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

Vasoneuronal signalling plays a causal role in migraine pathogenesis: the ‘Con’ argument

血管神经信号传导在偏头痛发病机制中起因果作用:反方论点

Beghi, Ettore; Derevyanko, K; Loder, E; Weizenbaum, E; Zidverc-Trajkovic, J; Pekmezovic, T; Radojicic, A; Podgorac, A; Sternic, N; Khan, I; Zafar, H; Ahmed, F; Palmisani, S; Smith, T; Arcioni, R; Mercieri, M; Vano, V; Tigano, S; Negro, A; Al-Kaisy, A; Martelletti, P; Sacco, S; Ornello, R; Ripa, P; Pistoia, F; Carolei, A; Christensen, AF; Esserlind, AL; Werge, T; Stefansson, H; Olesen, J; Sretenovic, S; Stanic, A; Mitrovic, A; Mostardini, C; Pauletti, G; Ahmed, F; Dikomitis, L; Zafar, HW; Goadsby, P; Paemeliere, K; Hung, CJ; Wu, CC; Hywel, B; Silver, N; Zaletel, M; Pretnar, J Oblak; Zvan, B; Perko, D; Grazzi, L; Usai, S; Bussone, G; Supronsinchai, W; Srikiatkhachorn, A; Bratbak, D; Nordgård, S; Stovner, L; Linde, M; Tronvik, E; Candan, F Un; Schulte, L; Sprenger, C; May, A; Vukasinovic, N; Jolic, S; Milosevic, V; Zivkovic, M; Slankamenac, P; Csepany, E; Toth, M; Janoska, D; Kellermann, I; Hajnal, B; Gyure, T; Bozsik, G; Ertsey, C; Sugrue, J; Thomkins, E; Ruttledge, M; Csepany, E; Toth, M; Janoska, D; Nagy, Z; Balogh, E; Gyüre, T; Bozsik, G; Ertsey, C; Hambardzumyan, HD; Manvelyan, HM; Mostardini, C; Nola, G; Giovanni, R; Avetisyan, A; Harutyunyan, AS; Vekilyan, HR; Karapetyan, AH; Gevorgyan, EM; Manvelyan, HM; Grosu, O; Moldovanu, I; Odobescu, S; Rotaru, L; Johnston, M; Jordan, SE; Charles, AC; Miller, S; Correia, F; Lagrata, S; Matharu, M; Pitino, R; Raieli, V; Consolo, F; La Franca, G; Puma, D; Santangelo, G; Vanadia, F; Tassorelli, C; Falzone, Y; De Icco, R; Cuzzoni, MG; Nappi, G; Sances, G; Gil-Gouveia, R; Oliveira, AG; Martins, IP; Vekilyan, HR; Karapetyan, AA; Karapetyan, AH; Gevorgyan, EM; Manvelyan, HM; Haghdoost, F; Gharzi, M; Faez, F; Hosseinzadeh, E; Zandifar, A; Zandifar, S; Javanmard, SH; Mosek, A; Dano, M; Fainmesser, Y; Hybloom, Z; Lambru, G; Shanahan, P; Davagnanam, I; Matharu, M; Braschinsky, M; Rakitin, A; Zmachinskaja, N; Zukovskaja, O; Saar, B; Karask, A; Sabre, L; Ljubisavljevic, S; Zidverc-Trajkovic, J; Kuqo, A; Kruja, J; Rao, K; Rekha, J; Mohan, S; Savi, L; Pinessi, L; Condello, C; Maarbjerg, S; Wolfram, F; Gozalov, A; Olesen, J; Bendtsen, L; Kristoffersen, ES; Lundqvist, C; Frich, JC; Sahin, HA; Turkel, Y; Sahin, EO; Ozbenli, T; Madsen, SK; Munksgaard, SB; Wienecke, T; Abramova, M; Novoselova, S; Stepanova, I; Shurupova, N; Burmeister, J; Holle, D; Bock, E; Ose, C; Diener, HC; Obermann, M; Genizi, J; Marom, D; Srugo, I; Kerem, N; Sawanyawisuth, K; Waranon, W; Pongtipakorn, K; Kongbunkiat, K; Limpawattana, P; Senthong, V; Chindaprasirt, J; Chotmongkol, V; Kanpittaya, J; Intapan, PM; Maleewong, W; Kitkhuandee, A; Nordgaard, JC; Kruse, LS; Moeller, M; Kruuse, C; Barloese, M; Jennum, P; Lund, N; Jensen, R; Hansen, J