A genome-wide association study identifies five loci influencing facial morphology in Europeans von Liu, Fan, van der Lijn, Fedde, Schurmann, Claudia, Zhu, Gu, Chakravarty, M Mallar, Hysi, Pirro G, Wollstein, Andreas, Lao, Oscar, de Bruijne, Marleen, Ikram, M Arfan, van der Lugt, Aad, Rivadeneira, Fernando, Uitterlinden, André G, Hofman, Albert, Niessen, Wiro J, Homuth, Georg, de Zubicaray, Greig, McMahon, Katie L, Thompson, Paul M, Daboul, Amro, Puls, Ralf, Hegenscheid, Katrin, Bevan, Liisa, Pausova, Zdenka, Medland, Sarah E, Montgomery, Grant W, Wright, Margaret J, Wicking, Carol, Boehringer, Stefan, Spector, Timothy D, Paus, Tomáš, Martin, Nicholas G, Biffar, Reiner, Kayser, Manfred

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Mendelian randomization indicates causal effects of estradiol levels on kidney function in males von Nasr, M Kamal, Schurmann, Claudia, Böttinger, Erwin P, Teumer, Alexander

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Apolipoprotein L1 Variants and Blood Pressure Traits in African Americans von Nadkarni, Girish N., MD, MPH, CPH, Galarneau, Geneviève, PhD, Ellis, Stephen B., MS, Nadukuru, Rajiv, MS, Zhang, Jinglan, PhD, Scott, Stuart A., PhD, Schurmann, Claudia, PhD, Li, Rongling, MD, PhD, MPH, Rasmussen-Torvik, Laura J., PhD, Kho, Abel N., MD, Hayes, M. Geoffrey, PhD, Pacheco, Jennifer A., MS, Manolio, Teri A., MD, PhD, Chisholm, Rex L., PhD, Roden, Dan M., MD, Denny, Joshua C., MD, MS, Kenny, Eimear E., PhD, Bottinger, Erwin P., MD

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Implementation and evaluation of personal genetic testing as part of genomics analysis courses in German universities von Slosarek, Tamara, Ibing, Susanne, Schormair, Barbara, Heyne, Henrike O, Böttinger, Erwin P, Andlauer, Till F M, Schurmann, Claudia

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Genetic identification of a common collagen disease in puerto ricans via identity-by-descent mapping in a health system von Belbin, Gillian Morven, Odgis, Jacqueline, Sorokin, Elena P, Yee, Muh-Ching, Kohli, Sumita, Glicksberg, Benjamin S, Gignoux, Christopher R, Wojcik, Genevieve L, Van Vleck, Tielman, Jeff, Janina M, Linderman, Michael, Schurmann, Claudia, Ruderfer, Douglas, Cai, Xiaoqiang, Merkelson, Amanda, Justice, Anne E, Young, Kristin L, Graff, Misa, North, Kari E, Peters, Ulrike, James, Regina, Hindorff, Lucia, Kornreich, Ruth, Edelmann, Lisa, Gottesman, Omri, Stahl, Eli Ea, Cho, Judy H, Loos, Ruth Jf, Bottinger, Erwin P, Nadkarni, Girish N, Abul-Husn, Noura S, Kenny, Eimear E

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Analyzing illumina gene expression microarray data from different tissues: methodological aspects of data analysis in the metaxpress consortium von Schurmann, Claudia, Heim, Katharina, Schillert, Arne, Blankenberg, Stefan, Carstensen, Maren, Dörr, Marcus, Endlich, Karlhans, Felix, Stephan B, Gieger, Christian, Grallert, Harald, Herder, Christian, Hoffmann, Wolfgang, Homuth, Georg, Illig, Thomas, Kruppa, Jochen, Meitinger, Thomas, Müller, Christian, Nauck, Matthias, Peters, Annette, Rettig, Rainer, Roden, Michael, Strauch, Konstantin, Völker, Uwe, Völzke, Henry, Wahl, Simone, Wallaschofski, Henri, Wild, Philipp S, Zeller, Tanja, Teumer, Alexander, Prokisch, Holger, Ziegler, Andreas

