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Mehta, Divya, Klengel, Torsten, Conneely, Karen N., Smith, Alicia K., Altmann, André, Pace, Thaddeus W., Rex-Haffner, Monika, Loeschner, Anne, Gonik, Mariya, Mercer, Kristina B., Bradley, Bekh, Muller-Myhsok, Bertram, Ressler, Kerry J. and Binder, Elisabeth B. (2013) Childhood maltreatment is associated with distinct genomic and epigenetic profiles in posttraumatic stress disorder. Proceedings of the National Academy of Sciences of the United States of America, 110 20: 8302-8307. doi:10.1073/pnas.1217750110     200 Cited 221 times in Scopus221 111
Xiao, Xiao, Wang, Lu, Wang, Chuang, Yuan, Ti-Fei, Zhou, Dongsheng, Zheng, Fanfan, Li, Lingyi, Grigoroiu-Serbanescu, Maria, Ikeda, Masashi, Iwata, Nakao, Takahashi, Atsushi, Kamatani, Yoichiro, Kubo, Michiaki, Preisig, Martin, Kutalik, Zoltán, Castelao, Enrique, Pistis, Giorgio, Amin, Najaf, Van Duijn, Cornelia M., Forstner, Andreas J., Strohmaier, Jana, Hecker, Julian, Schulze, Thomas G., Müller-Myhsok, Bertram, Reif, Andreas, Mitchell, Philip B., Martin, Nicholas G., Schofield, Peter R., Cichon, Sven, Nöthen, Markus M., Chang, Hong, Luo, Xiong-Jian, Fang, Yiru, Yao, Yong-Gang, Zhang, Chen, Rietschel, Marcella, Li, Ming, Advanced Collaborative Study of Mood Disorder (COSMO) Team and MooDS Bipolar Consortium (2017) Common variants at 2q11.2, 8q21.3, and 11q13.2 are associated with major mood disorders. Translational Psychiatry, 7 12: . doi:10.1038/s41398-017-0019-0     0 Cited 1 times in Scopus1 2
Nyholt, Dale R., Anttila, Verneri, Winsvold, Bendik S., Kurth, Tobias, Stefansson, Hreinn, Kallela, Mikko, Malik, Rainer, Vries, Boukje De, Terwindt, Gisela M., Ikram, M Arfan, Stam, Anine H., Ligthart, Lannie, Freilinger, Tobias, Alexander, Michael, Muller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Aromaa, Arpo, Eriksson, Johan G., Kaprio, Jaakko, Boomsma, Dorret I., Duijn, Cornelia Van, Raitakari, Olli, Järvelin, Marjo-Riitta, Zwart, John-Anker, Quaye, Lydia, Strachan, David P., Kubisch, Christian, Ferrari, Michel D., Van Den Maagdenberg, Arn M. J. M., Dichgans, Martin, Wessman, Maija, Smith, George Davey, Stefansson, Kari, Chasman, Daniel I. and Palotie, Aarno (2015) Concordance of genetic risk across migraine subgroups: impact on current and future genetic association studies. Cephalalgia, 35 6: 489-499. doi:10.1177/0333102414547784     14 Cited 15 times in Scopus15 1
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, Rietschel, Marcella, MooDS Consortium, and The Swedish Bipolar Study Group, (2016) Convergent lines of evidence support LRP8 as a susceptibility gene for psychosis. Molecular Neurobiology, 53 10: 6608-6619. doi:10.1007/s12035-015-9559-6     1 Cited 1 times in Scopus1 3
