Items where Author is "Nöthen, M. M."

2023

Budu-Aggrey, A. and Kilanowski, A. and Sobczyk, M. K. and Shringarpure, S. S. and Mitchell, R. and Reis, K. and Reigo, A. and Mägi, R. and Nelis, M. and Tanaka, N. and Brumpton, B. M. and Thomas, L. F. and Sole-Navais, P. and Flatley, C. and Espuela-Ortiz, A. and Herrera-Luis, E. and Lominchar, J. V. T. and Bork-Jensen, J. and Marenholz, I. and Arnau-Soler, A. and Jeong, A. and Fawcett, K. A. and Baurecht, H. and Rodriguez, E. and Alves, A. C. and Kumar, A. and Sleiman, P. M. and Chang, X. and Medina-Gomez, C. and Hu, C. and Xu, C. J. and Qi, C. and El-Heis, S. and Titcombe, P. and Antoun, E. and Fadista, J. and Wang, C. A. and Thiering, E. and Wu, B. and Kress, S. and Kothalawala, D. M. and Kadalayil, L. and Duan, J. and Zhang, H. and Hadebe, S. and Hoffmann, T. and Jorgenson, E. and Choquet, H. and Risch, N. and Njølstad, P. and Andreassen, O. A. and Johansson, S. and Almqvist, C. and Gong, T. and Ullemar, V. and Karlsson, R. and Magnusson, P. K. E. and Szwajda, A. and Burchard, E. G. and Thyssen, J. P. and Hansen, T. and Kårhus, L. L. and Dantoft, T. M. and Jeanrenaud, Acsn and Ghauri, A. and Arnold, A. and Homuth, G. and Lau, S. and Nöthen, M. M. and Hübner, N. and Imboden, M. and Visconti, A. and Falchi, M. and Bataille, V. and Hysi, P. and Ballardini, N. and Boomsma, D. I. and Hottenga, J. J. and Müller-Nurasyid, M. and Ahluwalia, T. S. and Stokholm, J. and Chawes, B. and Schoos, A. M. and Esplugues, A. and Bustamante, M. and Raby, B. and Arshad, S. and German, C. and Esko, T. and Milani, L. A. and Metspalu, A. and Terao, C. and Abuabara, K. and Løset, M. and Hveem, K. and Jacobsson, B. and Pino-Yanes, M. and Strachan, D. P. and Grarup, N. and Linneberg, A. and Lee, Y. A. and Probst-Hensch, N. and Weidinger, S. and Jarvelin, M. R. and Melén, E. and Hakonarson, H. and Irvine, A. D. and Jarvis, D. and Nijsten, T. and Duijts, L. and Vonk, J. M. and Koppelmann, G. H. and Godfrey, K. M. and Barton, S. J. and Feenstra, B. and Pennell, C. E. and Sly, P. D. and Holt, P. G. and Williams, L. K. and Bisgaard, H. and Bønnelykke, K. and Curtin, J. and Simpson, A. and Murray, C. and Schikowski, T. and Bunyavanich, S. and Weiss, S. T. and Holloway, J. W. and Min, J. L. and Brown, S. J. and Standl, M. and Paternoster, L.. (2023) European and multi-ancestry genome-wide association meta-analysis of atopic dermatitis highlights importance of systemic immune regulation. Nat Commun, 14. p. 6172.

2015

Nenadic, I. and Maitra, R. and Basmanav, F. B. and Schultz, C. C. and Lorenz, C. and Schachtzabel, C. and Smesny, S. and Nöthen, M. M. and Cichon, S. and Reichenbach, J. R. and Sauer, H. and Schlösser, R. G. M. and Gaser, C.. (2015) ZNF804A genetic variation (rs1344706) affects brain grey but not white matter in schizophrenia and healthy subjects. Psychological Medicine, 45 (1). pp. 143-152.