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Impact of common regulatory single-nucleotide variants on gene expression profiles in whole blood von Mehta, Divya, Heim, Katharina, Herder, Christian, Carstensen, Maren, Eckstein, Gertrud, Schurmann, Claudia, Homuth, Georg, Nauck, Matthias, Völker, Uwe, Roden, Michael, Illig, Thomas, Gieger, Christian, Meitinger, Thomas, Prokisch, Holger

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A functional brain-derived neurotrophic factor ( BDNF ) gene variant increases the risk of moderate-to-severe allergic rhinitis von Jin, Peng, BM, MSc, Andiappan, Anand Kumar, PhD, Quek, Jia Min, BSc, Lee, Bernett, PhD, Au, Bijin, BSc, Sio, Yang Yie, BSc, Irwanto, Astrid, PhD, Schurmann, Claudia, PhD, Grabe, Hans Jörgen, MD, Suri, Bani Kaur, PhD, Matta, Sri Anusha, BSc, Westra, Harm-Jan, PhD, Franke, Lude, PhD, Esko, Tonu, PhD, Sun, Liangdan, PhD, Zhang, Xuejun, PhD, Liu, Hong, PhD, Zhang, Furen, PhD, Larbi, Anis, PhD, Xu, Xin, MD, PhD, Poidinger, Michael, PhD, Liu, Jianjun, PhD, Chew, Fook Tim, PhD, Rotzschke, Olaf, PhD, Shi, Li, MD, PhD, Wang, De Yun, MD, PhD

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Mapping the genetic architecture of gene regulation in whole blood von Schramm, Katharina, Marzi, Carola, Schurmann, Claudia, Carstensen, Maren, Reinmaa, Eva, Biffar, Reiner, Eckstein, Gertrud, Gieger, Christian, Grabe, Hans-Jörgen, Homuth, Georg, Kastenmüller, Gabriele, Mägi, Reedik, Metspalu, Andres, Mihailov, Evelin, Peters, Annette, Petersmann, Astrid, Roden, Michael, Strauch, Konstantin, Suhre, Karsten, Teumer, Alexander, Völker, Uwe, Völzke, Henry, Wang-Sattler, Rui, Waldenberger, Melanie, Meitinger, Thomas, Illig, Thomas, Herder, Christian, Grallert, Harald, Prokisch, Holger

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Associations between Serum Sex Hormone Concentrations and Whole Blood Gene Expression Profiles in the General Population von Haring, Robin, Schurmann, Claudia, Homuth, Georg, Steil, Leif, Völker, Uwe, Völzke, Henry, Keevil, Brian G, Nauck, Matthias, Wallaschofski, Henri

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Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity von Walters, Robin G, Coin, Lachlan J M, Ruokonen, Aimo, de Smith, Adam J, El-Sayed Moustafa, Julia S, Jacquemont, Sebastien, Elliott, Paul, Esko, Tõnu, Hartikainen, Anna-Liisa, Laitinen, Jaana, Männik, Katrin, Martinet, Danielle, Meyre, David, Nauck, Matthias, Schurmann, Claudia, Sladek, Rob, Thorleifsson, Gudmar, Thorsteinsdóttir, Unnur, Valsesia, Armand, Waeber, Gerard, Zufferey, Flore, Balkau, Beverley, Pattou, François, Metspalu, Andres, Völzke, Henry, Vollenweider, Peter, Stefansson, Kári, Järvelin, Marjo-Riitta, Beckmann, Jacques S, Froguel, Philippe, Blakemore, Alexandra I F

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transferGWAS: GWAS of images using deep transfer learning von Kirchler, Matthias, Konigorski, Stefan, Norden, Matthias, Meltendorf, Christian, Kloft, Marius, Schurmann, Claudia, Lippert, Christoph

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Blood cis-eQTL analysis fails to identify novel association signals among sub-threshold candidates from genome-wide association studies in restless legs syndrome von Schulte, Eva C, Schramm, Katharina, Schurmann, Claudia, Lichtner, Peter, Herder, Christian, Roden, Michael, Gieger, Christian, Peters, Annette, Trenkwalder, Claudia, Högl, Birgit, Frauscher, Birgit, Berger, Klaus, Fietze, Ingo, Gross, Nadine, Stiasny-Kolster, Karin, Oertel, Wolfgang, Bachmann, Cornelius G, Paulus, Walter, Zimprich, Alexander, Völzke, Henry, Schminke, Ulf, Nauck, Matthias, Illig, Thomas, Meitinger, Thomas, Müller-Myhsok, Bertram, Prokisch, Holger, Winkelmann, Juliane

