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

A resource of induced pluripotent stem cell (iPSC) lines including clinical, genomic, and cellular data from genetically isolated families with mood and psychotic disorders

诱导性多能干细胞 (iPSC) 系资源,包括患有情绪障碍和精神病的遗传孤立家庭的临床、基因组和细胞数据

Sevilla D Detera-Wadleigh #, Layla Kassem #, Emily Besancon, Fabiana Lopes, Nirmala Akula, Heejong Sung, Meghan Blattner, Laura Sheridan, Ley Nadine Lacbawan, Joshua Garcia, Francis Gordovez, Katherine Hosey, Cassandra Donner, Claudio Salvini, Thomas Schulze, David T W Chen, Bryce England, Joanna Cr

Sodium valproate rescues expression of TRANK1 in iPSC-derived neural cells that carry a genetic variant associated with serious mental illness

丙戊酸钠可挽救携带与严重精神疾病相关的遗传变异的 iPSC 衍生神经细胞中 TRANK1 的表达

Xueying Jiang, Sevilla D Detera-Wadleigh, Nirmala Akula, Barbara S Mallon, Liping Hou, Tiaojiang Xiao, Gary Felsenfeld, Xinglong Gu, Francis J McMahon

Assessment of Response to Lithium Maintenance Treatment in Bipolar Disorder: A Consortium on Lithium Genetics (ConLiGen) Report

双相情感障碍锂维持治疗反应评估:锂遗传学联盟 (ConLiGen) 报告

Manchia, Mirko; Adli, Mazda; Akula, Nirmala; Ardau, Raffaella; Aubry, Jean-Michel; Backlund, Lena; Banzato, Claudio Em; Baune, Bernhard T; Bellivier, Frank; Bengesser, Susanne; Biernacka, Joanna M; Brichant-Petitjean, Clara; Bui, Elise; Calkin, Cynthia V; Cheng, Andrew Tai Ann; Chillotti, Caterina; Cichon, Sven; Clark, Scott; Czerski, Piotr M; Dantas, Clarissa; Zompo, Maria Del; Depaulo, J Raymond; Detera-Wadleigh, Sevilla D; Etain, Bruno; Falkai, Peter; Frisén, Louise; Frye, Mark A; Fullerton, Jan; Gard, Sébastien; Garnham, Julie; Goes, Fernando S; Grof, Paul; Gruber, Oliver; Hashimoto, Ryota; Hauser, Joanna; Heilbronner, Urs; Hoban, Rebecca; Hou, Liping; Jamain, Stéphane; Kahn, Jean-Pierre; Kassem, Layla; Kato, Tadafumi; Kelsoe, John R; Kittel-Schneider, Sarah; Kliwicki, Sebastian; Kuo, Po-Hsiu; Kusumi, Ichiro; Laje, Gonzalo; Lavebratt, Catharina; Leboyer, Marion; Leckband, Susan G; López Jaramillo, Carlos A; Maj, Mario; Malafosse, Alain; Martinsson, Lina; Masui, Takuya; Mitchell, Philip B; Mondimore, Frank; Monteleone, Palmiero; Nallet, Audrey; Neuner, Maria; Novák, Tomás; O'Donovan, Claire; Osby, Urban; Ozaki, Norio; Perlis, Roy H; Pfennig, Andrea; Potash, James B; Reich-Erkelenz, Daniela; Reif, Andreas; Reininghaus, Eva; Richardson, Sara; Rouleau, Guy A; Rybakowski, Janusz K; Schalling, Martin; Schofield, Peter R; Schubert, Oliver K; Schweizer, Barbara; Seemüller, Florian; Grigoroiu-Serbanescu, Maria; Severino, Giovanni; Seymour, Lisa R; Slaney, Claire; Smoller, Jordan W; Squassina, Alessio; Stamm, Thomas; Steele, Jo; Stopkova, Pavla; Tighe, Sarah K; Tortorella, Alfonso; Turecki, Gustavo; Wray, Naomi R; Wright, Adam; Zandi, Peter P; Zilles, David; Bauer, Michael; Rietschel, Marcella; McMahon, Francis J; Schulze, Thomas G; Alda, Martin

