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scopus: 7102222451

Nöthen, M.M.

(Markus Nöthen)


study association sample university control analysis genome-wide expression department disease table depression institute replication germany effect region research slc 6a genotype center genetic locus model genet signi individual result nature allele meta-analysi value figure population variant hippocampal rs 1545843 alzheimer patient medicine health nscl /p netherland number subject neuron psychiatry rotterdam brain genotyping cleft heart hospital chromosome stage illumina ficant european p values level depressive slc 6a expression stress volume gerad susceptibility factor german genomic discovery width disorder case-control genome-wide association study evidence recessive model epidemiology genotyped method -01




9 Most Recent Publications

Genetic determination of human facial morphology: Links between cleft-lips and normal variation (Article)
Boehringer, S. Lijn, F. van der Uitterlinden, A.G. Niessen, W.J. Breteler, M.M.B. Lugt, A. van der Würtz, R.P. Nöthen, M.M. Horsthemke, B. Wieczorek, D. Mangold, E. Kayser, M. Liu, F. Günther, M. Sinigerova, S. Nowak, S. Ludwig, K.U. Herberz, R. Klein, S. Hofman, A.
2011-11-01
Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease (Article)
Hollingworth, P. Harold, D. Dowzell, K. Tikka-Kleemola, P. Breteler, M.M.B. Ikram, M.A. DeStefano, A.L. Fitzpatrick, A.L. Lopez, O.L. Launer, L.J. Seshadri, S. Berr, C. Campion, D. Jones, N. Epelbaum, J. Dartigues, J.-F. Tzourio, C. Alperovitch, A. Lathrop, G.M. Feulner, T.M. Friedrich, P. Riehle, C. Krawczak, M. Schreiber, S. Stretton, A. Mayhaus, M. Nicolhaus, S. Wagenpfeil, S. Steinberg, S. Kallela, M. SnÆdal, J. Björnsson, S. Jonsson, P.V. Chouraki, V. Genier-Boley, B. Thomas, C. Hiltunen, M. Soininen, H. Combarros, O. Zelenika, D. Delepine, M. Bullido, M.J. Pasquier, F. Mateo, I. Frank-Garcia, A. Porcellini, E. Richards, A. Hanon, O. Coto, E. Alvarez, V. Bosco, P. Siciliano, G. Mancuso, M. Panza, F. Solfrizzi, V. Nacmias, B. Sorbi, S. Ivanov, D. Bossù, P. Piccardi, P. Arosio, B. Annoni, G. Seripa, D. Pilotto, A. Scarpini, E. Galimberti, D. Brice, A. Hannequin, D. Widdowson, C. Licastro, F. Holmans, P.A. Riemenschneider, M. Morgan, K. Younkin, S. Owen, M.J. O'Donovan, M. Amouyel, P. Williams, J. Chapman, J. Lovestone, S. Powell, J. Sims, R. Proitsi, P. Lupton, M.K. Brayne, C. Rubinsztein, D.C. Gill, M. Lawlor, B. Lynch, A. Brown, K. Passmore, P.A. Craig, D. Gerrish, A. McGuinness, B. Todd, S. Holmes, C. Mann, D. Smith, A.D. Beaumont, H. Warden, D.R. Wilcock, G.K. Love, S. Kehoe, P.G. Lambert, J.C. Hooper, N.M. Vardy, E.R.L.C. Hardy, J. Mead, S. Fox, N.C. Rossor, M. Collinge, J. Maier, W. Jessen, F. Rüther, E. Carrasquillo, M.M. Schürmann, B. Heun, R. Kölsch, H. Bussche, H. van den Heuser, I. Kornhuber, J. Wiltfang, J. Dichgans, M. Frölich, L. Hampel, H. Abraham, R. Gallacher, J. Hüll, M. Rujescu, D. Giegling, I. Goate, A.M. Kauwe, J.S.K. Cruchaga, C. Nowotny, P. Morris, J.C. Mayo, K. Hamshere, M.L. Sleegers, K. Bettens, K. Engelborghs, S. Deyn, P.P. de Broeckhoven, C. van Livingston, G. Bass, N.J. Gurling, H. McQuillin, A. Gwilliam, R. Pahwa, J.S. Deloukas, P. Al-Chalabi, A. Shaw, C.E. Tsolaki, M. Singleton, A.B. Guerreiro, R. Mühleisen, T.W. Nöthen, M.M. Moebus, S. Jöckel, K.-H. Moskvina, V. Klopp, N. Wichmann, H.E. Pankratz, V.S. Sando, S.B. Aasly, J.O. Barcikowska, M. Wszolek, Z.K. Dickson, D. Graff-Radford, N.R. Petersen, R.C.
