchini, Silvia; Fisher, Simon E.; Schumacher, Johannes; Nöthen, Markus M.; Müller-Myhsok, Bertram und Schulte-Körne, Gerd (2020): Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. In: Molecular psychiatry [PDF, 2MB]

Amare, Azmeraw T.; Schubert, Klaus Oliver; Hou, Liping; Clark, Scott R.; Papiol, Sergi; Heilbronner, Urs; Degenhardt, Franziska; Tekola-Ayele, Fasil; Hsu, Yi-Hsiang; Shekhtman, Tatyana; Adli, Mazda; Akula, Nirmala; Akiyama, Kazufumi; Ardau, Raffaella; Arias, Barbara; Aubry, Jean-Michel; Backlund, Lena; Bhattacharjee, Abesh Kumar; Bellivier, Frank; Benabarre, Antonio; Bengesser, Susanne; Biernacka, Joanna M.; Birner, Armin; Brichant-Petitjean, Clara; Cervantes, Pablo; Chen, Hsi-Chung; Chillotti, Caterina; Cichon, Sven; Cruceanu, Cristiana; Czerski, Piotr M.; Dalkner, Nina; Dayer, Alexandre; Zompo, Maria del; DePaulo, J. Raymond; Etain, Bruno; Falkai, Peter ORCID logoORCID: https://orcid.org/0000-0003-2873-8667; Forstner, Andreas J.; Frisen, Louise; Frye, Mark A.; Fullerton, Janice M.; Gard, Sebastien; Garnham, Julie S.; Goes, Fernando S.; Grigoroiu-Serbanescu, Maria; Grof, Paul; Hashimoto, Ryota; Hauser, Joanna; Herms, Stefan; Hoffmann, Per; Hofmann, Andrea; Jamain, Stephane; Jimenez, Esther; Kahn, Jean-Pierre; Kassem, Layla; Kuo, Po-Hsiu; Kato, Tadafumi; Kelsoe, John; Kittel-Schneider, Sarah; Kliwicki, Sebastian; König, Barbara; Kusumi, Ichiro; Laje, Gonzalo; Landen, Mikael; Lavebratt, Catharina; Leboyer, Marion; Leckband, Susan G.; Tortorella, Alfonso; Manchia, Mirko; Martinsson, Lina; McCarthy, Michael J.; McElroy, Susan; Colom, Francesc; Mitjans, Marina; Mondimore, Francis M.; Monteleone, Palmiero; Nievergelt, Caroline M.; Nöthen, Markus M.; Novak, Tomas; O'Donovan, Claire; Ozaki, Norio; Osby, Urban; Pfennig, Andrea; Potash, James B.; Reif, Andreas; Reininghaus, Eva; Rouleau, Guy A.; Rybakowski, Janusz K.; Schalling, Martin; Schofield, Peter R.; Schweizer, BarbaraW.; Severino, Giovanni; Shilling, Paul D.; Shimoda, Katzutaka; Simhandl, Christian; Slaney, Claire M.; Squassina, Alessio; Stamm, Thomas; Stopkova, Pavla; Maj, Mario; Turecki, Gustavo; Vieta, Eduard; Volkert, Julia; Witt, Stephanie; Wright, Adam; Zandi, Peter P.; Mitchell, Philip B.; Bauer, Michael; Alda, Martin; Rietschel, Marcella; McMahon, Francis J.; Schulze, Thomas G. und Baune, Bernhard T. (2018): Association of Polygenic Score for Schizophrenia and HLA Antigen and Inflammation Genes With Response to Lithium in Bipolar Affective Disorder A Genome-Wide Association Study. In: Jama Psychiatry, Bd. 75, Nr. 1: S. 65-74