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Mapping the human genetic architecture of COVID-19 von Niemi, Mari E. K., Karjalainen, Juha, Daly, Mark, Ganna, Andrea, Mehtonen, Juha, Cordioli, Mattia, Kaunisto, Mari, Pigazzini, Sara, Donner, Kati, Kivinen, Katja, Palotie, Aarno, Daly, Mark J., Liao, Rachel G., Kanai, Masahiro, Veerapen, Kumar, Minica, Camelia, Trankiem, Amy, Balaconis, Mary K., Nguyen, Huy, Solomonson, Matthew, Francioli, Laurent, Wang, Qingbo, Green, Robert C., Bryant, Sam, Finucane, Hilary, Martin, Alicia R., Zhou, Wei, Nkambule, Lindokuhle, Karczewski, Konrad J., Atkinson, Elizabeth G., Tsuo, Kristin, Baya, Nikolas, Turley, Patrick, Gupta, Rahul, Walters, Raymond K., Palmer, Duncan S., Sarma, Gopal, Cheng, Nathan, Lu, Wenhan, Churchhouse, Claire, Goldstein, Jacqueline, King, Daniel, Seed, Cotton, Neale, Benjamin M., Satterstrom, F. Kyle, Pathak, Gita A., Wendt, Frank R., Polimanti, Renato, Andrews, Shea J., Sloofman, Laura, Sealfon, Stuart C., Fernandez-Cadenas, Israel, Schulte, Eva C., Protzer, Ulrike, Striano, Pasquale, Coviello, Domenico A., Zara, Federico, Salpietro, Vincenzo, Iacomino, Michele, Scudieri, Paolo, Bocciardi, Renata, Minetti, Carlo, Vari, Maria Stella, Madia, Francesca, Marouli, Eirini, Kanoni, Stavroula, Moutsianas, Loukas, Karim, Mohd Anisul, Ghoussaini, Maya, Schwartzentruber, Jeremy, Dunham, Ian, Savage, Jeanne, Posthuma, Danielle, Tissink, Elleke, Uffelmann, Emil, Butler-Laporte, Guillaume, Richards, J. Brent, Nakanishi, Tomoko, Morrison, David R., Forgetta, Vincenzo, Ghosh, Biswarup, Laurent, Laetitia, Henry, Danielle, Abdullah, Tala, Adeleye, Olumide, Mamlouk, Noor, Kimchi, Nofar, Afrasiabi, Zaman, Rezk, Nardin, Vulesevic, Branka, Bouab, Meriem, Guzman, Charlotte, Petitjean, Louis, Tselios, Chris, Xue, Xiaoqing, Afilalo, Jonathan, Adra, Darin, Kim, Han-Na, Okada, Yukinori, Byun, Jinyoung

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Exome sequencing and characterization of 49,960 individuals in the UK Biobank von Van Hout, Cristopher V., Tachmazidou, Ioanna, Backman, Joshua D., Hoffman, Joshua D., Liu, Daren, Pandey, Ashutosh K., Gonzaga-Jauregui, Claudia, Khalid, Shareef, Ye, Bin, Banerjee, Nilanjana, Li, Alexander H., O’Dushlaine, Colm, Marcketta, Anthony, Staples, Jeffrey, Schurmann, Claudia, Hawes, Alicia, Maxwell, Evan, Barnard, Leland, Lopez, Alexander, Penn, John, Habegger, Lukas, Blumenfeld, Andrew L., Bai, Xiaodong, O’Keeffe, Sean, Yadav, Ashish, Praveen, Kavita, Jones, Marcus, Salerno, William J., Chung, Wendy K., Surakka, Ida, Willer, Cristen J., Hveem, Kristian, Leader, Joseph B., Carey, David J., Ledbetter, David H., Cardon, Lon, Yancopoulos, George D., Economides, Aris, Coppola, Giovanni, Shuldiner, Alan R., Balasubramanian, Suganthi, Cantor, Michael, Nelson, Matthew R., Whittaker, John, Reid, Jeffrey G., Marchini, Jonathan, Overton, John D., Scott, Robert A., Abecasis, Gonçalo R., Yerges-Armstrong, Laura, Baras, Aris

