P.4.d.011 Influence of DAT1 and DRD2 gene variants on antidepressant response in generalised anxiety disorder von Lohoff, F

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Methylomic profiling and replication implicates deregulation of PCSK9 in alcohol use disorder von Lohoff, F W, Sorcher, J L, Rosen, A D, Mauro, K L, Fanelli, R R, Momenan, R, Hodgkinson, C A, Vendruscolo, L F, Koob, G F, Schwandt, M, George, D T, Jones, I S, Holmes, A, Zhou, Z, Xu, M-J, Gao, B, Sun, H, Phillips, M J, Muench, C, Kaminsky, Z A

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Genome-wide association study of bipolar disorder in European American and African American individuals von Smith, E N, Bloss, C S, Badner, J A, Barrett, T, Belmonte, P L, Berrettini, W, Byerley, W, Coryell, W, Craig, D, Edenberg, H J, Eskin, E, Foroud, T, Gershon, E, Greenwood, T A, Hipolito, M, Koller, D L, Lawson, W B, Liu, C, Lohoff, F, McInnis, M G, McMahon, F J, Mirel, D B, Murray, S S, Nievergelt, C, Nurnberger, J, Nwulia, E A, Paschall, J, Potash, J B, Rice, J, Schulze, T G, Scheftner, W, Panganiban, C, Zaitlen, N, Zandi, P P, Zöllner, S, Schork, N J, Kelsoe, J R

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Interaction between polymorphisms in serotonin transporter (SLC6A4) and serotonin receptor 2A (HTR2A) genes predict treatment response to venlafaxine XR in generalized anxiety diso... von Lohoff, F W, Narasimhan, S, Rickels, K

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Case–control association analysis of polymorphisms in the delta-opioid receptor, OPRD1 , with cocaine and opioid addicted populations von Crist, R.C, Ambrose-Lanci, L.M, Vaswani, M, Clarke, T.K, Zeng, A, Yuan, C, Ferraro, T.N, Hakonarson, H, Kampman, K.M, Dackis, C.A, Pettinati, H.M, O’Brien, C.P, Oslin, D.W, Doyle, G.A, Lohoff, F.W, Berrettini, W.H

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Functional genetic variants in the vesicular monoamine transporter 1 modulate emotion processing von Lohoff, F W, Hodge, R, Narasimhan, S, Nall, A, Ferraro, T N, Mickey, B J, Heitzeg, M M, Langenecker, S A, Zubieta, J-K, Bogdan, R, Nikolova, Y S, Drabant, E, Hariri, A R, Bevilacqua, L, Goldman, D, Doyle, G A

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Confirmation of association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) gene and bipolar I disorder von Lohoff, F.W., Sander, T., Ferraro, T.N., Dahl, J.P., Gallinat, J., Berrettini, W.H.

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Genetic variation in OPRD1 and the response to treatment for opioid dependence with buprenorphine in European-American females von Clarke, T-K, Crist, R C, Ang, A, Ambrose-Lanci, L M, Lohoff, F W, Saxon, A J, Ling, W, Hillhouse, M P, Bruce, R D, Woody, G, Berrettini, W H

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VMAT1 deletion causes neuronal loss in the hippocampus and neurocognitive deficits in spatial discrimination von Multani, P.K, Hodge, R, Estévez, M.A, Abel, T, Kung, H, Alter, M, Brookshire, B, Lucki, I, Nall, A.H, Talbot, K, Doyle, G.A, Lohoff, F.W

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Exome sequence analysis of Finnish patients with clozapine-induced agranulocytosis von Tiwari, A K, Need, A C, Lohoff, F W, Zai, C C, Chowdhury, N I, Müller, D J, Putkonen, A, Repo-Tiihonen, E, Hallikainen, T, Anil Yağcıoğlu, A E, Tiihonen, J, Kennedy, J L, Meltzer, H Y

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Serotonin receptor 2A (HTR2A) gene polymorphism predicts treatment response to venlafaxine XR in generalized anxiety disorder von Lohoff, F W, Aquino, T D, Narasimhan, S, Multani, P K, Etemad, B, Rickels, K

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Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibility von Buono, R.J, Lohoff, F.W, Sander, T, Sperling, M.R, O’Connor, M.J, Dlugos, D.J, Ryan, S.G, Golden, G.T, Zhao, H, Scattergood, T.M, Berrettini, W.H, Ferraro, T.N

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Genetic association analyses of PDYN polymorphisms with heroin and cocaine addiction von Clarke, T.‐K., Ambrose‐Lanci, L., Ferraro, T. N., Berrettini, W. H., Kampman, K. M., Dackis, C. A., Pettinati, H. M., O’Brien, C. P., Oslin, D. W., Lohoff, F. W.

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Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy von Lenzen, K.P., Heils, A., Lorenz, S., Hempelmann, A., Höfels, S., Lohoff, F.W., Schmitz, B., Sander, T.

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Genetic dissection of intermale aggressive behavior in BALB/cJ and A/J mice von Dow, H. C., Kreibich, A. S., Kaercher, K. A., Sankoorikal, G. M. V., Pauley, E. D., Lohoff, F. W., Ferraro, T. N., Li, H., Brodkin, E. S.

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Confirmation of multiple seizure susceptibility QTLs on chromosome 15 in C57BL/6J and DBA/2J inbred mice von Ferraro, T N, Smith, G G, Schwebel, C L, Doyle, G A, Ruiz, S E, Oleynick, J U, Lohoff, F W, Berrettini, W H, Buono, R J

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Fine mapping of a seizure susceptibility locus on mouse Chromosome 1: nomination of Kcnj10 as a causative gene von Ferraro, Thomas N, Golden, Gregory T, Smith, George G, Martin, James F, Lohoff, Falk W, Gieringer, Tracy A, Zamboni, Deborah, Schwebel, Candice L, Press, Danielle M, Kratzer, Stephanie O, Zhao, Hongyu, Berrettini, Wade H, Buono, Russell J

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Quantitative trait loci for electrical seizure threshold mapped in C57BLKS/J and C57BL/10SnJ mice von Ferraro, T. N., Smith, G. G., Ballard, D., Zhao, H., Schwebel, C. L., Gupta, A., Rappaport, E. F., Ruiz, S. E., Lohoff, F. W., Doyle, G. A., Berrettini, W. H., Buono, R. J.

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Genetic Variants in the Vesicular Monoamine Transporter 1 (VMAT1/SLC18A1) and Neuropsychiatric Disorders von Lohoff, Falk W.

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Lack of Association Between an Interleukin 1 Beta (IL‐1β) Gene Variation and Refractory Temporal Lobe Epilepsy von Buono, Russell J., Ferraro, Thomas N., O'Connor, Michael J., Sperling, Michael R., Ryan, Stephen G., Scattergood, Theresa, Mulholland, Nicole, Gilmore, Joan, Lohoff, Falk W., Berrettini, Wade H.

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