TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies
ERHARDT, A, CZIBERE, L, HECK, A, PFISTER, H, ZIMMERMANN, P, LIEB, R, PÜTZ, B, UHR, M, WEBER, P, DEUSSING, J. M, GONIK, M, BUCK, M, ROESKE, D, KESSLER, M. S, FRANK, E, HOHOFF, C, DOMSCHKE, K, KRAKOWITZKY, P, MAIER, W, BANDELOW, B, JACOB, C, DECKERT, J, SCHREIBER, S, LUCAE, S, STROHMAIER, J, NÖTHEN, M, CICHON, S, RIETSCHEL, M, BETTECKEN, T, KECK, M. E, LANDGRAF, R, MÜLLER-MYHSOK, B, HOLSBOER, F, BINDER, E. B, UNSCHULD, P. G, RIPKE, S, SPECHT, M, KOHLI, M. A, KLOIBER, S, ISING, M
Published in Molecular psychiatry (01.06.2011)
Published in Molecular psychiatry (01.06.2011)
Get full text
Journal Article
The GABA transporter 1 (SLC6A1): a novel candidate gene for anxiety disorders
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.
Published in Journal of Neural Transmission (01.06.2009)
Published in Journal of Neural Transmission (01.06.2009)
Get full text
Journal Article
MS susceptibility is not affected by single nucleotide polymorphisms in the MMP9 gene
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
Published in Journal of neuroimmunology (15.02.2015)
Published in Journal of neuroimmunology (15.02.2015)
Get full text
Journal Article
IL2RA and IL7RA genes confer susceptibility for multiple sclerosis in two independent European populations
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
Published in Genes and immunity (01.04.2008)
Published in Genes and immunity (01.04.2008)
Get full text
Journal Article
Variants within the GABA transaminase (ABAT) gene region are associated with somatosensory evoked EEG potentials in families at high risk for affective disorders
Wegerer, M., Adena, S., Pfennig, A., Czamara, D., Sailer, U., Bettecken, T., Müller-Myhsok, B., Modell, S., Ising, M.
Published in Psychological medicine (01.06.2013)
Published in Psychological medicine (01.06.2013)
Get full text
Journal Article
Proteomic-based genotyping in a mouse model of trait anxiety exposes disease-relevant pathways
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
Published in Molecular psychiatry (01.07.2010)
Published in Molecular psychiatry (01.07.2010)
Get full text
Journal Article
Mitochondrial 12S rRNA susceptibility mutations in aminoglycoside-associated and idiopathic bilateral vestibulopathy
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.
Published in Biochemical and biophysical research communications (12.12.2008)
Published in Biochemical and biophysical research communications (12.12.2008)
Get full text
Journal Article
More CLEC16A gene variants associated with multiple sclerosis
Nischwitz, S., Cepok, S., Kroner, A., Wolf, C., Knop, M., Müller-Sarnowski, F., Pfister, H., Rieckmann, P., Hemmer, B., Ising, M., Uhr, M., Bettecken, T., Holsboer, F., Müller-Myhsok, B., Weber, F.
Published in Acta neurologica Scandinavica (01.06.2011)
Published in Acta neurologica Scandinavica (01.06.2011)
Get full text
Journal Article
Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample
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
Published in Journal of Neural Transmission (01.04.2007)
Published in Journal of Neural Transmission (01.04.2007)
Get full text
Journal Article
Evidence for associations between PDE4D polymorphisms and a subtype of neuroticism
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
Published in Molecular psychiatry (01.09.2008)
Published in Molecular psychiatry (01.09.2008)
Get full text
Journal Article
No association of sequence variants in the neuropeptide Y2 receptor (NPY2R) gene with early onset obesity in Germans
Wang, H-J, Wermter, A-K, Nguyen, T T, Scherag, A, Reichwald, K, Waldenmaier, B, Lichtner, P, Bettecken, T, Hebebrand, J, Hinney, A
Published in Hormone and metabolic research (01.11.2007)
Published in Hormone and metabolic research (01.11.2007)
Get more information
Journal Article
The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion
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
Published in American journal of human genetics (01.10.1989)
Get full text
Published in American journal of human genetics (01.10.1989)
Journal Article
Tetrasomy 21pter→q21.2 in a male infant without typical Down’s syndrome dysmorphic features but moderate mental retardation
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
Published in Journal of medical genetics (01.03.2004)
Published in Journal of medical genetics (01.03.2004)
Get full text
Journal Article
