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

Common and rare variant contributions to discontinuation of stimulant treatment in ADHD

常见和罕见变异对 ADHD 患者停止兴奋剂治疗的影响

Thirstrup, Janne Pia; Duan, Jinjie; Ribases Haro, Marta; Soler Artigas, Maria; Albiñana, Clara; Dalsgaard, Søren; Faraone, Stephen V; Werge, Thomas; Bybjerg-Grauholm, Jonas; Børglum, Anders D; Agerbo, Esben; Yao, Honghui; Chang, Zheng; Brikell, Isabell; Demontis, Ditte

Genome-wide association study of borderline personality disorder identifies 11 loci and highlights shared risk with mental and somatic disorders

全基因组关联研究发现边缘型人格障碍存在11个致病基因位点,并强调了其与精神和躯体疾病的共同风险。

Streit, Fabian; Awasthi, Swapnil; Hall, Alisha Sm; Braun, Alice; Niarchou, Maria; Marouli, Eirini; Babajide, Oladapo; Frank, Josef; Zillich, Lea; Callies, Carolin M; Avetyan, Diana; Zillich, Eric; Naamanka, Joonas; Gonzalez, Jean; Harder, Arvid; Lu, Yi; Aherrahrou, Zouhair; Ahmad, Zain-Ul-Abideen; Ask, Helga; Batzler, Anthony; Benros, Michael E; Brand-de Wilde, Odette M; Brunak, Søren; Bruun, Mie T; Christoffersen, Lea An; Colodro-Conde, Lucía; Coombes, Brandon J; Corfield, Elizabeth C; Dahmen, Norbert; Didriksen, Maria; Dinh, Khoa M; Djurovic, Srdjan; Dowsett, Joseph; Drange, Ole Kristian; Dukal, Helene; Edelmann, Susanne; Erikstrup, Christian; Espinola, Mariana K; Fassbinder, Eva; Faucon, Annika; de Sá, Diana S Ferreira; Foo, Jerome C; Gilles, Maria; Gutiérrez-Zotes, Alfonso; Hansen, Thomas F; Haraldsson, Magnus; Harper, R Patrick; Havdahl, Alexandra; Heilbronner, Urs; Herms, Stefan; Hjalgrim, Henrik; Hübel, Christopher; Jacob, Gitta A; Aagaard, Bitten; Jorgensen, Anders; Jungkunz, Martin; Kleindienst, Nikolaus; Knoblich, Nora; Koglin, Stefanie; Kraft, Julia; Krebs, Kristi; Lee, Christopher W; Lin, Yuhao; Lis, Stefanie; Lisoway, Amanda; Malogiannis, Ioannis A; Martinsen, Amy; Maslahati, Tolou; Merz, Katharina; Meyer-Lindenberg, Andreas; Mikkelsen, Susan; Mikkelsen, Christina; Mobascher, Arian; Muntané, Gerard; Oddsson, Asmundur; Ostrowski, Sisse R; Palviainen, Teemu; Pedersen, Ole Bv; Pedersen, Geir; Quinn, Liam; Reinhard, Matthias A; Ruths, Florian A; Schott, Björn H; Schredl, Michael; Schwarz, Emanuel; Schwarze, Cornelia E; Schwinn, Michael; Send, Tabea; Sigurdsson, Engilbert; Simon-Keller, Katja; Skuladottir, Astros T; Soler, Joaquim; Sonley, Anne; Sørensen, Erik; Stefansson, Hreinn; Straub, Peter; Suvisaari, Jaana; Tesli, Martin; Træholt, Jacob; Ullum, Henrik; Völker, Maja P; Walters, G Bragi; Wang, Rujia; Witt, Christian C; Zarbock, Gerhard; Zill, Peter; Zwart, John-Anker; Andreassen, Ole A; Arntz, Arnoud; Biernacka, Joanna M; Bohus, Martin; Breen, Gerome; Chapman, Alexander L; Cichon, Sven; Davis, Lea K; Deuschle, Michael; Euler, Sebastian; Herpertz, Sabine C; Hummelen, Benjamin; Jobst, Andrea; Kaprio, Jaakko; Kennedy, James L; Lehto, Kelli; Lieb, Klaus; Martorell, Lourdes; McMain, Shelley; Musil, Richard; Nieratschker, Vanessa; Nöthen, Markus M; Padberg, Frank; Palotie, Aarno; Pascual, Juan C; Perroud, Nader; Ramos-Quiroga, Josep A; Reichborn-Kjennerud, Ted; Ribases, Marta; Roepke, Stefan; Rujescu, Dan; Sanchez-Roige, Sandra; Schilling, Claudia; Schmahl, Christian; Stefansson, Kari; Thorgeirsson, Thorgeir E; Turecki, Gustavo; Vilella, Elisabet; Werge, Thomas; Winsvold, Bendik S; Wrege, Johannes; Rietschel, Marcella; Ripke, Stephan; Witt, Stephanie H

