Items where Author is "Binder, E. B."

2021

Min, J. L. and Hemani, G. and Hannon, E. and Dekkers, K. F. and Castillo-Fernandez, J. and Luijk, R. and Carnero-Montoro, E. and Lawson, D. J. and Burrows, K. and Suderman, M. and Bretherick, A. D. and Richardson, T. G. and Klughammer, J. and Iotchkova, V. and Sharp, G. and Al Khleifat, A. and Shatunov, A. and Iacoangeli, A. and McArdle, W. L. and Ho, K. M. and Kumar, A. and Soderhall, C. and Soriano-Tarraga, C. and Giralt-Steinhauer, E. and Kazmi, N. and Mason, D. and McRae, A. F. and Corcoran, D. L. and Sugden, K. and Kasela, S. and Cardona, A. and Day, F. R. and Cugliari, G. and Viberti, C. and Guarrera, S. and Lerro, M. and Gupta, R. and Bollepalli, S. and Mandaviya, P. and Zeng, Y. and Clarke, T. K. and Walker, R. M. and Schmoll, V. and Czamara, D. and Ruiz-Arenas, C. and Rezwan, F. I. and Marioni, R. E. and Lin, T. and Awaloff, Y. and Germain, M. and Aissi, D. and Zwamborn, R. and van Eijk, K. and Dekker, A. and van Dongen, J. and Hottenga, J. J. and Willemsen, G. and Xu, C. J. and Barturen, G. and Catala-Moll, F. and Kerick, M. and Wang, C. and Melton, P. and Elliott, H. R. and Shin, J. and Bernard, M. and Yet, I. and Smart, M. and Gorrie-Stone, T. and Bios Consortium, and Shaw, C. and Al Chalabi, A. and Ring, S. M. and Pershagen, G. and Melen, E. and Jimenez-Conde, J. and Roquer, J. and Lawlor, D. A. and Wright, J. and Martin, N. G. and Montgomery, G. W. and Moffitt, T. E. and Poulton, R. and Esko, T. and Milani, L. and Metspalu, A. and Perry, J. R. B. and Ong, K. K. and Wareham, N. J. and Matullo, G. and Sacerdote, C. and Panico, S. and Caspi, A. and Arseneault, L. and Gagnon, F. and Ollikainen, M. and Kaprio, J. and Felix, J. F. and Rivadeneira, F. and Tiemeier, H. and van, IJzendoorn M. H. and Uitterlinden, A. G. and Jaddoe, V. W. V. and Haley, C. and McIntosh, A. M. and Evans, K. L. and Murray, A. and Räikkönen, K. and Lahti, J. and Nohr, E. A. and Sorensen, T. I. A. and Hansen, T. and Morgen, C. S. and Binder, E. B. and Lucae, S. and Gonzalez, J. R. and Bustamante, M. and Sunyer, J. and Holloway, J. W. and Karmaus, W. and Zhang, H. and Deary, I. J. and Wray, N. R. and Starr, J. M. and Beekman, M. and van Heemst, D. and Slagboom, P. E. and Morange, P. E. and Trégouët, D. A. and Veldink, J. H. and Davies, G. E. and de Geus, E. J. C. and Boomsma, D. I. and Vonk, J. M. and Brunekreef, B. and Koppelman, G. H. and Alarcon-Riquelme, M. E. and Huang, R. C. and Pennell, C. E. and van Meurs, J. and Ikram, M. A. and Hughes, A. D. and Tillin, T. and Chaturvedi, N. and Pausova, Z. and Paus, T. and Spector, T. D. and Kumari, M. and Schalkwyk, L. C. and Visscher, P. M. and Davey Smith, G. and Bock, C. and Gaunt, T. R. and Bell, J. T. and Heijmans, B. T. and Mill, J. and Relton, C. L.. (2021) Genomic and phenotypic insights from an atlas of genetic effects on DNA methylation. Nature Genetics, 53 (9). pp. 1311-1321.