2014

Li, M. and Luo, X.-J. and Rietschel, M. and Lewis, C. M. and Mattheisen, M. and Müller-Myhsok, B. and Jamain, S. and Leboyer, M. and Landén, M. and Thompson, P. M. and Cichon, S. and Nöthen, M. M. and Schulze, T. G. and Sullivan, P. F. and Bergen, S. E. and Donohoe, G. and Morris, D. W. and Hargreaves, A. and Gill, M. and Corvin, A. and Hultman, C. and Toga, A. W. and Shi, L. and Lin, Q. and Shi, H. and Gan, L. and Meyer-Lindenberg, A. and Czamara, D. and Henry, C. and Etain, B. and Bis, J. C. and Ikram, M. A. and Fornage, M. and Debette, S. and Launer, L. J. and Seshadri, S. and Erk, S. and Walter, H. and Heinz, A. and Bellivier, F. and Stein, J. L. and Medland, S. E. and Arias Vasquez, A. and Hibar, D. P. and Franke, B. and Martin, N. G. and Wright, M. J. and MooDS Bipolar Consortium, and Swedish Bipolar Study Group, and Alzheimer's Disease Neuroimaging Initiative, and Enigma Consortium, and Charge Consortium, and Su, B.. (2014) Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility. Molecular Psychiatry, 19 (4). pp. 452-461.

Steinberg, S. and de Jong, S. and Mattheisen, M. and Costas, J. and Demontis, D. and Jamain, S. and Pietiläinen, O. P. H. and Lin, K. and Papiol, S. and Huttenlocher, J. and Sigurdsson, E. and Vassos, E. and Giegling, I. and Breuer, R. and Fraser, G. and Walker, N. and Melle, I. and Djurovic, S. and Agartz, I. and Tuulio-Henriksson, A. and Suvisaari, J. and Lönnqvist, J. and Paunio, T. and Olsen, L. and Hansen, T. and Ingason, A. and Pirinen, M. and Strengman, E. and Group, and Hougaard, D. M. and Ørntoft, T. and Didriksen, M. and Hollegaard, M. V. and Nordentoft, M. and Abramova, L. and Kaleda, V. and Arrojo, M. and Sanjuán, J. and Arango, C. and Etain, B. and Bellivier, F. and Méary, A. and Schürhoff, F. and Szoke, A. and Ribolsi, M. and Magni, V. and Siracusano, A. and Sperling, S. and Rossner, M. and Christiansen, C. and Kiemeney, L. A. and Franke, B. and van den Berg, L. H. and Veldink, J. and Curran, S. and Bolton, P. and Poot, M. and Staal, W. and Rehnstrom, K. and Kilpinen, H. and Freitag, C. M. and Meyer, J. and Magnusson, P. and Saemundsen, E. and Martsenkovsky, I. and Bikshaieva, I. and Martsenkovska, I. and Vashchenko, O. and Raleva, M. and Paketchieva, K. and Stefanovski, B. and Durmishi, N. and Pejovic Milovancevic, M. and Lecic Tosevski, D. and Silagadze, T. and Naneishvili, N. and Mikeladze, N. and Surguladze, S. and Vincent, J. B. and Farmer, A. and Mitchell, P. B. and Wright, A. and Schofield, P. R. and Fullerton, J. M. and Montgomery, G. W. and Martin, N. G. and Rubino, I. A. and van Winkel, R. and Kenis, G. and De Hert, M. and Réthelyi, J. M. and Bitter, I. and Terenius, L. and Jönsson, E. G. and Bakker, S. and van Os, J. and Jablensky, A. and Leboyer, M. and Bramon, E. and Powell, J. and Murray, R. and Corvin, A. and Gill, M. and Morris, D. and O'Neill, F. A. and Kendler, K. and Riley, B. and Wellcome Trust Case Control Consortium, and Craddock, N. and Owen, M. J. and O'Donovan, M. C. and Thorsteinsdottir, U. and Kong, A. and Ehrenreich, H. and Carracedo, A. and Golimbet, V. and Andreassen, O. A. and Børglum, A. D. and Mors, O. and Mortensen, P. B. and Werge, T. and Ophoff, R. A. and Nöthen, M. M. and Rietschel, M. and Cichon, S. and Ruggeri, M. and Tosato, S. and Palotie, A. and St Clair, D. and Rujescu, D. and Collier, D. A. and Stefansson, H. and Stefansson, K.. (2014) Common variant at 16p11.2 conferring risk of psychosis. Molecular Psychiatry, 19 (1). pp. 108-114.