Rosendahl, Jonas; Kirsten, Holger; Hegyi, Eszter; Kovacs, Peter; Weiss, Frank Ulrich; Laumen, Helmut; Lichtner, Peter; Ruffert, Claudia; Chen, Jian-Min; Masson, Emmanuelle; Beer, Sebastian; Zimmer, Constantin; Seltsam, Katharina; Alguel, Hana; Bühler, Florence; Bruno, Marco J.; Bugert, Peter; Burkhardt, Ralph; Cavestro, Giulia Martina; Cichoz-Lach, Halina; Farre, Antoni; Frank, Josef; Gambaro, Giovanni; Gimpfl, Sebastian; Grallert, Harald; Griesmann, Heidi; Gruetzmann, Robert; Hellerbrand, Claus; Hegyi, Peter; Hollenbach, Marcus; Iordache, Sevastitia; Jurkowska, Grazyna; Keim, Volker; Kiefer, Falk; Krug, Sebastian; Landt, Olfert; Di Leo, Milena; Lerch, Markus M.; Levy, Philippe; Löffler, Markus; Löhr, Matthias; Ludwig, Maren; Macek, Milan; Malats, Nuria; Malecka-Panas, Ewa; Malerba, Giovanni; Mann, Karl; Mayerle, Julia; Mohr, Sonja; te Morsche, Rene H. M.; Motyka, Marie; Müller, Sebastian; Müller, Thomas; Nöthen, Markus M.; Pedrazzoli, Sergio; Pereira, Stephen P.; Peters, Annette; Pfuetzer, Roland; Real, Francisco X.; Rebours, Vinciane; Ridinger, Monika; Rietschel, Marcella; Roesmann, Eva; Saftoiu, Adrian; Schneider, Alexander; Schulz, Hans-Ulrich; Soranzo, Nicole; Soyka, Michael; Simon, Peter; Skipworth, James; Stickel, Felix; Strauch, Konstantin; Stumvoll, Michael; Testoni, Pier Alberto; Toenjes, Anke; Werner, Lena; Werner, Jens; Wodarz, Norbert; Ziegler, Martin; Masamune, Atsushi; Moessner, Joachim; Ferec, Claude; Michl, Patrick; Drenth, Joost P. H.; Witt, Heiko; Scholz, Markus und Sahin-Toth, Miklos (2018): Genome-wide association study identifies inversion in the CTRB1-CTRB2 locus to modify risk for alcoholic and non-alcoholic chronic pancreatitis. In: Gut, Bd. 67, Nr. 10: S. 1855-1863 [PDF, 1MB]

Mühleisen, Thomas W.; Reinbold, Celine S.; Forstner, Andreas J.; Abramova, Lilia I.; Alda, Martin; Babadjanova, Gulja; Bauer, Michael; Brennan, Paul; Chuchalin, Alexander; Cruceanu, Cristiana; Czerski, Piotr M.; Degenhardt, Franziska; Fischer, Sascha B.; Fullerton, Janice M.; Gordon, Scott D.; Grigoroiu-Serbanescu, Maria; Grof, Paul; Hauser, Joanna; Hautzinger, Martin; Herms, Stefan; Hoffmann, Per; Kammerer-Ciernioch, Jutta; Khusnutdinova, Elza; Kogevinas, Manolis; Krasnova, Valery; Lacour, Andre; Laprise, Catherine; Leber, Markus; Lissowska, Jolanta; Lucae, Susanne; Maaser, Anna; Maier, Wolfgang; Martin, Nicholas G.; Mattheisen, Manuel; Mayoral, Fermin; McKay, James D.; Medland, Sarah E.; Mitchell, Philip B.; Moebus, Susanne; Montgomery, Grant W.; Müller-Myhsok, Bertram; Oruc, Lilijana; Pantelejeva, Galina; Pfennig, Andrea; Pojskic, Lejla; Polonikov, Alexey; Reif, Andreas; Rivas, Fabio; Rouleau, Guy A.; Schenk, Lorena M.; Schofield, Peter R.; Schwarz, Markus; Streit, Fabian; Strohmaier, Jana; Szeszenia-Dabrowska, Neonila; Tiganov, Alexander S.; Treutlein, Jens; Turecki, Gustavo; Vedder, Helmut; Witt, Stephanie H.; Schulze, Thomas G.; Rietschel, Marcella; Nöthen, Markus M. und Cichon, Sven (2018): Gene set enrichment analysis and expression pattern exploration implicate an involvement of neurodevelopmental processes in bipolar disorder. In: Journal of Affective Disorders, Bd. 228: S. 20-25