2017

Jukić, M. M. and Opel, N. and Ström, J. and Carrillo-Roa, T. and Miksys, S. and Novalen, M. and Renblom, A. and Sim, S. C. and Peñas-Lledó, E. M. and Courtet, P. and Llerena, A. and Baune, B. T. and de Quervain, D. J. and Papassotiropoulos, A. and Tyndale, R. F. and Binder, E. B. and Dannlowski, U. and Ingelman-Sundberg, M.. (2017) Elevated CYP2C19 expression is associated with depressive symptoms and hippocampal homeostasis impairment. Molecular Psychiatry, 22 (8). pp. 1155-1163.

Jukić, M. M. and Opel, N. and Ström, J. and Carrillo-Roa, T. and Miksys, S. and Novalen, M. and Renblom, A. and Sim, S. C. and Peñas-Lledó, E. M. and Courtet, P. and Llerena, A. and Baune, B. T. and de Quervain, D. J. and Papassotiropoulos, A. and Tyndale, R. F. and Binder, E. B. and Dannlowski, U. and Ingelman-Sundberg, M.. (2017) Elevated CYP2C19 expression is associated with depressive symptoms and hippocampal homeostasis impairment. Molecular Psychiatry, 22 (8). p. 1224.

2011

Erhardt, A. and Czibere, L. and Roeske, D. and Lucae, S. and Unschuld, P. G. and Ripke, S. and Kohli, M. A. and Kloiber, S. and Ising, M. and Heck, A. and Ellgas, A. and Pfister, H. and Lieb, R. and Puetz, B. and Uhr, M. and Hohoff, C. and Maier, W. and Bandelow, B. and Domschke, K. and Jacob, C. and Deckert, J. and Landgraf, R. and Bettecken, T. and Keck, M. E. and Müller-Myhsok, B. and Holsboer, F. and Binder, E. B.. (2011) TMEM132D : a new candidate for anxiety phenotypes - evidence from human and mouse studies. Molecular Psychiatry, Vol. 16, H. 6. pp. 647-663.

Erhardt, A. and Czibere, L. and Roeske, D. and Lucae, S. and Unschuld, P. G. and Ripke, S. and Specht, M. and Kohli, M. A. and Kloiber, S. and Ising, M. and Heck, A. and Pfister, H. and Zimmermann, P. and Lieb, R. and Pütz, B. and Uhr, M. and Weber, P. and Deussing, J. M. and Gonik, M. and Bunck, M. and Kebler, M. S. and Frank, E. and Hohoff, C. and Domschke, K. and Krakowitzky, P. and Maier, W. and Bandelow, B. and Jacob, C. and Deckert, J. and Schreiber, S. and Strohmaier, J. and Nöthen, M. and Cichon, S. and Rietschel, M. and Bettecken, T. and Keck, M. E. and Landgraf, R. and Müller-Myhsok, B. and Holsboer, F. and Binder, E. B.. (2011) TMEM132D, a new candidate for anxiety phenotypes: evidence from human and mouse studies. Molecular Psychiatry, 16 (6). pp. 647-663.

2009

Zimmermann, P. and Brueckl, T. and Pfister, H. and Lieb, R. and Wittchen, H. U. and Holsboer, F. and Ising, M. and Binder, E. B. and Uhr, M. and Nocon, A.. (2009) The interplay of variations in the FKBP5 gene and adverse life events in predicting the first onset of depression during a ten-year follow-up. Pharmacopsychiatry, Vol. 42, H. 5. p. 249.

2008

Erhardt, A. and Lucae, S. and Kern, N. and Unschuld, P. G. and Ising, M. and Lieb, R. and Uhr, M. and Hohoff, C. and Deckert, J. and Bandelow, B. and Maier, W. and Binder, E. B. and Müller-Myhsok, B. and Keck, M. E. and Holsboer, F.. (2008) Association of polymorphisms in the angiotensin-converting enzyme gene with syndromal panic attacks. Molecular Psychiatry, Vol. 13. pp. 242-243.

