TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies von Erhardt, A, Czibere, L, Roeske, D, Lucae, S, Unschuld, P G, Ripke, S, Specht, M, Kohli, M A, Kloiber, S, Ising, M, Heck, A, Pfister, H, Zimmermann, P, Lieb, R, Pütz, B, Uhr, M, Weber, P, Deussing, J M, Gonik, M, Bunck, M, Keßler, M S, Frank, E, Hohoff, C, Domschke, K, Krakowitzky, P, Maier, W, Bandelow, B, Jacob, C, Deckert, J, Schreiber, S, Strohmaier, J, Nöthen, M, Cichon, S, Rietschel, M, Bettecken, T, Keck, M E, Landgraf, R, Müller-Myhsok, B, Holsboer, F, Binder, E B

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The GABA transporter 1 (SLC6A1): a novel candidate gene for anxiety disorders von 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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MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene von 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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IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations von Weber, F, Fontaine, B, Cournu-Rebeix, I, Kroner, A, Knop, M, Lutz, S, Müller-Sarnowski, F, Uhr, M, Bettecken, T, Kohli, M, Ripke, S, Ising, M, Rieckmann, P, Brassat, D, Semana, G, Babron, M-C, Mrejen, S, Gout, C, Lyon-Caen, O, Yaouanq, J, Edan, G, Clanet, M, Holsboer, F, Clerget-Darpoux, F, Müller-Myhsok, B

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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 von Wegerer, M., Adena, S., Pfennig, A., Czamara, D., Sailer, U., Bettecken, T., Müller-Myhsok, B., Modell, S., Ising, M.

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Mitochondrial 12S rRNA susceptibility mutations in aminoglycoside-associated and idiopathic bilateral vestibulopathy von Elstner, M., Schmidt, C., Zingler, V.C., Prokisch, H., Bettecken, T., Elson, J.L., Rudolph, G., Bender, A., Halmagyi, G.M., Brandt, T., Strupp, M., Klopstock, T.

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Proteomic-based genotyping in a mouse model of trait anxiety exposes disease-relevant pathways von Ditzen, C, Varadarajulu, J, Czibere, L, Gonik, M, Targosz, B S, Hambsch, B, Bettecken, T, Keßler, M S, Frank, E, Bunck, M, Teplytska, L, Erhardt, A, Holsboer, F, Müller-Myhsok, B, Landgraf, R, Turck, C W

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Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample von Heiser, P, Dempfle, A, Friedel, S, Konrad, K, Hinney, A, Kiefl, H, Walitza, S, Bettecken, T, Saar, K, Linder, M, Warnke, A, Herpertz-Dahlmann, B, Schäfer, H, Remschmidt, H, Hebebrand, J

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Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways von O'Dushlaine, C., Rossin, L., Lee P., H., Duncan, L., Parikshak N., N., Newhouse, S., Ripke, S., Neale B., M., Purcell S., M., Posthuma, D., Nurnberger J., I., Lee S., H., Faraone S., V., Perlis R., H., Mowry B., J., Thapar, A., Goddard M., E., Witte J., S., Absher, D., Agartz, I., Akil, H., Amin, F., Andreassen O., A., Anjorin, A., Anney, R., Anttila, V., Arking D., E., Asherson, P., Azevedo M., H., Backlund, L., Badner J., A., Bailey A., J., Banaschewski, T., Barchas J., D., Barnes M., R., Barrett T., B., Bass, N., Battaglia, A., Bauer, M., Bayés, M., Bellivier, F., Bergen S., E., Berrettini, W., Betancur, Catalina, Bettecken, T., Biederman, J., Binder E., B., Black D., W., Blackwood D., H., Bloss C., S., Boehnke, M., Boomsma D., I., Breuer, R., Bruggeman, R., Cormican, P., Buccola N., G., Buitelaar J., K., Bunney W., E., Buxbaum J., D., Byerley W., F., Byrne E., M., Caesar, S., Cahn, W., Cantor R., M., Casas, M., Chakravarti, A., Chambert, K., Choudhury, K., Cichon, S., Mattheisen, M., Cloninger C., R., Collier D., A., Cook E., H., Coon, H., Cormand, B., Corvin, A., Coryell W., H., Craig D., W., Craig I., W., Crosbie, J., Cuccaro M., L., Curtis, D., Czamara, D., Datta, S., Dawson, G., Day, R., de Geus E., J., Degenhardt, F., Djurovic, S., Donohoe G., J., Doyle A., E., Duan, J., Dudbridge, F., Duketis, E., Ebstein R., P., Edenberg H., J., Elia, J., Ennis, S., Etain, B., Fanous, F.