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Auwera, Sandra van der; Teumer, Alexander; Hertel, Johannes; Homuth, Georg; Völker, Uwe; Lucht, Michael J.; Degenhardt, Franziska; Schulze, Thomas; Rietschel, Marcella; Nöthen, Markus M.; John, Ulrich; Nauck, Matthias und Grabe, Hans Jörgen (2016): The inverse link between genetic risk for schizophrenia and migraine through NMDA (N-methyl-D-aspartate) receptor activation via D-serine. In: European Neuropsychopharmacology, Bd. 26, Nr. 9: S. 1507-1515

Johnson, Emma C.; Bjelland, Douglas W.; Howrigan, Daniel P.; Abdellaoui, Abdel; Breen, Gerome; Borglum, Anders; Cichon, Sven; Degenhardt, Franziska; Forstner, Andreas J.; Frank, Josef; Genovese, Giulio; Heilmann-Heimbach, Stefanie; Herms, Stefan; Hoffman, Per; Maier, Wolfgang; Mattheisen, Manuel; Morris, Derek; Mowry, Bryan; Müller-Mhysok, Betram; Neale, Benjamin; Nenadic, Igor; Nöthen, Markus M.; O'Dushlaine, Colm; Rietschel, Marcella; Ruderfer, Douglas M.; Rujescu, Dan; Schulze, Thomas G.; Simonson, Matthew A.; Stahl, Eli; Strohmaier, Jana; Witt, Stephanie H.; Sullivan, Patrick F. und Keller, Matthew C. (2016): No Reliable Association between Runs of Homozygosity and Schizophrenia in a Well-Powered Replication Study.
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Kirsten, Holger; Scholz, Markus; Kovacs, Peter; Grallert, Harald; Peters, Annette; Strauch, Konstantin; Frank, Josef; Rietschel, Marcella; Nöthen, Markus M.; Witt, Heiko und Rosendahl, Jonas (2016): Genetic variants of lipase activity in chronic pancreatitis. In: Gut, Bd. 65, Nr. 1: S. 184-185 [PDF, 308kB]

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Li, Ming; Huang, Liang; Grigoroiu-Serbanescu, Maria; Bergen, Sarah E.; Landén, Mikael; Hultman, Christina M.; Forstner, Andreas J.; Strohmaier, Jana; Hecker, Julian; Schulze, Thomas G.; Müller-Myhsok, Bertram; Reif, Andreas; Mitchell, Philip B.; Martin, Nicholas G.; Cichon, Sven; Nöthen, Markus M.; Alkelai, Anna; Lerer, Bernard; Jamain, Stéphane; Leboyer, Marion; Bellivier, Frank; Etain, Bruno; Kahn, Jean-Pierre; Henry, Chantal und Rietschel, Marcella (2016): Convergent Lines of Evidence Support LRP8 as a Susceptibility Gene for Psychosis. In: Molecular Neurobiology, Bd. 53, Nr. 10: S. 6608-6619

Heilbronner, Urs; Gade, Katrin; Herms, Stefan; Strohmaier, Jana; Lang, Maren; Nöthen, Markus M.; Rietschel, Marcella; Schulze, Thomas G. und Degenhardt, Franziska (2016): Effect of copy number variant burden on Global Assessment of Functioning in schizophrenia. In: Psychiatric Genetics, Bd. 26, Nr. 4: S. 184-185

Degenhardt, Franziska; Heinemann, Barbara; Strohmaier, Jana; Pfohl, Marvin A.; Giegling, Ina; Hofmann, Andrea; Ludwig, Kerstin U.; Witt, Stephanie H.; Ludwig, Michael; Forstner, Andreas J.; Albus, Margot; Schwab, Sibylle G.; Borrmann-Hassenbach, Margitta; Lennertz, Leonard; Wagner, Michael; Hoffmann, Per; Rujescu, Dan; Maier, Wolfgang; Cichon, Sven; Rietschel, Marcella und Nöthen, Markus M. (2016): Identification of rare variants in KCTD13 at the schizophrenia risk locus 16p11.2. In: Psychiatric Genetics, Bd. 26, Nr. 6: S. 293-296

