A genome-wide association study implicates diacylglycerol kinase eta (DGKH) and several other genes in the etiology of bipolar disorder von Baum, A E, Akula, N, Cabanero, M, Cardona, I, Corona, W, Klemens, B, Schulze, T G, Cichon, S, Rietschel, M, Nöthen, M M, Georgi, A, Schumacher, J, Schwarz, M, Abou Jamra, R, Höfels, S, Propping, P, Satagopan, J, Detera-Wadleigh, S D, Hardy, J, McMahon, F J

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Infection fatality rate of SARS-CoV2 in a super-spreading event in Germany von Streeck, Hendrik, Schulte, Bianca, Kümmerer, Beate M., Richter, Enrico, Höller, Tobias, Fuhrmann, Christine, Bartok, Eva, Dolscheid-Pommerich, Ramona, Berger, Moritz, Wessendorf, Lukas, Eschbach-Bludau, Monika, Kellings, Angelika, Schwaiger, Astrid, Coenen, Martin, Hoffmann, Per, Stoffel-Wagner, Birgit, Nöthen, Markus M., Eis-Hübinger, Anna M., Exner, Martin, Schmithausen, Ricarda Maria, Schmid, Matthias, Hartmann, Gunther

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Genetic polymorphisms affecting telomere length and their association with cardiovascular disease in the Heinz-Nixdorf-Recall study von Tannemann, Nico, Erbel, Raimund, Nöthen, Markus M, Jöckel, Karl-Heinz, Pechlivanis, Sonali

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Two variants in Ankyrin 3 (ANK3) are independent genetic risk factors for bipolar disorder von Schulze, T G, Detera-Wadleigh, S D, Akula, N, Gupta, A, Kassem, L, Steele, J, Pearl, J, Strohmaier, J, Breuer, R, Schwarz, M, Propping, P, Nöthen, M M, Cichon, S, Schumacher, J, Rietschel, M, McMahon, F J

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Adaptor Protein Complex 4 Deficiency Causes Severe Autosomal-Recessive Intellectual Disability, Progressive Spastic Paraplegia, Shy Character, and Short Stature von JAMRA, Rami Abou, PHILIPPE, Orianne, MUNNICH, Arnold, STROM, Tim M, REIS, Andre, COLLEAUX, Laurence, RAAS-ROTHSCHILD, Annick, ECK, Sebastian H, GRAF, Elisabeth, BUCHERT, Rebecca, BORCK, Guntram, EKICI, Arif, BROCKSCHMIDT, Felix F, NÖTHEN, Markus M

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Exome Sequencing Identifies Biallelic MSH3 Germline Mutations as a Recessive Subtype of Colorectal Adenomatous Polyposis von Adam, Ronja, Spier, Isabel, Zhao, Bixiao, Kloth, Michael, Marquez, Jonathan, Hinrichsen, Inga, Kirfel, Jutta, Tafazzoli, Aylar, Horpaopan, Sukanya, Uhlhaas, Siegfried, Stienen, Dietlinde, Friedrichs, Nicolaus, Altmüller, Janine, Laner, Andreas, Holzapfel, Stefanie, Peters, Sophia, Kayser, Katrin, Thiele, Holger, Holinski-Feder, Elke, Marra, Giancarlo, Kristiansen, Glen, Nöthen, Markus M., Büttner, Reinhard, Möslein, Gabriela, Betz, Regina C., Brieger, Angela, Lifton, Richard P., Aretz, Stefan

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Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients von Frank, J, Lang, M, Witt, S H, Strohmaier, J, Rujescu, D, Cichon, S, Degenhardt, F, Nöthen, M M, Collier, D A, Ripke, S, Naber, D, Rietschel, M

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Breakthroughs in the genetics of orofacial clefting von Mangold, Elisabeth, Ludwig, Kerstin U, Nöthen, Markus M

