Publikationen

2013

257 Andreassen OA, Djurovic S, Thompson WK, Schork AJ, Kendler KS, O'Donovan MC, Rujescu D, Werge T, van de Bunt M, Morris AP, McCarthy MI; International Consortium for Blood Pressure GWAS; Diabetes Genetics Replication and Meta-analysis Consortium; Psychiatric Genomics Consortium Schizophrenia Working Group, Roddey JC, McEvoy LK, Desikan RS, Dale AM. Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors.  Am J Hum Genet. 2013 Feb 7;92(2):197-209. doi: 10.1016/j.ajhg.2013.01.001.

256 Bigdeli TB, Fanous AH, Riley BP, Reimers M; The Schizophrenia Psychiatric Genome-Wide Association Study (GWAS) Consortium (Ripke S, Sanders AR, Kendler KS, Levinson DF, Sklar P, Holmans PA, Lin DY, Duan J, Ophoff RA, Andreassen OA, Scolnick E, Cichon S, St Clair D, Corvin A, Gurling H, Werge T, Rujescu D, Blackwood DH, Pato CN, Malhotra AK, Purcell S, Dudbridge F, Neale BM, Rossin L, Visscher PM, Posthuma D, Ruderfer DM, Fanous A, Stefansson H, Steinberg S, Mowry BJ, Golimbet V, De Hert M, Jönsson EG, Bitter I, Pietiläinen OP, Collier DA, Tosato S, Agartz I, Albus M, Alexander M, Amdur RL, Amin F, Bass N, Bergen SE, Black DW, Børglum AD, Brown MA, Bruggeman R, Buccola NG, Byerley WF, Cahn W, Cantor RM, Carr VJ, Catts SV, Choudhury K, Cloninger CR, Cormican P, Craddock N, Danoy PA, Datta S, de Haan L, Demontis D, Dikeos D, Djurovic S, Donnelly P, Donohoe G, Duong L, Dwyer S, Fink-Jensen A, Freedman R, Freimer NB, Friedl M, Georgieva L, Giegling I, Gill M, Glenthøj B, Godard S, Hamshere M, Hansen M, Hansen T, Hartmann AM, Henskens FA, Hougaard DM, Hultman CM, Ingason A, Jablensky AV, Jakobsen KD, Jay M, Jürgens G, Kahn RS, Keller MC, Kenis G, Kenny E, Kim Y, Kirov GK, Konnerth H, Konte B, Krabbendam L, Krasucki R, Lasseter VK, Laurent C, Lawrence J, Lencz T, Lerer FB, Liang KY, Lichtenstein P, Lieberman JA, Linszen DH, Lönnqvist J, Loughland CM, Maclean AW, Maher BS, Maier W, Mallet J, Malloy P, Mattheisen M, Mattingsdal M, McGhee KA, McGrath JJ, McIntosh A, McLean DE, McQuillin A, Melle I, Michie PT, Milanova V, Morris DW, Mors O, Mortensen PB, Moskvina V, Muglia P, Myin-Germeys I, Nertney DA, Nestadt G, Nielsen J, Nikolov I, Nordentoft M, Norton N, Nöthen MM, O'Dushlaine CT, Olincy A, Olsen L, O'Neill FA, Orntoft TF, Owen MJ, Pantelis C, Papadimitriou G, Pato MT, Peltonen L, Petursson H, Pickard B, Pimm J, Pulver AE, Puri V, Quested D, Quinn EM, Rasmussen HB, Réthelyi JM, Ribble R, Rietschel M, Riley BP, Ruggeri M, Schall U, Schulze TG, Schwab SG, Scott RJ, Shi J, Sigurdsson E, Silverman JM, Spencer CC, Stefansson K, Strange A, Strengman E, Stroup TS, Suvisaari J, Terenius L, Thirumalai S, Thygesen JH, Timm S, Toncheva D, van den Oord E, van Os J, van Winkel R, Veldink J, Walsh D, Wang AG, Wiersma D, Wildenauer DB, Williams HJ, Williams NM, Wormley B, Zammit S, Sullivan PF, O'Donovan MC, Daly MJ, Gejman PV), Chen X, Kendler KS, Bacanu SA.  On schizophrenia as a 'disease of humanity'.  Schizophr Res. 2013 Jan;143(1):223-4. doi: 10.1016/j.schres.2012.10.036.

255 Børglum AD, Demontis D, Grove J, Pallesen J, Hollegaard MV, Pedersen CB, Hedemand A,Mattheisen M; GROUP investigators, Uitterlinden A, Nyegaard M, Orntoft T, Wiuf C, Didriksen M, Nordentoft M, Nöthen MM, Rietschel M, Ophoff RA, Cichon S, Yolken RH, Hougaard DM, Mortensen PB, Mors O.  Genome-wide study of association and interaction with maternal cytomegalovirus infection suggests new schizophrenia loci.  Mol Psychiatry. 2013 Jan 29. doi: 10.1038/mp.2013.2.

254 Chen, D. T., Jiang, X., Akula, N., Shugart, Y. Y., Wendland, J. R., Steele, C. J. M., Kassem, L., et al.  Genome-wide association study meta-analysis of European and Asian-ancestry samples identifies three novel loci associated with bipolar disorder.  Molecular psychiatry, 18(2), 195?205. doi:10.1038/mp.2011.157.

253 ng D, Asherson P, Azevedo MH, Backlund L, Badner JA, Banaschewski T, Barchas JD, Barnes MR, Bass N, Bauer M, Bellivier F, Bergen S, Berrettini W, Bettecken T, Biederman J, Binder EB, Black DW, Blackwood DH, Bloss CS, Boehnke M, Boomsma DI, Breen G, Breuer R, Buccola NG, Bunner WE, Burmeister M, Buxbaum JD, Byerley WF, Caesar S, Cantor RM, Chakravarti A, Chambert K, Choudhury K, Cichon S, Cloninger CR, Collier DA, Cook E, Coon H, Corvin A, Coryell WH, Craig DW, Craig IW, Curtis D, Czamara D, Daly M, Datta S, Day R, De Geus EJ, Degenhardt F, Devlin B, Djurovic S, Doyle AE, Duan J, Dudbridge F, Edenberg HJ, Elkin A, Etain B, Farmer AE, Ferreira MA, Ferrier IN, Flickinger M, Foroud T, Frank J, Franke B, Fraser C, Freedman R, Freimer NB, Friedl M, Frisén L, Gejman PV, Georgieva L, Gershon ES, Giegling I, Gill M, Gordon SD, Gordon-Smith K, Green EK, Greenwood TA, Gross M, Grozeva D, Guan W, Gurling H, Gustafsson O, Hakonarson H, Hamilton SP, Hamshere ML, Hansen TF, Hartmann AM, Hautzinger M, Heath AC, Henders AK, Herms S, Hickie IB, Hipolito M, Hoefels S, Holmans PA, Holsboer F, Hottenga JJ, Hultman CM, Ingason A, Ising M, Jamain S, Jones EG, Jones L, Jones I, Jung-Ying T, Kahler A, Kandaswamy R, Keller MC, Kelsoe JR, Kennedy JL, Kenny E, Kent L, Kim Y, Kirov GK, Knowles JA, Kohli MA, Koller DL, Konte B, Korszun A, Krasucki R, Kuntsi J, Kwan P, Landén M, Langstrom N, Lathrop M, Lawrence J, Lawson WB, Leboyer M, Lencz T, Lesch KP, Lewis CM, Li J, Lichtenstein P, Lieberman JA, Lin D, Liu C, Lohoff FW, Loo SK, Lucae S, MacIntyre D, Madden PA, Magnusson P, Mahon PB, Maier W, Malhotra AK, Martin NG, Mattheisen M, Matthews K, Mattingsdal M, McCarroll S, McGhee KA, McGough JJ, McGrath PJ, McGuffin P, McInnis MG, McIntosh A, McKinney R, McLean AW, McMahon FJ, McQuillin A, Medeiros H, Medland SE, Meier S, Melle I, Meng F, Middeldorp CM, Middleton L, Milanova V, Mitchell PB, Montgomery GW, Moran J, Morken G, Morris DW, Moskvina V, Mowry BJ, Muglia P, Mühleisen TW, Muir WJ, Müller-Myhsok B, Myers RM, Nelson SF, Nievergelt CM, Nikolov I, Nimgaonkar V, Nolen WA, Nöthen MM, Nwulia EA, Nyholt DR, O'Donovan MC, O'Dushlaine C, Oades RD, Olincy A, Olsen L, Ophoff RA, Osby U, Óskarsson H, Owen MJ, Palotie A, Pato MT, Pato CN, Penninx BP, Pergadia ML, Petursson H, Pickard BS, Pimm J, Piven J, Porgeirsson P, Posthuma D, Potash JB, Propping P, Puri V, Quested D, Quinn EM, Rasmussen HB, Raychaudhuri S, Rehnström K, Reif A, Rice J, Rossin L, Rothenberger A, Rouleau G, Ruderfer D, Rujescu D, Sanders AR, Schalling M, Schatzberg AF, Scheftner WA, Schellenberg G, Schofield PR, Schork NJ, Schumacher J, Schwarz MM, Scolnick E, Scott LJ, Shi J, Shi J, Shilling PD, Shyn SI, Sigurdsson E, Silverman JM, Sklar P, Slager SL, Smalley SL, Smit JH, Smith EN, Sonuga-Barke E, St Clair D, State M, Stefansson K, Stefansson H, Steffens M, Steinberg S, Steinhausen HC, Strauss J, Strohmaier J, Stroup TS, Sutcliffe J, Szatmari P, Szelinger S, Thirumalai S, Thompson RC, Tozzi F, Treutlein J, Uhr M, van den Oord EJ, Van Grootheest G, Vieland V, Vincent JB, Visscher PM, Watson SJ, Weissman MM, Werge T, Wienker TF, Willemsen G, Williamson R, Witt SH, Wray NR, Wright A, Xu W, Young AH, Zammit S, Zandi PP, Zhang P, Zitman FG, Zöllner S, Craddock N, Kendler K.   Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis.  Lancet. 2013 Apr 20;381(9875):1371-9.