Zhao, Huiying, Eising, Else, De Vries, Boukje, Vijfhuizen, Lisanne S., Anttila, Verneri, Winsvold, Bendik S., Kurth, Tobias, Stefansson, Hreinn, Kallela, Mikko, Malik, Rainer, Stam, Anine H., Arfan Ikram, M., Ligthart, Lannie, Freilinger, Tobias, Alexander, Michael, Müller-Myhsok, Bertram, Schreiber, Stefan, Meitinger, Thomas, Aromas, Arpo, Eriksson, Johan G., Boomsma, Dorret I., Van Duijn, Cornelia M., Zwart, John-Anker, Quaye, Lydia, Kubisch, Christian, Dichgans, Martin, Wessman, Maija, Stefansson, Kari, Chasman, Daniel I., Palotie, Aarno, Martin, Nicholas G., Montgomery, Grant W., Ferrari, Michel D., Terwindt, Gisela M., Van Den Maagdenberg, Arn M. J. M. and Nyholt, Dale R. (2016) Gene-based pleiotropy across migraine with aura and migraine without aura patient groups. Cephalalgia, 36 7: 648-657. doi:10.1177/0333102415591497     13 Cited 14 times in Scopus14 2
Amin, Najaf, Allebrandt, Karla V., van der Spek, Ashley, Müller-Myhsok, Bertram, Hek, Karin, Teder-Laving, Maris, Hayward, Caroline, Esko, Tõnu, van Mill, Josine G., Mbarek, Hamdi, Watson, Nathaniel F., Melville, Scott A., Del Greco, Fabiola M., Byrne, Enda M., Oole, Edwin, Kolcic, Ivana, Chen, Ting-hsu, Evans, Daniel S., Coresh, Josef, Vogelzangs, Nicole, Karjalainen, Juha, Willemsen, Gonneke, Gharib, Sina A., Zgaga, Lina, Mihailov, Evelin, Stone, Katie L., Campbell, Harry, Brouwer, Rutger W. W., Demirkan, Ayse, Isaacs, Aaron, Dogas, Zoran, Marciante, Kristin D., Campbell, Susan, Borovecki, Fran, Luik, Annemarie I., Li, Man, Hottenga, Jouke Jan, Huffman, Jennifer E., van den Hout, Mirjam C. G. N., Cummings, Steven R., Aulchenko, Yurii S., Gehrman, Philip R., Uitterlinden, André G., Wichmann, Heinz-Erich, Müller-Nurasyid, Martina, Fehrmann, Rudolf S. N., Montgomery, Grant W., Hofman, Albert, Kao, Wen Hong Linda, Oostra, Ben A., Wright, Alan F., Vink, Jacqueline M., Wilson, James F., Pramstaller, Peter P., Hicks, Andrew A., Polasek, Ozren, Punjabi, Naresh M., Redline, Susan, Psaty, Bruce M., Heath, Andrew C., Merrow, Martha, Tranah, Gregory J., Gottlieb, Daniel J., Boomsma, Dorret I., Martin, Nicholas G., Rudan, Igor, Tiemeier, Henning, van IJcken, Wilfred F. J., Penninx, Brenda W., Metspalu, Andres, Meitinger, Thomas, Franke, Lude, Roenneberg, Till and van Duijn, Cornelia M. (2016) Genetic variants in RBFOX3 are associated with sleep latency. European Journal of Human Genetics, 24 10: 1488-1495. doi:10.1038/ejhg.2016.31     10 Cited 9 times in Scopus9 7
ISGC, WTCCC2, Bellenguez, Céline, Bevan, Steve, Gschwendtner, Andreas, Spencer, Chris C. A., Burgess, Annette I., Pirinen, Matti, Jackson, Caroline A., Traylor, Matthew, Strange, Amy, Su, Zhan, Band, Gavin, Syme, Paul D., Malik, Rainer, Pera, Joanna, Norrving, Bo, Lemmens, Robin, Freeman, Colin, Schanz, Renata, James, Tom, Poole, Deborah, Murphy, Lee, Segal, Helen, Cortellini, Lynelle, Cheng, Yu-Ching, Woo, Daniel, Nalls, Michael A., Muller-Myhsok, Bertram, Meisinger, Christa, Seedorf, Udo, Ross-Adams, Helen, Boonen, Steven, Wloch-Kopec, Dorota, Valant, Valerie, Slark, Julia, Furie, Karen, Delavaran, Hossein, Langford, Cordelia, Deloukas, Panos, Edkins, Sarah, Hunt, Sarah, Gray, Emma, Dronov, Serge, Peltonen, Leena, Gretarsdottir, Solveig, Thorleifsson, Gudmar, Thorsteinsdottir, Unnur, Stefansson, Kari, Boncoraglio, Giorgio