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

Developmental convergence and divergence in human stem cell models of autism.

自闭症人类干细胞模型的发育趋同与分化。

Gordon Aaron, Yoon Se-Jin, Bicks Lucy K, Martín Jacqueline M, Pintacuda Greta, Arteaga Stephanie, Wamsley Brie, Guo Qiuyu, Elahi Lubayna, Dolmetsch Ricardo E, Bernstein Jonathan A, O'Hara Ruth, Hallmayer Joachim F, Lage Kasper, Pasca Sergiu P, Geschwind Daniel H

Cell-type specific global reprogramming of the transcriptome and epigenome in induced neurons with the 16p11.2 neuropsychiatric CNVs

16p11.2神经精神CNV诱导神经元中转录组和表观基因组的细胞类型特异性全局重编程

Ward, Thomas R; Qu, Ping-Ping; Leung, Louis C; Zhou, Bo; Muench, Kristin L; Khechaduri, Arineh; Plastini, Melanie J; Charlton, Carol A; Pattni, Reenal; Ho, Steve; Ho, Marcus; Huang, Yiling; Zhou, Patrick; Hallmayer, Joachim F; Mourrain, Philippe; Palmer, Theo D; Zhang, Xianglong; Urban, Alexander E

Gene dosage effects of 22q11.2 copy number variants on in-vivo measures of white matter axonal density and dispersion

22q11.2拷贝数变异的基因剂量效应对体内白质轴突密度和分散度的测量结果的影响

Boen, Rune; Villalón-Reina, Julio E; Kushan, Leila; O'Hora, Kathleen P; Fung, Hoki; Parker, Nadine; Akkouh, Ibrahim A; Alnæs, Dag; O'Hara, Ruth; Marzelli, Matthew John; Foland-Ross, Lara; Chick, Christina French; Cotto, Isabelle; Reiss, Allan L; Hallmayer, Joachim; Thompson, Paul M; Andreassen, Ole A; Sønderby, Ida E; Bearden, Carrie E

Psychiatric disorders converge on common pathways but diverge in cellular context, spatial distribution, and directionality of genetic effects