252 Degenhardt F, Priebe L, Strohmaier J, Herms S, Hoffmann P, Mattheisen M,Mössner R, Nenadic I, Sauer H, Rujescu D, Maier W, Schulze TG, Rietschel M,Nöthen MM, Cichon S.  No evidence for an involvement of copy number variation in ABCA13 in schizophrenia, bipolar disorder, or major depressive disorder.  Psychiatr Genet. 2013 Feb;23(1):45-6.

251 GENDEP Investigators; MARS Investigators; STAR*D Investigators; Collaborators: Uher R, Tansey KE, Rietschel M, Henigsberg N, Maier W, Mors O, Hauser J, Placentino A, Souery D, Farmer A, Aitchison KJ, Craig I, McGuffin P, Lewis CM, Ising M, Lucae S, Binder EB, Kloiber S, Holsboer F, Müller-Myhsok B, Ripke S, Hamilton SP, Soundy J, Laje G, McMahon FJ, Fava M, Rush A, Perlis RH.  Common genetic variation and antidepressant efficacy in major depressive disorder: a meta-analysis of three genome-wide pharmacogenetic studies.  Am J Psychiatry. 2013 Feb 1;170(2):207-17.

250 Guha S, Rees E, Darvasi A, Ivanov D, Ikeda M, Bergen SE, Magnusson PK,Cormican P, Morris D, Gill M, Cichon S, Rosenfeld JA, Lee A, Gregersen PK, Kane JM, Malhotra AK, Rietschel M, Nöthen MM, Degenhardt F, Priebe L, Breuer R, Strohmaier J, Ruderfer DM, Moran JL, Chambert KD, Sanders AR, Shi J, Kendler K, Riley B, O'Neill T, Walsh D, Malhotra D, Corvin A, Purcell S, Sklar P, Iwata N, Hultman CM, Sullivan PF, Sebat J, McCarthy S, Gejman PV, Levinson DF, Owen MJ, O'Donovan MC, Lencz T, Kirov G; Molecular Genetics of Schizophrenia Consortium; Wellcome Trust Case Control Consortium 2.  Implication of a rare deletion at distal 16p11.2 in schizophrenia. JAMA Psychiatry. 2013 Mar;70(3):253-60. doi: 10.1001/2013.jamapsychiatry.71.

249 Haenisch B, Herms S, Mattheisen M, Steffens M, Breuer R, Strohmaier J, Degenhardt F, Schmäl C, Lucae S, Maier W, Rietschel M, Nöthen MM, Cichon S.  Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder.  J Affect Disord. 2013 Apr 25;146(3):438-40.

248 Heinrich A, Lourdusamy A, Tzschoppe J, Vollstädt-Klein S, Bühler M, Steiner S, Bach C, Poustka L, Banaschewski T, Barker G, Büchel C, Conrod P, Garavan H, Gallinat J, Heinz A, Ittermann B, Loth E, Mann K, Martinot JL, Paus T, Pausova Z, Smolka M, Ströhle A, Struve M, Witt S, Flor H, Schumann G, Rietschel M, Nees F.  The risk variant in ODZ4 for bipolar disorder impacts on amygdala activation during reward processing.  Bipolar Disord. 2013 Apr 24. doi: 10.1111/bdi.12068.[Epub ahead of print]

247 Heinrich A, Nees F, Lourdusamy A, Tzschoppe J, Meier S, Vollstädt-Klein S,Fauth-Bühler M, Steiner S, Bach C, Poustka L, Banaschewski T, Barker GJ, Büchel C, Conrod PJ, Garavan H, Gallinat J, Heinz A, Ittermann B, Loth E, Mann K, Artiges E, Paus T, Lawrence C, Pausova Z, Smolka MN, Ströhle A, Struve M, Witt SH, Schumann G, Flor H, Rietschel M; The IMAGEN consortium.  From gene to brain to behavior: schizophrenia-associated variation in AMBRA1 alters impulsivity-related traits.  Eur J Neurosci. 2013 Apr 2. doi: 10.1111/ejn.12201. [Epub ahead of print]

246 Herold C, Mattheisen M, Lacour A, Vaitsiakhovich T, Angisch M, Drichel D, Becker T.  Integrated
genome-wide pathway association analysis with INTERSNP.  Hum Hered. 2012;73(2):63-72. doi: 10.1159/000336196.

245 Judy JT, Seifuddin F, Pirooznia M, Mahon PB; Bipolar Genome Study Consortium, Jancic D, Goes FS, Schulze T, Cichon S, Noethen M, Rietschel M, Depaulo JR Jr, Potash JB, Zandi PP.  Converging Evidence for Epistasis between ANK3 and Potassium Channel Gene KCNQ2 in Bipolar Disorder.  Front Genet. 2013 May 17;4:87.

244 Köttgen A, Albrecht E, Teumer A, Vitart V, Krumsiek J, Hundertmark C, Pistis G, Ruggiero D, O'Seaghdha CM, Haller T, Yang Q, Tanaka T, Johnson AD, Kutalik Z, Smith AV, Shi J, Struchalin M, Middelberg RP, Brown MJ, Gaffo AL, Pirastu N, Li G, Hayward C, Zemunik T, Huffman J, Yengo L, Zhao JH, Demirkan A, Feitosa MF, Liu X, Malerba G, Lopez LM, van der Harst P, Li X, Kleber ME, Hicks AA, Nolte IM, Johansson A, Murgia F, Wild SH, Bakker SJ, Peden JF, Dehghan A, Steri M, Tenesa A, Lagou V, Salo P, Mangino M, Rose LM, Lehtimäki T, Woodward OM, Okada Y, Tin A, Müller C, Oldmeadow C, Putku M, Czamara D, Kraft P, Frogheri L, Thun GA, Grotevendt A, Gislason GK, Harris TB, Launer LJ, McArdle P, Shuldiner AR, Boerwinkle E, Coresh J, Schmidt H, Schallert M, Martin NG, Montgomery GW, Kubo M, Nakamura Y, Tanaka T, Munroe PB, Samani NJ, Jacobs DR Jr, Liu K, D'Adamo P, Ulivi S, Rotter JI, Psaty BM, Vollenweider P, Waeber G, Campbell S, Devuyst O, Navarro P, Kolcic I, Hastie N, Balkau B, Froguel P, Esko T, Salumets A, Khaw KT, Langenberg C, Wareham NJ, Isaacs A, Kraja A, Zhang Q, Wild PS, Scott RJ, Holliday EG, Org E, Viigimaa M, Bandinelli S, Metter JE, Lupo A, Trabetti E, Sorice R, Döring A, Lattka E, Strauch K, Theis F, Waldenberger M, Wichmann HE, Davies G, Gow AJ, Bruinenberg M; LifeLines Cohort Study, Stolk RP, Kooner JS, Zhang W, Winkelmann BR, Boehm BO, Lucae S, Penninx BW, Smit JH, Curhan G, Mudgal P, Plenge RM, Portas L, Persico I, Kirin M, Wilson JF, Mateo Leach I, van Gilst WH, Goel A, Ongen H, Hofman A, Rivadeneira F, Uitterlinden AG, Imboden M, von Eckardstein A, Cucca F, Nagaraja R, Piras MG, Nauck M, Schurmann C, Budde K, Ernst F, Farrington SM, Theodoratou E, Prokopenko I, Stumvoll M, Jula A, Perola M, Salomaa V, Shin SY, Spector TD, Sala C, Ridker PM, Kähönen M, Viikari J, Hengstenberg C, Nelson CP; CARDIoGRAM Consortium; DIAGRAM Consortium; ICBP Consortium; MAGIC Consortium, Meschia JF, Nalls MA, Sharma P, Singleton AB, Kamatani N, Zeller T, Burnier M, Attia J, Laan M, Klopp N, Hillege HL, Kloiber S, Choi H, Pirastu M, Tore S, Probst-Hensch NM, Völzke H, Gudnason V, Parsa A, Schmidt R, Whitfield JB, Fornage M, Gasparini P, Siscovick DS, Pola?ek O, Campbell H, Rudan I, Bouatia-Naji N, Metspalu A, Loos RJ, van Duijn CM, Borecki IB, Ferrucci L, Gambaro G, Deary IJ, Wolffenbuttel BH, Chambers JC, März W, Pramstaller PP, Snieder H, Gyllensten U, Wright AF, Navis G, Watkins H, Witteman JC, Sanna S, Schipf S, Dunlop MG, Tönjes A, Ripatti S, Soranzo N, Toniolo D, Chasman DI, Raitakari O, Kao WH, Ciullo M, Fox CS, Caulfield M, Bochud M, Gieger C.  Genome-wide association analyses identify 18 new loci associated with serum urate concentrations.  Nat Genet. 2013 Feb;45(2):145-54.

