Genome-wide association study of recurrent major depressive disorder in two European case-control cohorts
Muglia, P, Tozzi, F, Galwey, N W, Francks, C, Upmanyu, R, Kong, X Q, Antoniades, A, Domenici, E, Perry, J, Rothen, S, Vandeleur, C L, Mooser, V, Waeber, G, Vollenweider, P, Preisig, M, Lucae, S, Müller-Myhsok, B, Holsboer, F, Middleton, L T, Roses, A D
Published in Molecular psychiatry (01.06.2010)
Published in Molecular psychiatry (01.06.2010)
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The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders
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
Published in Molecular psychiatry (01.02.2018)
Published in Molecular psychiatry (01.02.2018)
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Creatine supplementation in Parkinson disease: a placebo-controlled randomized pilot trial
Bender, A, Koch, W, Elstner, M, Schombacher, Y, Bender, J, Moeschl, M, Gekeler, F, Müller-Myhsok, B, Gasser, T, Tatsch, K, Klopstock, T
Published in Neurology (10.10.2006)
Published in Neurology (10.10.2006)
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TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies
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
Published in Molecular psychiatry (01.06.2011)
Published in Molecular psychiatry (01.06.2011)
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Autosomal dominant parkinsonism associated with variable synuclein and tau pathology
Wszolek, Z K, Pfeiffer, R F, Tsuboi, Y, Uitti, R J, McComb, R D, Stoessl, A J, Strongosky, A J, Zimprich, A, Müller-Myhsok, B, Farrer, M J, Gasser, T, Calne, D B, Dickson, D W
Published in Neurology (11.05.2004)
Published in Neurology (11.05.2004)
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First genome-wide association scan on neurophysiological endophenotypes points to trans-regulation effects on SLC2A3 in dyslexic children
Roeske, D, Ludwig, K U, Neuhoff, N, Becker, J, Bartling, J, Bruder, J, Brockschmidt, F F, Warnke, A, Remschmidt, H, Hoffmann, P, Müller-Myhsok, B, Nöthen, M M, Schulte-Körne, G
Published in Molecular psychiatry (01.01.2011)
Published in Molecular psychiatry (01.01.2011)
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Estimating the heritability of reporting stressful life events captured by common genetic variants
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.
Published in Psychological medicine (01.09.2013)
Published in Psychological medicine (01.09.2013)
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Replication and meta-analysis of TMEM132D gene variants in panic disorder
Erhardt, A, Akula, N, Schumacher, J, Czamara, D, Karbalai, N, Müller-Myhsok, B, Mors, O, Borglum, A, Kristensen, A S, Woldbye, D P D, Koefoed, P, Eriksson, E, Maron, E, Metspalu, A, Nurnberger, J, Philibert, R A, Kennedy, J, Domschke, K, Reif, A, Deckert, J, Otowa, T, Kawamura, Y, Kaiya, H, Okazaki, Y, Tanii, H, Tokunaga, K, Sasaki, T, Ioannidis, J P A, McMahon, F J, Binder, E B
Published in Translational psychiatry (04.09.2012)
Published in Translational psychiatry (04.09.2012)
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Polymorphisms in the DLG5 and OCTN cation transporter genes in Crohn’s disease
Török, H-P, Glas, J, Tonenchi, L, Lohse, P, Müller-Myhsok, B, Limbersky, O, Neugebauer, C, Schnitzler, F, Seiderer, J, Tillack, C, Brand, S, Brünnler, G, Jagiello, P, Epplen, J T, Griga, T, Klein, W, Schiemann, U, Folwaczny, M, Ochsenkühn, T, Folwaczny, C
Published in Gut (01.10.2005)
Published in Gut (01.10.2005)
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Polymorphisms in the angiotensin-converting enzyme gene are associated with unipolar depression, ACE activity and hypercortisolism
BAGHAI, T. C, BINDER, E. B, DEIML, T, UHR, M, ILLIG, T, WICHMANN, H.-E, MODELL, S, NOTHDURFTER, C, HOLSBOER, F, MÜLLER-MYHSOK, B, MÖLLER, H.-J, RUPPRECHT, R, SCHULE, C, BONDY, B, SALYAKINA, D, ESER, D, LUCAE, S, ZWANZGER, P, HABERGER, C, ZILL, P, ISING, M
Published in Molecular psychiatry (01.11.2006)
Published in Molecular psychiatry (01.11.2006)
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Single-nucleotide polymorphisms in HLA- and non-HLA genes associated with the development of antibodies to interferon-β therapy in multiple sclerosis patients
Weber, F, Cepok, S, Wolf, C, Berthele, A, Uhr, M, Bettecken, Th, Buck, D, Hartung, H P, Holsboer, F, Müller-Myhsok, B, Hemmer, B
Published in The pharmacogenomics journal (01.06.2012)
Published in The pharmacogenomics journal (01.06.2012)
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Supporting evidence for LRRTM1 imprinting effects in schizophrenia
Ludwig, K U, Mattheisen, M, Mühleisen, T W, Roeske, D, Schmäl, C, Breuer, R, Schulte-Körne, G, Müller-Myhsok, B, Nöthen, M M, Hoffmann, P, Rietschel, M, Cichon, S
Published in Molecular psychiatry (01.08.2009)
Published in Molecular psychiatry (01.08.2009)
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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
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)
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Somatization in major depression - clinical features and genetic associations
Klengel, T., Heck, A., Pfister, H., Brückl, T., Hennings, J. M., Menke, A., Czamara, D., Müller-Myhsok, B., Ising, M.
Published in Acta psychiatrica Scandinavica (01.10.2011)
Published in Acta psychiatrica Scandinavica (01.10.2011)
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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)
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Gender-stratified analysis of DLG5 R30Q in 4707 patients with Crohn disease and 4973 controls from 12 Caucasian cohorts
Browning, B L, Annese, V, Barclay, M L, Bingham, S A, Brand, S, Büning, C, Castro, M, Cucchiara, S, Dallapiccola, B, Drummond, H, Ferguson, L R, Ferraris, A, Fisher, S A, Gearry, R B, Glas, J, Henckaerts, L, Huebner, C, Knafelz, D, Lakatos, L, Lakatos, P L, Latiano, A, Liu, X, Mathew, C, Müller-Myhsok, B, Newman, W G, Nimmo, E R, Noble, C L, Palmieri, O, Parkes, M, Petermann, I, Rutgeerts, P, Satsangi, J, Shelling, A N, Siminovitch, K A, Török, H-P, Tremelling, M, Vermeire, S, Valvano, M R, Witt, H
Published in Journal of medical genetics (01.01.2008)
Published in Journal of medical genetics (01.01.2008)
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A susceptibility locus for Parkinson's disease maps to chromosome 2p13
Gasser, Thomas, Müller-Myhsok, Bertram, Wszolek, Zbigniew K, Oehlmann, Ralph, Calne, Donald B, Bonifati, Vincenzo, Bereznai, Benjamin, Fabrizio, Edito, Vieregge, Peter, Horstmann, Rolf D
Published in Nature genetics (01.03.1998)
Published in Nature genetics (01.03.1998)
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The P2RX7 polymorphism rs2230912 is associated with depression: A meta-analysis
Czamara, D., Müller-Myhsok, B., Lucae, S.
Published in Progress in neuro-psychopharmacology & biological psychiatry (02.03.2018)
Published in Progress in neuro-psychopharmacology & biological psychiatry (02.03.2018)
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