精神疾病虽然在共同的通路上有所关联,但在细胞环境、空间分布和基因效应的方向性方面却存在差异。

Engchuan, Worrawat; Shanta, Omar; Kumar, Kuldeep; MacDonald, Jeffrey R; Thiruvahindrapuram, Bhooma; Hamdan, Omar; Klein, Marieke; Maihofer, Adam; Guevara, James; Hong, Oanh; Huguet, Guillaume; Sacks, Molly; Ahangari, Mohammad; Feitosa, Rayssa M M W; Han, Kara; Mendes, Marla; Zhou, Xiaopu; Bautista, Nelson X; Pellecchia, Giovanna; Wang, Zhouzhi; Merico, Daniele; Yuen, Ryan K C; Trost, Brett; Sønderby, Ida; Adams, Mark J; Adolfsson, Rolf; Agartz, Ingrid; Aiello, Allison E; Alda, Martin; Allardyce, Judith; Amstadter, Ananda B; Andlauer, Till F M; Andreassen, Ole A; Artigas, María S; Austin, S Bryn; Ayub, Muhammad; Baker, Dewleen G; Bass, Nick; Baune, Bernhard T; Bayas, Maximilian; Berger, Klaus; Biernacka, Joanna M; Bigdeli, Tim; Bisson, Jonathan I; Blackwood, Douglas; Boks, Marco; Braff, David; Bramon, Elvira; Breen, Gerome; Brueckl, Tanja; Bryant, Richard A; Bulik, Cynthia M; Buxbaum, Joseph; Cairns, Murray J; Caldas-de-Almeida, Jose M; Campbell, Megan; Campion, Dominique; Carr, Vaughan J; Castelao, Enrique; Chaumette, Boris; Cichon, Sven; Cohen, David; Corvin, Aiden; Craddock, Nicholas; Crosbie, Jennifer; Czamara, Darrina; Dannlowski, Udo; Degenhardt, Franziska; Delahanty, Douglas L; Dempfle, Astrid; Desachy, Guillaume; Di Florio, Arianna; Dickerson, Faith B; Djurovic, Srdjan; Domschke, Katharina; Douglas, Lisa; Drange, Ole K; Duncan, Laramie E; Edenberg, Howard J; Esko, Tonu; Faraone, Steve; Feeny, Norah C; Forstner, Andreas J; Franke, Barbara; Frye, Mark; Fu, Dong-Jing; Fullerton, Janice M; Gareeva, Anna; Garvert, Linda; Gatt, Justine M; Gejman, Pablo; Geschwind, Daniel H; Giegling, Ina; Glatt, Stephen J; Glessner, Joe; Goes, Fernando S; Gordon-Smith, Katherine; Grabe, Hans; Green, Melissa J; Green, Michael F; Greenwood, Tiffany; Grigoroiu-Serbanescu, Maria; Gur, Raquel E; Gur, Ruben C; Guzman-Parra, Jose; Haavik, Jan; Hahn, Tim; Hakonarson, Hakon; Hallmayer, Joachim; Hamshere, Marian L; Hartmann, Annette M; Hassan, Arsalan; Hayward, Caroline; Hebebrand, Johannes; Hemmings, Sian M J; Herms, Stefan; Herrera-Rivero, Marisol; Hinney, Anke; Homuth, Georg; Ingason, Andrés; Ito, Lucas T; Iwata, Nakao; Jones, Ian; Jones, Lisa A; Jonsson, Lina; Jönsson, Erik G; Kahn, René S; Karlsson, Robert; Kaufman, Milissa L; Kelsoe, John R; Kennedy, James L; King, Anthony; Kircher, Tilo; Kirov, George; Knappskog, Per; Knowles, James A; Kobayashi, Nene; Koenen, Karestan C; Konte, Bettina; Korgaonkar, Mayuresh; Kowalec, Kaarina; Krebs, Marie-Odile; Landén, Mikael; Laurent-Levinson, Claudine; Lebois, Lauren A; Levinson, Doug; Lewis, Cathryn; Li, Qingqin; Liberzon, Israel; Light, Greg; Loo, Sandra K; Lu, Yi; Lucae, Susanne; Marmar, Charles; Martin, Nicholas G; Mayoral, Fermin; McIntosh, Andrew M; McLaughlin, Katie A; McLean, Samuel A; McQuillin, Andrew; Medland, Sarah E; Meyer-Lindenberg, Andreas; Milanova, Vihra; Mitchell, Philip B; Molina, Esther; Mowry, Bryan; Muller-Myhsok, Bertram; Mullins, Niamh; Murray, Robin; Nöthen, Markus M; Nurnberger, John I Jr; O'Connell, Kevin S; Ophoff, Roel A; Orcutt, Holly K; Owen, Michael J; Palotie, Aarno; Pato, Carlos; Pato, Michele; Pawlak, Joanna; Peters, Triinu; Petryshen, Tracey L; Pistis, Giorgio; Potash, James B; Powell, John; Preisig, Martin; Quested, Digby; Ramos-Quiroga, Josep A; Reif, Andreas; Ressler, Kerry J; Ribasés, Marta; Rietschel, Marcella; Risbrough, Victoria B; Rivera, Margarita; Rothbaum, Alex O; Rothbaum, Barbara O; Rujescu, Dan; Saito, Takeo; Sanders, Alan R; Schachar, Russell J; Schofield, Peter R; Schulte, Eva C; Schulze, Thomas G; Scott, Laura J; Seedat, Soraya; Sheerin, Christina; Shi, Jianxin; Sklar, Pamela; Smalley, Susan; Smeland, Olav B; Smoller, Jordan W; Sonuga-Barke, Edmund; Clair, David St; Steen, Nils Eiel; Stein, Dan; Stein, Frederike; Stein, Murray B; Streit, Fabian; Swerdlow, Neal; Thibaut, Florence; Thygesen, Johan H; Timerbulatov, Ilgiz; Toma, Claudio; Trapido, Edward; Tremblay, Micheline; Tsuang, Ming T; Uddin, Monica; Vawter, Marquis P; Vincent, John B; Völzke, Henry; Walters, James T; Weickert, Cynthia S; Weiss, Lauren A; Weissman, Myrna M; Werge, Thomas; Witt, Stephanie H; Xavier, Miguel; Yolken, Robert; Young, Ross M; Zayats, Tetyana; Zoellner, Lori A; Kendall, Kimberley; Riley, Brien; Wray, Naomi R; O'Donovan, Michael C; Sullivan, Patrick F; Sanchez-Roige, Sandra; Nievergelt, Caroline M; Jacquemont, Sébastien; Scherer, Stephen W; Sebat, Jonathan

Detection and analysis of complex structural variation in human genomes across populations and in brains of donors with psychiatric disorders.

对不同人群的人类基因组以及患有精神疾病的捐赠者大脑中的复杂结构变异进行检测和分析

Zhou Bo, Arthur Joseph G, Guo Hanmin, Kim Taeyoung, Huang Yiling, Pattni Reenal, Wang Tao, Kundu Soumya, Luo Jay X J, Lee HoJoon, Nachun Daniel C, Purmann Carolin, Monte Emma M, Weimer Annika K, Qu Ping-Ping, Shi Minyi, Jiang Lixia, Yang Xinqiong, Fullard John F, Bendl Jaroslav, Girdhar Kiran, Kim Minsu, Chen Xi, Greenleaf William J, Duncan Laramie, Ji Hanlee P, Zhu Xiang, Song Giltae, Montgomery Stephen B, Palejev Dean, Zu Dohna Heinrich, Roussos Panos, Kundaje Anshul, Hallmayer Joachim F, Snyder Michael P, Wong Wing H, Urban Alexander E