243 Lavebratt C, Olsson S, Backlund L, Frisén L, Sellgren C, Priebe L, Nikamo P, Träskman-Bendz L, Cichon S, Vawter MP, Osby U, Engberg G, Landén M, Erhardt S, Schalling M.  The KMO allele encoding Arg<sup>452</sup> is associated with psychotic features in bipolar disorder type 1, and with increased CSF KYNA level and reduced KMO expression.  Mol Psychiatry. 2013 Mar 5. doi: 10.1038/mp.2013.11.

242 Lennertz L, Franke PE, Grabe HJ, Rampacher F, Schulze-Rauschenbach S, Guttenthaler V, Ruhrmann S, Pukrop R, Klosterkötter J, Falkai P, Maier W, Wagner M, Mössner R The functional coding variant Asn107Ile of the neuropeptide S receptor gene (NPSR1) influences age at onset of obsessive-compulsive disorder. Int J Neuropsychopharmacol im Druck.

241 Levinson DF, Shi J, Wang K, Oh S, Riley B, Pulver AE, Wildenauer DB, Laurent C, Mowry BJ, Gejman PV, Owen MJ, Kendler KS, Nestadt G, Schwab SG, Mallet J, Nertney D, Sanders AR, Williams NM, Wormley B, Lasseter VK, Albus M, Godard-Bauché S, Alexander M, Duan J, O'Donovan MC, Walsh D, O'Neill A, Papadimitriou GN, Dikeos D, Maier W, Lerer B, Campion D, Cohen D, Jay M, Fanous A, Eichhammer P, Silverman JM, Norton N, Zhang N, Hakonarson H, Gao C, Citri A, Hansen M, Ripke S; Schizophrenia Psychiatric GWAS Consortium (Ripke S, Sanders AR, Kendler KS, Levinson DF, Sklar P, Holmans PA, Lin DY, Duan J, Ophoff RA, Andreassen OA, Scolnick E, Cichon S, St Clair D, Corvin A, Gurling H, Werge T, Rujescu D, Blackwood DH, Pato CN, Malhotra AK, Purcell S, Dudbridge F, Neale BM, Rossin L, Visscher PM, Posthuma D, Ruderfer DM, Fanous A, Stefansson H, Steinberg S, Mowry BJ, Golimbet V, De Hert M, Jönsson EG, Bitter I, Pietiläinen OP, Collier DA, Tosato S, Agartz I, Albus M, Alexander M, Amdur RL, Amin F, Bass N, Bergen SE, Black DW, Børglum AD, Brown MA, Bruggeman R, Buccola NG, Byerley WF, Cahn W, Cantor RM, Carr VJ, Catts SV, Choudhury K, Cloninger CR, Cormican P, Craddock N, Danoy PA, Datta S, de Haan L, Demontis D, Dikeos D, Djurovic S, Donnelly P, Donohoe G, Duong L, Dwyer S, Fink-Jensen A, Freedman R, Freimer NB, Friedl M, Georgieva L, Giegling I, Gill M, Glenthøj B, Godard S, Hamshere M, Hansen M, Hansen T, Hartmann AM, Henskens FA, Hougaard DM, Hultman CM, Ingason A, Jablensky AV, Jakobsen KD, Jay M, Jürgens G, Kahn RS, Keller MC, Kenis G, Kenny E, Kim Y, Kirov GK, Konnerth H, Konte B, Krabbendam L, Krasucki R, Lasseter VK, Laurent C, Lawrence J, Lencz T, Lerer FB, Liang KY, Lichtenstein P, Lieberman JA, Linszen DH, Lönnqvist J, Loughland CM, Maclean AW, Maher BS, Maier W, Mallet J, Malloy P, Mattheisen M, Mattingsdal M, McGhee KA, McGrath JJ, McIntosh A, McLean DE, McQuillin A, Melle I, Michie PT, Milanova V, Morris DW, Mors O, Mortensen PB, Moskvina V, Muglia P, Myin-Germeys I, Nertney DA, Nestadt G, Nielsen J, Nikolov I, Nordentoft M, Norton N, Nöthen MM, O'Dushlaine CT, Olincy A, Olsen L, O'Neill FA, Orntoft TF, Owen MJ, Pantelis C, Papadimitriou G, Pato MT, Peltonen L, Petursson H, Pickard B, Pimm J, Pulver AE, Puri V, Quested D, Quinn EM, Rasmussen HB, Réthelyi JM, Ribble R, Rietschel M, Riley BP, Ruggeri M, Schall U, Schulze TG, Schwab SG, Scott RJ, Shi J, Sigurdsson E, Silverman JM, Spencer CC, Stefansson K, Strange A, Strengman E, Stroup TS, Suvisaari J, Terenius L, Thirumalai S, Thygesen JH, Timm S, Toncheva D, van den Oord E, van Os J, van Winkel R, Veldink J, Walsh D, Wang AG, Wiersma D, Wildenauer DB, Williams HJ, Williams NM, Wormley B, Zammit S, Sullivan PF, O'Donovan MC, Daly MJ, Gejman PV), Dudbridge F, Holmans PA.  Genome-wide association study of multiplex schizophrenia pedigrees.  Am J Psychiatry 2012;169:963-973. Doi: 10.1176/appi.ajp.2012.11091423.

240 Li M, Luo XJ, Rietschel M, Lewis CM, Mattheisen M, Müller-Myhsok B, Jamain S, Leboyer M, Landén M, Thompson PM, Cichon S, Nöthen MM, Schulze TG, Sullivan PF, Bergen SE, Donohoe G, Morris DW, Hargreaves A, Gill M, Corvin A, Hultman C, Toga AW, Shi L, Lin Q, Shi H, Gan L, Meyer-Lindenberg A, Czamara D, Henry C, Etain B, Bis JC, Ikram MA, Fornage M, Debette S, Launer LJ, Seshadri S, Erk S, Walter H, Heinz A, Bellivier F, Stein JL, Medland SE, Arias Vasquez A, Hibar DP, Franke B,  Martin NG, Wright MJ; MooDS Bipolar Consortium, Strohmaier J, Breuer R, Meier S, Mühleisen TW, Degenhardt FA, Hoffmann P, Herms S, Schwarz M, Vedder H, Kammerer-Ciernioch J, Reif A, Sasse J, Bauer M, Zwick S, Hautzinger M, Wright A, Mitchell PB, Fullerton JM, Schofield PR, Montgomery GW, Martin NG, Czerski PM, Hauser J, Schumacher J, Maier W, Propping P; The Swedish Bipolar Study Group, Backlund L, Frisén L, Lavebratt C, Schalling M, Osby U; The Alzheimer?s Disease Neuroimaging Initiative; ENIGMA Consortium; CHARGE Consortium, Su B.  Allelic differences between Europeans and Chinese for CREB1 SNPs and their implications in gene expression regulation, hippocampal structure and function, and bipolar disorder susceptibility.  Mol Psychiatry. 2013 Apr 9. doi: 10.1038/mp.2013.37. [Epub ahead of print].

239 LLudwig, K. U., P. Samann, M. Alexander, J. Becker, J. Bruder, K. Moll, D. Spieler, M. Czisch, A. Warnke, S. J. Docherty, O. S. Davis, R. Plomin, M. M. Nothen, K. Landerl, B. Muller-Myhsok, P. Hoffmann, J. Schumacher, G. Schulte-Korne, and D. Czamara.  A common variant in Myosin-18B contributes to mathematical abilities in children with dyslexia and intraparietal sulcus variability in adults.  Transl Psychiatry. 2013 Feb 19;3:e229. doi: 10.1038/tp.2012.148..

238 Major Depressive Disorder Working Group of the Psychiatric GWAS Consortium, Ripke S, Wray NR, Lewis CM, Hamilton SP, Weissman MM, Breen G, Byrne EM, Blackwood DH, Boomsma DI, Cichon S, Heath AC, Holsboer F, Lucae S, Madden PA, Martin NG, McGuffin P, Muglia P, Noethen MM, Penninx BP, Pergadia ML, Potash JB, Rietschel M, Lin D, Müller-Myhsok B, Shi J, Steinberg S, Grabe HJ, Lichtenstein P, Magnusson P, Perlis RH, Preisig M, Smoller JW, Stefansson K, Uher R, Kutalik Z, Tansey KE, Teumer A, Viktorin A, Barnes MR, Bettecken T, Binder EB, Breuer R, Castro VM, Churchill SE, Coryell WH, Craddock N, Craig IW, Czamara D, De Geus EJ, Degenhardt F, Farmer AE, Fava M, Frank J, Gainer VS, Gallagher PJ, Gordon SD, Goryachev S, Gross M, Guipponi M, Henders AK, Herms S, Hickie IB, Hoefels S, Hoogendijk W, Hottenga JJ, Iosifescu DV, Ising M, Jones I, Jones L, Jung-Ying T, Knowles JA, Kohane IS, Kohli MA, Korszun A, Landen M, Lawson WB, Lewis G, Macintyre D, Maier W, Mattheisen M, McGrath PJ, McIntosh A, McLean A, Middeldorp CM, Middleton L, Montgomery GM, Murphy SN, Nauck M, Nolen WA, Nyholt DR, O'Donovan M, Oskarsson H, Pedersen N, Scheftner WA, Schulz A, Schulze TG, Shyn SI, Sigur.  A mega-analysis of genome-wide association studies for major depressive disorder.  Mol Psychiatry. 2013 Apr;18(4):497-511.