2011-05-01
The Neuronal Transporter Gene SLC6A15 Confers Risk to Major Depression (Article)
Kohli, M.A. Lucae, S. Hoehn, D. Specht, M. Menke, A. Hennings, J. Heck, A. Wolf, C. Ising, M. Schreiber, S. Czisch, M. Müller, M.B. Saemann, P.G. Uhr, M. Bettecken, T. Becker, A. Schramm, J. Rietschel, M. Maier, W. Bradley, B. Ressler, K.J. Nöthen, M.M. Cichon, S. Schmidt, M.V. Craig, I.W. Breen, G. Lewis, C.M. Hofman, A. Tiemeier, H. Tikka-Kleemola, P. Holsboer, F. Müller-Myhsok, B. Binder, E.B. Demirkan, A. Hek, K. Czamara, D. Alexander, M. Salyakina, D. Ripke, S.
2011-04-28
The Neuronal Transporter Gene SLC6A15 Confers Risk to Major Depression (Article)
Kohli, M.A. Lucae, S. Hoehn, D. Specht, M. Menke, A. Hennings, J. Heck, A. Wolf, C. Ising, M. Schreiber, S. Czisch, M. Müller, M.B. Saemann, P.G. Uhr, M. Bettecken, T. Becker, A. Schramm, J. Rietschel, M. Maier, W. Bradley, B. Ressler, K.J. Nöthen, M.M. Cichon, S. Schmidt, M.V. Craig, I.W. Breen, G. Lewis, C.M. Hofman, A. Tiemeier, H. Duijn, C.M. van Holsboer, F. Müller-Myhsok, B. Binder, E.B. Demirkan, A. Hek, K. Czamara, D. Alexander, M. Salyakina, D. Ripke, S.
2011-04-01
Large-scale association analysis identifies 13 new susceptibility loci for coronary artery disease (Article)
Schunkert, H. König, I.R. Absher, D. Peters, A. Peyvandi, F. Qu, L. Quyyumi, A.A. Rader, D.J. Rallidis, L.S. Rice, C. Rosendaal, F.R. Rubin, D. Salomaa, V. Aherrahrou, Z. Sampietro, M.L. Sandhu, M.S. Schadt, E.E. Scḧsignfer, A. Schillert, A. Schreiber, S. Schrezenmeir, J. Schwartz, S.M. Siscovick, D.S. Sivananthan, M. Allayee, H. Sivapalaratnam, S. Smith, A.V. Snoep, J.D. Soranzo, N. Spertus, J.A. Stark, K. Stirrups, K. Stoll, M. Tang, W.H.W. Tennstedt, S. Altshuler, D. Thorgeirsson, G. Thorleifsson, G. Tomaszewski, M. Uitterlinden, A.G. Rij, A.M. van Voight, B.F. Wareham, N.J. Wells, G. Wichmann, H.E. Wild, P.S. Anand, S.S. Willenborg, C. Witteman, J.C.M. Wright, B.J. Ye, S. Zeller, T. Ziegler, A. Cambien, F. Goodall, A.H. Cupples, L.A. Quertermous, T. Andersen, K. Mäsignrz, W. Hengstenberg, C. Blankenberg, S. Ouwehand, W.H. Hall, A.S. Kastelein, J.J.P. Deloukas, P. Thompson, J.R. Stefansson, K. Roberts, R. Anderson, J.L. Thorsteinsdottir, U. O'Donnell, C.J. McPherson, R. Erdmann, J. Samani, N.J. Ardissino, D. Ball, S.G. Balmforth, A.J. Kathiresan, S. Barnes, T.A. Becker, D.M. Berger, K. Bis, J.C. Boekholdt, S.M. Boerwinkle, E. Braund, P.S. Brown, M.J. Burnett, M.S. Buysschaert, I. Reilly, M.P. Carlquist, J.F. Chen, L. Cichon, S. Codd, V. Davies, R.W. Dedoussis, G.V. Dehghan, A. Demissie, S Devaney, J. Diemert, P. Assimes, T.L. Do, R. Doering, A. Eifert, S. Mokhtari, N.E.E. Ellis, S.G. Elosua, R. Engert, J.C. Epstein, S.E. Faire, U. de Fischer, M. Holm, H. Folsom, A.R. Freyer, J. Gigante, B. Girelli, D. Gretarsdottir, S. Gudnason, V. Gulcher, J.R. Halperin, E. Hammond, N. Hazen, S.L. Preuss, M. Hofman, A. Horne, B.D. Illig, T. Iribarren, C. Jones, G.T. Jukema, J.W. Kaiser, M.A. Kaplan, R. Khaw, K-T. Knowles, J.W. Stewart, A.F.R. Kolovou, G. Kong, A. Laaksonen, R. Lambrechts, D. Leander, K. Lettre, G. Li, X. Lieb, W. Loley, C. Lotery, A.J. Barbalic, M. Mannucci, P.M. Maouche, S. Martinelli, N. McKeown, P.P. Meisinger, C. Meitinger, T. Melander, O. Merlini, P.A. Mooser, V. Morgan, T. Gieger, C. Mühleisen, T.W. Muhlestein, J.B. Münzel, T. Musunuru, K. Nahrstaedt, J. Nelson, C.P. Nöthen, M.M. Olivieri, O. Patel, R.S. Patterson, C.C.