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Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure von Henry, Albert, Roselli, Carolina, Sveinbjörnsson, Garðar, Fatemifar, Ghazaleh, Hedman, Åsa K., Morley, Michael P., Helgadottir, Anna, Verweij, Niek, Dehghan, Abbas, Almgren, Peter, Andersson, Charlotte, Backman, Joshua D., Biggs, Mary L., Brandimarto, Jeffrey, Buckbinder, Leonard, Carey, David J., Chasman, Daniel I., Chen, Xu, Chung, Jonathan, Cook, James P., Delgado, Graciela E., Denaxas, Spiros, Dörr, Marcus, Dudley, Samuel C., Esko, Tõnu, Finan, Chris, Gottdiener, John S., Gross, Stefan, Guðbjartsson, Daníel F., Gutmann, Rebecca, Haggerty, Christopher M., Hyde, Craig L., Ingelsson, Erik, Jukema, J. Wouter, Kavousi, Maryam, Khaw, Kay-Tee, Kleber, Marcus E., Køber, Lars, Koekemoer, Andrea, Langenberg, Claudia, Lind, Lars, Lotta, Luca A., Luan, Jian’an, März, Winfried, Melander, Olle, Mordi, Ify R., Morgan, Thomas, Morris, Andrew D., Morris, Andrew P., Morrison, Alanna C., Nelson, Christopher P., Niessner, Alexander, Niiranen, Teemu, O’Donoghue, Michelle L., Owens, Anjali T., Parry, Helen M., Perola, Markus, Rice, Kenneth M., Ridker, Paul M., Rotter, Jerome I., Salo, Perttu, Salomaa, Veikko, Smelser, Diane T., Stender, Steen, Stott, David J., Tammesoo, Mari-Liis, Taylor, Kent D., Teder-Laving, Maris, Thorsteinsdottir, Unnur, Torp-Pedersen, Christian, Trompet, Stella, Tyl, Benoit, Uitterlinden, Andre G., Veluchamy, Abirami, Völker, Uwe, Voors, Adriaan A., Wareham, Nicholas J., Waterworth, Dawn, Weiss, Raul, Wiggins, Kerri L., Yerges-Armstrong, Laura M., Yu, Bing, Zannad, Faiez, Zhao, Jing Hua, Hemingway, Harry, McMurray, John J. V., Yang, Jian, Visscher, Peter M., Malarstig, Anders, Holm, Hilma, Sattar, Naveed, Holmes, Michael V., Cappola, Thomas P., Hingorani, Aroon D., Kuchenbaecker, Karoline, Ellinor, Patrick T., Smith, J. Gustav, Vasan, Ramachandran S., Swerdlow, Daniel I., Lumbers, R. Thomas

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Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation von Kitajima, Hidetoshi, Kim, Young Jin, Horikoshi, Momoko, Moon, Sanghoon, Robertson, Neil R., Nano, Jana, Lamri, Amel, Nakatochi, Masahiro, Graff, Mariaelisa, Yao, Jie, Bielak, Lawrence F., Hai, Yang, Schmidt, Ellen M., Nousome, Darryl, Trompet, Stella, Ahmad, Meraj, Noordam, Raymond, Lim, Victor J. Y., Joo, Yoonjung Yoonie, Prins, Bram Peter, Chen, Guanjie, Jensen, Richard A., Kabagambe, Edmond K., Xiang, Anny H., Flanagan, Jack, Adair, Linda S., Akiyama, Masato, Bertoni, Alain, Chee, Miao-Li, Chen, Shyh-Huei, Chen, Yuan-Tsong, Das, Swapan K., de Silva, H. Janaka, Eckardt, Kai-Uwe, Evans, Daniel S., Evans, Michele K., Franco, Oscar H., Fuchsberger, Christian, Genter, Pauline, Goodarzi, Mark O., Gordon-Larsen, Penny, Gorkin, David, Guo, Yu, Howard, Annie-Green, Hung, Yi-Jen, Hwang, Mi Yeong, Ingelsson, Martin, Jonas, Jost B., Jørgensen, Torben, Kamatani, Yoichiro, Kasturiratne, Anuradhani, Katsuya, Tomohiro, Keaton, Jacob M., Kho, Abel N., Khor, Chiea-Chuen, Läll, Kristi, Li-Gao, Ruifang, Liu, Jianjun, Luan, Jian’an, Luo, Xi, Lyssenko, Valeriya, Metspalu, Andres, Morris, Andrew D., Nalls, Michael A., Ntalla, Ioanna, Sattar, Naveed, Shi, Jinxiu, Shriner, Daniel, Stilp, Adrienne M., Takahashi, Atsushi, Taylor, Kent D., Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Varma, Rohit, Yamamoto, Ken, Yoon, Kyungheon, Yusuf, Salim, Zheng, Wei, Cho, Yoon Shin, Lind, Lars, Province, Michael A., Zonderman, Alan B., Becker, Diane M., Yokota, Mitsuhiro, Chen, Yii-Der Ida, Ma, Ronald C. W., Chandak, Giriraj R., Sale, Michèle M., Shu, Xiao-Ou, Jukema, J. Wouter, McKean-Cowdin, Roberta, Kooner, Jaspal S., North, Kari E., Florez, Jose C., Maeda, Shiro, Stefansson, Kari, Mohlke, Karen L., Gloyn, Anna L., Below, Jennifer E., Rotter, Jerome I.

