The GABA transporter 1 (SLC6A1): a novel candidate gene for anxiety disorders by Thoeringer, C. K., Ripke, S., Unschuld, P. G., Lucae, S., Ising, M., Bettecken, T., Uhr, M., Keck, M. E., Mueller-Myhsok, B., Holsboer, F., Binder, E. B., Erhardt, A.

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Risk conferring genes in multiple sclerosis by Nischwitz, S., Müller-Myhsok, B., Weber, F.

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Estimating the heritability of reporting stressful life events captured by common genetic variants by Power, R. A., Wingenbach, T., Cohen-Woods, S., Uher, R., Ng, M. Y., Butler, A. W., Ising, M., Craddock, N., Owen, M. J., Korszun, A., Jones, L., Jones, I., Gill, M., Rice, J. P., Maier, W., Zobel, A., Mors, O., Placentino, A., Rietschel, M., Lucae, S., Holsboer, F., Binder, E. B., Keers, R., Tozzi, F., Muglia, P., Breen, G., Craig, I. W., Müller-Myhsok, B., Kennedy, J. L., Strauss, J., Vincent, J. B., Lewis, C. M., Farmer, A. E., McGuffin, P.

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Familiality and SNP heritability of age at onset and episodicity in major depressive disorder by Ferentinos, P., Koukounari, A., Power, R., Rivera, M., Uher, R., Craddock, N., Owen, M. J., Korszun, A., Jones, L., Jones, I., Gill, M., Rice, J. P., Ising, M., Maier, W., Mors, O., Rietschel, M., Preisig, M., Binder, E. B., Aitchison, K. J., Mendlewicz, J., Souery, D., Hauser, J., Henigsberg, N., Breen, G., Craig, I. W., Farmer, A. E., Müller-Myhsok, B., McGuffin, P., Lewis, C. M.

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MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene by Nischwitz, S, Wolf, C, Andlauer, T.F.M, Czamara, D, Zettl, U.K, Rieckmann, P, Buck, D, Ising, M, Bettecken, T, Mueller-Myhsok, B, Weber, F

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Variants within the GABA transaminase (ABAT) gene region are associated with somatosensory evoked EEG potentials in families at high risk for affective disorders by Wegerer, M., Adena, S., Pfennig, A., Czamara, D., Sailer, U., Bettecken, T., Müller-Myhsok, B., Modell, S., Ising, M.

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Somatization in major depression - clinical features and genetic associations by Klengel, T., Heck, A., Pfister, H., Brückl, T., Hennings, J. M., Menke, A., Czamara, D., Müller-Myhsok, B., Ising, M.

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Investigation of 17 candidate genes for personality traits confirms effects of the HTR2A gene on novelty seeking by Heck, A., Lieb, R., Ellgas, A., Pfister, H., Lucae, S., Roeske, D., Pütz, B., Müller‐Myhsok, B., Uhr, M., Holsboer, F., Ising, M.

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Genome-wide meta-analysis of ascertainment and symptom structures of major depression in case-enriched and community cohorts by Adams, Mark J, Thorp, Jackson G, Jermy, Bradley S, Kwong, Alex S F, Kõiv, Kadri, Grotzinger, Andrew D, Nivard, Michel G, Marshall, Sally, Milaneschi, Yuri, Baune, Bernhard T, Müller-Myhsok, Bertram, Penninx, Brenda W J H, Boomsma, Dorret I, Levinson, Douglas F, Breen, Gerome, Pistis, Giorgio, Grabe, Hans J, Tiemeier, Henning, Berger, Klaus, Rietschel, Marcella, Magnusson, Patrik K, Uher, Rudolf, Hamilton, Steven P, Lucae, Susanne, Lehto, Kelli, Li, Qingqin S, Byrne, Enda M, Hickie, Ian B, Martin, Nicholas G, Medland, Sarah E, Wray, Naomi R, Tucker-Drob, Elliot M, Lewis, Cathryn M, McIntosh, Andrew M, Derks, Eske M

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An Extensive Comparison of Quantitative Trait Loci Mapping Methods by Kleensang, A., Franke, D., Alcaïs, A., Abel, L., Müller-Myhsok, B., Ziegler, A.

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A locus on 2p12 containing the co-regulated MRPL19 and C2ORF3 genes is associated to dyslexia by Anthoni, Heidi, Zucchelli, Marco, Matsson, Hans, Müller-Myhsok, Bertram, Fransson, Ingegerd, Schumacher, Johannes, Massinen, Satu, Onkamo, Päivi, Warnke, Andreas, Griesemann, Heide, Hoffmann, Per, Nopola-Hemmi, Jaana, Lyytinen, Heikki, Schulte-Körne, Gerd, Kere, Juha, Nöthen, Markus M., Peyrard-Janvid, Myriam

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The P2RX7 polymorphism rs2230912 is associated with depression: A meta-analysis by Czamara, D., Müller-Myhsok, B., Lucae, S.