Hou, Liping; Bergen, Sarah E.; Akula, Nirmala; Song, Jie; Hultman, Christina M.; Landén, Mikael; Adli, Mazda; Alda, Martin; Ardau, Raffaella; Arias, Bárbara; Aubry, Jean-Michel; Backlund, Lena; Badner, Judith A.; Barrett, Thomas B.; Bauer, Michael; Baune, Bernhard T.; Bellivier, Frank; Benabarre, Antonio; Bengesser, Susanne; Berrettini, Wade H.; Bhattacharjee, Abesh Kumar; Biernacka, Joanna M.; Birner, Armin; Bloss, Cinnamon S.; Brichant-Petitjean, Clara; Bui, Elise T.; Byerley, William; Cervantes, Pablo; Chillotti, Caterina; Cichon, Sven; Colom, Francesc; Coryell, William; Craig, David W.; Cruceanu, Cristiana; Czerski, Piotr M.; Davis, Tony; Dayer, Alexandre; Degenhardt, Franziska; Del Zompo, Maria; DePaulo, J. Raymond; Edenberg, Howard J.; Étain, Bruno; Falkai, Peter ORCID logoORCID: https://orcid.org/0000-0003-2873-8667; Foroud, Tatiana; Forstner, Andreas J.; Frisen, Louise; Frye, Mark A.; Fullerton, Janice M.; Gard, Sébastien; Garnham, Julie S.; Gershon, Elliot S.; Goes, Fernando S.; Greenwood, Tiffany A.; Grigoroiu-Serbanescu, Maria; Hauser, Joanna; Heilbronner, Urs; Heilmann-Heimbach, Stefanie; Herms, Stefan; Hipolito, Maria; Hitturlingappa, Shashi; Hoffmann, Per; Hofmann, Andrea; Jamain, Stephane; Jiménez, Esther; Kahn, Jean-Pierre; Kassem, Layla; Kelsoe, John R.; Kittel-Schneider, Sarah; Kliwicki, Sebastian; Koller, Daniel L.; König, Barbara; Lackner, Nina; Laje, Gonzalo; Lang, Maren; Lavebratt, Catharina; Lawson, William B.; Leboyer, Marion; Leckband, Susan G.; Liu, Chunyu; Maaser, Anna; Mahon, Pamela B.; Maier, Wolfgang; Maj, Mario; Manchia, Mirko; Martinsson, Lina; McCarthy, Michael J.; McElroy, Susan L.; McInnis, Melvin G.; McKinney, Rebecca; Mitchell, Philip B.; Mitjans, Marina; Mondimore, Francis M.; Monteleone, Palmiero; Mühleisen, Thomas W.; Nievergelt, Caroline M.; Nöthen, Markus M.; Novak, Tomas; Nurnberger, John I.; Nwulia, Evaristus A.; Ösby, Urban; Pfennig, Andrea; Potash, James B.; Propping, Peter; Reif, Andreas; Reininghaus, Eva; Rice, John; Rietschel, Marcella; Rouleau, Guy A.; Rybakowski, Janusz K.; Schalling, Martin; Scheftner, William A.; Schofield, Peter R.; Schork, Nicholas J.; Schulze, Thomas G.; Schumacher, Johannes; Schweizer, Barbara W.; Severino, Giovanni; Shekhtman, Tatyana; Shilling, Paul D.; Simhandl, Christian; Slaney, Claire M.; Smith, Erin N.; Squassina, Alessio; Stamm, Thomas; Stopkova, Pavla; Streit, Fabian; Strohmaier, Jana; Szelinger, Szabolcs; Tighe, Sarah K.; Tortorella, Alfonso; Turecki, Gustavo; Vieta, Eduard; Volkert, Julia; Witt, Stephanie H.; Wright, Adam; Zandi, Peter P.; Zhang, Peng; Zollner, Sebastian und McMahon, Francis J. (2016): Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder. In: Human Molecular Genetics, Bd. 25, Nr. 15: S. 3383-3394