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Systematic identification of trans eQTLs as putative drivers of known disease associations von Westra, Harm-Jan, Peters, Marjolein J, Esko, Tõnu, Yaghootkar, Hanieh, Schurmann, Claudia, Kettunen, Johannes, Christiansen, Mark W, Fairfax, Benjamin P, Schramm, Katharina, Powell, Joseph E, Zhernakova, Alexandra, Zhernakova, Daria V, Veldink, Jan H, Van den Berg, Leonard H, Karjalainen, Juha, Withoff, Sebo, Uitterlinden, André G, Hofman, Albert, Rivadeneira, Fernando, 't Hoen, Peter A C, Reinmaa, Eva, Fischer, Krista, Nelis, Mari, Milani, Lili, Melzer, David, Ferrucci, Luigi, Singleton, Andrew B, Hernandez, Dena G, Nalls, Michael A, Homuth, Georg, Nauck, Matthias, Radke, Dörte, Völker, Uwe, Perola, Markus, Salomaa, Veikko, Brody, Jennifer, Suchy-Dicey, Astrid, Gharib, Sina A, Enquobahrie, Daniel A, Lumley, Thomas, Montgomery, Grant W, Makino, Seiko, Prokisch, Holger, Herder, Christian, Roden, Michael, Grallert, Harald, Meitinger, Thomas, Strauch, Konstantin, Li, Yang, Jansen, Ritsert C, Visscher, Peter M, Knight, Julian C, Psaty, Bruce M, Ripatti, Samuli, Teumer, Alexander, Frayling, Timothy M, Metspalu, Andres, van Meurs, Joyce B J, Franke, Lude

