Items where Author is "Lucae, S."

Yes

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.

Direk, N. and Williams, S. and Smith, J. A. and Ripke, S. and Air, T. and Amare, A. T. and Amin, N. and Baune, B. T. and Bennett, D. A. and Blackwood, D. H. and Boomsma, D. and Breen, G. and Buttenschon, H. N. and Byrne, E. M. and Borglum, A. D. and Castelao, E. and Cichon, S. and Clarke, T. K. and Cornelis, M. C. and Dannlowski, U. and De Jager, P. L. and Demirkan, A. and Domenici, E. and van Duijn, C. M. and Dunn, E. C. and Eriksson, J. G. and Esko, T. and Faul, J. D. and Ferrucci, L. and Fornage, M. and de Geus, E. and Gill, M. and Gordon, S. D. and Grabe, H. J. and van Grootheest, G. and Hamilton, S. P. and Hartman, C. A. and Heath, A. C. and Hek, K. and Hofman, A. and Homuth, G. and Horn, C. and Jan Hottenga, J. and Kardia, S. L. and Kloiber, S. and Koenen, K. and Kutalik, Z. and Ladwig, K. H. and Lahti, J. and Levinson, D. F. and Lewis, C. M. and Lewis, G. and Li, Q. S. and Llewellyn, D. J. and Lucae, S. and Lunetta, K. L. and MacIntyre, D. J. and Madden, P. and Martin, N. G. and McIntosh, A. M. and Metspalu, A. and Milaneschi, Y. and Montgomery, G. W. and Mors, O. and Mosley, T. H. and Jr., and Murabito, J. M. and Muller-Myhsok, B. and Nothen, M. M. and Nyholt, D. R. and O'Donovan, M. C. and Penninx, B. W. and Pergadia, M. L. and Perlis, R. and Potash, J. B. and Preisig, M. and Purcell, S. M. and Quiroz, J. A. and Raikkonen, K. and Rice, J. P. and Rietschel, M. and Rivera, M. and Schulze, T. G. and Shi, J. and Shyn, S. and Sinnamon, G. C. and Smit, J. H. and Smoller, J. W. and Snieder, H. and Tanaka, T. and Tansey, K. E. and Teumer, A. and Uher, R. and Umbricht, D. and Van der Auwera, S. and Ware, E. B. and Weir, D. R. and Weissman, M. M. and Willemsen, G. and Yang, J. and Zhao, W. and Tiemeier, H. and Sullivan, P. F.. (2016) An Analysis of Two Genome-wide Association Meta-analyses Identifies a New Locus for Broad Depression Phenotype. Biological Psychiatry, 83 (5). pp. 322-329.

Schwantes-An, T. H. and Zhang, J. and Chen, L. S. and Hartz, S. M. and Culverhouse, R. C. and Chen, X. and Coon, H. and Frank, J. and Kamens, H. M. and Konte, B. and Kovanen, L. and Latvala, A. and Legrand, L. N. and Maher, B. S. and Melroy, W. E. and Nelson, E. C. and Reid, M. W. and Robinson, J. D. and Shen, P. H. and Yang, B. Z. and Andrews, J. A. and Aveyard, P. and Beltcheva, O. and Brown, S. A. and Cannon, D. S. and Cichon, S. and Corley, R. P. and Dahmen, N. and Degenhardt, L. and Foroud, T. and Gaebel, W. and Giegling, I. and Glatt, S. J. and Grucza, R. A. and Hardin, J. and Hartmann, A. M. and Heath, A. C. and Herms, S. and Hodgkinson, C. A. and Hoffmann, P. and Hops, H. and Huizinga, D. and Ising, M. and Johnson, E. O. and Johnstone, E. and Kaneva, R. P. and Kendler, K. S. and Kiefer, F. and Kranzler, H. R. and Krauter, K. S. and Levran, O. and Lucae, S. and Lynskey, M. T. and Maier, W. and Mann, K. and Martin, N. G. and Mattheisen, M. and Montgomery, G. W. and Muller-Myhsok, B. and Murphy, M. F. and Neale, M. C. and Nikolov, M. A. and Nishita, D. and Nothen, M. M. and Nurnberger, J. and Partonen, T. and Pergadia, M. L. and Reynolds, M. and Ridinger, M. and Rose, R. J. and Rouvinen-Lagerstrom, N. and Scherbaum, N. and Schmal, C. and Soyka, M. and Stallings, M. C. and Steffens, M. and Treutlein, J. and Tsuang, M. and Wall, T. L. and Wodarz, N. and Yuferov, V. and Zill, P. and Bergen, A. W. and Chen, J. and Cinciripini, P. M. and Edenberg, H. J. and Ehringer, M. A. and Ferrell, R. E. and Gelernter, J. and Goldman, D. and Hewitt, J. K. and Hopfer, C. J. and Iacono, W. G. and Kaprio, J. and Kreek, M. J. and Kremensky, I. M. and Madden, P. A. and McGue, M. and Munafo, M. R. and Philibert, R. A. and Rietschel, M. and Roy, A. and Rujescu, D. and Saarikoski, S. T. and Swan, G. E. and Todorov, A. A. and Vanyukov, M. M. and Weiss, R. B. and Bierut, L. J. and Saccone, N. L.. (2016) Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts. Behavior Genetics, 46 (2). pp. 151-169.