Li, Ming; Luo, Xiong-jian; Landén, Mikael; Bergen, Sarah E.; Hultman, Christina M.; Li, Xiao; Zhang, Wen; Yao, Yong-Gang; Zhang, Chen; Liu, Jiewei; Mattheisen, Manuel; Cichon, Sven; Mühleisen, Thomas W.; Degenhardt, Franziska A.; Nöthen, Markus M.; Schulze, Thomas G.; Grigoroiu-Serbanescu, Maria; Li, Hao; Fuller, Chris K.; Chen, Chunhui; Dong, Qi; Chen, Chuansheng; Jamain, Stéphane; Leboyer, Marion; Bellivier, Frank; Etain, Bruno; Kahn, Jean-Pierre; Henry, Chantal; Preisig, Martin; Kutalik, Zoltán; Castelao, Enrique; Wright, Adam; Mitchell, Philip B.; Fullerton, Janice M.; Schofield, Peter R.; Montgomery, Grant W.; Medland, Sarah E.; Gordon, Scott D.; Martin, Nicholas G.; Rietschel, Marcella; Liu, Chunyu; Kleinman, Joel E.; Hyde, Thomas M.; Weinberger, Daniel R. und Su, Bing (2016): Impact of a cis-associated gene expression SNP on chromosome 20q11.22 on bipolar disorder susceptibility, hippocampal structure and cognitive performance. In: British Journal of Psychiatry, Bd. 208, Nr. 2: S. 128-137

Li, Jin; Jørgensen, Silje F.; Maggadottir, S. Melkorka; Bakay, Marina; Warnatz, Klaus; Glessner, Joseph; Pandey, Rahul; Salzer, Ulrich; Schmidt, Reinhold E.; Perez, Elena; Resnick, Elena; Goldacker, Sigune; Buchta, Mary; Witte, Torsten; Padyukov, Leonid; Videm, Vibeke; Folseraas, Trine; Atschekzei, Faranaz; Elder, James T.; Nair, Rajan P.; Winkelmann, Juliane; Gieger, Christian; Nöthen, Markus M.; Büning, Carsten; Brand, Stephan; Sullivan, Kathleen E.; Orange, Jordan S.; Fevang, Børre; Schreiber, Stefan; Lieb, Wolfgang; Aukrust, Pål; Chapel, Helen; Cunningham-Rundles, Charlotte; Franke, Andre; Karlsen, Tom H.; Grimbacher, Bodo; Hakonarson, Hakon; Hammarström, Lennart und Ellinghaus, Eva (2015): Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells. In: Nature Communications, Bd. 6, 6804 [PDF, 807kB]

Juraeva, Dilafruz; Haenisch, Britta; Zapatka, Marc; Frank, Josef; Witt, Stephanie H.; Muehleisen, ThomasW.; Treutlein, Jens; Strohmaier, Jana; Meier, Sandra; Degenhardt, Franziska; Giegling, Ina; Ripke, Stephan; Leber, Markus; Lange, Christoph; Schulze, ThomasG.; Mössner, Rainald; Nenadic, Igor; Sauer, Heinrich; Rujescu, Dan; Maier, Wolfgang; Borglum, Anders; Ophoff, Roel; Cichon, Sven; Nöthen, Markus M.; Rietschel, Marcella; Mattheisen, Manuel und Brors, Benedikt (2014): Integrated Pathway-Based Approach Identifies Association between Genomic Regions at CTCF and CACNB2 and Schizophrenia.
In: PLOS Genetics 10(6), e1004345 [PDF, 2MB]