Ablation of Mrds1/Ofcc1 induces hyper-γ-glutamyl transpeptidasemia without abnormal head development and schizophrenia-relevant behaviors in mice

在小鼠中,Mrds1/Ofcc1基因缺失可诱导高γ-谷氨酰转肽血症,但不会引起头部发育异常和精神分裂症相关行为。

Ohnishi, Tetsuo; Yamada, Kazuo; Watanabe, Akiko; Ohba, Hisako; Sakaguchi, Toru; Honma, Yota; Iwayama, Yoshimi; Toyota, Tomoko; Maekawa, Motoko; Watanabe, Kazutada; Detera-Wadleigh, Sevilla D; Wakana, Shigeharu; Yoshikawa, Takeo

The International Consortium on Lithium Genetics (ConLiGen): an initiative by the NIMH and IGSLI to study the genetic basis of response to lithium treatment

国际锂遗传学联盟(ConLiGen):由美国国立精神卫生研究院(NIMH)和国际锂离子学会(IGSLI)联合发起,旨在研究锂治疗反应的遗传基础。

Schulze, Thomas G; Alda, Martin; Adli, Mazda; Akula, Nirmala; Ardau, Raffaella; Bui, Elise T; Chillotti, Caterina; Cichon, Sven; Czerski, Piotr; Del Zompo, Maria; Detera-Wadleigh, Sevilla D; Grof, Paul; Gruber, Oliver; Hashimoto, Ryota; Hauser, Joanna; Hoban, Rebecca; Iwata, Nakao; Kassem, Layla; Kato, Tadafumi; Kittel-Schneider, Sarah; Kliwicki, Sebastian; Kelsoe, John R; Kusumi, Ichiro; Laje, Gonzalo; Leckband, Susan G; Manchia, Mirko; Macqueen, Glenda; Masui, Takuya; Ozaki, Norio; Perlis, Roy H; Pfennig, Andrea; Piccardi, Paola; Richardson, Sara; Rouleau, Guy; Reif, Andreas; Rybakowski, Janusz K; Sasse, Johanna; Schumacher, Johannes; Severino, Giovanni; Smoller, Jordan W; Squassina, Alessio; Turecki, Gustavo; Young, L Trevor; Yoshikawa, Takeo; Bauer, Michael; McMahon, Francis J

Autistic-like phenotypes in Cadps2-knockout mice and aberrant CADPS2 splicing in autistic patients

Cadps2基因敲除小鼠表现出类似自闭症的表型,自闭症患者体内存在异常的CADPS2剪接

Sadakata, Tetsushi; Washida, Miwa; Iwayama, Yoshimi; Shoji, Satoshi; Sato, Yumi; Ohkura, Takeshi; Katoh-Semba, Ritsuko; Nakajima, Mizuho; Sekine, Yukiko; Tanaka, Mika; Nakamura, Kazuhiko; Iwata, Yasuhide; Tsuchiya, Kenji J; Mori, Norio; Detera-Wadleigh, Sevilla D; Ichikawa, Hironobu; Itohara, Shigeyoshi; Yoshikawa, Takeo; Furuichi, Teiichi

Polymorphisms at the G72/G30 gene locus, on 13q33, are associated with bipolar disorder in two independent pedigree series

位于13q33的G72/G30基因位点的多态性与两个独立的家系系列中的双相情感障碍相关。

Hattori, Eiji; Liu, Chunyu; Badner, Judith A; Bonner, Tom I; Christian, Susan L; Maheshwari, Manjula; Detera-Wadleigh, Sevilla D; Gibbs, Richard A; Gershon, Elliot S