A Twin Study of Altered White Matter Heritability in Youth With Autism Spectrum Disorder

自闭症谱系障碍青少年白质遗传性改变的双胞胎研究

Hegarty, John P 2nd; Monterrey, Julio C; Tian, Qiyuan; Cleveland, Sue C; Gong, Xinyi; Phillips, Jennifer M; Wolke, Olga N; McNab, Jennifer A; Hallmayer, Joachim F; Reiss, Allan L; Hardan, Antonio Y; Lazzeroni, Laura C

Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy

发作性睡病风险基因位点概述了T细胞自身免疫和感染诱因在发作性睡病中的作用

Ollila, Hanna M; Sharon, Eilon; Lin, Ling; Sinnott-Armstrong, Nasa; Ambati, Aditya; Yogeshwar, Selina M; Hillary, Ryan P; Jolanki, Otto; Faraco, Juliette; Einen, Mali; Luo, Guo; Zhang, Jing; Han, Fang; Yan, Han; Dong, Xiao Song; Li, Jing; Zhang, Jun; Hong, Seung-Chul; Kim, Tae Won; Dauvilliers, Yves; Barateau, Lucie; Lammers, Gert Jan; Fronczek, Rolf; Mayer, Geert; Santamaria, Joan; Arnulf, Isabelle; Knudsen-Heier, Stine; Bredahl, May Kristin Lyamouri; Thorsby, Per Medbøe; Plazzi, Giuseppe; Pizza, Fabio; Moresco, Monica; Crowe, Catherine; Van den Eeden, Stephen K; Lecendreux, Michel; Bourgin, Patrice; Kanbayashi, Takashi; Martínez-Orozco, Francisco J; Peraita-Adrados, Rosa; Benetó, Antonio; Montplaisir, Jacques; Desautels, Alex; Huang, Yu-Shu; Jennum, Poul; Nevsimalova, Sona; Kemlink, David; Iranzo, Alex; Overeem, Sebastiaan; Wierzbicka, Aleksandra; Geisler, Peter; Sonka, Karel; Honda, Makoto; Högl, Birgit; Stefani, Ambra; Coelho, Fernando Morgadinho; Mantovani, Vilma; Feketeova, Eva; Wadelius, Mia; Eriksson, Niclas; Smedje, Hans; Hallberg, Pär; Hesla, Per Egil; Rye, David; Pelin, Zerrin; Ferini-Strambi, Luigi; Bassetti, Claudio L; Mathis, Johannes; Khatami, Ramin; Aran, Adi; Nampoothiri, Sheela; Olsson, Tomas; Kockum, Ingrid; Partinen, Markku; Perola, Markus; Kornum, Birgitte R; Rueger, Sina; Winkelmann, Juliane; Miyagawa, Taku; Toyoda, Hiromi; Khor, Seik-Soon; Shimada, Mihoko; Tokunaga, Katsushi; Rivas, Manuel; Pritchard, Jonathan K; Risch, Neil; Kutalik, Zoltan; O'Hara, Ruth; Hallmayer, Joachim; Ye, Chun Jimmie; Mignot, Emmanuel J

Sleep architecture is associated with core symptom severity in autism spectrum disorder

睡眠结构与自闭症谱系障碍的核心症状严重程度相关

Kawai, Makoto; Buck, Casey; Chick, Christina F; Anker, Lauren; Talbot, Lisa; Schneider, Logan; Linkovski, Omer; Cotto, Isabelle; Parker-Fong, Kai; Phillips, Jennifer; Hardan, Antonio Y; Hallmayer, Joachim; O'Hara, Ruth

Mutations in human DNA methyltransferase DNMT1 induce specific genome-wide epigenomic and transcriptomic changes in neurodevelopment

人类 DNA 甲基转移酶 DNMT1 突变会在神经发育过程中引发特定的全基因组表观基因组和转录组变化

Kasey N Davis, Ping-Ping Qu, Shining Ma, Ling Lin, Melanie Plastini, Niklas Dahl, Giuseppe Plazzi, Fabio Pizza, Ruth O'Hara, Wing Hung Wong, Joachim Hallmayer, Emmanuel Mignot, Xianglong Zhang, Alexander E Urban

Preparing the Next Generation of Academic Researchers During the Pandemic: Lessons from a National Mental Health Research Postdoctoral Fellowship

疫情期间培养下一代学术研究人员:来自国家心理健康研究博士后奖学金项目的经验教训

Hantke, Nathan C; Samarina, Viktoriya; Hallmayer, Joachim; Anker, Lauren; O'Hara, Ruth; Beaudreau, Sherry A