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Salivary cortisol response to psychosocial stress in the late evening depends on CRHR1 genotype by Weeger, J., Ising, M., Müller-Myhsok, B., Uhr, M., Schmidt, U., Steiger, A.

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Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology by Zimprich, Alexander, Biskup, Saskia, Leitner, Petra, Lichtner, Peter, Farrer, Matthew, Lincoln, Sarah, Kachergus, Jennifer, Hulihan, Mary, Uitti, Ryan J., Calne, Donald B., Stoessl, A.Jon, Pfeiffer, Ronald F., Patenge, Nadja, Carbajal, Iria Carballo, Vieregge, Peter, Asmus, Friedrich, Müller-Myhsok, Bertram, Dickson, Dennis W., Meitinger, Thomas, Strom, Tim M., Wszolek, Zbigniew K., Gasser, Thomas

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Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia by Witt, S H, Streit, F, Jungkunz, M, Frank, J, Awasthi, S, Reinbold, C S, Treutlein, J, Forstner, A J, Dietl, L, Schwarze, C E, Strohmaier, J, Adolfsson, R, Air, T M, Akil, H, Alda, M, Bass, N J, Bauer, M, Biernacka, J M, Blackwood, D H R, Boks, M P, Børglum, A D, Borrmann-Hassenbach, M, Budde, M, Cervantes, P, Cruceanu, C, Curtis, D, Czerski, P M, Dannlowski, U, Davis, T, de Geus, E J C, Di Florio, A, Djurovic, S, Edenberg, H J, Etain, B, Fischer, S B, Frye, M A, Fullerton, J M, Gade, K, Gershon, E S, Gordon-Smith, K, Grabe, H J, Green, E K, Greenwood, T A, Grigoroiu-Serbanescu, M, Guzman-Parra, J, Hall, L S, Hauser, J, Hoffmann, P, Hottenga, J-J, Juréus, A, Kahn, R S, Kammerer-Ciernioch, J, Kloiber, S, Knott, S V, Landén, M, Leboyer, M, Lissowska, J, Martin, N G, Mayoral-Cleries, F, McElroy, S L, McIntosh, A M, McQuillin, A, Middeldorp, C M, Mitchell, P B, Morken, G, Mors, O, Müller-Myhsok, B, Myers, R M, Nievergelt, C M, Nurnberger, J I, O'Donovan, M C, Ophoff, R, Penninx, B W J H, Pfennig, A, Potash, J B, Preisig, M, Rivas, F, Rouleau, G A, Schofield, P R, Schulze, T G, Schwarz, M, Scott, L, Strauss, J, Turecki, G, Van der Auwera, S, Vedder, H, Vincent, J B, Willemsen, G, Witt, C C, Wray, N R, Tadic, A, Dahmen, N, Schott, B H, Cichon, S, Nöthen, M M, Ripke, S, Mobascher, A, Rujescu, D, Schmahl, C, Bohus, M

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The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders by Chang, H, Hoshina, N, Zhang, C, Ma, Y, Cao, H, Wang, Y, Wu, D-d, Bergen, S E, Landén, M, Hultman, C M, Preisig, M, Kutalik, Z, Castelao, E, Grigoroiu-Serbanescu, M, Forstner, A J, Strohmaier, J, Hecker, J, Schulze, T G, Müller-Myhsok, B, Reif, A, Mitchell, P B, Martin, N G, Schofield, P R, Cichon, S, Nöthen, M M, Walter, H, Erk, S, Heinz, A, Amin, N, van Duijn, C M, Meyer-Lindenberg, A, Tost, H, Xiao, X, Yamamoto, T, Rietschel, M, Li, M

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The variant Arg110Gln of human IL-13 is associated with an immunologically hyper-reactive form of onchocerciasis (sowda) by Hoerauf, Achim, Kruse, Susanne, Brattig, Norbert W., Heinzmann, Andrea, Mueller-Myhsok, Bertram, Deichmann, Klaus A.

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1112 MiRNA-expression in primary tumours allows to discriminate metastasized from non-metastasized seminoma by Ruf, C.G.A, Schmelz, H-U, Port, M, Matthies, C, Meineke, V, Mueller-Myhsok, B, Wagner, W, Abend, M

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Genetic risk prediction and neurobiological understanding of alcoholism by Levey, D F, Le-Niculescu, H, Frank, J, Ayalew, M, Jain, N, Kirlin, B, Learman, R, Winiger, E, Rodd, Z, Shekhar, A, Schork, N, Kiefe, F, Wodarz, N, Müller-Myhsok, B, Dahmen, N, Nöthen, M, Sherva, R, Farrer, L, Smith, A H, Kranzler, H R, Rietschel, M, Gelernter, J, Niculescu, A B

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Restless legs syndrome in Czech patients with multiple sclerosis: An epidemiological and genetic study by Vávrová, J, Kemlink, D, Šonka, K, Havrdová, E, Horáková, D, Pardini, B, Müller-Myhsok, B, Winkelmann, J

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