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

Meta-analysis of genome-wide association studies for personality

人格全基因组关联研究的荟萃分析

de Moor, M H M; Costa, P T; Terracciano, A; Krueger, R F; de Geus, E J C; Toshiko, T; Penninx, B W J H; Esko, T; Madden, P A F; Derringer, J; Amin, N; Willemsen, G; Hottenga, J-J; Distel, M A; Uda, M; Sanna, S; Spinhoven, P; Hartman, C A; Sullivan, P; Realo, A; Allik, J; Heath, A C; Pergadia, M L; Agrawal, A; Lin, P; Grucza, R; Nutile, T; Ciullo, M; Rujescu, D; Giegling, I; Konte, B; Widen, E; Cousminer, D L; Eriksson, J G; Palotie, A; Peltonen, L; Luciano, M; Tenesa, A; Davies, G; Lopez, L M; Hansell, N K; Medland, S E; Ferrucci, L; Schlessinger, D; Montgomery, G W; Wright, M J; Aulchenko, Y S; Janssens, A C J W; Oostra, B A; Metspalu, A; Abecasis, G R; Deary, I J; Räikkönen, K; Bierut, L J; Martin, N G; van Duijn, C M; Boomsma, D I

Expanding the range of ZNF804A variants conferring risk of psychosis

扩大ZNF804A变异体的范围,这些变异体与精神病风险相关

Steinberg, S; Mors, O; Børglum, A D; Gustafsson, O; Werge, T; Mortensen, P B; Andreassen, O A; Sigurdsson, E; Thorgeirsson, T E; Böttcher, Y; Olason, P; Ophoff, R A; Cichon, S; Gudjonsdottir, I H; Pietiläinen, O P H; Nyegaard, M; Tuulio-Henriksson, A; Ingason, A; Hansen, T; Athanasiu, L; Suvisaari, J; Lonnqvist, J; Paunio, T; Hartmann, A; Jürgens, G; Nordentoft, M; Hougaard, D; Norgaard-Pedersen, B; Breuer, R; Möller, H-J; Giegling, I; Glenthøj, B; Rasmussen, H B; Mattheisen, M; Bitter, I; Réthelyi, J M; Sigmundsson, T; Fossdal, R; Thorsteinsdottir, U; Ruggeri, M; Tosato, S; Strengman, E; Kiemeney, L A; Melle, I; Djurovic, S; Abramova, L; Kaleda, V; Walshe, M; Bramon, E; Vassos, E; Li, T; Fraser, G; Walker, N; Toulopoulou, T; Yoon, J; Freimer, N B; Cantor, R M; Murray, R; Kong, A; Golimbet, V; Jönsson, E G; Terenius, L; Agartz, I; Petursson, H; Nöthen, M M; Rietschel, M; Peltonen, L; Rujescu, D; Collier, D A; Stefansson, H; St Clair, D; Stefansson, K

Copy number variations of chromosome 16p13.1 region associated with schizophrenia

16p13.1染色体区域的拷贝数变异与精神分裂症相关

Ingason, A; Rujescu, D; Cichon, S; Sigurdsson, E; Sigmundsson, T; Pietiläinen, O P H; Buizer-Voskamp, J E; Strengman, E; Francks, C; Muglia, P; Gylfason, A; Gustafsson, O; Olason, P I; Steinberg, S; Hansen, T; Jakobsen, K D; Rasmussen, H B; Giegling, I; Möller, H-J; Hartmann, A; Crombie, C; Fraser, G; Walker, N; Lonnqvist, J; Suvisaari, J; Tuulio-Henriksson, A; Bramon, E; Kiemeney, L A; Franke, B; Murray, R; Vassos, E; Toulopoulou, T; Mühleisen, T W; Tosato, S; Ruggeri, M; Djurovic, S; Andreassen, O A; Zhang, Z; Werge, T; Ophoff, R A; Rietschel, M; Nöthen, M M; Petursson, H; Stefansson, H; Peltonen, L; Collier, D; Stefansson, K; St Clair, D M

Hostility in adolescents and adults: a genome-wide association study of the Young Finns

青少年和成年人的敌意:芬兰青年人群的全基因组关联研究

Merjonen, P; Keltikangas-Järvinen, L; Jokela, M; Seppälä, I; Lyytikäinen, L-P; Pulkki-Råback, L; Kivimäki, M; Elovainio, M; Kettunen, J; Ripatti, S; Kähönen, M; Viikari, J; Palotie, A; Peltonen, L; Raitakari, O T; Lehtimäki, T

Design, recruitment, logistics, and data management of the GEHA (Genetics of Healthy Ageing) project