2011-02-01
Common variants in KCNN3 are associated with lone atrial fibrillation (Article)
Ellinor, P.T. Lunetta, K.L. Fox, E.R. Darbar, D. Smith, N.L. Schnabel, R. Soliman, E.Z. Rice, K. Wagoner, D.R. van Beckmann, B.M. Noord, C. van Wang, T.J. Glazer, N.L. Ehret, G.B. Rotter, J.I. Hazen, S.L. Steinbeck, G. Launer, L.J. Harris, T.B. Makino, S. Nelis, M. Milan, D.J. Perz, S. Pfeufer, A. Esko, T. Köttgen, A. Moebus, S. Newton-Cheh, C. Li, M. Möhlenkamp, S. Linda Kao, W.H. Vasan, R.S. Nöthen, M.M. MacRae, C.A. Alonso, A. Stricker, B.H.Ch. Hofman, A. Uitterlinden, A.G. Levy, D. Boerwinkle, E. Metspalu, A. Topol, E.J. Chakravarti, A. Gudnason, V. Psaty, B.M. Chung, M.K. Roden, D.M. Meitinger, T. Wichmann, H.E. Witteman, J.C.M. Barnard, J. Arking, D.E. Benjamin, E.J. Heckbert, S.R. Kääb, S. Sinner, M.F. Bakker, P.I.W. de Mueller, M. Lubitz, S.A.
2010-03-01
Genome-wide association study identifies two susceptibility loci for nonsyndromic cleft lip with or without cleft palate (Article)
Mangold, E. Ludwig, K.U. Steffens, M. Barth, S. Kluck, N. Paul, A. Becker, J. Lauster, C. Schmidt, G. Braumann, B. Scheer, M. Reich, R.H. Birnbaum, S. Hemprich, A. Pötzsch, B. Blaumeiser, B. Moebus, S. Krawczak, M. Schreiber, S. Meitinger, T. Wichmann, H.E. Steegers-Theunissen, R.P.M. Kramer, F.J. Baluardo, C. Cichon, S. Propping, P. Wienker, T.F. Knapp, M. Rubini, M. Mossey, P.A. Hoffmann, P. Nöthen, M.M. Ferrian, M. Herms, S. Reutter, H. Assis, N.A. de Chawa, T.A. Mattheisen, M.
2010-01-01
Genome-wide association study identifies 19p13.3 (UNC13A) and 9p21.2 as susceptibility loci for sporadic amyotrophic lateral sclerosis (Article)
Es, M.A. van Veldink, J.H. Kooi, A.J. van der Visser, M. de Dahlberg, C. Estrada Gil, J.K. Rivadeneira Ramirez, F. Hofman, A. Zwarts, M.J. Doormaal, P.T.C. van Rujescu, D. Strengman, E. Saris, C.G. Giegling, I. Muglia, P. Tomik, B. Slowik, A. Uitterlinden, A.G. Hendrich, C. Waibel, S. Meyer, T. Ludolph, A.C. Glass, J.D. Blauw, H.M. Purcell, S. Cichon, S. Nöthen, M.M. Wichmann, H.E. Schreiber, S. Vermeulen, S.H.H.M. Kiemeney, L.A.L.M. Wokke, J.H.J. Cronin, S. Mclaughlin, R.L. Vught, P.W. van Hardiman, O. Fumoto, K. Pasterkamp, R.J. Meininger, V. Melki, J. Leigh, P.N. Shaw, C.E. Landers, J.E. Al-Chalabi, A. Brown Jr, R.H. Birve, A. Robberecht, W. Andersen, P.M. Ophoff, R.A. Berg, L.H. van den Lemmens, R. Schelhaas, H.J. Groen, E.J. Huisman, M.H.B.
2009-10-01
Key susceptibility locus for nonsyndromic cleft lip with or without cleft palate on chromosome 8q24 (Article)
Birnbaum, S. Ludwig, K.U. Barth, S. Freudenberg, J. Lauster, C. Schmidt, G. Scheer, M. Braumann, B. Bergé, S.J. Reich, R.H. Schiefke, F. Hemprich, A. Reutter, H. Pötzsch, B. Moebus, S. Horsthemke, B. Kramer, F.J. Wienker, T.F. Mossey, P.A. Propping, P. Cichon, S. Hoffmann, P. Knapp, M. Herms, S. Nöthen, M.M. Mangold, E. Steffens, M. Rubini, M. Baluardo, C. Ferrian, M. Almeida de Assis, N. Alblas, M.A.
2009-04-01