Møller; Goadsby, PJ; Charles, A; Khalil, M; Zafar, H; Ahmed, F; Grazzi, L; Usai, S; Bussone, G; Sava, S; Baschi, R; Vecchio, E; De Pasqua, V; Schoenen, J; Magis, D; Kovacevic, N Milovanovic; Zaric, N; Savic, M; Harutyunyan, AS; Avetisyan, AY; Vekilyan, HR; Karapetyan, AH; Gevorgyan, EM; Manvelyan, HM; Gao, Y; Drew, P; Prabhakar, P; Arkush, L; Scott, R; Aylett, S; Akhmadeeva, L; Valeeva, D; Naprienko, M; Goldobina, L; Rayanova, G; Veytsman, B; Torabzadeh, N; Asadnia, S; Azar, F Sepehrian; Zamanlu, M; Mohammadi, NAVA; Caruana, G; Bertozzi, N; Grieco, MP; Raposio, E; Togha, M; Taghdiri, F; Jahromi, S Razeghi; Zafar, H; Khalil, M; Ahmed, F; Kruja, J; Alimehmeti, I; Dobi, D; Kuqo, A; Mijo, S; Grabova, S; Rakacolli, M; Skorobogatykh, K; Azimova, J; Sergeev, A; Klimov, E; Tabeeva, G; Fokina, N; Korobeynikova, L; Kokaeva, Z; Kivellos, S; Skifti, S; Vithoulkas, G; Ansari, H; Lisotto, C; Mainardi, F; Maggioni, F; Zanchin, G; Vigàno, A; Bogdanov, VB; Noirhomme, Q; Guy, N; Dallel, R; Laureys, S; Phillips, C; Schoenen, J; Chatchaisak, D; Chetsawang, B; le Grand, SM; Govitrapong, P; Srikiatkhachorn, A; Pradhan, A; McGuire, B; Charles, A; Fischer, M; Wille, G; Klien, S; Broessner, G; Lampl, C; Haider, B; Schweiger, C; Tachibana, H; Danno, D; Abramova, MF; Stepanova, IA; Novoselova, SN; Eftekhari, S; Warfvinge, K; Blixt, F; Edvinsson, L; Watanabe, Y; Tateno, H; Hirata, K; Mainardi, F; Maggioni, F; Lisotto, C; Zanchin, G; Danno, D; Tachibana, H; Nesbitt, A; Marin, J; Goadsby, P; Viana, M; Tassorelli, C; Allena, M; Nappi, G; Antonaci, F; Quintas, MS; Neto, JL; Pereira-Monteiro, J; Barros, J; Sequeiros, J; Sousa, A; Alonso, I; Lemos, C; Cosentino, G; Paladino, P; Fierro, B; Brighina, F; Christian, CL; Ikawa, M; Ikawa, M; Mack, J; Squier, W; Savi, LT; Condello, V; Bert, F; Pinessi, L; Kim, BK; Stanic, I; Sretenovic, LJ; Larrosa, D; Benavente, L; Calleja, S; Gonzalez-Delgado, M; Pascual, J; Carotenuto, M; Antinolfi, L; Faraldo, MA; Di Dona, A; Esposito, M; Nicolodi, M; Hougaard, A; Amin, FM; Hauge, AW; Ashina, M; Olesen, J; Prabhakar, P; Simpson, JC; Matsumori, Y; Fujiwara, S; Piazza, F; Chiappedi, M; Maffioletti, E; Galli, F; Spada, G; Nappi, G; Balottin, U; Labruijere, S; Ramirez Rosas, MB; De Vries, R; Danser, AHJ; MaassenVanDenBrink, A; Kalashyan, R; Voiticovschi-Iosob, C; Moldovanu, I; Shi, L; Rao, S; Sun, H; Wild, K; Xu, C; Caspersen, N; Hirsvang, JR; Kroell, L; Jadidi, F; Baad-Hansen, L; Svensson, P; Jensen, R; Sergeev, A; Mesherina, M; Tabeeva, G; Sacco, Simona; Carolei, Antonio; Karsan, Nazia; Goadsby, Peter J