237 Mattheisen M, Mühleisen TW, Strohmaier J, Treutlein J, Nenadic I, Alblas M, Meier S, Degenhardt F, Herms S, Hoffmann P, Witt SH, Giegling I, Sauer H, Schulze TG, Rujescu D, Nöthen MM, Rietschel M, Cichon S.  Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia.  Schizophr Res. 2012 Nov;141(2-3):262-5. doi: 10.1016/j.schres.2012.08.027.

236 Meier S, Strohmaier J, Breuer R, Mattheisen M, Degenhardt F, Mühleisen TW, Schulze TG, Nöthen MM, Cichon S, Rietschel M, Wüst S.  Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder.  Int J Neuropsychopharmacol. 2013 Apr;16(3):549-56. doi: 10.1017/S1461145712000697.

235 Menke A, Klengel T, Rubel J, Brückl T, Pfister H, Lucae S, Uhr M, Holsboer F, Binder EB.  Genetic variation in FKBP5 associated with the extent of stress hormone dysregulation in major depression.  Genes Brain Behav. 2013 Apr;12(3):289-96.

234 Mühleisen TW, Mattheisen M, Strohmaier J, Degenhardt F, Priebe L, Schultz CC, Breuer R, Meier S, Hoffmann P; GROUP Investigators, Rivandeneira F, Hofman A, Uitterlinden AG, Moebus S, Gieger C, Emeny R, Ladwig KH, Wichmann HE, Schwarz M, Kammerer-Ciernioch J, Schlösser RG, Nenadic I, Sauer H, Mössner R, Maier W, Rujescu D, Lange C, Ophoff RA, Schulze TG, Rietschel M, Nöthen MM, Cichon S.  Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder.  Schizophr Res. 2012 Jun;138(1):69-73. doi: 10.1016/j.schres.2012.03.007.

233 Otte DM, Barcena de Arellano ML, Bilkei-Gorzo A, Albayram O, Imbeault S, Jeung H, Alferink J, Zimmer A. Effects of chronic D-serine elevation on animal models of depression and anxiety-related behavior PLoS One. 2013 Jun 21;8(6):e67131. Print 2013.

232 Paulus FM, Bedenbender J, Krach S, Pyka M, Krug A, Sommer J, Mette M, Nöthen MM, Witt SH, Rietschel M, Kircher T, Jansen A.  Association of rs1006737 in CACNA1C with alterations in prefrontal activation and fronto-hippocampal connectivity.  Hum Brain Mapp. 2013 Feb 13. doi: 10.1002/hbm.22244. [Epub ahead of print].

231 Pernhorst K, van Loo KM, von Lehe M, Priebe L, Cichon S, Herms S, Hoffmann P, Helmstaedter C, Sander T, Schoch S, Becker AJ.  Rs6295 promoter variants of the serotonin type 1A receptor are differentially activated by c-Jun in vitro and correlate to transcript levels in human epileptic brain tissue.  Brain Res. 2013 Mar 7;1499:136-44. doi: 10.1016/j.brainres.2012.12.045.                                                                                                                                                                                                                                                                                                                                                                                                                                                                                
230 Petrakis S, Schaefer MH, Wanker EE, Andrade-Navarro MA Aggregation of polyQ-extended proteins is promoted by interaction with their natural coiled-coil partners.  BioEssays 35 (6): 503-507.

229 SSchork AJ, Thompson WK, Pham P, Torkamani A, Roddey JC, Sullivan PF, Kelsoe JR, O'Donovan MC, Furberg H; Tobacco and Genetics Consortium; Bipolar Disorder Psychiatric Genomics Consortium; Schizophrenia Psychiatric Genomics Consortium, Schork NJ, Andreassen OA, Dale AM; Collaborators: Absher D, Agudo A, Almgren P, Ardissino D, Assimes TL, Bandinelli S, Barzan L, Bencko V, Benhamou S, Benjamin EJ, Bernardinelli L, Bis J, Boehnke M, Boerwinkle E, Boomsma DI, Brennan P, Canova C, Castellsagué X, Chanock S, Chasman D, Conway DI, Dackor J, de Geus EJ, Duan J, Elosua R, Everett B, Fabianova E, Ferrucci L, Foretova L, Fortmann SP, Franceschini N, Frayling T, Furberg C, Gejman PV, Groop L, Gu F, Guralnik J, Hankinson SE, Haritunians T, Healy C, Hofman A, Holcátová I, Hunter DJ, Hwang SJ, Ioannidis JP, Iribarren C, Jackson AU, Janout V, Kaprio J, Kim Y, Kjaerheim K, Knowles JW, Kraft P, Ladenvall C, Lagiou P, Lanthrop M, Lerman C, Levinson DF, Levy D, Li MD, Lin DY, Lips EH, Lissowska J, Lowry R, Lucas G, Macfarlane TV, Maes H, Mannucci PM, Mates D, Mauri F, McGovern JA, McKay JD, McKnight B, Melander O, Merlini PA, Milaneschi Y, Mohlke KL, O'Donnell CJ, Pare G, Penninx BW, Perry J, Posthuma D, Preis SR, Psaty B, Quertermous T, Ramachandran VS, Richiardi L, Ridker P, Rose J, Rudnai P, Salomaa V, Sanders AR, Schwartz SM, Shi J, Smit JH, Stringham HM, Szeszenia-Dabrowska N, Tanaka T, Taylor K, Thacker E, Thornton L, Tiemeier H, Tuomilehto J, Uitterlinden AG, van Duijn CM, Vink JM, Vogelzangs N, Voight BF, Walter S, Willemsen G, Zaridze D, Znaor A, Absher D, Akil H, Anjorin A, Backlund L, Badner JA, Barchas JD, Barrett TB, Bass N, Bauer M, Bellivier F, Bergen SE, Berrettini W, Blackwood D, Bloss CS, Boehnke M, Breen G, Breuer R, Bunner WE, Burmeister M, Byerley W, Caesar S, Chambert K, Cichon S, St Clair D, Collier DA, Corvin A, Coryell WH, Craddock N, Craig DW, Daly M, Day R, Degenhardt F, Djurovic S, Dudbridge F, Edenberg HJ, Elkin A, Etain B, Farmer AE, Ferreira MA, Ferrier I, Flickinger M, Foroud T, Frank J, Fraser C, Frisén L, Gershon ES, Gill M, Gordon-Smith K, Green EK, Greenwood TA, Grozeva D, Guan W, Gurling H, Gustafsson Ó, Hamshere ML, Hautzinger M, Herms S, Hipolito M, Holmans PA, Hultman CM, Jamain S, Jones EG, Jones I, Jones L, Kandaswamy R, Kennedy JL, Kirov GK, Koller DL, Kwan P, Landén M, Langstrom N, Lathrop M, Lawrence J, Lawson WB, Leboyer M, Lee PH, Li J, Lichtenstein P, Lin D, Liu C, Lohoff FW, Lucae S, Mahon PB, Maier W, Martin NG, Mattheisen M, Matthews K, Mattingsdal M, McGhee KA, McGuffin P, McInnis MG, McIntosh A, McKinney R, McLean AW, McMahon FJ, McQuillin A, Meier S, Melle I, Meng F, Mitchell PB, Montgomery GW, Moran J, Morken G, Morris DW, Moskvina V, Muglia P, Mühleisen TW, Muir WJ, Müller-Myhsok B, Myers RM, Nievergelt CM, Nikolov I, Nimgaonkar V, Nöthen MM, Nurnberger JI, Nwulia EA, O'Dushlaine C, Osby U, Óskarsson H, Owen MJ, Petursson H, Pickard BS, Porgeirsson P, Potash JB, Propping P, Purcell SM, Quinn E, Raychaudhuri S, Rice J, Rietschel M, Ruderfer D, Schalling M, Schatzberg AF, Scheftner WA, Schofield PR, Schulze TG, Schumacher J, Schwarz MM, Scolnick E, Scott LJ, Shilling PD, Sigurdsson E, Sklar P, Smith EN, Stefansson H, Stefansson K, Steffens M, Steinberg S, Strauss J, Strohmaier J, Szelinger S, Thompson RC, Tozzi F, Treutlein J, Vincent JB, Watson SJ, Wienker TF, Williamson R, Witt SH, Wright A, Xu W, Young AH, Zandi PP, Zhang P, Zöllner S, Agartz I, Albus M, Alexander M, Amdur RL, Amin F, Bass N, Bitter I, Black DW, Børglum AD, Brown MA, Bruggeman R, Buccola NG, Byerley WF, Cahn W, Cantor RM, Carr VJ, Catts SV, Choudhury K, Cloninger C, Cormican P, Danoy PA, Datta S, DeHert M, Demontis D, Dikeos D, Donnelly P, Donohoe G, Duan J, Duong L, Dwyer S, Fanous A, Fink-Jensen A, Freedman R, Freimer NB, Friedl M, Gejman PV, Georgieva L, Giegling I, Glenthøj B, Godard S, Golimbet V, de Haan L, Hansen M, Hansen T, Hartmann AM, Henskens FA, Hougaard DM, Ingason A, Jablensky AV, Jakobsen KD, Jay M, Jönsson EG, Jürgens G, Kahn RS, Keller MC, Kendler KS, Kenis G, Kenny E, Kim Y, Konnerth H, Konte B, Krabbendam L, Krasucki R, Lasseter VK, Laurent C, Lencz T, Lerer F, Levinson DF, Liang KY, Lieberman JA, Linszen DH, Lönnqvist J, Loughland CM, Maclean AW, Maher BS, Malhotra AK, Mallet J, Malloy P, McGrath JJ, McLean DE, Michie PT, Milanova V, Mors O, Mortensen PB, Mowry BJ, Myin-Germeys I, Neale B, Nertney DA, Nestadt G, Nielsen J, Nordentoft M, Norton N, O'Neill F, Olincy A, Olsen L, Ophoff RA, Ørntoft TF, van Os J, Pantelis C, Papadimitriou G, Pato CN, Pato MT, Peltonen L, Pickard B, Pietiläinen OP, Pimm J, Posthuma D, Pulver AE, Puri V, Quested D, Rasmussen HB, Réthelyi JM, Ribble R, Riley BP, Rossin L, Ruggeri M, Rujescu D, Sanders AR, Schall U, Schwab SG, Scolnick E, Scott RJ, Shi J, Silverman JM, Spencer CC, Strange A, Strengman E, Stroup T, Suvisaari J, Terenius L, Thirumalai S, Timm S, Toncheva D, Tosato S, van den Oord EJ, Veldink J, Visscher PM, Walsh D, Wang AG, Werge T, Wiersma D, Wildenauer DB, Williams HJ, Williams NM, van Winkel R, Wormley B, Zammit S.  All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs.  PLoS Genet. 2013 Apr;9(4):e1003449.