GEHA(健康老龄化遗传学)项目的设计、招募、后勤和数据管理

Skytthe, A; Valensin, S; Jeune, B; Cevenini, E; Balard, F; Beekman, M; Bezrukov, V; Blanche, H; Bolund, L; Broczek, K; Carru, C; Christensen, K; Christiansen, L; Collerton, J C; Cotichini, R; de Craen, A J M; Dato, S; Davies, K; De Benedictis, G; Deiana, L; Flachsbart, F; Gampe, J; Gilbault, C; Gonos, E S; Haimes, E; Hervonen, A; Hurme, M A; Janiszewska, D; Jylhä, M; Kirkwood, T B L; Kristensen, P; Laiho, P; Leon, A; Marchisio, A; Masciulli, R; Nebel, A; Passarino, G; Pelicci, G; Peltonen, L; Perola, M; Poulain, M; Rea, I M; Remacle, J; Robine, J M; Schreiber, S; Scurti, M; Sevini, F; Sikora, E; Skouteri, A; Slagboom, P E; Spazzafumo, L; Stazi, M A; Toccaceli, V; Toussaint, O; Törnwall, O; Vaupel, J W; Voutetakis, K; Franceschi, C

Findings from bipolar disorder genome-wide association studies replicate in a Finnish bipolar family-cohort

双相情感障碍全基因组关联研究的结果在芬兰双相情感障碍家族队列中得到重复验证

Ollila, H M; Soronen, P; Silander, K; Palo, O M; Kieseppä, T; Kaunisto, M A; Lönnqvist, J; Peltonen, L; Partonen, T; Paunio, T

Meta-analysis of 32 genome-wide linkage studies of schizophrenia

对32项精神分裂症全基因组连锁研究的荟萃分析

Ng, M Y M; Levinson, D F; Faraone, S V; Suarez, B K; DeLisi, L E; Arinami, T; Riley, B; Paunio, T; Pulver, A E; Irmansyah; Holmans, P A; Escamilla, M; Wildenauer, D B; Williams, N M; Laurent, C; Mowry, B J; Brzustowicz, L M; Maziade, M; Sklar, P; Garver, D L; Abecasis, G R; Lerer, B; Fallin, M D; Gurling, H M D; Gejman, P V; Lindholm, E; Moises, H W; Byerley, W; Wijsman, E M; Forabosco, P; Tsuang, M T; Hwu, H-G; Okazaki, Y; Kendler, K S; Wormley, B; Fanous, A; Walsh, D; O'Neill, F A; Peltonen, L; Nestadt, G; Lasseter, V K; Liang, K Y; Papadimitriou, G M; Dikeos, D G; Schwab, S G; Owen, M J; O'Donovan, M C; Norton, N; Hare, E; Raventos, H; Nicolini, H; Albus, M; Maier, W; Nimgaonkar, V L; Terenius, L; Mallet, J; Jay, M; Godard, S; Nertney, D; Alexander, M; Crowe, R R; Silverman, J M; Bassett, A S; Roy, M-A; Mérette, C; Pato, C N; Pato, M T; Roos, J Louw; Kohn, Y; Amann-Zalcenstein, D; Kalsi, G; McQuillin, A; Curtis, D; Brynjolfson, J; Sigmundsson, T; Petursson, H; Sanders, A R; Duan, J; Jazin, E; Myles-Worsley, M; Karayiorgou, M; Lewis, C M

Common candidate gene variants are associated with QT interval duration in the general population

常见候选基因变异与一般人群的QT间期持续时间相关

Marjamaa, A; Newton-Cheh, C; Porthan, K; Reunanen, A; Lahermo, P; Väänänen, H; Jula, A; Karanko, H; Swan, H; Toivonen, L; Nieminen, M S; Viitasalo, M; Peltonen, L; Oikarinen, L; Palotie, A; Kontula, K; Salomaa, V

Replication of restless legs syndrome loci in three European populations

在三个欧洲人群中复制不宁腿综合征基因位点

Kemlink, D; Polo, O; Frauscher, B; Gschliesser, V; Högl, B; Poewe, W; Vodicka, P; Vavrova, J; Sonka, K; Nevsimalova, S; Schormair, B; Lichtner, P; Silander, K; Peltonen, L; Gieger, C; Wichmann, H E; Zimprich, A; Roeske, D; Müller-Myhsok, B; Meitinger, T; Winkelmann, J

Trait components provide tools to dissect the genetic susceptibility of migraine

性状成分为剖析偏头痛的遗传易感性提供了工具

Anttila, V; Kallela, M; Oswell, G; Kaunisto, M A; Nyholt, D R; Hamalainen, E; Havanka, H; Ilmavirta, M; Terwilliger, J; Sobel, E; Peltonen, L; Kaprio, J; Farkkila, M; Wessman, M; Palotie, A