Staff

TOP 5 publications:

1. Peterson RE, Kuchenbaecker K, Walters RK, Chen CY, Popejoy AB, Periyasamy S, Lam M, Iyegbe C, Strawbridge RJ, Brick L, Carey CE, Martin AR, Meyers JL, Su J, Chen J, Edwards AC, Kalungi A, Koen N, Majara L, Schwarz, Prof. Ph.D E, Smoller JW, Stahl EA, Sullivan PF, Vassos E, Mowry B, Prieto ML, Cuellar-Barboza A, Bigdeli TB, Edenberg HJ, Huang H, Duncan LE. Genome-wide Association Studies in Ancestrally Diverse Populations: Opportunities, Methods, Pitfalls, and Recommendations.Cell. 2019 179(3):589-603.
2. García-Marín LM, Campos AI, Diaz-Torres S, Rabinowitz JA, Ceja Z, Mitchell BL, Grasby KL, Thorp JG, Agartz I, Alhusaini S, Ames D, Amouyel P, Andreassen OA, Arfanakis K, Arias-Vásquez A, Armstrong NJ, Athanasiu L, Bastin ME, Beiser AS, Bennett DA, Bis JC, Boks MPM, Boomsma DI, Brodaty H, Brouwer RM, Buitelaar JK, Burkhardt R, Cahn W, Calhoun VD, Carmichael OT, Chakravarty M, Chen Q, Ching CR, Cichon S, Crespo-Facorro B, Crivello F, Dale AM, Smith GD, de Geus EJC, De Jager PL, de Zubicaray GI, Debette S, Decarli C, Depondt C, Desrivieres S, Djurovic S, Ehrlich S, Erk S, Espeseth T, Fernández G, Filippi I, Fisher SE, Fleischman DA, Fletcher E, Fornage M, Forstner AJ, Francks C, Franke B, Ge T, Goldman AL, Grabe HJ, Green RC, Grimm O, Groenewold NA, Gruber O, Gudnason V, Håberg AK, Haukvik UK, Heinz A, Hibar DP, Hilal S, Himali JJ, Ho BC, Hoehn DF, Hoekstra PJ, Hofer E, Hoffmann W, Holmes AJ, Homuth G, Hosten N, Ikram MK, Ipser JC, Jack CR, Jahanshad N, Jönsson EG, Kahn RS, Kanai R, Klein M, Knol MJ, Launer LJ, Lawrie SM, Hellard SL, Lee PH, Lemaitre H, Li S, Liewald DC, Lin H, Longstreth WT, Lopez OL, Luciano M, Maillard P, Marquand AF, Martin NG, Martinot JL, Mather KA, Mattay VS, McMahon KL, Mecocci P, Melle I, Meyer-Lindenberg A, Mirza-Schreiber N, Milaneschi Y, Mosley TH, Mühleisen TW, Müller-Myhsok B, Maniega SM, Nauck M, Nho K, Niessen WJ, Nöthen MM, Nyquist PA, Oosterlaan J, Pandolfo M, Paus T, Pausova Z, Penninx BWJH, Pike GB, Psaty BM, Pütz B, Reppermund S, Rietschel MD, Risacher SL, Romanczuk-Seiferth N, Romero-Garcia R, Roshchupkin GV, Rotter JI, Sachdev PS, Sämann PG, Saremi A, Sargurupremraj M, Saykin AJ, Schmaal L, Schmidt H, Schmidt R, Schofield PR, Scholz M, Schumann G, Schwarz E, Shen L, Shin J, Sisodiya SM, Smith AV, Smoller JW, Soininen HS, Steen VM, Stein DJ, Stein JL, Thomopoulos SI, Toga AW, Tordesillas-Gutierrez D, Trollor JN, Valdes-Hernandez MC, Van T Ent D, van Bokhoven H, van der Meer D, van der Wee NJ, Vázquez-Bourgon J, Veltman DJ, Vernooij MW, Villringer A, Vinke LN, Völzke H, Walter H, Wardlaw JM, Weinberger DR, Weiner MW, Wen W, Westlye LT, Westman E, White T, Witte AV, Wolf C, Yang J, Zwiers MP, Ikram MA, Seshadri S, Thompson PM, Satizabal CL, Medland SE, Rentería ME. Genomic analysis of intracranial and subcortical brain volumes yields polygenic scores accounting for variation across ancestries.Nat Genet. 2024 56(11):2333-2344. Epub 2024 Oct 21.