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Genetic regulatory effects modified by immune activation contribute to autoimmune disease associations von Kim-Hellmuth, Sarah, Bechheim, Matthias, Pütz, Benno, Mohammadi, Pejman, Nédélec, Yohann, Giangreco, Nicholas, Becker, Jessica, Kaiser, Vera, Fricker, Nadine, Beier, Esther, Boor, Peter, Castel, Stephane E., Nöthen, Markus M., Barreiro, Luis B., Pickrell, Joseph K., Müller-Myhsok, Bertram, Lappalainen, Tuuli, Schumacher, Johannes, Hornung, Veit

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Familial occurrence of systemic mast cell activation disease von Molderings, Gerhard J, Haenisch, Britta, Bogdanow, Manuela, Fimmers, Rolf, Nöthen, Markus M

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Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness von Hochfeld, Lara M., Bertolini, Marta, Broadley, David, Botchkareva, Natalia V., Betz, Regina C., Schoch, Susanne, Nothen, Markus M., Heilmann-Heimbach, Stefanie

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A genome-wide association study confirms PNPLA3 and identifies TM6SF2 and MBOAT7 as risk loci for alcohol-related cirrhosis von Buch, Stephan, Stickel, Felix, Trépo, Eric, Way, Michael, Herrmann, Alexander, Nischalke, Hans Dieter, Brosch, Mario, Rosendahl, Jonas, Berg, Thomas, Ridinger, Monika, Rietschel, Marcella, McQuillin, Andrew, Frank, Josef, Kiefer, Falk, Schreiber, Stefan, Lieb, Wolfgang, Soyka, Michael, Semmo, Nasser, Aigner, Elmar, Datz, Christian, Schmelz, Renate, Brückner, Stefan, Zeissig, Sebastian, Stephan, Anna-Magdalena, Wodarz, Norbert, Devière, Jacques, Clumeck, Nicolas, Sarrazin, Christoph, Lammert, Frank, Gustot, Thierry, Deltenre, Pierre, Völzke, Henry, Lerch, Markus M, Mayerle, Julia, Eyer, Florian, Schafmayer, Clemens, Cichon, Sven, Nöthen, Markus M, Nothnagel, Michael, Ellinghaus, David, Huse, Klaus, Franke, Andre, Zopf, Steffen, Hellerbrand, Claus, Moreno, Christophe, Franchimont, Denis, Morgan, Marsha Y, Hampe, Jochen

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High Frequencies of De Novo CNVs in Bipolar Disorder and Schizophrenia von Malhotra, Dheeraj, McCarthy, Shane, Michaelson, Jacob J., Vacic, Vladimir, Burdick, Katherine E., Yoon, Seungtai, Cichon, Sven, Corvin, Aiden, Gary, Sydney, Gershon, Elliot S., Gill, Michael, Karayiorgou, Maria, Kelsoe, John R., Krastoshevsky, Olga, Krause, Verena, Leibenluft, Ellen, Levy, Deborah L., Makarov, Vladimir, Bhandari, Abhishek, Malhotra, Anil K., McMahon, Francis J., Nöthen, Markus M., Potash, James B., Rietschel, Marcella, Schulze, Thomas G., Sebat, Jonathan

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Direct Conversion of Fibroblasts into Stably Expandable Neural Stem Cells von Thier, Marc, Wörsdörfer, Philipp, Lakes, Yenal B., Gorris, Raphaela, Herms, Stefan, Opitz, Thoralf, Seiferling, Dominic, Quandel, Tamara, Hoffmann, Per, Nöthen, Markus M., Brüstle, Oliver, Edenhofer, Frank

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Imputation of orofacial clefting data identifies novel risk loci and sheds light on the genetic background of cleft lip ± cleft palate and cleft palate only von Ludwig, Kerstin U, Böhmer, Anne C, Bowes, John, Nikolic, Miloš, Ishorst, Nina, Wyatt, Niki, Hammond, Nigel L, Gölz, Lina, Thieme, Frederic, Barth, Sandra, Schuenke, Hannah, Klamt, Johanna, Spielmann, Malte, Aldhorae, Khalid, Rojas-Martinez, Augusto, Nöthen, Markus M, Rada-Iglesias, Alvaro, Dixon, Michael J, Knapp, Michael, Mangold, Elisabeth