228 Suter B, Fontaine JF, Yildirimman R, Rasko T, Schaefer MH, Rasche A, Porras P, Vazquez-Alvarez BM, Russ J, Rau K, Foulle R, Zenkner M, Saar K, Herwig R, Andrade-Navarro MA, Wanker EE.  Development and application of a DNA microarray-based yeast two-hybrid system.  Nucleic Acids Research 41 (3): 1496-507.

227 Terwisscha van Scheltinga AF, Bakker SC, van Haren NE, Derks EM,Buizer-Voskamp JE, Boos HB, Cahn W, Hulshoff Pol HE, Ripke S, Ophoff RA, Kahn RS; Psychiatric Genome-wide Association Study Consortium; Collaborators: Ripke S, Sanders AR, Kendler KS, Levinson DF, Sklar P, Holmans PA, Lin DY, Duan J, Ophoff RA, Andreassen OA, Scolnick E, Cichon S, St Clair D, Corvin A, Gurling H, Werge T, Rujescu D, Blackwood DH, Pato CN, Malhotra AK, Purcell S, Dudbridge F, Neale BM, Rossin L, Visscher PM, Posthuma D, Ruderfer DM, Fanous A, Stefansson H, Steinberg S, Mowry BJ, Golimbet V, De Hert M, Jonsson EG, Bitter I, Pietiläinen OP, Collier DA, Tosato S, Agartz I, Albus M, Alexander M, Amdur RL, Amin F, Bass N, Bergen SE, Black DW, Børglum AD, Brown MA, Bruggeman R, Buccola NG, Byerley WF, Cahn W, Cantor RM, Carr VJ, Catts SV, Choudhury K, Cloninger C, Cormican P, Craddock N, Danoy PA, Datta S, de Haan L, Demontis D, Dikeos D, Djurovic S, Donnelly P, Donohoe G, Duong L, Dwyer S, Fink-Jensen A, Freedman R, Freimer NB, Friedl M, Georgieva L, Giegline I, Gill M, Glenthøj B, Godard S, Hamshere M, Hansen M, Hansen T, Hartmann AM, Henskens FA, Hougaard DM, Hultman CM, Ingason A, Jablensky AV, Jakobsen KD, Jay M, Jürgens G, Kahn RS, Keller MC, Kenis G, Kenny E, Kim Y, Kirov GK, Konnerth H, Konte B, Krabbendam L, Krasucki R, Lasseter VK, Laurent C, Lawrence J, Lencz T, Lerer F, Liang KY, Lichtenstein P, Lieberman JA, Linszen DH, Lönnqvist J, Loughland CM, Maclean AW, Maher BS, Maier W, Mallet J, Malloy P, Mattheisen M, Mattingsdal M, McGhee KA, McGrath JJ, McIntosh A, McLean DE, McQuillin A, Melle I, Michie PT, Milanova V, Morris DW, Mors O, Mortensen PB, Moskvina V, Muglia P, Myin-Germeys I, Nertney DA, Nestadt G, Nielsen J, Nikolov I, Nordentoft M, Norton N, Nöthen MM, O'Dushlaine C, Olincy A, Olsen L, O'Neill F, Ørntoft TF, Owen MJ, Pantelis C, Papadimitriou G, Pato MT, Peltonen L, Petursson H, Pickard B, Pimm J, Pulver AE, Puri V, Quested D, Quinn EM, Rasmussen HB, Réthelyi JM, Ribble R, Rietschel M, Riley BP, Ruggeri M, Schall U, Schulze TG, Schwab SG, Scott RJ, Shi J, Sigurdsson E, Silverman JM, Spencer CC, Stefansson K, Strange A, Strengman E, Stroup TS, Suvisaari J, Terenius L, Thirumalai S, Thygesen JH, Timm S, Toncheva D, van den Oord E, van Os J, van Winkel R, Veldink J, Walsh D, Wang AG, Wiersma D, Wildenauer DB, Williams HJ, Williams NM, Wormley B, Zammit S, Sullivan PF, O'Donovan MC, Daly MJ, Gejman PV.   Genetic schizophrenia risk variants jointly modulate total brain and white matter volume.  Biol Psychiatry. 2013 Mar 15;73(6):525-31.

226 Wang X.D., Su Y.-A., Wagner K.V., Avrabos C., Scharf S.H., Hartmann J., Wolf M., Liebl C., Kuehne C., Wurst W., Holsboer F., Eder M., Deussing J.M., Mueller M.B., Schmidt M.V.  Nectin-3 Links CRHR1 Signaling to Stress-Induced Memory Deficits and Spine Loss.  Nat Neurosci. 2013 Jun;16(6):706-13. doi: 10.1038/nn.3395. Epub 2013 May 5.

2012

225 Adhikari K, AlChawa T, Ludwig K, Mangold E, Laird N, Lange C. Is it rare or common?  Genet Epidemiol. 2012 Jul;36(5):419-29. doi: 10.1002/gepi.21637.
 
224 Bis JC. et al., Enhancing Neuro Imaging Genetics through Meta-Analysis (ENIGMA) Consortium (2012).  Common variants at 12q14 and 12q24 are associated with hippocampal volume.  Nat Genetics, 44 (5): 545-551.                                                         
 
223 Breu J, Touma C, Hölter SM, Knapman A, Wurst W, Deussing JM.  Urocortin 2 modulates aspects of social behaviour in mice.  Behav Brain Res. 2012 Aug 1;233(2):331-6.

222 Carrera N, Arrojo M, Sanjuán J, Ramos-Rios R, Paz E, Suárez-Rama JJ, Páramo M, Agra S, Brenlla J, Martinez S, Rivero O, Collier DA, Palotie A, Cichon S, Nöthen MM, Rietschel M, Rujescu D, Stefansson H, Steinberg S, Sigurdsson E, Clair DS, Tosato S, Werge T, Stefansson K, González JC, Valero J, Gutiérrez-Zotes A, Labad A, Martorell L, Vilella E, Carracedo A, Costas J Association study of nonsynonymous single nucleotide polymorphisms in schizophrenia.  Biol Psychiatry 71:169-177. doi.org/10.1016/j.biopsych.2011.09.032.

221 Christoforou A, Dondrup M, Mattingsdal M, Mattheisen M, Giddaluru S, Nöthen MM, Rietschel M, Cichon S, Djurovic S, Andreassen OA, Jonassen I, Steen VM, Puntervoll P, Le Hellard S. Linkage-Disequilibrium-Based Binning Affects the Interpretation of GWASs. Am J Hum Genet. 2012 Apr 6;90(4):727-33. Epub 2012 Mar 22.

220 Collins AL, Kim Y, Szatkiewicz JP, Bloom RJ, Hilliard CE, Quackenbush CR, Meier S, Rivas F, Mayoral F, Cichon S, Nöthen MM, Rietschel M, Sullivan PF.  Identifying bipolar disorder susceptibility loci in a densely affected pedigree.  Mol Psychiatry. 2012 Dec 18. doi: 10.1038/mp.2012.176.

