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CHROMATIN ACCESSIBILITY MAPPING IN HIPSC IMPLICATES FUNCTIONAL GWAS RISK VARIANTS AND TARGET GENES FOR NEUROPSYCHIATRIC DISORDERS AND ALZHEIMER'S DISEASE Zhang, Siwei; Zhang, Hanwen; Kozlova, Alena; Forrest, Marc; Zhou, Yifan; Bagchi, Vikram; Dos Santos, Marc; Wood, Whitney; Li, Lexi; Sanders, Alan; Pang, Zhiping; He, Xin; Penzes, Peter; Duan, Jubao 分享 收藏
Multiple genes in a single GWAS risk locus synergistically mediate aberrant synaptic development and function in human neurons 单个GWAS风险基因座中的多个基因协同介导人类神经元的异常突触发育和功能 Zhang, Siwei; Zhang, Hanwen; Forrest, Marc P.; Zhou, Yifan; Sun, Xiaotong; Bagchi, Vikram A.; Kozlova, Alena; Santos, Marc Dos; Piguel, Nicolas H.; Dionisio, Leonardo E.; Sanders, Alan R.; Pang, Zhiping P.; He, Xin; Penzes, Peter; Duan, Jubao 分享 收藏
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Excitatory Dysfunction Drives Network and Calcium Handling Deficits in 16p11.2 Duplication Schizophrenia Induced Pluripotent Stem Cell- Derived Neurons Parnell, Euan; Culotta, Lorenza; Forrest, Marc P.; Jalloul, Hiba A.; Eckman, Blair L.; Loizzo, Daniel D.; Horan, Katherine K. E.; Dos Santos, Marc; Piguel, Nicolas H.; Tai, Derek J. C.; Zhang, Hanwen; Gertler, Tracy S.; Simkin, Dina; Sanders, Alan R.; Talkowski, Michael E.; V. Gejman, Pablo; Kiskinis, Evangelos; Duan, Jubao; Penzes, Peter 分享 收藏
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Rescue of neuropsychiatric phenotypes in a mouse model of 16p11.2 duplication syndrome by genetic correction of an epilepsy network hub Forrest, Marc P.; Dos Santos, Marc; Piguel, Nicolas H.; Wang, Yi-Zhi; Hawkins, Nicole A.; Bagchi, Vikram A.; Dionisio, Leonardo E.; Yoon, Sehyoun; Simkin, Dina; Martin-de-Saavedra, Maria Dolores; Gao, Ruoqi; Horan, Katherine E.; George Jr, Alfred L.; LeDoux, Mark S.; Kearney, Jennifer A.; Savas, Jeffrey N.; Penzes, Peter 分享 收藏
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Impaired OTUD7A-dependent Ankyrin regulation mediates neuronal dysfunction in mouse and human models of the 15q13.3 microdeletion syndrome OTUD7A-dependent锚蛋白调节受损介导15 q13.3微缺失综合征小鼠和人类模型的神经元功能障碍 Unda, Brianna K.; Chalil, Leon; Yoon, Sehyoun; Kilpatrick, Savannah; Irwin, Courtney; Xing, Sansi; Murtaza, Nadeem; Cheng, Anran; Brown, Chad; Afonso, Alexandria; McCready, Elizabeth; Ronen, Gabriel M.; Howe, Jennifer; Caye-Eude, Aurelie; Verloes, Alain; Doble, Brad W.; Faivre, Laurence; Vitobello, Antonio; Scherer, Stephen W.; Lu, Yu; Penzes, Peter; Singh, Karun K. 分享 收藏
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Shed CNTNAP2 ectodomain is detectable in CSF and regulates Ca2+ homeostasis and network synchrony via PMCA2/ATP2B2 Martin-de-Saavedra, M. Dolores; Dos Santos, Marc; Culotta, Lorenza; Varea, Olga; Spielman, Benjamin P.; Parnell, Euan; Forrest, Marc P.; Gao, Ruoqi; Yoon, Sehyoun; McCoig, Emmarose; Jalloul, Hiba A.; Myczek, Kristoffer; Khalatyan, Natalia; Hall, Elizabeth A.; Turk, Liam S.; Sanz-Clemente, Antonio; Comoletti, Davide; Lichtenthaler, Stefan F.; Burgdorf, Jeffrey S.; Barbolina, Maria V.; Savas, Jeffrey N.; Penzes, Peter 分享 收藏
A Kalirin missense mutation enhances dendritic RhoA signaling and leads to regression of cortical dendritic arbors across development Grubisha, Melanie J.; Sun, Tao; Eisenman, Leanna; Erickson, Susan L.; Chou, Shinnyi; Helmer, Cassandra D.; Trudgen, Melody T.; Ding, Ying; Homanics, Gregg E.; Penzes, Peter; Wills, Zachary P.; Sweet, Robert A. 分享 收藏
CHROMATIN ACCESSIBILITY MAPPING REVEALS COMPOUND GENETIC EFFECTS AT A SCHIZOPHRENIA GWAS RISK LOCUS IMPAIRING NEURODEVELOPMENT AND SYNAPTIC FUNCTION IN HUMAN NEURONS Zhang, Siwei; Zhang, Hanwen; Forrest, Marc; Zhou, Yifan; Bagchi, Vikram; Kozlova, Alena; Dos Santos, Marc; Piguel, Nicholas; Dionisio, Leonardo; Sanders, Alan; Pang, Zhiping; He, Xin; Penzes, Peter; Duan, Jubao 分享 收藏
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Dyshomeostatic modulation of Ca2+-activated K+ channels in a human neuronal model of KCNQ2 encephalopathy Simkin, Dina; Marshall, Kelly A.; Vanoye, Carlos G.; Desai, Reshma R.; Bustos, Bernabe, I; Piyevsky, Brandon N.; Ortega, Juan A.; Forrest, Marc; Robertson, Gabriella L.; Penzes, Peter; Laux, Linda C.; Lubbe, Steven J.; Millichap, John J.; George, Alfred L., Jr.; Kiskinis, Evangelos 分享 收藏