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

Effects of BDNF Val(66)Met genotype and schizophrenia familial risk on a neural functional network for cognitive control in humans

BDNF Val(66)Met 基因型和精神分裂症家族风险对人类认知控制神经功能网络的影响

Schweiger, J I; Bilek, E; Schäfer, A; Braun, U; Moessnang, C; Harneit, A; Post, P; Otto, K; Romanczuk-Seiferth, N; Erk, S; Wackerhagen, C; Mattheisen, M; Mühleisen, T W; Cichon, S; Nöthen, M M; Frank, J; Witt, S H; Rietschel, M; Heinz, A; Walter, H; Meyer-Lindenberg, A; Tost, H

The protocadherin 17 gene affects cognition, personality, amygdala structure and function, synapse development and risk of major mood disorders

原钙黏蛋白17基因影响认知、人格、杏仁核结构和功能、突触发育以及罹患严重情绪障碍的风险。

Chang, H; Hoshina, N; Zhang, C; Ma, Y; Cao, H; Wang, Y; Wu, D-D; Bergen, S E; Landén, M; Hultman, C M; Preisig, M; Kutalik, Z; Castelao, E; Grigoroiu-Serbanescu, M; Forstner, A J; Strohmaier, J; Hecker, J; Schulze, T G; Müller-Myhsok, B; Reif, A; Mitchell, P B; Martin, N G; Schofield, P R; Cichon, S; Nöthen, M M; Walter, H; Erk, S; Heinz, A; Amin, N; van Duijn, C M; Meyer-Lindenberg, A; Tost, H; Xiao, X; Yamamoto, T; Rietschel, M; Li, M

Genetic effects influencing risk for major depressive disorder in China and Europe

遗传因素对中国和欧洲重度抑郁症风险的影响

Bigdeli, T B; Ripke, S; Peterson, R E; Trzaskowski, M; Bacanu, S-A; Abdellaoui, A; Andlauer, T F M; Beekman, A T F; Berger, K; Blackwood, D H R; Boomsma, D I; Breen, G; Buttenschøn, H N; Byrne, E M; Cichon, S; Clarke, T-K; Couvy-Duchesne, B; Craddock, N; de Geus, E J C; Degenhardt, F; Dunn, E C; Edwards, A C; Fanous, A H; Forstner, A J; Frank, J; Gill, M; Gordon, S D; Grabe, H J; Hamilton, S P; Hardiman, O; Hayward, C; Heath, A C; Henders, A K; Herms, S; Hickie, I B; Hoffmann, P; Homuth, G; Hottenga, J-J; Ising, M; Jansen, R; Kloiber, S; Knowles, J A; Lang, M; Li, Q S; Lucae, S; MacIntyre, D J; Madden, P A F; Martin, N G; McGrath, P J; McGuffin, P; McIntosh, A M; Medland, S E; Mehta, D; Middeldorp, C M; Milaneschi, Y; Montgomery, G W; Mors, O; Müller-Myhsok, B; Nauck, M; Nyholt, D R; Nöthen, M M; Owen, M J; Penninx, B W J H; Pergadia, M L; Perlis, R H; Peyrot, W J; Porteous, D J; Potash, J B; Rice, J P; Rietschel, M; Riley, B P; Rivera, M; Schoevers, R; Schulze, T G; Shi, J; Shyn, S I; Smit, J H; Smoller, J W; Streit, F; Strohmaier, J; Teumer, A; Treutlein, J; Van der Auwera, S; van Grootheest, G; van Hemert, A M; Völzke, H; Webb, B T; Weissman, M M; Wellmann, J; Willemsen, G; Witt, S H; Levinson, D F; Lewis, C M; Wray, N R; Flint, J; Sullivan, P F; Kendler, K S

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

全基因组关联研究揭示边缘型人格障碍与双相情感障碍、重度抑郁症和精神分裂症存在遗传重叠

Witt, S H; Streit, F; Jungkunz, M; Frank, J; Awasthi, S; Reinbold, C S; Treutlein, J; Degenhardt, F; Forstner, A J; Heilmann-Heimbach, S; Dietl, L; Schwarze, C E; Schendel, D; Strohmaier, J; Abdellaoui, A; Adolfsson, R; Air, T M; Akil, H; Alda, M; Alliey-Rodriguez, N; Andreassen, O A; Babadjanova, G; Bass, N J; Bauer, M; Baune, B T; Bellivier, F; Bergen, S; Bethell, A; Biernacka, J M; Blackwood, D H R; Boks, M P; Boomsma, D I; Børglum, A D; Borrmann-Hassenbach, M; Brennan, P; Budde, M; Buttenschøn, H N; Byrne, E M; Cervantes, P; Clarke, T-K; Craddock, N; Cruceanu, C; Curtis, D; Czerski, P M; Dannlowski, U; Davis, T; de Geus, E J C; Di Florio, A; Djurovic, S; Domenici, E; Edenberg, H J; Etain, B; Fischer, S B; Forty, L; Fraser, C; Frye, M A; Fullerton, J M; Gade, K; Gershon, E S; Giegling, I; Gordon, S D; Gordon-Smith, K; Grabe, H J; Green, E K; Greenwood, T A; Grigoroiu-Serbanescu, M; Guzman-Parra, J; Hall, L S; Hamshere, M; Hauser, J; Hautzinger, M; Heilbronner, U; Herms, S; Hitturlingappa, S; Hoffmann, P; Holmans, P; Hottenga, J-J; Jamain, S; Jones, I; Jones, L A; Juréus, A; Kahn, R S; Kammerer-Ciernioch, J; Kirov, G; Kittel-Schneider, S; Kloiber, S; Knott, S V; Kogevinas, M; Landén, M; Leber, M; Leboyer, M; Li, Q S; Lissowska, J; Lucae, S; Martin, N G; Mayoral-Cleries, F; McElroy, S L; McIntosh, A M; McKay, J D; McQuillin, A; Medland, S E; Middeldorp, C M; Milaneschi, Y; Mitchell, P B; Montgomery, G W; Morken, G; Mors, O; Mühleisen, T W; Müller-Myhsok, B; Myers, R M; Nievergelt, C M; Nurnberger, J I; O'Donovan, M C; Loohuis, L M O; Ophoff, R; Oruc, L; Owen, M J; Paciga, S A; Penninx, B W J H; Perry, A; Pfennig, A; Potash, J B; Preisig, M; Reif, A; Rivas, F; Rouleau, G A; Schofield, P R; Schulze, T G; Schwarz, M; Scott, L; Sinnamon, G C B; Stahl, E A; Strauss, J; Turecki, G; Van der Auwera, S; Vedder, H; Vincent, J B; Willemsen, G; Witt, C C; Wray, N R; Xi, H S; Tadic, A; Dahmen, N; Schott, B H; Cichon, S; Nöthen, M M; Ripke, S; Mobascher, A; Rujescu, D; Lieb, K; Roepke, S; Schmahl, C; Bohus, M; Rietschel, M

