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

Distinct metabolic signatures of Alzheimer's and Parkinson's disease revealed through genetic overlap

通过基因重叠揭示阿尔茨海默病和帕金森病的独特代谢特征

Stinson, Sara E; Shadrin, Alexey A; Rahman, Zillur; Rødevand, Linn; Broce, Iris J; Selbæk, Geir; Stefansson, Hreinn; Haavik, Jan; Parker, Nadine; Koch, Elise; Frei, Oleksandr; O'Connell, Kevin S; Smeland, Olav B; Djurovic, Srdjan; Dale, Anders M; van der Meer, Dennis; Andreassen, Ole A

A low frequency damaging SORCS2 variant identified in a family with ADHD compromises receptor stability and quenches activity.

在一个患有 ADHD 的家庭中发现了一种低频有害的 SORCS2 变异,这种变异会损害受体稳定性并抑制其活性。

Kaas Mathias, Dinesen Sarah Broholt, Ahlgreen Ole, Madsen Peder, Mølgaard Simon, Dalby Anders, Gustafsen Camilla, Olsen Ditte, Duan Jinjie, Vilstrup Joachim, Lende Jonas, Nordestgaard Sanne, Zayats Tetyana, Knappskog Per Morten, Johansson Stefan, Neckelmann Gesche, Franke Barbara, Thirup Søren, Børglum Anders, Reif Andreas, Vægter Christian, Demontis Ditte, Haavik Jan, Glerup Simon, Skeldal Sune

Author Correction: Effects of electroconvulsive therapy on hippocampal longitudinal axis and its association with cognitive side effects

作者更正:电休克疗法对海马纵轴的影响及其与认知副作用的关系

Ousdal, Olga Therese; Argyelan, Miklos; Laroy, Maarten; Anand, Amit; Bouckaert, Filip; Camprodon, Joan A; Cano, Marta; Cardoner, Narcis; Dannlowski, Udo; Dols, Annemiek; Emsell, Louise; Espinoza, Randall; Hebbrecht, Kaat; Hurlemann, René; Jorgensen, Martin; Kiebs, Maximilian; Kishimoto, Taishiro; Narr, Katherine L; Nordanskog, Pia; Opel, Nils; Redlich, Ronny; Rhebergen, Didi; Sartorius, Alexander; Schrijvers, Didier; Sienaert, Pascal; Soriano-Mas, Carles; Takamiya, Akihiro; Ten Doesschate, Freek; Tendolkar, Indira; Urretavizcaya, Mikel; van Diermen, Linda; van Eijndhoven, Philip; van Wingen, Guido; van Waarde, Jeroen; Vandenbulcke, Mathieu; Verdijk, Joey; Wade, Benjamin S C; Antoine, Yrondi; Brekke, Njål; Prudic, Joan; McClintock, Shawn; Kessler, Ute; Bartsch, Hauke; Odegaard, Ketil; Haavik, Jan; Hammar, Åsa; Abbott, Christopher; Oltedal, Leif

Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder

全基因组分析确定了30个与强迫症相关的基因位点

Strom, Nora I; Gerring, Zachary F; Galimberti, Marco; Yu, Dongmei; Halvorsen, Matthew W; Abdellaoui, Abdel; Rodriguez-Fontenla, Cristina; Sealock, Julia M; Bigdeli, Tim; Coleman, Jonathan R; Mahjani, Behrang; Thorp, Jackson G; Bey, Katharina; Burton, Christie L; Luykx, Jurjen J; Zai, Gwyneth; Alemany, Silvia; Andre, Christine; Askland, Kathleen D; Bäckman, Julia; Banaj, Nerisa; Barlassina, Cristina; Nissen, Judith Becker; Bienvenu, O Joseph; Black, Donald; Bloch, Michael H; Børte, Sigrid; Bosch, Rosa; Breen, Michael; Brennan, Brian P; Brentani, Helena; Buxbaum, Joseph D; Bybjerg-Grauholm, Jonas; Byrne, Enda M; Cabana-Dominguez, Judit; Camarena, Beatriz; Camarena, Adrian; Cappi, Carolina; Carracedo, Angel; Casas, Miguel; Cavallini, Maria Cristina; Ciullo, Valentina; Cook, Edwin H; Crosby, Jesse; Cullen, Bernadette A; De Schipper, Elles J; Delorme, Richard; Djurovic, Srdjan; Elias, Jason A; Estivill, Xavier; Falkenstein, Martha J; Fundin, Bengt T; Garner, Lauryn; Gironda, Christina; Goes, Fernando S; Grados, Marco A; Grove, Jakob; Guo, Wei; Haavik, Jan; Hagen, Kristen; Harrington, Kelly; Havdahl, Alexandra; Höffler, Kira D; Hounie, Ana G; Hucks, Donald; Hultman, Christina; Janecka, Magdalena; Jenike, Eric; Karlsson, Elinor K; Kelley, Kara; Klawohn, Julia; Krasnow, Janice E; Krebs, Kristi; Lange, Christoph; Lanzagorta, Nuria; Levey, Daniel; Lindblad-Toh, Kerstin; Macciardi, Fabio; Maher, Brion; Mathes, Brittany; McArthur, Evonne; McGregor, Nathaniel; McLaughlin, Nicole C; Meier, Sandra; Miguel, Euripedes C; Mulhern, Maureen; Nestadt, Paul S; Nurmi, Erika L; O'Connell, Kevin S; Osiecki, Lisa; Ousdal, Olga Therese; Palviainen, Teemu; Pedersen, Nancy L; Piras, Fabrizio; Piras, Federica; Potluri, Sriramya; Rabionet, Raquel; Ramirez, Alfredo; Rauch, Scott; Reichenberg, Abraham; Riddle, Mark A; Ripke, Stephan; Rosário, Maria C; Sampaio, Aline S; Schiele, Miriam A; Skogholt, Anne Heidi; Sloofman, Laura G; Smit, Jan; Artigas, María Soler; Thomas, Laurent F; Tifft, Eric; Vallada, Homero; van Kirk, Nathanial; Veenstra-VanderWeele, Jeremy; Vulink, Nienke N; Walker, Christopher P; Wang, Ying; Wendland, Jens R; Winsvold, Bendik S; Yao, Yin; Zhou, Hang; Agrawal, Arpana; Alonso, Pino; Berberich, Götz; Bucholz, Kathleen K; Bulik, Cynthia M; Cath, Danielle; Denys, Damiaan; Eapen, Valsamma; Edenberg, Howard; Falkai, Peter; Fernandez, Thomas V; Fyer, Abby J; Gaziano, J M; Geller, Dan A; Grabe, Hans J; Greenberg, Benjamin D; Hanna, Gregory L; Hickie, Ian B; Hougaard, David M; Kathmann, Norbert; Kennedy, James; Lai, Dongbing; Landén, Mikael; Hellard, Stéphanie Le; Leboyer, Marion; Lochner, Christine; McCracken, James T; Medland, Sarah E; Mortensen, Preben B; Neale, Benjamin M; Nicolini, Humberto; Nordentoft, Merete; Pato, Michele; Pato, Carlos; Pauls, David L; Piacentini, John; Pittenger, Christopher; Posthuma, Danielle; Ramos-Quiroga, Josep Antoni; Rasmussen, Steven A; Richter, Margaret A; Rosenberg, David R; Ruhrmann, Stephan; Samuels, Jack F; Sandin, Sven; Sandor, Paul; Spalletta, Gianfranco; Stein, Dan J; Stewart, S Evelyn; Storch, Eric A; Stranger, Barbara E; Turiel, Maurizio; Werge, Thomas; Andreassen, Ole A; Børglum, Anders D; Walitza, Susanne; Hveem, Kristian; Hansen, Bjarne K; Rück, Christian; Martin, Nicholas G; Milani, Lili; Mors, Ole; Reichborn-Kjennerud, Ted; Ribasés, Marta; Kvale, Gerd; Mataix-Cols, David; Domschke, Katharina; Grünblatt, Edna; Wagner, Michael; Zwart, John-Anker; Breen, Gerome; Nestadt, Gerald; Kaprio, Jaakko; Arnold, Paul D; Grice, Dorothy E; Knowles, James A; Ask, Helga; Verweij, Karin J; Davis, Lea K; Smit, Dirk J; Crowley, James J; Scharf, Jeremiah M; Stein, Murray B; Gelernter, Joel; Mathews, Carol A; Derks, Eske M; Mattheisen, Manuel

A burden of rare copy number variants in obsessive-compulsive disorder

强迫症中罕见拷贝数变异的负担

Halvorsen, Matthew W; de Schipper, Elles; Bäckman, Julia; Strom, Nora I; Hagen, Kristen; Lindblad-Toh, Kerstin; Karlsson, Elinor K; Pedersen, Nancy L; Wallert, John; Bulik, Cynthia M; Fundín, Bengt; Landén, Mikael; Kvale, Gerd; Hansen, Bjarne; Haavik, Jan; Mattheisen, Manuel; Rück, Christian; Mataix-Cols, David; Crowley, James J

Epigenetic and blood markers associated with response to electroconvulsive therapy in patients with depressive disorders

表观遗传学和血液标志物与抑郁症患者对电休克疗法的反应相关

Stavrum, Anne-Kristin; Sirignano, Lea; Frid, Leila M; Frank, Josef; Foo, Jerome C; Spindola, Leticia M; Höffler, Kira D; Oedegaard, Ketil J; Haavik, Jan; Rietschel, Marcella; Witt, Stephanie H; Kessler, Ute; Oltedal, Leif; Le Hellard, Stéphanie

Local patterns of genetic sharing between neuropsychiatric and insulin resistance-related conditions