B., Parati, Eugenio A., Attia, John, Holliday, Elizabeth, Levi, Chris, Franzosi, Maria-Grazia, Goel, Anuj, Helgadottir, Anna, Blackwell, Jenefer M., Bramon, Elvira, Brown, Matthew A., Casas, Juan P., Corvin, Aiden, Duncanson, Audrey, Jankowski, Janusz, Mathew, Christopher G., Palmer, Colin N. A., Plomin, Robert, Rautanen, Anna, Sawcer, Stephen J., Trembath, Richard C., Viswanathan, Ananth C., Wood, Nicholas W., Worrall, Bradford B., Kittner, Steven J., Kissela, Brett, Mitchell, Braxton D., Meschia, James F., Thijs, Vincent, Lindgren, Arne, Macleod, Mary Joan, Slowik, Agnieszka, Walters, Matthew, Rosand, Jonathan, Sharma, Pankaj, Farrall, Martin, Sudlow, Cathie L. M., Rothwell, Peter M., Dichgans, Martin, Donnelly, Peter and Markus, Hugh S. (2012) Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke. Nature Genetics, 44 3: 328-333. doi:10.1038/ng.1081     216 Cited 247 times in Scopus247 34
Anttila, Verneri, Stefansson, Hreinn, Kallela, Mikko, Todt, Unda, Terwindt, Gisela M., Calafato, M Stella, Nyholt, Dale R., Dimas, Antigone S., Freilinger, Tobias, Müller-Myhsok, Bertram, Artto, Ville, Inouye, Michael, Alakurtti, Kirsi, Kaunisto, Mari A., Hämäläinen, Eija, De Vries, Boukje, Stam, Anine H., Weller, Claudia M., Heinze, Axel, Heinze-Kuhn, Katja, Goebel, Ingrid, Borck, Guntram, Göbel, Hartmut, Steinberg, Stacy, Wolf, Christiane, Björnsson, Asgeir, Gudmundsson, Gretar, Kirchmann, Malene, Hauge, Anne, Werge, Thomas, Schoenen, Jean, Eriksson, Johan G., Hagen, Knut, Stovner, Lars, Wichmann, H-Erich, Meitinger, Thomas, Alexander, Michael, Moebus, Susanne, Schreiber, Stefan, Aulchenko, Yurii S., Breteler, Monique M. B., Uitterlinden, Andre G., Hofman, Albert, Van Duijn, Cornelia M., Tikka-Kleemola, Päivi, Vepsäläinen, Salli, Lucae, Susanne, Tozzi, Federica, Muglia, Pierandrea, Barrett, Jeffrey, Kaprio, Jaakko, Färkkilä, Markus, Peltonen, Leena, Stefansson, Kari, Zwart, John-Anker, Ferrari, Michel D., Olesen, Jes, Daly, Mark, Wessman, Maija, Van Den Maagdenberg, Arn M.J.M., Dichgans, Martin, Kubisch, Christian, Dermitzakis, Emmanouil T., Frants, Rune R. and Palotie, Aarno (2010) Genome-wide association study of migraine implicates a common susceptibility variant on 8q22.1. Nature Genetics, 42 10: 869-873. doi:10.1038/ng.652     216 Cited 239 times in Scopus239 37
Chang, Hong, Li, Lingyi, Peng, Tao, 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., Jamain, Stéphane, Leboyer, Marion, Bellivier, Frank, Etain, Bruno, Kahn, Jean-Pierre, Henry, Chantal, Rietschel, Marcella, Backlund, Lena, Frisén, Louise, Lavebratt, Catharina, Schalling, Martin, Ösby, Urban, Mühleisen, Thomas W., Leber, Markus, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel, Hofmann, Andrea, Breuer, René, Meier, Sandra, Herms, Stefan, Hoffmann, Per, Lacour, André, Witt, Stephanie H., Streit, Fabian, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Wright, Adam, Fullerton, Janice M., Schofield, Peter R., Montgomery, Grant W., Medland, Sarah E., Gordon, Scott D., Becker, Tim, Schumacher, Johannes, Propping, Peter, Xiao, Xiao, Li, Ming, The Swedish Bipolar Study Group and MooDS Consortium (2017) Identification of a bipolar disorder vulnerable gene CHDH at 3p21.1. Molecular Neurobiology, 54 7: 5166-5176. doi:10.1007/s12035-016-0041-x     0 0 3