Forstner, A. J. and Hofmann, A. and Maaser, A. and Sumer, S. and Khudayberdiev, S. and Muhleisen, T. W. and Leber, M. and Schulze, T. G. and Strohmaier, J. and Degenhardt, F. and Treutlein, J. and Mattheisen, M. and Schumacher, J. and Breuer, R. and Meier, S. and Herms, S. and Hoffmann, P. and Lacour, A. and Witt, S. H. and Reif, A. and Muller-Myhsok, B. and Lucae, S. and Maier, W. and Schwarz, M. and Vedder, H. and Kammerer-Ciernioch, J. and Pfennig, A. and Bauer, M. and Hautzinger, M. and Moebus, S. and Priebe, L. and Sivalingam, S. and Verhaert, A. and Schulz, H. and Czerski, P. M. and Hauser, J. and Lissowska, J. and Szeszenia-Dabrowska, N. and Brennan, P. and McKay, J. D. and Wright, A. and Mitchell, P. B. and Fullerton, J. M. and Schofield, P. R. and Montgomery, G. W. and Medland, S. E. and Gordon, S. D. and Martin, N. G. and Krasnov, V. and Chuchalin, A. and Babadjanova, G. and Pantelejeva, G. and Abramova, L. I. and Tiganov, A. S. and Polonikov, A. and Khusnutdinova, E. and Alda, M. and Cruceanu, C. and Rouleau, G. A. and Turecki, G. and Laprise, C. and Rivas, F. and Mayoral, F. and Kogevinas, M. and Grigoroiu-Serbanescu, M. and Propping, P. and Becker, T. and Rietschel, M. and Cichon, S. and Schratt, G. and Nothen, M. M.. (2015) Genome-wide analysis implicates microRNAs and their target genes in the development of bipolar disorder. Translational Psychiatry , 5. e678.

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.

Heck, A. and Lieb, R. and Ellgas, A. and Pfister, H. and Lucae, S. and Roeske, D. and Pütz, B. and Müller-Myhsok, B. and Uhr, M. and Holsboer, F. and Ising, M.. (2009) Investigation of 17 candidate genes for personality traits confirms effects of the HTR2A gene on novelty seeking. Genes, Brain and Behavior, 8 (4). pp. 464-472.

Heck, A. and Lieb, R. and Unschuld, P. G. and Ellgas, A. and Pfister, H. and Lucae, S. and Erhardt, A. and Himmerich, H. and Horstmann, S. and Kloiber, S. and Ripke, S. and Müller-Myhsok, B. and Bettecken, T. and Uhr, M. and Holsboer, F. and Ising, M.. (2008) Evidence for associations between PDE4D polymorphisms and a subtype of neuroticism. Molecular Psychiatry, 13 (9). pp. 831-832.

Unschuld, P. G. and Ising, M. and Erhardt, A. and Lucae, S. and Kohli, M. and Kloiber, S. and Salyakina, D. and Thoeringer, C. K. and Kern, N. and Lieb, R. and Uhr, M. and Binder, E. and Müller-Myhsok, B. and Holsboer, F. and Keck, M. E.. (2008) Polymorphisms in the galanin gene are associated with symptom-severity in female patients suffering from panic disorder. Journal of affective disorders, Vol. 105, H. 1-3. pp. 177-184.

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.

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.

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.

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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.