神经精神疾病与胰岛素抵抗相关疾病之间基因共享的局部模式

Fanelli, Giuseppe; Franke, Barbara; Fabbri, Chiara; Werme, Josefin; Erdogan, Izel; De Witte, Ward; Poelmans, Geert; Ruisch, I Hyun; Reus, Lianne Maria; van Gils, Veerle; Jansen, Willemijn J; Vos, Stephanie J B; Alam, Kazi Asraful; Martinez, Aurora; Haavik, Jan; Wimberley, Theresa; Dalsgaard, Søren; Fóthi, Ábel; Barta, Csaba; Fernandez-Aranda, Fernando; Jimenez-Murcia, Susana; Berkel, Simone; Matura, Silke; Salas-Salvadó, Jordi; Arenella, Martina; Serretti, Alessandro; Mota, Nina Roth; Bralten, Janita

Penetrance of Neurodevelopmental Copy Number Variants Is Associated With Variations in Cortical Morphology

神经发育拷贝数变异的穿透率与皮质形态变异相关

Silva, Ana I; Sønderby, Ida E; Kirov, George; Abdellaoui, Abdel; Agartz, Ingrid; Ames, David; Armstrong, Nicola J; Artiges, Eric; Banaschewski, Tobias; Bassett, Anne S; Bearden, Carrie E; Blangero, John; Boen, Rune; Boomsma, Dorret I; Bülow, Robin; Butcher, Nancy J; Calhoun, Vince; Campbell, Linda E; Chow, Eva W C; Ciufolini, Simone; Craig, Michael C; Crespo-Farroco, Benedicto; Cunningham, Adam C; Dalvie, Shareefa; Daly, Eileen; Dazzan, Paola; de Geus, Eco J C; de Zubicaray, Greig I; Doherty, Joanne L; Donohoe, Gary; Drakesmith, Mark; Espeseth, Thomas; Frouin, Vincent; Garavan, Hugh; Glahn, David C; Goodrich-Hunsaker, Naomi J; Gowland, Penny A; Grabe, Hans J; Grigis, Antoine; Gudbrandsen, Maria; Gutman, Boris A; Haavik, Jan; Håberg, Asta K; Hall, Jeremy; Heinz, Andreas; Hohmann, Sarah; Hottenga, Jouke-Jan; Jacquemont, Sébastien; Jahanshad, Neda; Jonas, Rachel K; Jones, Derek K; Jönsson, Erik G; Koops, Sanne; Kumar, Kuldeep; Le Hellard, Stephanie; Lemaitre, Herve; Liu, Jingyu; Lundervold, Astri J; Martinot, Jean-Luc; Mather, Karen A; McDonald-McGinn, Donna M; McMahon, Katie L; McRae, Allan F; Medland, Sarah E; Moreau, Clara A; Murphy, Kieran C; Murphy, Declan; Murray, Robin M; Nees, Frauke; Owen, Michael J; Paillère Martinot, Marie-Laure; Orfanos, Diimitri Papadopoulos; Paus, Tomas; Poustka, Luise; Marques, Tiago Reis; Roalf, David R; Sachdev, Perminder S; Scheffler, Freda; Schmitt, J Eric; Schumann, Gunter; Steen, Vidar M; Stein, Dan J; Strike, Lachlan T; Teumer, Alexander; Thalamuthu, Anbupalam; Thomopoulos, Sophia I; Tordesillas-Gutiérrez, Diana; Trollor, Julian N; Uhlmann, Anne; Vajdi, Ariana; van 't Ent, Dennis; van Amelsvoort, Therese; van den Bree, Marianne B M; van der Meer, Dennis; Vázquez-Bourgon, Javier; Villalón-Reina, Julio E; Völker, Uwe; Völzke, Henry; Vorstman, Jacob A S; Westlye, Lars T; Williams, Nigel; Wittfeld, Katharina; Wright, Margaret J; Thompson, Paul M; Andreassen, Ole A; Linden, David E J

Optimizing genetic ancestry adjustment in DNA methylation studies: a comparative analysis of approaches

优化DNA甲基化研究中的遗传祖源调整:方法比较分析

Höffler, Kira D; Katrinli, Seyma; Halvorsen, Matthew W; Stavrum, Anne-Kristin; O'Connell, Kevin S; Shadrin, Alexey; Djurovic, Srdjan; Andreassen, Ole A; Crowley, James J; Haavik, Jan; Hagen, Kristen; Kvale, Gerd; Ressler, Kerry; Hansen, Bjarne; Soares, Jair C; Fries, Gabriel R; Smith, Alicia K; Le Hellard, Stéphanie

Association Between Polygenic Risk and Symptom Severity Change After Cognitive Behavioral Therapy for Obsessive-Compulsive Disorder

多基因风险与强迫症认知行为疗法后症状严重程度变化之间的关联

Bäckman, Julia; Wallert, John; Halvorsen, Matthew; Roelstraete, Bjorn; de Schipper, Elles; Strom, Nora I; Eide, Thorstein Olsen; Höffler, Kira D; Mattheisen, Manuel; Hansen, Bjarne; Kvale, Gerd; Hagen, Kristen; Haavik, Jan; Mataix-Cols, David; Rück, Christian; Crowley, James J