219 de Jong S, van Eijk KR, Zeegers DW, Strengman E, Janson E, Veldink JH, van den Berg LH, Cahn W, Kahn RS, Boks MP, Ophoff RA; The PGC Schizophrenia (GWAS) Consortium: St Clair D, Cichon S, Rietschel M, Nöthen MM, Maier W, Schulze TG, Mattheisen M, Kirov GK, O'Donovan MC, Holmans PA, Georgieva L, Nikolov I, Williams HJ, Toncheva D, Milanova V, Owen MJ, O'Donovan MC, Craddock N, Holmans PA, Hamshere M, Williams HJ, Moskvina V, Dwyer S, Georgieva L, Zammit S, Owen MJ, Kirov GK, Sullivan PF, Lin DY, van den Oord E, Kim Y, Stroup T, Lieberman JA, Hansen T, Ingason A, Olsen L, Schmock H, Skjødt C, Thygesen JH, Rosengren A, Werge T, Morris DW, O'Dushlaine CT, Kenny E, Quinn EM, Gill M, Corvin A, Blackwood DH, McGhee KA, Pickard B, Malloy P, Maclean AW, McIntosh A, Gejman PV, Sanders AR, Duan J, Levinson DF, Shi J, Buccola NG, Mowry BJ, Freedman R, Amin F, Black DW, Silverman JM, Byerley WF, Cloninger C, Giegling I, Hartmann AM, Konnerth H, Friedl M, Konte B, Muglia P, Rujescu D, Pato MT, Pato CN, Fanous A, Hultman CM, Lichtenstein P, Bergen SE, Purcell S, Scolnick E, Sklar P, Sullivan PF, Djurovic S, Mattingsdal M, Agartz I, Melle I, Andreassen OA, Ophoff RA, Cantor RM, Freimer NB, Kahn RS, Linszen DH, van Os J, Wiersma D, Bruggeman R, Cahn W, de Haan L, Krabbendam L, Myin-Germeys I, Strengman E, McQuillin A, Choudhury K, Datta S, Pimm J, Thirumalai S, Puri V, Krasucki R, Lawrence J, Quested D, Bass N, Gurling H, Malhotra AK, Lencz T.  Expression QTL analysis of top loci from GWAS meta-analysis highlights additional schizophrenia candidate genes.  Eur J Hum Genet. 2012 Sep;20(9):1004-8. doi: 10.1038/ejhg.2012.38.
 
218 Dedic N, Touma C, Romanowski CP, Schieven M, Kühne C, Ableitner M, Lu A, Holsboer F, Wurst W, Kimura M, Deussing JM. Assessing Behavioural Effects of Chronic HPA Axis Activation Using Conditional CRH-Overexpressing Mice. Cell Mol Neurobiol.  2012 Jul;32(5):815-28. Epub 2011 Dec 25.

217 Degenhardt F, Priebe L, Herms S, Mattheisen M, Mühleisen TW, Meier S, Moebus S, Strohmaier J, Groß M, Breuer R, Lange C, Hoffmann P, Meyer-Lindenberg A, Heinz A, Walter H, Lucae S, Wolf C, Müller-Myhsok B, Holsboer F, Maier W, Rietschel M, Nöthen MM, Cichon S. Association between copy number variants in 16p11.2 and major depressive disorder in a German case-control sample. Am J Med Genet B Neuropsychiatr Genet. 2012 Apr;159B(3):263-73. doi: 10.1002/ajmg.b.32034. Epub 2012 Feb 17.

216 Derks EM, Vorstman JA, Ripke S, Kahn RS; Schizophrenia Psychiatric Genomic Consortium (Craddock N, Holmans PA, Hamshere M, Williams HJ, Moskvina V, Dwyer S, Georgieva L, Zammit S, Owen MJ, Sullivan PF, Lin DY, van den Oord E, Kim Y, Stroup TS, Lieberman JA, St Clair D, Kirov GK, O'Donovan MC, Holmans PA, Georgieva L, Nikolov I, Williams HJ, Toncheva D, Milanova V, Owen MJ, Morris DW, O'Dushlaine CT, Kenny E, Quinn EM, Gill M, Corvin A, Blackwood DH, McGhee KA, Pickard B, Malloy P, Maclean AW, McIntosh A, McQuillin A, Choudhury K, Datta S, Pimm J, Thirumalai S, Puri V, Krasucki R, Lawrence J, Quested D, Bass N, Gurling H, Pato MT, Pato CN, Fanous A, Hultman CM, Lichtenstein P, Bergen SE, Purcell S, Scolnick E, Sklar P, Sullivan PF, Gejman PV, Sanders AR, Duan J, Levinson DF, Shi J, Buccola NG, Mowry BJ, Freedman R, Amin F, Black DW, Black DW, Silverman JM, Byerley WF, Cloninger C, Cichon S, Rietschel M, Nöthen MM, Maier W, Schulze TG, Mattheisen M, Hansen T, Olsen L, Jakobsen KD, Schmock H, Skjødt C, Rosengren A, Høffding LK, Thygersen JH, Vangkilde A, Werge T, Giegling I, Hartmann AM, Konnerth H, Friedl M, Konte B, Muglia P, Rujescu D, Djurovic S, Mattingsdal M, Agartz I, Melle I, Andreassen OA, Ophoff RA, Cantor RM, Freimer NB, Kahn RS, Linszen DH, van Os J, Wiersma D, Bruggeman R, Cahn W, de Haan L, Krabbendam L, Myin-Germeys I, Strengman E, Malhotra AK, Lencz T, Ripke S, Daly MJ, Holmans PA, Lin DY, Purcell S, Dudbridge F, Neale BM, Rossin L, Visscher PM, Posthuma D, Ruderfer DM, Kendler KS, Fanous A, O'Donovan MC), Ophoff RA.  Investigation of the genetic association between quantitative measures of psychosis and schizophrenia: a polygenic risk score analysis.  PLoS One. 2012;7(6):e37852. doi: 10.1371/journal.pone.0037852.                                                                    
 
215 Di Benedetto B, Kühn R, Nothdurfter C, Rein T, Wurst W, Rupprecht R. N-desalkylquetiapine activates ERK1/2 to induce GDNF release in C6 glioma cells: a putative cellular mechanism for quetiapine as antidepressant. Neuropharmacology. 2012 Jan;62(1):209-16. Epub 2011 Jul 13.

214 Ditzen C, Tang N, Jastorff AM, Teplytska L, Yassouridis A, Maccarrone G, Uhr M, Bronisch T, Miller CA, Holsboer F, Turck CW.  Cerebrospinal fluid biomarkers for major depression confirm relevance of associated pathophysiology.  Neuropsychopharmacology 2012 Mar, 37(4):1013-1025. doi: 10.1038/npp.2011.285.

213 Ersland KM, Christoforou A, Stansberg C, Espeseth T, Mattheisen M, Mattingsdal M, Hardarson GA, Hansen T, Fernandes CP, Giddaluru S, Breuer R, Strohmaier J, Djurovic S, Nöthen MM, Rietschel M, Lundervold AJ, Werge T, Cichon S, Andreassen OA, Reinvang I, Steen VM, LeHellard S.   Gene-based analysis of regionally enriched cortical genes in GWAS data sets of cognitive traits and psychiatric disorders.  PLoS ONE 7(2): e31687. doi:10.1371/journal.pone.0031687.

212 Etain B, Dumaine A, Bellivier F, Pagan C, Francelle L, Goubran-Botros H, Moreno S, Deshommes J, Moustafa K, Le Dudal K, Mathieu F, Henry C, Kahn JP, Launay JM, Mühleisen TW, Cichon S, Bourgeron T, Leboyer M, Jamain S.  Genetic and functional abnormalities of the melatonin biosynthesis pathway in patients with bipolar disorder.  Hum Mol Genet. 2012 Sep 15;21(18):4030-7. doi: 10.1093/hmg/dds227.
 
211 Fier H, Won S, Prokopenko D, AlChawa T, Ludwig KU, Fimmers R, Silverman EK, Pagano M, Mangold E, Lange C.  'Location, Location, Location': a spatial approach for rare variant analysis and an application to a study on non-syndromic cleft lip with or without cleft palate.  Bioinformatics. 2012 Dec 1;28(23):3027-33. doi: 10.1093/bioinformatics/bts568.

210 Filiou MD, Teplytska L, Otte DM, Zimmer A, Turck CW.  Myelination and oxidative stress alterations in the cerebellum of the G72/G30 transgenic schizophrenia mouse model.  J Psychiatr Res. 2012 Oct;46(10):1359-1365. doi: 10.1016/j.jpsychires.2012.07.004.

209 Frank J, Cichon S, Treutlein J, Ridinger M, Mattheisen M, Hoffmann P, Herms S, Wodarz N, Soyka M, Zill P, Maier W, Mössner R, Gaebel W, Dahmen N, Scherbaum N, Schmäl C, Steffens M, Lucae S, Ising M, Müller-Myhsok B, Nöthen MM, Mann K, Kiefer F, Rietschel M.  Genome-wide significant association between alcohol dependence and a variant in the ADH gene cluster.  Addict Biol. 2012 Jan;17(1):171-80. doi: 10.1111/j.1369-1600.2011.00395.                                                                                 
 
208 Freilinger, T., V. Anttila, V. B. de, R. Malik, M. Kallela, G. M. Terwindt, P. Pozo-Rosich, B. Winsvold, D. R. Nyholt, W. P. van Oosterhout, V. Artto, U. Todt, E. Hamalainen, J. Fernandez-Morales, M. A. Louter, M. A. Kaunisto, J. Schoenen, O. Raitakari, T. Lehtimaki, M. Vila-Pueyo, H. Gobel, E. Wichmann, C. Sintas, A. G. Uitterlinden, A. Hofman, F. Rivadeneira, A. Heinze, E. Tronvik, C. M. van Duijn, J. Kaprio, B. Cormand, M. Wessman, R. R. Frants, T. Meitinger, B. Muller-Myhsok, J. A. Zwart, M. Farkkila, A. Macaya, M. D. Ferrari, C. Kubisch, A. Palotie, M. Dichgans, and A. M. van den Maagdenberg.  Genome-wide association analysis identifies susceptibility loci for migraine without aura.  Nat Genet. 2012 Jun 10;44(7):777-82. doi: 10.1038/ng.2307.