Escott-Price, Valentina; Bellenguez, Céline; Wang, Li-San; Choi, Seung-Hoan; Harold, Denise; Jones, Lesley; Holmans, Peter; Gerrish, Amy; Vedernikov, Alexey; Richards, Alexander; DeStefano, Anita L.; Lambert, Jean-Charles; Ibrahim-Verbaas, Carla A.; Naj, Adam C.; Sims, Rebecca; Jun, Gyungah; Bis, Joshua C.; Beecham, Gary W.; Grenier-Boley, Benjamin; Russo, Giancarlo; Thornton-Wells, Tricia A.; Denning, Nicola; Smith, Albert V.; Chouraki, Vincent; Thomas, Charlene; Ikram, M. Arfan; Zelenika, Diana; Vardarajan, Badri N.; Kamatani, Yoichiro; Lin, Chiao-Feng; Schmidt, Helena; Kunkle, Brian; Dunstan, Melanie L.; Vronskaya, Maria; Johnson, Andrew D.; Ruiz, Agustin; Bihoreau, Marie-Thérèse; Reitz, Christiane; Pasquier, Florence; Hollingworth, Paul; Hanon, Olivier; Fitzpatrick, Annette L.; Buxbaum, Joseph D.; Campion, Dominique; Crane, Paul K.; Baldwin, Clinton; Becker, Tim; Gudnason, Vilmundur; Cruchaga, Carlos; Craig, David; Amin, Najaf; Berr, Claudine; Lopez, Oscar L.; De Jager, Philip L.; Deramecourt, Vincent; Johnston, Janet A.; Evans, Denis; Lovestone, Simon; Letenneur, Luc; Hernandez, Isabel; Rubinsztein, David C.; Eiriksdottir, Gudny; Sleegers, Kristel; Goate, Alison M.; Fievet, Nathalie; Huentelman, Matthew J.; Gill, Michael; Brown, Kristelle; Kamboh, M. Ilyas; Keller, Lina; Barberger-Gateau, Pascale; McGuinness, Bernadette; Larson, Eric B.; Myers, Amanda J.; Dufouil, Carole; Todd, Stephen; Wallon, David; Love, Seth; Rogaeva, Ekaterina; Gallacher, John; St George-Hyslop, Peter; Clarimon, Jordi; Lleo, Alberto; Bayer, Anthony; Tsuang, Debby W.; Yu, Lei; Tsolaki, Magda; Bossu, Paola; Spalletta, Gianfranco; Proitsi, Petra; Collinge, John; Sorbi, Sandro; Garcia, Florentino Sanchez; Fox, Nick C.; Hardy, John; Deniz Naranjo, Maria Candida; Bosco, Paolo; Clarke, Robert; Brayne, Carol; Galimberti, Daniela; Scarpini, Elio; Bonuccelli, Ubaldo; Mancuso, Michelangelo; Siciliano, Gabriele; Moebus, Susanne; Mecocci, Patrizia; Del Zompo, Maria; Maier, Wolfgang; Hampel, Harald; Pilotto, Alberto; Frank-Garcia, Ana; Panza, Francesco; Solfrizzi, Vincenzo; Caffarra, Paolo; Nacmias, Benedetta; Perry, William; Mayhaus, Manuel; Lannfelt, Lars; Hakonarson, Hakon; Pichler, Sabrina; Carrasquillo, Minerva M.; Ingelsson, Martin; Beekly, Duane; Alvarez, Victoria; Zou, Fanggeng; Valladares, Otto; Younkin, Steven G.; Coto, Eliecer; Hamilton-Nelson, Kara L.; Gu, Wei; Razquin, Cristina; Pastor, Pau; Mateo, Ignacio; Owen, Michael J.; Faber, Kelley M.; Jonsson, Palmi V.; Combarros, Onofre; O'Donovan, Michael C.; Cantwell, Laura B.; Soininen, Hilkka; Blacker, Deborah; Mead, Simon; Mosley, Thomas H.; Bennett, David A.; Harris, Tamara B.; Fratiglioni, Laura; Holmes, Clive; de Bruijn, Renee F. A. G.; Passmore, Peter; Montine, Thomas J.; Bettens, Karolien; Rotter, Jerome I.; Brice, Alexis; Morgan, Kevin; Foroud, Tatiana M.; Kukull, Walter A.; Hannequin, Didier; Powell, John F.; Nalls, Michael A.; Ritchie, Karen; Lunetta, Kathryn L.; Kauwe, John S. K.; Boerwinkle, Eric; Riemenschneider, Matthias; Boada, Merce; Hiltunen, Mikko; Martin, Eden R.; Schmidt, Reinhold; Rujescu, Dan; Dartigues, Jean-Francois; Mayeux, Richard; Tzourio, Christophe; Hofman, Albert; Nöthen, Markus M.; Graff, Caroline; Psaty, Bruce M.; Haines, Jonathan L.; Lathrop, Mark; Pericak-Vance, Margaret A.; Launer, Lenore J.; Broeckhoven, Christine Van; Farrer, Lindsay A.; Duijn, Cornelia M. van; Ramirez, Alfredo; Seshadri, Sudha; Schellenberg, Gerard D.; Amouyel, Philippe und Williams, Julie (2014): Gene-Wide Analysis Detects Two New Susceptibility Genes for Alzheimer's Disease.
In: PLOS ONE 9(6), e94661 [PDF, 1MB]

