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Cell-type specific global reprogramming of the transcriptome and epigenome in induced neurons with the 16p11.2 neuropsychiatric CNVs 携带16p11.2神经精神领域CNV的诱导神经元中，细胞类型特异性的转录组和表观基因组全局重编程。 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. 分享 收藏
LONG-READ RNA ISOFORM MAP OF THE HUMAN BRAIN (ISOHUB) Lin, Xiao; Hadas, Yoav; Hadjimichael, Evi; Li, Ling; Monte, Emma; Koornstra, Eline; Shieh, Annie; van Bakel, Harm; Snyder, Michael; Hallmayer, Joachim; Wang, Xusheng; Liu, Chunyu; Urban, Alexander; Pinto, Dalila 分享 收藏
IMPLICATION OF COMPLEX STRUCTURAL GENOME VARIATION IN THE GENETIC ARCHITECTURE OF NEUROPSYCHIATRIC DISORDERS: INSIGHTS FROM HUMAN POPULATION ANALYSIS AND FROM POSTMORTEM BRAINS OF INDIVIDUALS WITH PSYCHIATRIC DISORDERS 复杂结构基因组变异在神经精神疾病遗传结构中的意义: 来自人群分析和精神疾病个体死后大脑的见解 Zhou, Bo; Arthur, Joseph; Guo, Hanmin; Kim, Taeyoung; Huang, Yiling; Pattni, Reenal; Song, Giltae; Palejev, Dean; Dohna, Heinrich; Roussos, Panos; Kundaje, Anshul; Hallmayer, Joachim; Snyder, Michael; Wong, Wing; Urban, Alexander 分享 收藏
A Twin Study of Altered White Matter Heritability in Youth With Autism Spectrum Disorder Hegarty, John P., II; 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. 分享 收藏
Mutations in human DNA methyltransferase DNMT1 induce specific genome-wide epigenomic and transcriptomic changes in neurodevelopment Davis, Kasey N.; Qu, Ping-Ping; Ma, Shining; Lin, Ling; Plastini, Melanie; Dahl, Niklas; Plazzi, Giuseppe; Pizza, Fabio; O'Hara, Ruth; Wong, Wing Hung; Hallmayer, Joachim; Mignot, Emmanuel; Zhang, Xianglong; Urban, Alexander E. 分享 收藏
Sleep architecture is associated with core symptom severity in autism spectrum disorder 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 分享 收藏
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Increased activation product of complement 4 protein in plasma of individuals with schizophrenia Kalinowski, Agnieszka; Liliental, Joanna; Anker, Lauren A.; Linkovski, Omer; Culbertson, Collin; Hall, Jacob N.; Pattni, Reenal; Sabatti, Chiara; Noordsy, Douglas; Hallmayer, Joachim F.; Mellins, Elizabeth D.; Ballon, Jacob S.; O'Hara, Ruth; Levinson, Douglas F.; Urban, Alexander E. 分享 收藏
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Network Effects of the 15q13.3 Microdeletion on the Transcriptome and Epigenome in Human- Induced Neurons Zhang, Siming; Zhang, Xianglong; Purmann, Carolin; Ma, Shining; Shrestha, Anima; Davis, Kasey N.; Ho, Marcus; Huang, Yiling; Pattni, Reenal; Hung, Wing; Bernstein, Jonathan A.; Hallmayer, Joachim; Urban, Alexer E. 分享 收藏
Brain health registry GenePool study: A novel approach to online genetics research Fockler, Juliet; Kwang, Winnie; Ashford, Miriam T.; Flenniken, Derek; Hwang, Joshua; Truran, Diana; Mackin, R. Scott; Jin, Chengshi; O'Hara, Ruth; Hallmayer, Joachim F.; Yesavage, Jerome A.; Weiner, Michael W.; Nosheny, Rachel L. 分享 收藏
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Neuronal defects in a human cellular model of 22q11.2 deletion syndrome 22 q11.2缺失综合征的人类细胞模型中的神经元缺陷 Khan, Themasap A.; Revah, Omer; Gordon, Aaron; Yoon, Se-Jin; Krawisz, Anna K.; Goold, Carleton; Sun, Yishan; Kim, Chul Hoon; Tian, Yuan; Li, Min-Yin; Schaepe, Julia M.; Ikeda, Kazuya; Amin, Neal D.; Sakai, Noriaki; Yazawa, Masayuki; Kushan, Leila; Nishino, Seiji; Porteus, Matthew H.; Rapoport, Judith L.; Bernstein, Jonathan A.; O'Hara, Ruth; Bearden, Carrie E.; Hallmayer, Joachim F.; Huguenard, John R.; Geschwind, Daniel H.; Dolmetsch, Ricardo E.; Pasca, Sergiu P. 分享 收藏
The5-HTTLPRlong allele predicts two-year longitudinal increases in cortisol and declines in verbal memory in older adults Hirst, Rayna B.; Jordan, Joshua T.; Rose, Sophia Miryam Schussler-Fiorenza; Schneider, Logan; Kawai, Makoto; Gould, Christine E.; Anker, Lauren; Chick, Christina F.; Beaudreau, Sherry A.; Hallmayer, Joachim; O'Hara, Ruth 分享 收藏
Genetic and environmental influences on corticostriatal circuits in twins with autism Hegarty, John P., II; Lazzeroni, Laura C.; Raman, Mira M.; Hallmayer, Joachim F.; Cleveland, Sue C.; Wolke, Olga N.; Phillips, Jennifer M.; Reiss, Allan L.; Hardan, Antonio Y. 分享 收藏
Integrated functional genomic analyses of Klinefelter and Turner syndromes reveal global network effects of altered X chromosome dosage Zhang, Xianglong; Hong, David; Ma, Shining; Ward, Thomas; Ho, Marcus; Pattni, Reenal; Duren, Zhana; Stankov, Atanas; Shrestha, Sharon Bade; Hallmayer, Joachim; Wong, Wing Hung; Reiss, Allan L.; Urban, Alexander E. 分享 收藏
Brain Development in School-Age and Adolescent Girls: Effects of Turner Syndrome, Estrogen Therapy, and Genomic Imprinting O'Donoghue, Stefani; Green, Tamar; Ross, Judith L.; Hallmayer, Joachim; Lin, Xiaoyan; Jo, Booil; Huffman, Lynne C.; Hong, David S.; Reiss, Allan L. 分享 收藏
COMPARATIVE FUNCTIONAL GENOMICS ANALYSES OF THE 16P11.2 DELETION AND DUPLICATION CNVS IN A HUMAN IPSC-TO-INDUCED NEURON MODEL Zhang, Xianglong; Thomas, Ward; Leung, Louis; Zhou, Bo; Muench, Kristin; Plastini, Melanie; Pattni, Reenal; Ho, Steve; Ho, Marcus; Huang, Yiling; Hallmayer, Joachim; Mourrain, Philippe; Palmer, Theo; Urban, Alexander 分享 收藏
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