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Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus von Jacquemont, Sébastien, Reymond, Alexandre, Walters, Robin G., Kutalik, Zoltán, Valsesia, Armand, Belfiore, Marco, Bouquillon, Sonia, Campion, Dominique, de Vries, Bert B. A., Esko, Tõnu, Hoyer, Juliane, Jarvelin, Marjo-Riitta, Frank Kooy, R., Kurg, Ants, Le Caignec, Cédric, Männik, Katrin, Platt, Orah S., Sanlaville, Damien, Wu, Bai-lin, Yu, Yongguo, Addor, Marie-Claude, Antonarakis, Stylianos E., Arveiler, Benoît, Barth, Magalie, Bergmann, Sven, Bernardini, Laura, Blaumeiser, Bettina, Bonneau, Dominique, Brunner, Han G., Cailley, Dorothée, Chrast, Jacqueline, Coutton, Charles, Cuisset, Jean-Marie, de Freminville, Bénédicte, Demeer, Bénédicte, Descamps, Dominique, Disciglio, Vittoria, Doco-Fenzy, Martine, Dubourg, Christèle, El-Sayed Moustafa, Julia S., Faivre, Laurence, Ferrarini, Alessandra, Fisher, Richard, Flori, Elisabeth, Forer, Lukas, Gaillard, Dominique, Gimelli, Stefania, Gimelli, Giorgio, Grabe, Hans J., Hartikainen, Anna-Liisa, Heron, Délphine, Homuth, Georg, Isidor, Bertrand, Jaillard, Sylvie, Jaros, Zdenek, Jiménez-Murcia, Susana, Joly Helas, Géraldine, Jonveaux, Philippe, Kaksonen, Satu, Kroisel, Peter M., Kronenberg, Florian, Labalme, Audrey, Legallic, Solenn, Lewis, Suzanne, Lucas, Josette, MacDermot, Kay D., Marshall, Christian, McCarthy, Mark I., Meitinger, Thomas, Merla, Giuseppe, Morice-Picard, Fanny, Mucciolo, Mafalda, Nauck, Matthias, Nordgren, Ann, Pasquier, Laurent, Petit, Florence, Plessis, Ghislaine, Paolo Ramelli, Gian, Rauch, Anita, Ravazzolo, Roberto, Roetzer, Katharina M., Rooryck, Caroline, Schurmann, Claudia, Stavropoulos, Dimitri J., Tengström, Carola, Tinahones, Francisco J., Vincent-Delorme, Catherine, Visvikis-Siest, Sophie, Vollenweider, Peter, Völzke, Henry, Vulto-van Silfhout, Anneke T., Waeber, Gérard, Wallgren-Pettersson, Carina, Witwicki, Robert M., Andrieux, Joris, Estivill, Xavier, Gusella, James F., Stefansson, Kari, Beckmann, Jacques S., Froguel, Philippe

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A second update on mapping the human genetic architecture of COVID-19 von Jansen, Philip, Nakanishi, Tomoko, Priest, James, Turebayeva, Gulsimzhan, Bouab, Meriem, Bourque, Guillaume, Tse, Sze Man, Faucon, Annika B, Jensen, Björn-Erik Ole, Bals, Robert, Noor, Abdul, Liontos, Angelos, Azuure, Clinton, Blanco-Grau, Albert, Casalone, Elisabetta, Bellelli, Giuseppe, Kurihara, Hayato, Farré, Xavier, Hunkapiller, Julie, Kim, Jin Yong, Lee, Ji Yeon, Jung, Keum Ji, Bretherick, Andrew D, Ostermann, Marlies, Ryan, Lucy, Briton, Kate, Cutler, Sean, Springle, Philippa, Goodwin, Emma, Tibke, Clare, Farley, Sean, Bradley-Potts, Joanne, Whileman, Amanda, Kaye, Callum, Preston, Stephen, Cupitt, Jason, Jakkula, Srinivas, Lamb, Thomas, Hudson, Anne, Clark, Richard, Hudig, Lisa, Roberts, Abigail, Slevin, Kathryn, Thomas, Vicky, Chisholm, Catherine, Scanlon, Jeremy, Jones, Helen, Riches, Joanne, Anderson, Susan, Davies, Rhys, Tebbutt, Julie, Conyngham, Jo-Anna, Hobden, Gillian, Collier, Dawn, Durga, Latha, Wilson, Alison, Finnell, Jez, Serrano-Ruiz, Alfredo, Turner, Patricia, Turney, Sharon, Tutt, Gabriella, Varghese, Mathew, Stuart, Carmel, Wood, Stephen, Cother, Naiara, Brady, Ailbhe, Arden, Tracie, Capps, Nigel, Lennon, Liz, Joseph, Sibet, Jennings, Claire, Revill, Adam, Fletcher, Jo, Sutherland, Isobel, Kaye, Duncan, Whitbread, Jennifer, Hector, Gemma, Goddard, Peter, Lauder, Christen, Oosthuyzen, Wilna, Szoor-Mcelhinney, Helen, Upadhyay, Kamlesh J, Joshi, Chaitanya G, Kabata, Hiroki, Mikami, Yohei, Sonobe, Kazunari, Tateno, Hiroki, Yoshihara, Tomoyuki, Kuwahara, Naota, Sugiura, Hisatoshi, Ishihara, Sayoko, Ismail, Said I, Feng, Yen-Chen Anne, Castano, Luis, Ceballos, Francisco C, Aguado, Jose María, Carbonell, Cristina, Werge, Thomas, Wilson, Daniel J, Serra-Llovich, Alex

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