Contribution of Common Genetic Variants to Risk of Early-Onset Ischemic Stroke

常见遗传变异对早发性缺血性卒中风险的影响

Jaworek, Thomas; Xu, Huichun; Gaynor, Brady J; Cole, John W; Rannikmae, Kristiina; Stanne, Tara M; Tomppo, Liisa; Abedi, Vida; Amouyel, Philippe; Armstrong, Nicole D; Attia, John; Bell, Steven; Benavente, Oscar R; Boncoraglio, Giorgio B; Butterworth, Adam; Carcel-Marquez, Jara; Chen, Zhengming; Chong, Michael; Cruchaga, Carlos; Cushman, Mary; Danesh, John; Debette, Stéphanie; Duggan, David J; Durda, Jon Peter; Engstrom, Gunnar; Enzinger, Chris; Faul, Jessica D; Fecteau, Natalie S; Fernandez-Cadenas, Israel; Gieger, Christian; Giese, Anne-Katrin; Grewal, Raji P; Grittner, Ulrike; Havulinna, Aki S; Heitsch, Laura; Hochberg, Marc C; Holliday, Elizabeth; Hu, Jie; Ilinca, Andreea; Irvin, Marguerite R; Jackson, Rebecca D; Jacob, Mina A; Rabionet, Raquel; Jimenez-Conde, Jordi; Johnson, Julie A; Kamatani, Yoichiro; Kardia, Sharon L R; Koido, Masaru; Kubo, Michiaki; Lange, Leslie; Lee, Jin-Moo; Lemmens, Robin; Levi, Christopher R; Li, Jiang; Li, Liming; Lin, Kuang; Lopez, Haley; Luke, Sothear; Maguire, Jane; McArdle, Patrick F; McDonough, Caitrin W; Meschia, James F; Metso, Tiina; Müller-Nurasyid, Martina; O'Connor, Timothy D; O'Donnell, Martin; Peddareddygari, Leema R; Pera, Joanna; Perry, James A; Peters, Annette; Putaala, Jukka; Ray, Debashree; Rexrode, Kathryn; Ribases, Marta; Rosand, Jonathan; Rothwell, Peter M; Rundek, Tatjana; Ryan, Kathleen A; Sacco, Ralph L; Salomaa, Veikko; Sanchez-Mora, Cristina; Schmidt, Reinhold; Sharma, Pankaj; Slowik, Agnieszka; Smith, Jennifer A; Smith, Nicholas L; Wassertheil-Smoller, Sylvia; Söderholm, Martin; Stine, O Colin; Strbian, Daniel; Sudlow, Cathie L M; Tatlisumak, Turgut; Terao, Chikashi; Thijs, Vincent; Torres-Aguila, Nuria P; Trégouët, David-Alexandre; Tuladhar, Anil M; Veldink, Jan H; Walters, Robin G; Weir, David R; Woo, Daniel; Worrall, Bradford B; Hong, Charles C; Ross, Owen A; Zand, Ramin; Leeuw, Frank-Erik de; Lindgren, Arne G; Pare, Guillaume; Anderson, Christopher D; Markus, Hugh S; Jern, Christina; Malik, Rainer; Dichgans, Martin; Mitchell, Braxton D; Kittner, Steven J

