Novel epigenetic molecular therapies for imprinting disorders

por Wang, Sung Eun, Jiang, Yong-hui
Publicado 2023

Cellular and Circuitry Bases of Autism: Lessons Learned from the Temporospatial Manipulation of Autism Genes in the Brain

por Hulbert, Samuel W., Jiang, Yong-hui
Publicado 2017

Synaptic Plasticity in Mouse Models of Autism Spectrum Disorders

por Chung, Leeyup, Bey, Alexandra L., Jiang, Yong-Hui
Publicado 2012

Environmental enrichment has minimal effects on behavior in the Shank3 complete knockout model of autism spectrum disorder

por Hulbert, Samuel W., Bey, Alexandra L., Jiang, Yong‐hui
Publicado 2018

Systematic reconstruction of autism biology from massive genetic mutation profiles

por Luo, Weijun, Zhang, Chaolin, Jiang, Yong-hui, Brouwer, Cory R.
Publicado 2018

Transcriptional and functional complexity of Shank3 provides a molecular framework to understand the phenotypic heterogeneity of SHANK3 causing autism and Shank3 mutant mice

por Wang, Xiaoming, Xu, Qiong, Bey, Alexandra L, Lee, Yoonji, Jiang, Yong-hui
Publicado 2014

SHANK3 in vagal sensory neurons regulates body temperature, systemic inflammation, and sepsis

por Zhang, Linlin, Bang, Sangsu, He, Qianru, Matsuda, Megumi, Luo, Xin, Jiang, Yong-Hui, Ji, Ru-Rong
Publicado 2023

Estimation on risk of spontaneous abortions by genomic disorders from a meta‐analysis of microarray results on large case series of pregnancy losses

por Peng, Gang, Zhou, Qinghua, Chai, Hongyan, Wen, Jiadi, Zhao, Hongyu, Taylor, Hugh S., Jiang, Yong‐Hui, Li, Peining
Publicado 2023

Role of PUF60 gene in Verheij syndrome: a case report of the first Chinese Han patient with a de novo pathogenic variant and review of the literature

por Xu, Qiong, Li, Chun-yang, Wang, Yi, Li, Hui-ping, Wu, Bing-bing, Jiang, Yong-hui, Xu, Xiu
Publicado 2018

Inhibition of Trpv4 rescues circuit and social deficits unmasked by acute inflammatory response in a Shank3 mouse model of Autism

por Tzanoulinou, Stamatina, Musardo, Stefano, Contestabile, Alessandro, Bariselli, Sebastiano, Casarotto, Giulia, Magrinelli, Elia, Jiang, Yong-hui, Jabaudon, Denis, Bellone, Camilla
Publicado 2022

Genomic analysis of the chromosome 15q11-q13 Prader-Willi syndrome region and characterization of transcripts for GOLGA8E and WHCD1L1 from the proximal breakpoint region

por Jiang, Yong-hui, Wauki, Kekio, Liu, Qian, Bressler, Jan, Pan, Yanzhen, Kashork, Catherine D, Shaffer, Lisa G, Beaudet, Arthur L
Publicado 2008

CRISPR/Cas9-induced shank3b mutant zebrafish display autism-like behaviors

por Liu, Chun-xue, Li, Chun-yang, Hu, Chun-chun, Wang, Yi, Lin, Jia, Jiang, Yong-hui, Li, Qiang, Xu, Xiu
Publicado 2018

Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing

por Wang, Yimin, Du, Xiaonan, Bin, Rao, Yu, Shanshan, Xia, Zhezhi, Zheng, Guo, Zhong, Jianmin, Zhang, Yunjian, Jiang, Yong-hui, Wang, Yi
Publicado 2017

Corrigendum: Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing

por Wang, Yimin, Du, Xiaonan, Bin, Rao, Yu, Shanshan, Xia, Zhezhi, Zheng, Guo, Zhong, Jianmin, Zhang, Yunjian, Jiang, Yong-hui, Wang, Yi
Publicado 2017

Altered Ultrasonic Vocalization and Impaired Learning and Memory in Angelman Syndrome Mouse Model with a Large Maternal Deletion from Ube3a to Gabrb3

por Jiang, Yong-hui, Pan, Yanzhen, Zhu, Li, Landa, Luis, Yoo, Jong, Spencer, Corinne, Lorenzo, Isabel, Brilliant, Murray, Noebels, Jeffrey, Beaudet, Arthur L.
Publicado 2010

A genomic copy number variant analysis implicates the MBD5 and HNRNPU genes in Chinese children with infantile spasms and expands the clinical spectrum of 2q23.1 deletion

por Du, Xiaonan, An, Yu, Yu, Lifei, Liu, Renchao, Qin, Yanrong, Guo, Xiaohong, Sun, Daokan, Zhou, Shuizhen, Wu, Bailin, Jiang, Yong-hui, Wang, Yi
Publicado 2014

The importance of managing the patient and not the gene: expanded phenotype of GLE1-associated arthrogryposis

por Tan, Queenie K.-G., McConkie-Rosell, Allyn, Juusola, Jane, Gustafson, Kathryn E., Pizoli, Carolyn E., Buckley, Anne F., Jiang, Yong-hui
Publicado 2017

Loss of miR-23b/27b/24-1 Cluster Impairs Glucose Tolerance via Glycolysis Pathway in Mice

por Jiang, Yong-Hui, Man, Yuan-Yuan, Liu, Yue, Yin, Chang-Jian, Li, Jia-Lin, Shi, Huang-Cong, Zhao, Han, Zhao, Shi-Gang
Publicado 2021

Cross-Cultural Revision and Psychometric Properties of the Chinese Version of the Autism Spectrum Rating Scale (2–5 Years)

por Zhou, Hao, Li, Chunpei, Luo, Xuerong, Wu, Lijie, Huang, Yi, Zhang, Lan, Zou, Xiaobing, Xu, Xiu, Jiang, Yong-Hui, Yan, Weili, Wang, Yi
Publicado 2018

Severe multisystem pathology, metabolic acidosis, mitochondrial dysfunction, and early death associated with an X-linked AIFM1 variant

por Moss, Tonya, May, Melanie, Flanagan-Steet, Heather, Caylor, Raymond, Jiang, Yong-Hui, McDonald, Marie, Friez, Michael, McConkie-Rosell, Allyn, Steet, Richard
Publicado 2021