Luo, X.-J. and Li, M. and Huang, L. and Steinberg, S. and Mattheisen, M. and Liang, G. and Donohoe, G. and Shi, Y. and Chen, C. and Yue, W. and Alkelai, A. and Lerer, B. and Li, Z. and Yi, Q. and Rietschel, M. and Cichon, S. and Collier, D. A. and Tosato, S. and Suvisaari, J. and Rujescu, Dan and Golimbet, V. and Silagadze, T. and Durmishi, N. and Milovancevic, M. P. and Stefansson, H. and Schulze, T. G. and Nöthen, M. M. and Chen, C. and Lyne, R. and Morris, D. W. and Gill, M. and Corvin, A. and Zhang, D. and Dong, Q. and Moyzis, R. K. and Stefansson, K. and Sigurdsson, E. and Hu, F. and MooDS SCZ Consortium, and Su, B. and Gan, L.. (2014) Convergent lines of evidence support CAMKK2 as a schizophrenia susceptibility gene. Molecular Psychiatry, 19 (7). pp. 774-783.

Arking, D. E. and Pulit, S. L. and Crotti, L. and van der Harst, P. and Munroe, P. B. and Koopmann, T. T. and Sotoodehnia, N. and Rossin, E. J. and Morley, M. and Wang, X. and Johnson, A. D. and Lundby, A. and Gudbjartsson, D. F. and Noseworthy, P. A. and Eijgelsheim, M. and Bradford, Y. and Tarasov, K. V. and Dörr, M. and Müller-Nurasyid, M. and Lahtinen, A. M. and Nolte, I. M. and Smith, A. V. and Bis, J. C. and Isaacs, A. and Newhouse, S. J. and Evans, D. S. and Post, W. S. and Waggott, D. and Lyytikäinen, L. P. and Hicks, A. A. and Eisele, L. and Ellinghaus, D. and Hayward, C. and Navarro, P. and Ulivi, S. and Tanaka, T. and Tester, D. J. and Chatel, S. and Gustafsson, S. and Kumari, M. and Morris, R. W. and Naluai, ÅT and Padmanabhan, S. and Kluttig, A. and Strohmer, B. and Panayiotou, A. G. and Torres, M. and Knoflach, M. and Hubacek, J. A. and Slowikowski, K. and Raychaudhuri, S. and Kumar, R. D. and Harris, T. B. and Launer, L. J. and Shuldiner, A. R. and Alonso, A. and Bader, J. S. and Ehret, G. and Huang, H. and Kao, W. H. and Strait, J. B. and Macfarlane, P. W. and Brown, M. and Caulfield, M. J. and Samani, N. J. and Kronenberg, F. and Willeit, J. and CARe Consortium, and Cogent Consortium, and Smith, J. G. and Greiser, K. H. and Meyer zu Schwabedissen, H. and Werdan, K. and Carella, M. and Zelante, L. and Heckbert, S. R. and Psaty, B. M. and Rotter, J. I. and Kolcic, I. and Polašek, O. and Wright, A. F. and Griffin, M. and Daly, M. J. and Dcct/Edic, and Arnar, D. O. and Hólm, H. and Thorsteinsdottir, U. and eMerge Consortium, and Denny, J. C. and Roden, D. M. and Zuvich, R. L. and Emilsson, V. and Plump, A. S. and Larson, M. G. and O'Donnell, C. J. and Yin, X. and Bobbo, M. and D'Adamo, A. P. and Iorio, A. and Sinagra, G. and Carracedo, A. and Cummings, S. R. and Nalls, M. A. and Jula, A. and Kontula, K. K. and Marjamaa, A. and Oikarinen, L. and Perola, M. and Porthan, K. and Erbel, R. and Hoffmann, P. and Jöckel, K. H. and Kälsch, H. and Nöthen, M. M. and Hrgen Consortium, and den Hoed, M. and Loos, R. J. and Thelle, D. S. and Gieger, C. and Meitinger, T. and Perz, S. and Peters, A. and Prucha, H. and Sinner, M. F. and Waldenberger, M. and de Boer, R. A. and Franke, L. and van der Vleuten, P. A. and Beckmann, B. M. and Martens, E. and Bardai, A. and Hofman, N. and Wilde, A. A. and Behr, E. R. and Dalageorgou, C. and Giudicessi, J. R. and Medeiros-Domingo, A. and Barc, J. and Kyndt, F. and Probst, V. and Ghidoni, A. and Insolia, R. and Hamilton, R. M. and Scherer, S. W. and Brandimarto, J. and Margulies, K. and Moravec, C. E. and del Greco, M. F. and Fuchsberger, C. and O'Connell, J. R. and Lee, W. K. and Watt, G. C. and Campbell, H. and Wild, S. H. and El Mokhtari, N. E. and Frey, N. and Asselbergs, F. W. and Mateo Leach, I. and Navis, G. and van den Berg, M. P. and van Veldhuisen, D. J. and Kellis, M. and Krijthe, B. P. and Franco, O. H. and Hofman, A. and Kors, J. A. and Uitterlinden, A. G. and Witteman, J. C. and Kedenko, L. and Lamina, C. and Oostra, B. A. and Abecasis, G. R. and Lakatta, E. G. and Mulas, A. and Orrú, M. and Schlessinger, D. and Uda, M. and Markus, M. R. and Völker, U. and Snieder, H. and Spector, T. D. and Ärnlöv, J. and Lind, L. and Sundström, J. and Syvänen, A. C. and Kivimaki, M. and Kähönen, M. and Mononen, N. and Raitakari, O. T. and Viikari, J. S. and Adamkova, V. and Kiechl, S. and Brion, M. and Nicolaides, A. N. and Paulweber, B. and Haerting, J. and Dominiczak, A. F. and Nyberg, F. and Whincup, P. H. and Hingorani, A. D. and Schott, J. J. and Bezzina, C. R. and Ingelsson, E. and Ferrucci, L. and Gasparini, P. and Wilson, J. F. and Rudan, I. and Franke, A. and Mühleisen, T. W. and Pramstaller, P. P. and Lehtimäki, T. J. and Paterson, A. D. and Parsa, A. and Liu, Y. and van Duijn, C. M. and Siscovick, D. S. and Gudnason, V. and Jamshidi, Y. and Salomaa, V. and Felix, S. B. and Sanna, S. and Ritchie, M. D. and Stricker, B. H. and Stefansson, K. and Boyer, L. A. and Cappola, T. P. and Olsen, J. V. and Lage, K. and Schwartz, P. J. and Kääb, S. and Chakravarti, A. and Ackerman, M. J. and Pfeufer, A. and de Bakker, P. I. and Newton, C.. (2014) Genetic association study of QT interval highlights role for calcium signaling pathways in myocardial repolarization. Nature genetics, Vol. 46, H. 8. pp. 826-836.