Functional neuroimaging effects of recently discovered genetic risk loci for schizophrenia and polygenic risk profile in five RDoC subdomains.

最近发现的精神分裂症遗传风险位点和五种 RDoC 子域中的多基因风险特征的功能神经影像学效应

Erk S, Mohnke S, Ripke S, Lett T A, Veer I M, Wackerhagen C, Grimm O, Romanczuk-Seiferth N, Degenhardt F, Tost H, Mattheisen M, Mühleisen T W, Charlet K, Skarabis N, Kiefer F, Cichon S, Witt S H, Nöthen M M, Rietschel M, Heinz A, Meyer-Lindenberg A, Walter H

Mutational spectrum of the SERPING1 gene in Swiss patients with hereditary angioedema

瑞士遗传性血管性水肿患者中SERPING1基因的突变谱

Steiner, U C; Keller, M; Schmid, P; Cichon, S; Wuillemin, W A

GWAS for executive function and processing speed suggests involvement of the CADM2 gene

针对执行功能和处理速度的全基因组关联研究(GWAS)表明,CADM2基因参与其中。

Ibrahim-Verbaas, C A; Bressler, J; Debette, S; Schuur, M; Smith, A V; Bis, J C; Davies, G; Trompet, S; Smith, J A; Wolf, C; Chibnik, L B; Liu, Y; Vitart, V; Kirin, M; Petrovic, K; Polasek, O; Zgaga, L; Fawns-Ritchie, C; Hoffmann, P; Karjalainen, J; Lahti, J; Llewellyn, D J; Schmidt, C O; Mather, K A; Chouraki, V; Sun, Q; Resnick, S M; Rose, L M; Oldmeadow, C; Stewart, M; Smith, B H; Gudnason, V; Yang, Q; Mirza, S S; Jukema, J W; deJager, P L; Harris, T B; Liewald, D C; Amin, N; Coker, L H; Stegle, O; Lopez, O L; Schmidt, R; Teumer, A; Ford, I; Karbalai, N; Becker, J T; Jonsdottir, M K; Au, R; Fehrmann, Rsn; Herms, S; Nalls, M; Zhao, W; Turner, S T; Yaffe, K; Lohman, K; van Swieten, J C; Kardia, Slr; Knopman, D S; Meeks, W M; Heiss, G; Holliday, E G; Schofield, P W; Tanaka, T; Stott, D J; Wang, J; Ridker, P; Gow, A J; Pattie, A; Starr, J M; Hocking, L J; Armstrong, N J; McLachlan, S; Shulman, J M; Pilling, L C; Eiriksdottir, G; Scott, R J; Kochan, N A; Palotie, A; Hsieh, Y-C; Eriksson, J G; Penman, A; Gottesman, R F; Oostra, B A; Yu, L; DeStefano, A L; Beiser, A; Garcia, M; Rotter, J I; Nöthen, M M; Hofman, A; Slagboom, P E; Westendorp, Rgj; Buckley, B M; Wolf, P A; Uitterlinden, A G; Psaty, B M; Grabe, H J; Bandinelli, S; Chasman, D I; Grodstein, F; Räikkönen, K; Lambert, J-C; Porteous, D J; Price, J F; Sachdev, P S; Ferrucci, L; Attia, J R; Rudan, I; Hayward, C; Wright, A F; Wilson, J F; Cichon, S; Franke, L; Schmidt, H; Ding, J; de Craen, Ajm; Fornage, M; Bennett, D A; Deary, I J; Ikram, M A; Launer, L J; Fitzpatrick, A L; Seshadri, S; van Duijn, C M; Mosley, T H

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

Identification of increased genetic risk scores for schizophrenia in treatment-resistant patients

识别难治性精神分裂症患者中升高的遗传风险评分

Frank, J; Lang, M; Witt, S H; Strohmaier, J; Rujescu, D; Cichon, S; Degenhardt, F; Nöthen, M M; Collier, D A; Ripke, S; Naber, D; Rietschel, M

Evaluating historical candidate genes for schizophrenia

评估精神分裂症的历史候选基因

Farrell, M S; Werge, T; Sklar, P; Owen, M J; Ophoff, R A; O'Donovan, M C; Corvin, A; Cichon, S; Sullivan, P F