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Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs von Lee, S Hong, Ripke, Stephan, Neale, Benjamin M, Faraone, Stephen V, Purcell, Shaun M, Perlis, Roy H, Mowry, Bryan J, Thapar, Anita, Goddard, Michael E, Witte, John S, Absher, Devin, Agartz, Ingrid, Akil, Huda, Amin, Farooq, Andreassen, Ole A, Anjorin, Adebayo, Anney, Richard, Anttila, Verneri, Arking, Dan E, Asherson, Philip, Azevedo, Maria H, Backlund, Lena, Badner, Judith A, Bailey, Anthony J, Banaschewski, Tobias, Barchas, Jack D, Barnes, Michael R, Barrett, Thomas B, Bass, Nicholas, Battaglia, Agatino, Bauer, Michael, Bayés, Mònica, Bellivier, Frank, Bergen, Sarah E, Berrettini, Wade, Betancur, Catalina, Bettecken, Thomas, Biederman, Joseph, Binder, Elisabeth B, Black, Donald W, Blackwood, Douglas H R, Bloss, Cinnamon S, Boehnke, Michael, Boomsma, Dorret I, Breen, Gerome, Breuer, René, Bruggeman, Richard, Cormican, Paul, Buccola, Nancy G, Buitelaar, Jan K, Bunney, William E, Buxbaum, Joseph D, Byerley, William F, Byrne, Enda M, Caesar, Sian, Cahn, Wiepke, Cantor, Rita M, Casas, Miguel, Chakravarti, Aravinda, Chambert, Kimberly, Choudhury, Khalid, Cichon, Sven, Cloninger, C Robert, Collier, David A, Cook, Edwin H, Coon, Hilary, Cormand, Bru, Corvin, Aiden, Coryell, William H, Craig, David W, Craig, Ian W, Crosbie, Jennifer, Cuccaro, Michael L, Curtis, David, Czamara, Darina, Datta, Susmita, Dawson, Geraldine, Day, Richard, De Geus, Eco J, Degenhardt, Franziska, Djurovic, Srdjan, Donohoe, Gary J, Doyle, Alysa E, Duan, Jubao, Dudbridge, Frank, Duketis, Eftichia, Ebstein, Richard P, Edenberg, Howard J, Elia, Josephine, Ennis, Sean, Etain, Bruno, Fanous, Ayman, Farmer, Anne E, Ferrier, I Nicol, Flickinger, Matthew, Fombonne, Eric, Foroud, Tatiana, Frank, Josef, Franke, Barbara, Fraser, Christine

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A mega-analysis of genome-wide association studies for major depressive disorder von Ripke, Stephan, Wray, Naomi R, Lewis, Cathryn M, Hamilton, Steven P, Weissman, Myrna M, Breen, Gerome, Byrne, Enda M, Blackwood, Douglas H R, Boomsma, Dorret I, Cichon, Sven, Heath, Andrew C, Holsboer, Florian, Lucae, Susanne, Madden, Pamela A F, Martin, Nicholas G, McGuffin, Peter, Muglia, Pierandrea, Noethen, Markus M, Penninx, Brenda P, Pergadia, Michele L, Potash, James B, Rietschel, Marcella, Lin, Danyu, Müller-Myhsok, Bertram, Shi, Jianxin, Steinberg, Stacy, Grabe, Hans J, Lichtenstein, Paul, Magnusson, Patrik, Perlis, Roy H, Preisig, Martin, Smoller, Jordan W, Stefansson, Kari, Uher, Rudolf, Kutalik, Zoltan, Tansey, Katherine E, Teumer, Alexander, Viktorin, Alexander, Barnes, Michael R, Bettecken, Thomas, Binder, Elisabeth B, Breuer, René, Castro, Victor M, Churchill, Susanne E, Coryell, William H, Craddock, Nick, Craig, Ian W, Czamara, Darina, De Geus, Eco J, Degenhardt, Franziska, Farmer, Anne E, Fava, Maurizio, Frank, Josef, Gainer, Vivian S, Gallagher, Patience J, Gordon, Scott D, Goryachev, Sergey, Gross, Magdalena, Guipponi, Michel, Henders, Anjali K, Herms, Stefan, Hickie, Ian B, Hoefels, Susanne, Hoogendijk, Witte, Hottenga, Jouke Jan, Iosifescu, Dan V, Ising, Marcus, Jones, Ian, Jones, Lisa, Jung-Ying, Tzeng, Knowles, James A, Kohane, Isaac S, Kohli, Martin A, Korszun, Ania, Landen, Mikael, Lawson, William B, Lewis, Glyn, Macintyre, Donald, Maier, Wolfgang, Mattheisen, Manuel, McGrath, Patrick J, McIntosh, Andrew, McLean, Alan, Middeldorp, Christel M, Middleton, Lefkos, Montgomery, Grant M, Murphy, Shawn N, Nauck, Matthias, Nolen, Willem A, Nyholt, Dale R, O'Donovan, Michael, Oskarsson, Högni, Pedersen, Nancy, Scheftner, William A, Schulz, Andrea, Schulze, Thomas G, Shyn, Stanley I, Sigurdsson, Engilbert, Slager, Susan L, Smit, Johannes H