Forstner, Andreas J., Hecker, Julian, Hofmann, Andrea, Maaser, Anna, Reinbold, Céline S., Mühleisen, Thomas W., Leber, Markus, Strohmaier, Jana, Degenhardt, Franziska, Treutlein, Jens, Mattheisen, Manuel, Schumacher, Johannes, Streit, Fabian, Meier, Sandra, Herms, Stefan, Hoffmann, Per, Lacour, André, Witt, Stephanie H., Reif, Andreas, Müller-Myhsok, Bertram, Lucae, Susanne, Maier, Wolfgang, Schwarz, Markus, Vedder, Helmut, Kammerer-Ciernioch, Jutta, Pfennig, Andrea, Bauer, Michael, Hautzinger, Martin, Moebus, Susanne, Schenk, Lorena M., Fischer, Sascha B., Sivalingam, Sugirthan, Czerski, Piotr M., Hauser, Joanna, Lissowska, Jolanta, Szeszenia-Dabrowska, Neonila, Brennan, Paul, McKay, James D., Wright, Adam, Mitchell, Philip B., Fullerton, Janice M., Schofield, Peter R., Montgomery, Grant W., Medland, Sarah E., Gordon, Scott D., Martin, Nicholas G., Krasnov, Valery, Chuchalin, Alexander, Babadjanova, Gulja, Pantelejeva, Galina, Abramova, Lilia I., Tiganov, Alexander S., Polonikov, Alexey, Khusnutdinova, Elza, Alda, Martin, Cruceanu, Cristiana, Rouleau, Guy A., Turecki, Gustavo, Laprise, Catherine, Rivas, Fabio, Mayoral, Fermin, Kogevinas, Manolis, Grigoroiu-Serbanescu, Maria, Becker, Tim, Schulze, Thomas G., Rietschel, Marcella, Cichon, Sven, Fier, Heide and Nöthen, Markus M. (2017) Identification of shared risk loci and pathways for bipolar disorder and schizophrenia. PLoS ONE, 12 2: e0171595. doi:10.1371/journal.pone.0171595     12 Cited 14 times in Scopus14 9
Becker, Jessica, May, Andrea, Gerges, Christian, Anders, Mario, Veits, Lothar, Weise, Katharina, Czamara, Darina, Lyros, Orestis, Manner, Hendrik, Terheggen, Grischa, Venerito, Marino, Noder, Tania, Mayershofer, Rupert, Hofer, Jan-Hinnerk, Karch, Hans-Werner, Ahlbrand, Constantin J., Arras, Michael, Hofer, Sebastian, Mangold, Elisabeth, Heilmann-Heimbach, Stefanie, Heinrichs, Sophie K. M., Hess, Timo, Kiesslich, Ralf, Izbicki, Jakob R., Hölscher, Arnulf H., Bollschweiler, Elfriede, Malfertheiner, Peter, Lang, Hauke, Moehler, Markus, Lorenz, Dietmar, Müller-Myhsok, Bertram, Ott, Katja, Schmidt, Thomas, Whiteman, David C., Vaughan, Thomas L., Nöthen, Markus M., Hackelsberger, Andreas, Schumacher, Brigitte, Pech, Oliver, Vashist, Yogesh, Vieth, Michael, Weismüller, Josef, Neuhaus, Horst, Rösch, Thomas, Ell, Christian, Gockel, Ines and Schumacher, Johannes (2015) Supportive evidence for FOXP1, BARX1, and FOXF1 as genetic risk loci for the development of esophageal adenocarcinoma. Cancer Medicine, 4 11: 1700-1704. doi:10.1002/cam4.500     11 Cited 10 times in Scopus10 1