Jarick, I. and Volckmar, A. L. and Pütter, C. and Pechlivanis, S. and Nguyen, T. T. and Dauvermann, M. R. and Beck, S. and Albayrak, Ö. and Scherag, S. and Gilsbach, S. and Cichon, S. and Hoffmann, P. and Degenhardt, F. and Nöthen, M. M. and Schreiber, S. and Wichmann, H.-E. and Jöckel, K.-H. and Heinrich, J. and Tiesler, C. M. T. and Faraone, S. V. and Walitza, S. and Sinzig, J. and Freitag, C. and Meyer, J. and Herpertz-Dahlmann, B. and Lehmkuhl, G. and Renner, T. J. and Warnke, A. and Romanos, M. and Lesch, K.-P. and Reif, A. and Schimmelmann, B. G. and Hebebrand, J. and Scherag, A. and Hinney, A.. (2014) Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder. Molecular Psychiatry, 19 (1). pp. 115-121.

Børglum, A. D. and Demontis, D. and Grove, J. and Pallesen, J. and Hollegaard, M. V. and Pedersen, C. B. and Hedemand, A. and Mattheisen, M. and Group investigators, and Uitterlinden, A. and Nyegaard, M. and Ørntoft, T. and Wiuf, C. and Didriksen, M. and Nordentoft, M. and Nöthen, M. M. and Rietschel, M. and Ophoff, R. A. and Cichon, S. and Yolken, R. H. and Hougaard, D. M. and Mortensen, P. B. and Mors, O.. (2014) Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci. Molecular Psychiatry, 19 (3). pp. 325-333.

2000

Schulze, T. G. and Müller, D. J. and Krauss, H. and Scherk, H. and Ohlraun, S. and Syagailo, Y. V. and Windemuth, C. and Neidt, H. and Grässle, M. and Papassotiropoulos, A. and Heun, R. and Nöthen, M. M. and Maier, W. and Lesch, K. P. and Rietschel, M.. (2000) Association between a functional polymorphism in the monoamine oxidase A gene promoter and major depressive disorder. American journal of medical genetics, Vol. 96, no. 6. pp. 801-803.

1999

Kühn, K. U. and Meyer, K. and Nöthen, M. M. and Gänsicke, M. and Papassotiropoulos, A. and Maier, W.. (1999) Allelic variants of dopamine receptor D4 (DRD4) and serotonin receptor 5HT2c (HTR2c) and temperament factors : replication tests. American journal of medical genetics, Vol. 88, no. 2. pp. 168-172.