Pharmacogenetic drug use in young danish individuals with severe mental disorders

丹麦年轻重度精神障碍患者的药物遗传学用药

Buyvalenko, U V; Pokrovskaya, E V; Sousa, S M; Areias, D; Dionísio, R; Portela, C; Leitão, F; Oliveira, N; Lunenburg, C; Ishtiak-Ahmed, K; Werge, T; Gasse, C

Genetic risk scores and family history as predictors of schizophrenia in Nordic registers

北欧登记数据中遗传风险评分和家族史作为精神分裂症预测指标

Lu, Y; Pouget, J G; Andreassen, O A; Djurovic, S; Esko, T; Hultman, C M; Metspalu, A; Milani, L; Werge, T; Sullivan, P F

15q13.3 homozygous knockout mouse model display epilepsy-, autism- and schizophrenia-related phenotypes.

15q13.3纯合敲除小鼠模型表现出癫痫、自闭症和精神分裂症相关的表型

Forsingdal A, Fejgin K, Nielsen V, Werge T, Nielsen J

Associations between social cognition, skills, and function and subclinical negative and positive symptoms in 22q11.2 deletion syndrome

22q11.2缺失综合征患者的社会认知、技能和功能与亚临床阴性和阳性症状之间的关联

Vangkilde, A; Jepsen, J R M; Schmock, H; Olesen, C; Arnarsdóttir, S; Baaré, W F C; Plessen, K J; Didriksen, M; Siebner, H R; Werge, T; Olsen, L

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

Common variant at 16p11.2 conferring risk of psychosis

16p11.2 上的常见变异会增加患精神病的风险

Steinberg, S; de Jong, S; Mattheisen, M; Costas, J; Demontis, D; Jamain, S; Pietiläinen, O P H; Lin, K; Papiol, S; Huttenlocher, J; Sigurdsson, E; Vassos, E; Giegling, I; Breuer, R; Fraser, G; Walker, N; Melle, I; Djurovic, S; Agartz, I; Tuulio-Henriksson, A; Suvisaari, J; Lönnqvist, J; Paunio, T; Olsen, L; Hansen, T; Ingason, A; Pirinen, M; Strengman, E; Hougaard, D M; Orntoft, T; Didriksen, M; Hollegaard, M V; Nordentoft, M; Abramova, L; Kaleda, V; Arrojo, M; Sanjuán, J; Arango, C; Etain, B; Bellivier, F; Méary, A; Schürhoff, F; Szoke, A; Ribolsi, M; Magni, V; Siracusano, A; Sperling, S; Rossner, M; Christiansen, C; Kiemeney, L A; Franke, B; van den Berg, L H; Veldink, J; Curran, S; Bolton, P; Poot, M; Staal, W; Rehnstrom, K; Kilpinen, H; Freitag, C M; Meyer, J; Magnusson, P; Saemundsen, E; Martsenkovsky, I; Bikshaieva, I; Martsenkovska, I; Vashchenko, O; Raleva, M; Paketchieva, K; Stefanovski, B; Durmishi, N; Pejovic Milovancevic, M; Lecic Tosevski, D; Silagadze, T; Naneishvili, N; Mikeladze, N; Surguladze, S; Vincent, J B; Farmer, A; Mitchell, P B; Wright, A; Schofield, P R; Fullerton, J M; Montgomery, G W; Martin, N G; Rubino, I A; van Winkel, R; Kenis, G; De Hert, M; Réthelyi, J M; Bitter, I; Terenius, L; Jönsson, E G; Bakker, S; van Os, J; Jablensky, A; Leboyer, M; Bramon, E; Powell, J; Murray, R; Corvin, A; Gill, M; Morris, D; O'Neill, F A; Kendler, K; Riley, B; Craddock, N; Owen, M J; O'Donovan, M C; Thorsteinsdottir, U; Kong, A; Ehrenreich, H; Carracedo, A; Golimbet, V; Andreassen, O A; Børglum, A D; Mors, O; Mortensen, P B; Werge, T; Ophoff, R A; Nöthen, M M; Rietschel, M; Cichon, S; Ruggeri, M; Tosato, S; Palotie, A; St Clair, D; Rujescu, D; Collier, D A; Stefansson, H; Stefansson, K

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

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia

全基因组关联研究数据挖掘和独立重复验证表明,心肌病相关基因5 (CMYA5) 是精神分裂症的风险基因。

Chen, X; Lee, G; Maher, B S; Fanous, A H; Chen, J; Zhao, Z; Guo, A; van den Oord, E; Sullivan, P F; Shi, J; Levinson, D F; Gejman, P V; Sanders, A; Duan, J; Owen, M J; Craddock, N J; O'Donovan, M C; Blackman, J; Lewis, D; Kirov, G K; Qin, W; Schwab, S; Wildenauer, D; Chowdari, K; Nimgaonkar, V; Straub, R E; Weinberger, D R; O'Neill, F A; Walsh, D; Bronstein, M; Darvasi, A; Lencz, T; Malhotra, A K; Rujescu, D; Giegling, I; Werge, T; Hansen, T; Ingason, A; Nöethen, M M; Rietschel, M; Cichon, S; Djurovic, S; Andreassen, O A; Cantor, R M; Ophoff, R; Corvin, A; Morris, D W; Gill, M; Pato, C N; Pato, M T; Macedo, A; Gurling, H M D; McQuillin, A; Pimm, J; Hultman, C; Lichtenstein, P; Sklar, P; Purcell, S M; Scolnick, E; St Clair, D; Blackwood, D H R; Kendler, K S