207 Ganea K, Menke A, Schmidt MV, Lucae S, Rammes G, Liebl C, Harbich D, Sterlemann V, Storch C, Uhr M, Holsboer F, Binder EB, Sillaber I, Müller MB.  Convergent animal and human evidence suggests the activin/inhibin pathway to be involved in antidepressant response.  Transl Psychiatry. 2012 Oct 23;2:e177.
 
206 Gladwin TE, Derks EM; Genetic Risk and Outcome of Psychosis (GROUP), Rietschel M, Mattheisen M, Breuer R, Schulze TG, Nöthen MM, Levinson D, Shi J, Gejman PV, Cichon S, Ophoff RA.  Segment-wise genome-wide association analysis identifies a candidate region associated with schizophrenia in three independent samples.  PLoS One. 2012;7(6):e38828. doi: 10.1371/journal.pone.0038828.

205 Goes, F. S., Hamshere, M. L., Seifuddin, F., Pirooznia, M., Belmonte-Mahon, P., Breuer, R., Schulze, T., et al.  Genome-wide association of mood-incongruent psychotic bipolar disorder.  Transl psychiatry, 2012, 2, e180. doi:10.1038/tp.2012.106.

204 Graf C, Kuehne C, Panhuysen M, Puetz B, Weber P, Holsboer F, Wurst W, Deussing JM.  Corticotropin-releasing hormone regulates common target genes with divergent functions in corticotrope and neuronal cells.  Mol Cell Endocrinol. 2012 Oct 15;362(1-2):29-38.

203 Haenisch B, Herms S, Mattheisen M, Steffens M, Breuer R, Strohmaier J, Degenhardt F, Schmäl C, Lucae S, Maier W, Rietschel M, Nöthen MM, Cichon S.  Genome-wide association data provide further support for an association between 5-HTTLPR and major depressive disorder.  J Affect Disord. 2013 Apr 25;146(3):438-40. doi: 10.1016/j.jad.2012.08.001.

202 Hammer C, Cichon S, Mühleisen TW, Haenisch B, Degenhardt F, Mattheisen M, Breuer R, Witt SH, Strohmaier J, Oruc L, Rivas F, Babadjanova G, Grigoroiu-Serbanescu M, Hauser J, Röth R, Rappold G, Rietschel M, Nöthen MM, Niesler B.  Replication of functional serotonin receptor type 3A and B variants in bipolar affective disorder: a European multicenter study.  Transl Psychiatry. 2012 Apr 17;2:e103. doi: 10.1038/tp.2012.30.

201 Hamshere ML, Walters JT, Smith R, Richards AL, Green E, Grozeva D, Jones I, Forty L, Jones L, Gordon-Smith K, Riley B, O'Neill T, Kendler KS, Sklar P, Purcell S, Kranz J; The Schizophrenia Psychiatric Genome-wide Association Study Consortium (PGC): Schizophrenia Psychiatric Genome-Wide Association Study Consortium: St Clair D, Cichon S, Rietschel M, Nöthen MM, Maier W, Schulze TG, Mattheisen M, Kirov GK, O'Donovan MC, Holmans PA, Georgieva L, Nikolov I, Williams HJ, Toncheva D, Milanova V, Owen MJ, O'Donovan MC, Craddock N, Holmans PA, Hamshere M, Williams HJ, Moskvina V, Dwyer S, Georgieva L, Zammit S, Owen MJ, Kirov GK, Sullivan PF, Lin DY, van den Oord E, Kim Y, Stroup T, Lieberman JA, Hansen T, Ingason A, Olsen L, Schmock H, Skjødt C, Thygesen JH, Rosengren A, Werge T, Morris DW, O'Dushlaine CT, Kenny E, Quinn EM, Gill M, Corvin A, Blackwood DH, McGhee KA, Pickard B, Malloy P, Maclean AW, McIntosh A, Gejman PV, Sanders AR, Duan J, Levinson DF, Shi J, Buccola NG, Mowry BJ, Freedman R, Amin F, Black DW, Silverman JM, Byerley WF, Cloninger C, Giegling I, Hartmann AM, Konnerth H, Friedl M, Konte B, Muglia P, Rujescu D, Pato MT, Pato CN, Fanous A, Hultman CM, Lichtenstein P, Bergen SE, Purcell S, Scolnick E, Sklar P, Sullivan PF, Djurovic S, Mattingsdal M, Agartz I, Melle I, Andreassen OA, Ophoff RA, Cantor RM, Freimer NB, Kahn RS, Linszen DH, van Os J, Wiersma D, Bruggeman R, Cahn W, de Haan L, Krabbendam L, Myin-Germeys I, Strengman E, McQuillin A, Choudhury K, Datta S, Pimm J, Thirumalai S, Puri V, Krasucki R, Lawrence J, Quested D, Bass N, Gurling H, Malhotra AK, Lencz T., Wellcome Trust Case Control Consortium+ (WTCCC+), Wellcome Trust Case Control Consortium 2 (WTCCC2), Morris D, Gill M, Holmans P, Craddock N, Corvin A, Owen MJ, O'Donovan MC.  Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.  Mol Psychiatry. 2012 May 22. doi: 10.1038/mp.2012.67.
 
200 Hartz SM, Short SE, Saccone NL, Culverhouse R, Chen L, Schwantes-An TH, Coon H, Han Y, Stephens SH, Sun J, Chen X, Ducci F, Dueker N, Franceschini N, Frank J, Geller F, Gubjartsson D, Hansel NN, Jiang C, Keskitalo-Vuokko K, Liu Z, Lyytikainen LP, Michel M, Rawal R, Rosenberger A, Scheet P, Shaffer JR, Teumer A, Thompson JR, Vink JM, Vogelzangs N, Wenzlaff AS, Wheeler W, Xiao X, Yang BZ, Aggen SH, Balmforth AJ, Baumeister SE, Beaty T, Bennett S, Bergen AW, Boyd HA, Broms U, Campbell H, Chatterjee N, Chen J, Cheng YC, Cichon S, Couper D, Cucca F, Dick DM, Foroud T, Furberg H, Giegling I, Gu F, Hall AS, Hallfors J, Han S, Hartmann AM, Hayward C, Heikkila K, Hewitt JK, Hottenga JJ, Jensen MK, Jousilahti P, Kaakinen M, Kittner SJ, Konte B, Korhonen T, Landi MT, Laatikainen T, Leppert M, Levy SM, Mathias RA, McNeil DW, Medland SE, Montgomery GW, Muley T, Murray T, Nauck M, North K, Pergadia M, Polasek O, Ramos EM, Ripatti S, Risch A, Ruczinski I, Rudan I, Salomaa V, Schlessinger D, Styrkarsdottir U, Terracciano A, Uda M, Willemsen G, Wu X, Abecasis G, Barnes K, Bickeboller H, Boerwinkle E, Boomsma DI, Caporaso N, Duan J, Edenberg HJ, Francks C, Gejman PV, Gelernter J, Grabe HJ, Hops H, Jarvelin MR, Viikari J, Kahonen M, Kendler KS, Lehtimaki T, Levinson DF, Marazita ML, Marchini J, Melbye M, Mitchell BD, Murray JC, Nothen MM, Penninx BW, Raitakari O, Rietschel M, Rujescu D, Samani NJ, Sanders AR, Schwartz AG, Shete S, Shi J, Spitz M, Stefansson K, Swan GE, Thorgeirsson T, Volzke H, Wei Q, Wichmann HE, Amos CI, Breslau N, Cannon DS, Ehringer M, Grucza R, Hatsukami D, Heath A, Johnson EO, Kaprio J, Madden P, Martin NG, Stevens VL, Stitzel JA, Weiss RB, Kraft P, Bierut LJ  Increased Genetic Vulnerability to Smoking at CHRNA5 in Early-Onset Smokers.  Arch Gen Psychiatry 69:854-60.
 
199 Haß J, Walton E, Kirsten H, Liu J, Priebe L, Wolf C, Karbalai N, Gollub R, White T, Rößner V,  Scholz M, Cichon S, Calhoun V, Ehrlich S.  A genome-wide association study suggests novel loci associated with a schizophrenia-related brain-based phenotype.  PLoS One. 2013 Jun 21;8(6):e64872. Print 2013.

198 Håvik B, Degenhardt FA, Johansson S, Fernandes CP, Hinney A, Scherag A, Lybæk H, Djurovic S, Christoforou A, Ersland KM, Giddaluru S, O'Donovan MC, Owen MJ, Craddock N, Mühleisen TW,Mattheisen M, Schimmelmann BG, Renner T, Warnke A, Herpertz-Dahlmann B, Sinzig J, Albayrak Ö, Rietschel M, Nöthen MM, Bramham CR, Werge T, Hebebrand J, Haavik J, Andreassen OA, Cichon S, Steen VM, Le Hellard S.  DCLK1 variants are associated across schizophrenia and attention deficit/hyperactivity disorder.  PLoS One. 2012;7(4):e35424. doi: 10.1371/journal.pone.0035424.

