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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext

Defective glycosylation of coagulation factor XII underlies hereditary angioedema type III von Björkqvist, Jenny, de Maat, Steven, Lewandrowski, Urs, Di Gennaro, Antonio, Oschatz, Chris, Schönig, Kai, Nöthen, Markus M, Drouet, Christian, Braley, Hal, Nolte, Marc W, Sickmann, Albert, Panousis, Con, Maas, Coen, Renné, Thomas

Volltext

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

Volltext

Molecular monitoring of short- and long-term transcriptional effects of hair growth stimulating agents von Henne, Sabrina K, Hochfeld, Lara M, Bartmann, Werner, Welss, Thomas, Nöthen, Markus M, Heilmann-Heimbach, Stefanie

Volltext

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

Volltext

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

Volltext

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, Nöthen, Markus M, Heilmann-Heimbach, Stefanie

Volltext

Socioeconomic position interacts with the genetic effect of a CRP gene common variant to influence C-reactive protein values von Cheaib, Miriam, Hornung, Nicola, Dragano, Nico, Frank, Mirjam, Hoffmann, Per, Nöthen, Markus M., Erbel, Raimund, Stang, Andreas, Schmidt, Börge

Volltext

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

Volltext

Dihydropyrimidine Dehydrogenase Testing prior to Treatment with 5-Fluorouracil, Capecitabine, and Tegafur: A Consensus Paper von Wörmann, Bernhard, Bokemeyer, Carsten, Burmeister, Thomas, Köhne, Claus-Henning, Schwab, Matthias, Arnold, Dirk, Blohmer, Jens-Uwe, Borner, Markus, Brucker, Sara, Cascorbi, Ingolf, Decker, Thomas, de Wit, Maike, Dietz, Andreas, Einsele, Hermann, Eisterer, Wolfgang, Folprecht, Gunnar, Hilbe, Wolfgang, Hoffmann, Jürgen, Knauf, Wolfgang, Kunzmann, Volker, Largiadèr, Carlo R., Lorenzen, Sylvie, Lüftner, Diana, Moehler, Markus, Nöthen, Markus M., Pox, Christian, Reinacher-Schick, Anke, Scharl, Anton, Schlegelberger, Brigitte, Seufferlein, Thomas, Sinn, Marianne, Stroth, Matthias, Tamm, Ingo, Trümper, Lorenz, Wilhelm, Martin, Wöll, Ewald, Hofheinz, Ralf-Dieter

Volltext

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

Volltext

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

Volltext

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

Volltext

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

Volltext