Keck, M. E. and Kern, N. and Erhardt, A. and Unschuld, P. G. and Ising, M. and Salyakina, D. and Müller, M. B. and Knorr, C. C. and Lieb, R. and Hohoff, C. and Krakowitzky, P. and Maier, W. and Bandelow, B. and Fritze, J. and Deckert, J. and Holsboer, F. and Müller-Myhsok, B. and Binder, E. B.. (2008) Combined effects of exonic polymorphisms in CRHR1 and AVPR1B genes in a case/control study for panic disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 147B, H. 7. pp. 1196-1204.

2007

Thoeringer, C. K. and Binder, E. B. and Salyakina, D. and Erhardt, A. and Ising, M. and Unschuld, P. G. and Kern, N. and Lucae, S. and Brueckl, T. M. and Mueller, B. M. and Fuchs, B. and Puetz, B. and Lieb, R. and Uhr, M. and Holsboer, F. and Mulller-Myshok, B. and Keck, M. E.. (2007) Association of a Met88Val diazepam binding inhibitor (DBI) gene polymorphism and anxiety disorders with panic attacks. Journal of psychiatric research, Vol. 41, H. 7. pp. 579-584.

Erhardt, A. and Lucae, S. and Unschuld, P. G. and Ising, M. and Kern, N. and Salyakina, D. and Lieb, R. and Uhr, M. and Binder, E. B. and Keck, M. E. and Müller-Myhsok, B. and Holsboer, F.. (2007) Association of polymorphisms in P2RX7 and CaMKKb with anxiety disorders. Journal of affective disorders, Vol. 101, H. 1-3. pp. 159-168.

Unschuld, P. G. and Ising, M. and Erhardt, A. and Lucae, S. and Kloiber, S. and Kohli, M. and Salyakina, D. and Welt, T. and Kern, N. and Lieb, R. and Uhr, M. and Binder, E. B. and Müller-Myhsok, B. and Holsboer, F. and Keck, M. E.. (2007) Polymorphisms in the serotonin receptor gene HTR2A are associated with quantitative traits in panic disorder. American journal of medical genetics. Part B, Neuropsychiatric genetics, Vol. 144B, H. 4. pp. 424-429.

2006

Lucae, S. and Salyakina, D. and Barden, N. and Harvey, M. and Gagné, B. and Labbé, M. and Binder, E. B. and Uhr, M. and Paez-Pereda, M. and Sillaber, I. and Ising, M. and Brückl, T. and Lieb, R. and Holsboer, F. and Müller-Myhsok, B.. (2006) P2RX7, a gene coding for a purinergic ligand-gated ion channel, is associated with major depressive disorder. Human molecular genetics, Vol. 15, H. 16. pp. 2438-2445.

2004

Binder, E. B. and Salyakina, D. and Lichtner, P. and Wochnik, G. M. and Ising, M. and Pütz, B. and Papiol, S. and Seaman, S. and Lucae, S. and Kohli, M. A. and Nickel, T. and Künzel, H. E. and Fuchs, B. and Majer, M. and Pfennig, A. and Kern, N. and Brunner, J. and Modell, S. and Baghai, T. and Deiml, T. and Zill, P. and Bondy, B. and Rupprecht, R. and Messer, T. and Köhnlein, O. and Dabitz, H. and Brückl, T. and Müller, N. and Pfister, H. and Lieb, R. and Mueller, J. C. and Lohmussar, E. and Strom, T. and Bettecken, T. and Meitinger, T. and Uhr, M. and Rein, T. and Holsboer, F. and Müller-Myhsok, B.. (2004) Polymorphisms in FKBP5 are associated with increased recurrence of depressive episodes and rapid response to antidepressant treatment. Nature genetics, Vol. 36, H. 12. pp. 1319-1325.