Search Results - "Lohoff, F.W"

Case–control association analysis of polymorphisms in the delta-opioid receptor, OPRD1 , with cocaine and opioid addicted populations by 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

“…Abstract Background Addiction susceptibility and treatment responsiveness are greatly influenced by genetic factors. Sequence variation in genes involved in…”
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VMAT1 deletion causes neuronal loss in the hippocampus and neurocognitive deficits in spatial discrimination by 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

“…Highlights ► VMAT1 is expressed in mouse brain. ► Deletion of VMAT1 results in reduced neurogenesis and apoptosis in the hippocampus. ► VMAT2 expression is not…”
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Association between variation in the human KCNJ10 potassium ion channel gene and seizure susceptibility by 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

“…Purpose: Our research program uses genetic linkage and association analysis to identify human seizure sensitivity and resistance alleles. Quantitative trait…”
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P.6.c.004 Association between the val158met polymorphism in the catechol-o-methyltransferase (comt) gene and cocaine dependence by Lohoff, F.W, Weller, A.E, Bloch, P.J, Ferraro, T.N, Kampman, K.M, Pettinati, H.M, Oslin, D.W, Dackis, C.A, O'Brien, C.P, Berrettini, W.H

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Interaction between polymorphisms in serotonin transporter genes predict treatment response to venlafaxine XR in generalized anxiety disorder by Lohoff, F.W, Narasimhan, S, Rickels, K

“…Variation in genes involved in serotonergic signaling is thought to be associated with antidepressant treatment response in generalized anxiety disorder (GAD)…”
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Serotonin receptor 2A (HTR2A) gene polymorphism predicts treatment response to venlafaxine XR in generalized anxiety disorder by Lohoff, F W, Aquino, T D, Narasimhan, S, Multani, P K, Etemad, B, Rickels, K

“…Generalized anxiety disorder (GAD) is a chronic psychiatric disorder with significant morbidity and mortality. Antidepressant drugs are the preferred choice…”
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Genetic variation in OPRD1 and the response to treatment for opioid dependence with buprenorphine in European-American females by 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

“…Two commonly prescribed treatments for opioid addiction are methadone and buprenorphine. Although these drugs show some efficacy in treating opioid dependence,…”
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Confirmation of association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) gene and bipolar I disorder by Lohoff, F.W., Sander, T., Ferraro, T.N., Dahl, J.P., Gallinat, J., Berrettini, W.H.

“…Recent studies have indicated that the brain‐derived neurotrophic factor (BDNF) gene is involved in the etiology of bipolar disorder (BPD). Two family‐based…”
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Exome sequence analysis of Finnish patients with clozapine-induced agranulocytosis by 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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Functional genetic variants in the vesicular monoamine transporter 1 modulate emotion processing by 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

“…Emotional behavior is in part heritable and often disrupted in psychopathology. Identification of specific genetic variants that drive this heritability may…”
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Supportive evidence for an allelic association of the human KCNJ10 potassium channel gene with idiopathic generalized epilepsy by Lenzen, K.P., Heils, A., Lorenz, S., Hempelmann, A., Höfels, S., Lohoff, F.W., Schmitz, B., Sander, T.

“…Quantitative trait loci (QTL) mapping in mice revealed a seizure-related QTL ( Szs1), for which the inward-rectifying potassium channel Kcnj10 is the most…”
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