Karagiannidis, Iordanis; Dehning, Sandra; Sandor, Paul; Tarnok, Zsanett; Rizzo, Renata; Wolanczyk, Tomasz; Madruga-Garrido, Marcos; Hebebrand, Johannes; Nöthen, Markus M.; Lehmkuhl, Gerd; Farkas, Luca; Nagy, Peter; Szymanska, Urszula; Anastasiou, Zachos; Stathias, Vasileios; Androutsos, Christos; Tsironi, Vaia; Koumoula, Anastasia; Barta, Csaba; Zill, Peter; Mir, Pablo; Müller, Norbert; Barr, Cathy und Paschou, Peristera (November 2013): Support of the histaminergic hypothesis in Tourette Syndrome: association of the histamine decarboxylase gene in a large sample of families. In: Journal of Medical Genetics, Bd. 50, Nr. 11: S. 760-764 [PDF, 368kB]

Jones, Lesley; Holmans, Peter A.; Hamshere, Marian L.; Harold, Denise; Moskvina, Valentina; Ivanov, Dobril; Pocklington, Andrew; Abraham, Richard; Hollingworth, Paul; Sims, Rebecca; Gerrish, Amy; Pahwa, Jaspreet Singh; Jones, Nicola; Stretton, Alexandra; Morgan, Angharad R.; Lovestone, Simon; Powell, John; Proitsi, Petroula; Lupton, Michelle K.; Brayne, Carol; Rubinsztein, David C.; Gill, Michael; Lawlor, Brian; Lynch, Aoibhinn; Morgan, Kevin; Brown, Kristelle S.; Passmore, Peter A.; Craig, David; McGuinness, Bernadette; Todd, Stephen; Holmes, Clive; Mann, David; Smith, A. David; Love, Seth; Kehoe, Patrick G.; Mead, Simon; Fox, Nick; Rossor, Martin; Collinge, John; Maier, Wolfgang; Jessen, Frank; Schürmann, Britta; Heun, Reinhard; Kölsch, Heike; van den Bussche, Hendrik; Heuser, Isabella; Peters, Oliver; Kornhuber, Johannes; Wiltfang, Jens; Dichgans, Martin; Frölich, Lutz; Hampel, Harald; Hüll, Michael; Rujescu, Dan; Goate, Alison M.; Kauwe, John S. K.; Cruchaga, Carlos; Nowotny, Petra; Morris, John C.; Mayo, Kevin; Livingston, Gill; Bass, Nicholas J.; Gurling, Hugh; McQuillin, Andrew; Gwilliam, Rhian; Deloukas, Panos; Al-Chalabi, Ammar; Shaw, Christopher E; Singleton, Andrew B; Guerreiro, Rita; Mühleisen, Thomas W.; Nöthen, Markus M.; Moebus, Susanne; Jöckel, Karl-Heinz; Klopp, Norman; Wichmann, Heinz-Erich; Rüther, Eckhard; Carrasquillo, Minerva M.; Pankratz, V. Shane; Younkin, Steven G.; Hardy, John; O'Donovan, Michael C.; Owen, Michael J. und Williams, Julie (2010): Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease.
In: PLOS ONE 5(11), e13950 [PDF, 151kB]

Schumacher, Johannes; Hoffmann, Per; Schmäl, Christine; Schulte-Körne, Gerd und Nöthen, Markus M. (2007): Genetics of dyslexia: the evolving landscape. In: Journal of Medical Genetics, Bd. 44: S. 289-297 [PDF, 192kB]

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