Exploring the overlap between alopecia areata and major depressive disorder: Epidemiological and genetic perspectives von Foo, J. C., Redler, S., Forstner, A. J., Basmanav, F. B., Pethukova, L., Guo, J., Streit, F., Witt, S. H., Sirignano, L., Zillich, L., Awasthi, S., Ripke, S., Christiano, A. M., Tesch, F., Schmitt, J., Nöthen, M. M., Betz, R. C., Rietschel, M., Frank, J.

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Functional implications of novel ADAM10 mutations in reticulate acropigmentation of Kitamura von Ralser, D.J., Lestringant, G.G., Du‐Thanh, A., Kokordelis, P., Fischer, J., Basmanav, F.B.Ünalan, Wolf, S., Thiele, H., Altmüller, J., Nürnberg, P., Oji, V., Fritz, G., Frank, J., Betz, R.C.

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

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Parent-of-origin Effect in Alopecia Areata: A Large-scale Pedigree Study von Redler, Silke, Basmanav, F Buket Ü, Blaumeiser, Bettina, Bartels, Natalie Garcia, Lutz, Gerhard, Tafazzoli, Aylar, Kruse, Roland, Wolff, Hans, Böhm, Markus, Blume-Peytavi, Ulrike, Becker, Tim, Nöthen, Markus M, Betz, Regina C

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Investigation of the involvement of MIR185 and its target genes in the development of schizophrenia von Forstner, Andreas J., MD, Basmanav, F. Buket, MSc, Mattheisen, Manuel, MD, GROUP Investigators, MSc, Böhmer, Anne C., PhD, Hollegaard, Mads V., BAS, Janson, Esther, MSc, Strengman, Eric, MSc, Priebe, Lutz, MD, Degenhardt, Franziska, PhD, Hoffmann, Per, MSc, Herms, Stefan, MD, Maier, Wolfgang, MD, Mössner, Rainald, MD, Rujescu, Dan, PhD, Ophoff, Roel A., PhD, Moebus, Susanne, MD, DMSc, Mortensen, Preben B., MD, PhD, Børglum, Anders D., MD, DSc, Hougaard, David M., MSc, Frank, Josef, PhD, Witt, Stephanie H., MD, Rietschel, Marcella, PhD, Zimmer, Andreas, MD, Nöthen, Markus M., PhD, Miró, Xavier, PhD, Cichon, Sven

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

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Systematic Integration of Brain eQTL and GWAS Identifies ZNF323 as a Novel Schizophrenia Risk Gene and Suggests Recent Positive Selection Based on Compensatory Advantage on Pulmona... von Luo, Xiong-Jian, Mattheisen, Manuel, Li, Ming, Huang, Liang, Rietschel, Marcella, Børglum, Anders D, Als, Thomas D, van den Oord, Edwin J, Aberg, Karolina A, Mors, Ole, Mortensen, Preben Bo, Luo, Zhenwu, Degenhardt, Franziska, Cichon, Sven, Schulze, Thomas G, Nöthen, Markus M, Su, Bing, Zhao, Zhongming, Gan, Lin, Yao, Yong-Gang

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Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe von Rietschel, M, Mattheisen, M, Degenhardt, F, Mühleisen, T W, Kirsch, P, Esslinger, C, Herms, S, Demontis, D, Steffens, M, Strohmaier, J, Haenisch, B, Breuer, R, Czerski, P M, Giegling, I, Strengman, E, Schmael, C, Mors, O, Mortensen, P B, Hougaard, D M, Ørntoft, T, Kapelski, P, Priebe, L, Basmanav, F B, Forstner, A J, Hoffmann, P, Meier, S, Nikitopoulos, J, Moebus, S, Alexander, M, Mössner, R, Wichmann, H-E, Schreiber, S, Rivandeneira, F, Hofman, A, Uitterlinden, A G, Wienker, T F, Schumacher, J, Hauser, J, Maier, W, Cantor, R M, Erk, S, Schulze, T G, Craddock, N, Owen, M J, O'Donovan, M C, Børglum, A D, Rujescu, D, Walter, H, Meyer-Lindenberg, A, Nöthen, M M, Ophoff, R A, Cichon, S

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Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe von Rietschel, M, Mattheisen, M, Degenhardt, F, GROUP Investigators, Mühleisen, T.W, Kirsch, P, Esslinger, C, Herms, S, Demontis, D, Steffens, M, Strohmaier, J, Haenisch, B, Breuer, R, Czerski, P.M, Giegling, I, Strengman, E, Schmael, C, Mors, O, Mortensen, P.B, Hougaard, D.M, Ørntoft, T, Kapelski, P, Priebe, L, Basmanav, F.F, Forstner, A.J, Hoffman, P, Meier, S, Nikitopoulos, J, Moebus, S, Alexander, Lee, Mössner, R, Wichmann, H.-E, Schreiber, S, Rivandeneira, F, Hofman, A, Uitterlinden, A.G, Wienker, T.F, Schumacher, J, Hauser, J, Maier, W, Cantor, R.M, Erk, S, Schulze, T.G, SGENE-plus Consortium, Craddock, N, Owen, M.J, O'Donovan, M.C, Børglum, A.D, Rujescu, D, Walter, H, Meyer-Lindenberg, A, Nöthen, N.M, Ophoff, R.A, Cichon, S

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