3. Frangou S, Schwarz E, Meyer-Lindenberg A, IMAGEMEND . Identifying multimodal signatures associated with symptom clusters: the example of the IMAGEMEND project.World Psychiatry. 2016 15(2):179-80.
4. Streit F, Awasthi S, Hall ASM, Braun A, Niarchou M, Marouli E, Babajide O, Frank J, Zillich L, Callies CM, Avetyan D, Zillich E, Naamanka J, Gonzalez J, Harder A, Lu Y, Aherrahrou Z, Ahmad ZU, Ask H, Batzler A, Benros ME, Brand-de Wilde OM, Brunak S, Bruun MT, Christoffersen LAN, Colodro-Conde L, Coombes BJ, Corfield EC, Dahmen N, Didriksen M, Dinh KM, Djurovic S, Dowsett J, Drange OK, Dukal H, Edelmann S, Erikstrup C, Espinola MK, Fassbinder E, Faucon A, Ferreira de Sá DS, Foo JC, Gilles M, Gutiérrez-Zotes A, Hansen TF, Haraldsson M, Harper RP, Havdahl A, Heilbronner U, Herms S, Hjalgrim H, Hübel C, Jacob GA, Aagaard B, Jorgensen A, Jungkunz M, Kleindienst N, Knoblich N, Koglin S, Kraft J, Krebs K, Lee CW, Lin Y, Lis S, Lisoway A, Malogiannis IA, Martinsen A, Maslahati T, Merz K, Meyer-Lindenberg A, Mikkelsen S, Mikkelsen C, Mobascher A, Muntané G, Oddsson A, Ostrowski SR, Palviainen T, Pedersen OBV, Pedersen G, Quinn L, Reinhard MA, Ruths FA, Schott BH, Schredl M, Schwarz E, Schwarze CE, Schwinn M, Send TS, Sigurdsson E, Simon-Keller K, Skuladottir AT, Soler J, Sonley A, Sørensen E, Stefansson H, Straub P, Suvisaari J, Tesli M, Træholt J, Ullum H, Völker MP, Walters GB, Wang R, Witt CC, Zarbock G, Zill P, Zwart JA, DBDS Genomic Consortium DBDS Genomic Consortium, GLAD Study GLAD Study, HUNT All-In Psychiatry , Andreassen OA, Arntz A, Biernacka JM, Bohus M, Breen G, Chapman AL, Cichon S, Davis LK, Deuschle M, Euler S, Herpertz SC, Hummelen B, Jobst A, Kaprio J, Kennedy JL, Lehto K, Lieb K, Martorell L, McMain S, Musil R, Nieratschker V, Nöthen MM, Padberg F, Palotie A, Pascual JC, Perroud N, Ramos-Quiroga JA, Reichborn-Kjennerud T, Ribasés M, Roepke S, Rujescu D, Sanchez-Roige S, Schilling C, Schmahl C, Stefansson K, Thorgeirsson TE, Turecki G, Vilella E, Werge T, Winsvold BS, Wrege J, Rietschel M, Ripke S, Witt S. Genome-wide association analyses of borderline personality disorder identify 11 loci and highlight shared risk with mental and somatic disorders.Nat Genet. 2026 Jul 20. [Epub ahead of print].
5. Chen J, Zang Z, Braun U, Schwarz K, Harneit A, Kremer T, Ma R, Schweiger J, Mössnang C, Geiger-Primo L, Cao H, Degenhardt F, Nöthen MM, Tost H, Meyer-Lindenberg A, Schwarz, Prof. Ph.D E. Association of a Reproducible Epigenetic Risk Profile for Schizophrenia With Brain Methylation and Function.JAMA Psychiatry. 2020 77(6):628-636. Epub 2020 Feb 12.