Brain structural and functional substrates of ADGRL3 (latrophilin 3) haplotype in attention-deficit/hyperactivity disorder

注意力缺陷/多动障碍中ADGRL3(latrophilin 3)单倍型的脑结构和功能基础

Moreno-Alcázar, Ana; Ramos-Quiroga, Josep A; Ribases, Marta; Sánchez-Mora, Cristina; Palomar, Gloria; Bosch, Rosa; Salavert, Josep; Fortea, Lydia; Monté-Rubio, Gemma C; Canales-Rodríguez, Erick J; Milham, Michael P; Castellanos, F Xavier; Casas, Miquel; Pomarol-Clotet, Edith; Radua, Joaquim

Subtype Specificity of Genetic Loci Associated With Stroke in 16 664 Cases and 32 792 Controls

16664例卒中患者和32792例对照中与卒中相关的基因位点的亚型特异性

Traylor, Matthew; Anderson, Christopher D; Rutten-Jacobs, Loes C A; Falcone, Guido J; Comeau, Mary E; Ay, Hakan; Sudlow, Cathie L M; Xu, Huichun; Mitchell, Braxton D; Cole, John W; Rexrode, Kathryn; Jimenez-Conde, Jordi; Schmidt, Reinhold; Grewal, Raji P; Sacco, Ralph; Ribases, Marta; Rundek, Tatjana; Rosand, Jonathan; Dichgans, Martin; Lee, Jin-Moo; Langefeld, Carl D; Kittner, Steven J; Markus, Hugh S; Woo, Daniel; Malik, Rainer

GWAS of lifetime cannabis use reveals new risk loci, genetic overlap with psychiatric traits, and a causal influence of schizophrenia

终生大麻使用情况的全基因组关联研究揭示了新的风险位点、与精神疾病特征的遗传重叠以及精神分裂症的因果影响

Pasman, Joëlle A; Verweij, Karin J H; Gerring, Zachary; Stringer, Sven; Sanchez-Roige, Sandra; Treur, Jorien L; Abdellaoui, Abdel; Nivard, Michel G; Baselmans, Bart M L; Ong, Jue-Sheng; Ip, Hill F; van der Zee, Matthijs D; Bartels, Meike; Day, Felix R; Fontanillas, Pierre; Elson, Sarah L; de Wit, Harriet; Davis, Lea K; MacKillop, James; Derringer, Jaime L; Branje, Susan J T; Hartman, Catharina A; Heath, Andrew C; van Lier, Pol A C; Madden, Pamela A F; Mägi, Reedik; Meeus, Wim; Montgomery, Grant W; Oldehinkel, A J; Pausova, Zdenka; Ramos-Quiroga, Josep A; Paus, Tomas; Ribases, Marta; Kaprio, Jaakko; Boks, Marco P M; Bell, Jordana T; Spector, Tim D; Gelernter, Joel; Boomsma, Dorret I; Martin, Nicholas G; MacGregor, Stuart; Perry, John R B; Palmer, Abraham A; Posthuma, Danielle; Munafò, Marcus R; Gillespie, Nathan A; Derks, Eske M; Vink, Jacqueline M

Live fast, die young? A review on the developmental trajectories of ADHD across the lifespan

及时行乐,英年早逝?关于注意力缺陷多动障碍(ADHD)终生发展轨迹的回顾

Franke, Barbara; Michelini, Giorgia; Asherson, Philip; Banaschewski, Tobias; Bilbow, Andrea; Buitelaar, Jan K; Cormand, Bru; Faraone, Stephen V; Ginsberg, Ylva; Haavik, Jan; Kuntsi, Jonna; Larsson, Henrik; Lesch, Klaus-Peter; Ramos-Quiroga, J Antoni; Réthelyi, János M; Ribases, Marta; Reif, Andreas

Two-stage case-control association study of dopamine-related genes and migraine

多巴胺相关基因与偏头痛的两阶段病例对照关联研究

Corominas, Roser; Ribases, Marta; Camiña, Montserrat; Cuenca-León, Ester; Pardo, Julio; Boronat, Susana; Sobrido, María-Jesús; Cormand, Bru; Macaya, Alfons