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Hypomorphic Mutations in PGAP2, Encoding a GPI-Anchor-Remodeling Protein, Cause Autosomal-Recessive Intellectual Disability von Hansen, Lars, Tawamie, Hasan, Murakami, Yoshiko, Mang, Yuan, ur Rehman, Shoaib, Buchert, Rebecca, Schaffer, Stefanie, Muhammad, Safia, Bak, Mads, Nöthen, Markus M., Bennett, Eric P., Maeda, Yusuke, Aigner, Michael, Reis, André, Kinoshita, Taroh, Tommerup, Niels, Baig, Shahid Mahmood, Abou Jamra, Rami

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G protein-coupled receptor P2Y5 and its ligand LPA are involved in maintenance of human hair growth von Pasternack, Sandra M, Molderings, Gerhard J, Voss, Katrin, Betz, Regina C, Nöthen, Markus M, Aboud, Khalid Al, Lee, Young-Ae, Hillmer, Axel M, Ramirez, Alfredo, Rüschendorf, Franz, Nürnberg, Peter, Franz, Thomas, von Kügelgen, Ivar

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Common variants on 8p12 and 1q24.2 confer risk of schizophrenia von Shi, Yongyong, Li, Zhiqiang, Xu, Qi, Wang, Ti, Li, Tao, Shen, Jiawei, Zhang, Fengyu, Chen, Jianhua, Zhou, Guoquan, Ji, Weidong, Li, Baojie, Xu, Yifeng, Liu, Dengtang, Wang, Peng, Yang, Ping, Liu, Benxiu, Sun, Wensheng, Wan, Chunling, Qin, Shengying, He, Guang, Steinberg, Stacy, Cichon, Sven, Werge, Thomas, Sigurdsson, Engilbert, Tosato, Sarah, Palotie, Aarno, Nöthen, Markus M, Rietschel, Marcella, Ophoff, Roel A, Collier, David A, Rujescu, Dan, Clair, David St, Stefansson, Hreinn, Stefansson, Kari, Ji, Jue, Wang, Qingzhong, Li, Wenjin, Zheng, Linqing, Zhang, Hairong, Feng, Guoyin, He, Lin

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genome-wide association study of alcohol dependence von Bierut, Laura J, Agrawal, Arpana, Bucholz, Kathleen K, Doheny, Kimberly F, Laurie, Cathy, Pugh, Elizabeth, Fisher, Sherri, Fox, Louis, Howells, William, Bertelsen, Sarah, Hinrichs, Anthony L, Almasy, Laura, Breslau, Naomi, Culverhouse, Robert C, Dick, Danielle M, Edenberg, Howard J, Foroud, Tatiana, Grucza, Richard A, Hatsukami, Dorothy, Hesselbrock, Victor, Johnson, Eric O, Kramer, John, Krueger, Robert F, Kuperman, Samuel, Lynskey, Michael, Mann, Karl, Neuman, Rosalind J, Nöthen, Markus M, Nurnberger, John I. Jr, Porjesz, Bernice, Ridinger, Monika, Saccone, Nancy L, Saccone, Scott F, Schuckit, Marc A, Tischfield, Jay A, Wang, Jen C, Rietschel, Marcella, Goate, Alison M, Rice, John P

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Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder von Jarick, I, Volckmar, A-L, Pütter, C, Pechlivanis, S, Nguyen, T T, Dauvermann, M R, Beck, S, Albayrak, Ö, Scherag, S, Gilsbach, S, Cichon, S, Hoffmann, P, Degenhardt, F, Nöthen, M M, Schreiber, S, Wichmann, H-E, Jöckel, K-H, Heinrich, J, Tiesler, C M T, Faraone, S V, Walitza, S, Sinzig, J, Freitag, C, Meyer, J, Herpertz-Dahlmann, B, Lehmkuhl, G, Renner, T J, Warnke, A, Romanos, M, Lesch, K-P, Reif, A, Schimmelmann, B G, Hebebrand, J, Scherag, A, Hinney, A

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