197 JJang MH, Kitabatake Y, Kang E, Jun H, Pletnikov MV, Christian KM, Hen R, Lucae S, Binder EB, Song H, Ming GI.  Secreted frizzled-related protein 3 (sFRP3) regulates antidepressant responses in mice and humans.  Mol Psychiatry. 2012 Dec 4. doi: 10.1038/mp.2012.158. [Epub ahead of print]

196 Kam-Thong, T., C. A. Azencott, L. Cayton, B. Putz, A. Altmann, N. Karbalai, P. G. Samann, B. Scholkopf, B. Muller-Myhsok, and K. M. Borgwardt.  GLIDE: GPU-based linear regression for detection of epistasis.  Hum Hered 2012;73:220?236, DOI:10.1159/000341885.

195 Keers R, Pedroso I, Breen G, Aitchison KJ, Nolan PM, Cichon S, Nöthen MM, Rietschel M, Schalkwyk LC, Fernandes C.  Reduced anxiety and depression-like behaviours in the circadian period mutant mouse afterhours.  PLoS One. 2012;7(6):e38263. doi: 10.1371/journal.pone.0038263.

194 Keller MC, Simonson MA, Ripke S, Neale BM, Gejman PV, Howrigan DP, Lee SH, Lencz T, Levinson DF, Sullivan PF Runs of homozygosity implicate autozygosity as a schizophrenia risk factor.  PLoS Genet. 2012;8(4):e1002656. doi: 10.1371/journal.pgen.1002656.

193 Kloiber S, Czamara D, Karbalai N, Müller-Myhsok B, Hennings J, Holsboer F, Lucae S. ANK3 and CACNA1C--missing genetic link for bipolar disorder and major depressive disorder in two German case-control samples. J Psychiatr Res. 2012 Aug;46(8):973-9. doi: 10.1016/j.jpsychires.2012.04.017. Epub 2012 May 29

192 Kloiber S, Ripke S, Kohli MA, Reppermund S, Salyakina D, Uher R, McGuffin P, Perlis RH, Hamilton SP, Pütz B, Hennings J, Brückl T, Klengel T, Bettecken T, Ising M, Uhr M, Dose T, Unschuld PG, Zihl J, Binder E, Müller-Myhsok B, Holsboer F, Lucae S.  Resistance to antidepressant treatment is associated with polymorphisms in the leptin gene, decreased leptin mRNA expression, and decreased leptin serum levels.  Eur Neuropsychopharmacol. 2012 Sep 28. doi:pii: S0924-977X(12)00228-3. 10.1016/j.euroneuro.2012.08.010. [Epub ahead of print]
 
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189 Lennertz L, Wagner M, Wölwer W, Schuhmacher A, Frommann I, Berning J, Schulze-Rauschenbach S, Landsberg MW, Steinbrecher A, Alexander M, Franke PE, Pukrop R, Ruhrmann S, Bechdolf A, Gaebel W, Klosterkötter J, Häfner H, Maier W, Mössner R. A promoter variant of SHANK1 affects auditory working memory in schizophrenia patients and in subjects clinically at risk for psychosis. Eur Arch Psychiatry Clin Neurosci. 2012 Mar;262(2):117-24.

188 Li M, Wang Y, Zheng XB, Ikeda M, Iwata N, Luo XJ, Chong SA, Lee J, Rietschel M, Zhang F, Müller-Myhsok B, Cichon S, Weinberger DR, Mattheisen M, Schulze TG, Martin NG, Mitchell PB, Schofield PR, Liu JJ, Su B; MooDS Consortium. Meta-analysis and brain imaging data support the involvement of VRK2 (rs2312147) in schizophrenia susceptibility. Schizophr Res. 2012 Dec;142(1-3):200-5. doi: 10.1016/j.schres.2012.10.008.

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186 Mattheisen M, Mühleisen TW, Strohmaier J, Treutlein J, Nenadic I, Alblas M, Meier S, Degenhardt F, Herms S, Hoffmann P, Witt SH, Giegling I, Sauer H, Schulze TG, Rujescu D, Nöthen MM, Rietschel M, Cichon S.  Genetic variation at the synaptic vesicle gene SV2A is associated with schizophrenia. S Schizophr Res. 2012 Nov;141(2-3):262-5. doi: 10.1016/j.schres.2012.08.027.

185 Meesters C, Leber M, Herold C, Angisch M, Mattheisen M, Drichel D, Lacour A, Becker T. Quick,  'imputation-free' meta-analysis with proxy-SNPs.  BMC Bioinformatics. 2012 Sep 12;13:231. doi: 10.1186/1471-2105-13-231.

184 Meier S, Mattheisen M, Vassos E, Strohmaier J, Treutlein J, Josef F, Breuer R, Degenhardt F, Mühleisen TW, Müller-Myhsok B, Steffens M, Schmael C, McMahon FJ; Bipolar Disorder Genome Study (BiGS) Consortium, Nöthen MM, Cichon S, Schulze TG, Rietschel M, Kelsoe JR, Greenwood TA, Nievergelt CM, Barrett TB, McKinney R, Shilling PD, Schork NJ, Smith EN, Bloss CS, Nurnberger J, Edenberg HJ, Foroud T, Koller DL, Gershon ES, Liu CY, Badner JA, Scheftner W, Lawson WB, Nwulia EA, Hipolito M, Coryell W, Rice J, Byerley W, McMahon F, Chen DT, Schulze TG, Berrettini W, Potash JB, Zandi PP, Mahon PB, McInnis M, Craig D, Szelinger S. Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1.  Transl Psychiatry. 2012 Sep 25;2:e165.

183 Meier S, Mattheisen M, Vassos E, Strohmaier J, Treutlein J, Josef F, Breuer R, Degenhardt F, Mühleisen TW, Müller-Myhsok B, Steffens M, Schmael C, McMahon FJ; Bipolar Disorder Genome Study (BiGS) Consortium, Nöthen MM, Cichon S, Schulze TG, Rietschel M, Kelsoe JR, Greenwood TA, Nievergelt CM, Barrett TB, McKinney R, Shilling PD, Schork NJ, Smith EN, Bloss CS, Nurnberger J, Edenberg HJ, Foroud T, Koller DL, Gershon ES, Liu CY, Badner JA, Scheftner W, Lawson WB, Nwulia EA, Hipolito M, Coryell W, Rice J, Byerley W, McMahon F, Chen DT, Schulze TG, Berrettini W, Potash JB, Zandi PP, Mahon PB, McInnis M, Craig D, Szelinger S.  Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1.  Transl Psychiatry. 2012 Sep 25;2:e165. doi: 10.1038/tp.2012.81.

182 Meier S, Strohmaier J, Breuer R, Mattheisen M, Degenhardt F, Muhleisen TW, Schulze TG, Nothen MM, Cichon S, Rietschel M, Wust S  Neuregulin 3 is associated with attention deficits in schizophrenia and bipolar disorder.  Int J Neuropsychopharmacol:1-8.

181 Menke A, Arloth J, Pütz B, Weber P, Klengel T, Mehta D, Gonik M, Rex-Haffner M, Rubel J, Uhr M, Lucae S, Deussing JM, Müller-Myhsok B, Holsboer F, Binder EB.  Dexamethasone Stimulated Gene Expression in Peripheral Blood is a Sensitive Marker for Glucocorticoid Receptor Resistance in Depressed Patients.  Neuropsychopharmacology. 2012 May;37(6):1455-64.

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179 Menke A, Sämann P, Kloiber S, Czamara D, Lucae S, Hennings J, Heck A, Kohli MA, Czisch M, Müller-Myhsok B, Holsboer F, Binder EB.  Polymorphisms within the metabotropic glutamate receptor 1 gene are associated with depression phenotypes.  Psychoneuroendocrinology. 2012 Apr;37(4):565-75.

178 Miró X, Meier S, Dreisow ML, Frank J, Strohmaier J, Breuer R, Schmäl C, Albayram Ö, Pardo-Olmedilla MT, Mühleisen TW, Degenhardt FA, Mattheisen M, Reinhard I, Bilkei-Gorzo A, Cichon S, Seidenbecher C, Rietschel M, Nöthen MM, Zimmer A.  Studies in humans and mice implicate neurocan in the etiology of mania.  Am J Psychiatry. 2012 Sep;169(9):982-90. doi: 10.1176/appi.ajp.2012.11101585.

177 Mössner R, Schuhmacher A, Wagner M, Lennertz L, Steinbrecher A, Quednow BB, Rujescu D, Rietschel M, Maier W.  The schizophrenia risk gene ZNF804A influences the antipsychotic response of positive schizophrenia symptoms.  Eur Arch Psychiatry Clin Neurosci. 2012 Apr;262(3):193-7. doi: 10.1007/s00406-011-0235-1.

176 Mühleisen TW, Mattheisen M, Strohmaier J, Degenhardt F, Priebe L, Schultz CC, Breuer R, Meier S, Hoffmann P; GROUP Investigators, Rivandeneira F, Hofman A, Uitterlinden AG, Moebus S, Gieger C, Emeny R, Ladwig KH, Wichmann HE, Schwarz M, Kammerer-Ciernioch J, Schlösser RG, Nenadic I, Sauer H, Mössner R, Maier W, Rujescu D, Lange C, Ophoff RA, Schulze TG, Rietschel M, Nöthen MM, Cichon S. Association between schizophrenia and common variation in neurocan (NCAN), a genetic risk factor for bipolar disorder. Schizophr Res. 2012 Apr 10. [Epub ahead of print]

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