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
Grimm, T, Meng, G, Liechti-Gallati, S, Bettecken, T, Müller, C R, Müller, B
Published in Journal of medical genetics (01.03.1994)
Published in Journal of medical genetics (01.03.1994)
Get full text
Journal Article
Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs
Faraone, Stephen V, Absher, Devin, Akil, Huda, Arking, Dan E, Badner, Judith A, Barchas, Jack D, Barrett, Thomas B, Battaglia, Agatino, Bayés, Mònica, Bergen, Sarah E, Bettecken, Thomas, Biederman, Joseph, Buitelaar, Jan K, Byerley, William F, Caesar, Sian, Cahn, Wiepke, Chakravarti, Aravinda, Cichon, Sven, Cook, Edwin H, Corvin, Aiden, Coryell, William H, Crosbie, Jennifer, Curtis, David, Doyle, Alysa E, Elia, Josephine, Ennis, Sean, Fanous, Ayman, Farmer, Anne E, Ferrier, I Nicol, Foroud, Tatiana, Freedman, Robert, Gershon, Elliot S, Giegling, Ina, Gordon, Scott D, Gross, Magdalena, Gurling, Hugh, Hipolito, Maria, Jones, Edward G, Jones, Lisa, Kahn, René S, Kent, Lindsey, Kim, Yunjung, Kohli, Martin A, Krasucki, Robert, Lawson, William B, Li, Jun, Lin, Dan-Yu, Lowe, Jennifer K, Magnusson, Patrik K E, Mahon, Pamela B, Mane, Shrikant M, McCarroll, Steven A, McGough, James J, McInnis, Melvin G, McKinney, Rebecca, McMahon, Francis J, Medeiros, Helena, Middeldorp, Christel M, Miranda, Ana, Monaco, Anthony P, Morris, Derek W, Morrow, Eric M, Müller-Myhsok, Bertram, Nikolov, Ivan, Nolen, Willem A, Nurnberger, John I, Nyholt, Dale R, Parr, Jeremy R, Pato, Carlos N, Piven, Joseph, Rossin, Lizzy, Sanders, Stephan J, Schalling, Martin, Scheftner, William A, Schellenberg, Gerard D, Schumacher, Johannes, Schwarz, Markus, Shilling, Paul D, Smit, Johannes H, Sonuga-Barke, Edmund J S, St Clair, David, Steffens, Michael, Steinhausen, Hans-Christoph, Strohmaier, Jana, Szatmari, Peter, Thompson, Robert C, Uhr, Manfred, Van Grootheest, Gerard, Vicente, Astrid M, Vincent, John B, Weissman, Myrna M, Wijsman, Ellen M, Williams, Nigel, Willsey, A Jeremy, Zöllner, Sebastian, Sklar, Pamela, O'Donovan, Michael C, Craddock, Nicholas, Sullivan, Patrick F, Kendler, Kenneth S
Published in Nature genetics (01.09.2013)
Published in Nature genetics (01.09.2013)
Get full text
Journal Article
Web Resource
Consciousness disturbances in megalencephalic leukoencephalopathy with subcortical cysts
Bugiani, M, Moroni, I, Bizzi, A, Nardocci, N, Bettecken, T, Gärtner, J, Uziel, G
Published in Neuropediatrics (01.08.2003)
Published in Neuropediatrics (01.08.2003)
Get more information
Journal Article
Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways
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.
Published in Nature neuroscience (01.02.2015)
Published in Nature neuroscience (01.02.2015)
Get full text
Journal Article
A mega-analysis of genome-wide association studies for major depressive disorder
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, 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, Kutalik, Zoltan, Teumer, Alexander, Viktorin, Alexander, Barnes, Michael R, Bettecken, Thomas, Binder, Elisabeth B, 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, Gallagher, Patience J, Gordon, Scott D, Goryachev, Sergey, Gross, Magdalena, Henders, Anjali K, Herms, Stefan, Hickie, Ian B, Hoefels, Susanne, Hoogendijk, Witte, Iosifescu, Dan V, Ising, Marcus, Jones, Ian, Jones, Lisa, Jung-Ying, Tzeng, Knowles, James A, Kohli, Martin A, Korszun, Ania, Landen, Mikael, Lawson, William B, Lewis, Glyn, Macintyre, Donald, Maier, Wolfgang, McIntosh, Andrew, McLean, Alan, Middeldorp, Christel M, Middleton, Lefkos, Montgomery, Grant M, Murphy, Shawn N, Nauck, Matthias, Nolen, Willem A, 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, Stefansson, Hreinn, Steffens, Michael, Thorgeirsson, Thorgeir, Treutlein, Jens, Uhr, Manfred, van den Oord, Edwin J C G, Van Grootheest, Gerard, Völzke, Henry, Weilburg, Jeffrey B, Willemsen, Gonneke, Daly, Mark, Levinson, Douglas F, Sullivan, Patrick F
Published in Molecular psychiatry (01.04.2013)
Published in Molecular psychiatry (01.04.2013)
Get full text
Journal Article
Reduced amplification efficiency of KIAA0027/MLC1 alleles: implications for the molecular diagnosis of megalencephalic leukoencephalopathy with subcortical cysts
Bettecken, T., Rubie, C., Lichtner, P., Siekiera, M., Meitinger, T., Stöber, G.
Published in Molecular and cellular probes (01.10.2002)
Published in Molecular and cellular probes (01.10.2002)
Get full text
Journal Article