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Evidence for associations between PDE4D polymorphisms and a subtype of neuroticism von Heck, A, Lieb, R, Unschuld, P G, Ellgas, A, Pfister, H, Lucae, S, Erhardt, A, Himmerich, H, Horstmann, S, Kloiber, S, Ripke, S, Müller-Myhsok, B, Bettecken, T, Uhr, M, Holsboer, F, Ising, M

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Polymorphisms in the Drug Transporter Gene ABCB1 Predict Antidepressant Treatment Response in Depression von Uhr, Manfred, Tontsch, Alina, Namendorf, Christian, Ripke, Stephan, Lucae, Susanne, Ising, Marcus, Dose, Tatjana, Ebinger, Martin, Rosenhagen, Marcus, Kohli, Martin, Kloiber, Stefan, Salyakina, Daria, Bettecken, Thomas, Specht, Michael, Pütz, Benno, Binder, Elisabeth B., Müller-Myhsok, Bertram, Holsboer, Florian

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Sequence fossils, triplet expansion, and reconstruction of earliest codons von Trifonov, E.N., Bettecken, T.

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No Association of Sequence Variants in the Neuropeptide Y2 Receptor (NPY2R) Gene with Early Onset Obesity in Germans von Wang, H-J., Wermter, A-K., Nguyen, T. T., Scherag, A., Reichwald, K., Waldenmaier, B., Lichtner, P., Bettecken, T., Hebebrand, J., Hinney, A.

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Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment von Binder, Elisabeth B, Salyakina, Daria, Lichtner, Peter, Wochnik, Gabriele M, Ising, Marcus, Pütz, Benno, Papiol, Sergi, Seaman, Shaun, Lucae, Susanne, Kohli, Martin A, Nickel, Thomas, Künzel, Heike E, Fuchs, Brigitte, Majer, Matthias, Pfennig, Andrea, Kern, Nikola, Brunner, Jürgen, Modell, Sieglinde, Baghai, Thomas, Deiml, Tobias, Zill, Peter, Bondy, Brigitta, Rupprecht, Rainer, Messer, Thomas, Köhnlein, Oliver, Dabitz, Heike, Brückl, Tanja, Müller, Nina, Pfister, Hildegard, Lieb, Roselind, Mueller, Jakob C, Lõhmussaar, Elin, Strom, Tim M, Bettecken, Thomas, Meitinger, Thomas, Uhr, Manfred, Rein, Theo, Holsboer, Florian, Muller-Myhsok, Bertram

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The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion von KOENIG, M, BEGGS, A. H, DE LA CHAPELLE, A, KIURU, A, SAVONTAUS, M.-L, GILGENKRANTZ, H, RECAN, D, CHELLY, J, KAPLAN, J.-C, COVONE, A. E, ARCHIDIACONO, N, ROMEO, G, MOYER, M, SCHERPF, S, HEINDRICH, K, BETTECKEN, T, MENG, G, MÜLLER, C. R, LINDÖF, M, KAARIAINEN, H

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Tetrasomy 21pter→q21.2 in a male infant without typical Down’s syndrome dysmorphic features but moderate mental retardation von Rost, I, Fiegler, H, Fauth, C, Carr, P, Bettecken, T, Kraus, J, Meyer, C, Enders, A, Wirtz, A, Meitinger, T, Carter, N P, Speicher, M R

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On the origin of deletions and point mutations in Duchenne muscular dystrophy: most deletions arise in oogenesis and most point mutations result from events in spermatogenesis von Grimm, T, Meng, G, Liechti-Gallati, S, Bettecken, T, Müller, C R, Müller, B

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Consciousness Disturbances in Megalencephalic Leukoencephalopathy with Subcortical Cysts von Bugiani, M., Moroni, I., Bizzi, A., Nardocci, N., Bettecken, T., Gärtner, J., Uziel, G.

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