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

Aberrant pace of cortical neuron development in brain organoids from patients with 22q11.2 deletion syndrome-associated schizophrenia

22q11.2缺失综合征相关精神分裂症患者脑类器官中皮质神经元发育速度异常

Sneha B Rao ,Zhixiong Sun ,Francesco Brundu ,Yannan Chen ,Yan Sun ,Huixiang Zhu ,Robert J Shprintzen ,Raju Tomer ,Raul Rabadan ,Kam W Leong ,Sander Markx ,Steven A Kushner ,Bin Xu ,Joseph A Gogos

A rare variant in GPR156 associated with depression in a Mennonite pedigree causes habenula hyperactivity and stress sensitivity in mice

在门诺派家族中发现的一种与抑郁症相关的GPR156罕见变异会导致小鼠缰核过度活跃和应激敏感性。

Miller, Bradley R; Gonzaga-Jauregui, Claudia; Brigatti, Karlla W; de Jong, Job; Breese, Robert S; Ko, Seung Yeon; Puffenberger, Erik G; Van Hout, Cristopher; Young, Millie; Luna, Victor M; Staples, Jeffrey; First, Michael B; Gregoire, Hilledna J; Dwork, Andrew J; Pefanis, Evangelos; McCarthy, Shane; Brydges, Susannah; Rojas, Jose; Ye, Bin; Stahl, Eli; Di Gioia, Silvio Alessandro; Hen, René; Elwood, Kevin; Rosoklija, Gorazd; Li, Dadong; Mellis, Scott; Carey, David; Croll, Susan D; Overton, John D; Macdonald, Lynn E; Economides, Aris N; Shuldiner, Alan R; Chuhma, Nao; Rayport, Stephen; Amin, Najaf; Kushner, Steven A; Alessandri-Haber, Nicole; Markx, Sander; Strauss, Kevin A

An antisense oligonucleotide-based strategy to ameliorate cognitive dysfunction in the 22q11.2 Deletion Syndrome

一种基于反义寡核苷酸的策略,用于改善22q11.2缺失综合征的认知功能障碍

Pratibha Thakur # ,Martin Lackinger # ,Anastasia Diamantopoulou ,Sneha Rao ,Yijing Chen ,Khakima Khalizova ,Annie Ferng ,Curt Mazur ,Holly Kordasiewicz ,Robert J Shprintzen ,Sander Markx ,Bin Xu ,Joseph A Gogos

Genomic and Transcriptomic Signatures of SETD1A Disruption in Human Excitatory Neuron Development and Psychiatric Disease Risk.

SETD1A 基因破坏在人类兴奋性神经元发育和精神疾病风险中的基因组和转录组特征

Sun Zhixiong, Zhu Huixiang, He Xiaofu, Lendemeijer Bas, Wang Zanxu, Fan Jack, Sun Yan, Zhang Zhiguo, Markx Sander, Kushner Steven A, Xu Bin, Gogos Joseph A

Prevalence and incidence measures for schizophrenia among commercial health insurance and medicaid enrollees

商业健康保险和医疗补助参保者中精神分裂症的患病率和发病率

Finnerty, Molly T; Khan, Atif; You, Kai; Wang, Rui; Gu, Gyojeong; Layman, Deborah; Chen, Qingxian; Elhadad, Noémie; Joshi, Shalmali; Appelbaum, Paul S; Lencz, Todd; Markx, Sander; Kushner, Steven A; Rzhetsky, Andrey

Inhibition of Abl Kinase by Imatinib Can Rescue the Compromised Barrier Function of 22q11.2DS Patient-iPSC-Derived Blood-Brain Barriers

伊马替尼抑制 Abl 激酶可挽救 22q11.2DS 患者 iPSC 衍生的血脑屏障受损的屏障功能

Yunfei Li, Zhixiong Sun, Huixiang Zhu, Yan Sun, David B Shteyman, Sander Markx, Kam W Leong, Bin Xu, Bingmei M Fu

Aberrant pace of cortical neuron development in brain organoids from patients with 22q11.2 deletion syndrome and schizophrenia

22q11.2 缺失综合征和精神分裂症患者脑类器官皮质神经元发育速度异常

Sneha B Rao, Francesco Brundu, Yannan Chen, Yan Sun, Huixiang Zhu, Robert J Shprintzen, Raju Tomer, Raul Rabadan, Kam W Leong, Sander Markx, Bin Xu, Joseph A Gogos

An in vitro model of neuronal ensembles

神经元群的体外模型

M Angeles Rabadan ,Estanislao Daniel De La Cruz ,Sneha B Rao ,Yannan Chen ,Cheng Gong ,Gregg Crabtree ,Bin Xu ,Sander Markx ,Joseph A Gogos ,Rafael Yuste ,Raju Tomer

Cortical overgrowth in a preclinical forebrain organoid model of CNTNAP2-associated autism spectrum disorder

CNTNAP2 相关自闭症谱系障碍的临床前前脑类器官模型中的皮质过度生长

Job O de Jong, Ceyda Llapashtica, Matthieu Genestine, Kevin Strauss, Frank Provenzano, Yan Sun, Huixiang Zhu, Giuseppe P Cortese, Francesco Brundu, Karlla W Brigatti, Barbara Corneo, Bianca Migliori, Raju Tomer, Steven A Kushner, Christoph Kellendonk, Jonathan A Javitch, Bin Xu, Sander Markx

High-impact rare genetic variants in severe schizophrenia

严重精神分裂症中的高影响罕见基因变异

Zoghbi, Anthony W; Dhindsa, Ryan S; Goldberg, Terry E; Mehralizade, Aydan; Motelow, Joshua E; Wang, Xinchen; Alkelai, Anna; Harms, Matthew B; Lieberman, Jeffrey A; Markx, Sander; Goldstein, David B