日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

No association between peripheral serotonin-gene-related DNA methylation and brain serotonin neurotransmission in the healthy and depressed state

在健康状态和抑郁状态下,外周血清素基因相关DNA甲基化与脑内血清素神经传递之间无关联。

Bruzzone, S E P; Ozenne, B; Fisher, P M; Ortega, G; Jensen, P S; Dam, V H; Svarer, C; Knudsen, G M; Lesch, K P; Frokjaer, V G

Longitudinal analyses of the DNA methylome in deployed military servicemen identify susceptibility loci for post-traumatic stress disorder

对已部署军人DNA甲基化组的纵向分析发现了创伤后应激障碍的易感基因位点

Rutten, B P F; Vermetten, E; Vinkers, C H; Ursini, G; Daskalakis, N P; Pishva, E; de Nijs, L; Houtepen, L C; Eijssen, L; Jaffe, A E; Kenis, G; Viechtbauer, W; van den Hove, D; Schraut, K G; Lesch, K-P; Kleinman, J E; Hyde, T M; Weinberger, D R; Schalkwyk, L; Lunnon, K; Mill, J; Cohen, H; Yehuda, R; Baker, D G; Maihofer, A X; Nievergelt, C M; Geuze, E; Boks, M P M

In Memoriam: Dennis L. Murphy, MD – Neuropsychopharmacologist, Scientifc Mentor, and Friend

谨此缅怀:丹尼斯·L·墨菲医学博士——神经精神药理学家、科学导师及挚友

Clifford, David B; Lesch, K P

Genetically driven brain serotonin deficiency facilitates panic-like escape behavior in mice

基因驱动的脑内血清素缺乏会促进小鼠出现类似恐慌的逃避行为。

Waider, J; Popp, S; Lange, M D; Kern, R; Kolter, J F; Kobler, J; Donner, N C; Lowe, K R; Malzbender, J H; Brazell, C J; Arnold, M R; Aboagye, B; Schmitt-Böhrer, A; Lowry, C A; Pape, H C; Lesch, K P

Serotonergic modulation of 'waiting impulsivity' is mediated by the impulsivity phenotype in humans

血清素对“等待冲动”的调节是由人类的冲动表型介导的。

Neufang, S; Akhrif, A; Herrmann, C G; Drepper, C; Homola, G A; Nowak, J; Waider, J; Schmitt, A G; Lesch, K-P; Romanos, M

Exome chip analyses in adult attention deficit hyperactivity disorder

成人注意力缺陷多动障碍的外显子芯片分析

Zayats, T; Jacobsen, K K; Kleppe, R; Jacob, C P; Kittel-Schneider, S; Ribasés, M; Ramos-Quiroga, J A; Richarte, V; Casas, M; Mota, N R; Grevet, E H; Klein, M; Corominas, J; Bralten, J; Galesloot, T; Vasquez, A A; Herms, S; Forstner, A J; Larsson, H; Breen, G; Asherson, P; Gross-Lesch, S; Lesch, K P; Cichon, S; Gabrielsen, M B; Holmen, O L; Bau, C H D; Buitelaar, J; Kiemeney, L; Faraone, S V; Cormand, B; Franke, B; Reif, A; Haavik, J; Johansson, S

CO2 exposure as translational cross-species experimental model for panic

二氧化碳暴露作为恐慌症的跨物种转化实验模型

Leibold, N K; van den Hove, D L A; Viechtbauer, W; Buchanan, G F; Goossens, L; Lange, I; Knuts, I; Lesch, K P; Steinbusch, H W M; Schruers, K R J

MAOA gene hypomethylation in panic disorder-reversibility of an epigenetic risk pattern by psychotherapy

惊恐障碍中MAOA基因低甲基化——心理治疗可逆转表观遗传风险模式

Ziegler, C; Richter, J; Mahr, M; Gajewska, A; Schiele, M A; Gehrmann, A; Schmidt, B; Lesch, K-P; Lang, T; Helbig-Lang, S; Pauli, P; Kircher, T; Reif, A; Rief, W; Vossbeck-Elsebusch, A N; Arolt, V; Wittchen, H-U; Hamm, A O; Deckert, J; Domschke, K

Cadherin-13, a risk gene for ADHD and comorbid disorders, impacts GABAergic function in hippocampus and cognition

钙黏蛋白-13是注意力缺陷多动障碍及相关疾病的风险基因,它会影响海马体的GABA能功能和认知功能。

Rivero, O; Selten, M M; Sich, S; Popp, S; Bacmeister, L; Amendola, E; Negwer, M; Schubert, D; Proft, F; Kiser, D; Schmitt, A G; Gross, C; Kolk, S M; Strekalova, T; van den Hove, D; Resink, T J; Nadif Kasri, N; Lesch, K P

Genome-wide analysis of rare copy number variations reveals PARK2 as a candidate gene for attention-deficit/hyperactivity disorder

全基因组罕见拷贝数变异分析揭示PARK2是注意力缺陷/多动障碍的候选基因

Jarick, I; Volckmar, A-L; Pütter, C; Pechlivanis, S; Nguyen, T T; Dauvermann, M R; Beck, S; Albayrak, Ö; Scherag, S; Gilsbach, S; Cichon, S; Hoffmann, P; Degenhardt, F; Nöthen, M M; Schreiber, S; Wichmann, H-E; Jöckel, K-H; Heinrich, J; Tiesler, C M T; Faraone, S V; Walitza, S; Sinzig, J; Freitag, C; Meyer, J; Herpertz-Dahlmann, B; Lehmkuhl, G; Renner, T J; Warnke, A; Romanos, M; Lesch, K-P; Reif, A; Schimmelmann, B G; Hebebrand, J; Scherag, A; Hinney, A