The scientist’s investigation covers issues in Genetics, Angelman syndrome, UBE3A, Neuroscience and Gene. By researching both Genetics and Uniparental disomy, he produces research that crosses academic boundaries. His research integrates issues of Regulation of gene expression, Congenital disease, Imprinting and Happy puppet syndrome in his study of Angelman syndrome.
The study incorporates disciplines such as Genetic model, Mutant and Endocrinology in addition to UBE3A. His study in Neuroscience is interdisciplinary in nature, drawing from both Mutation, Long-term potentiation and Autism. His work is dedicated to discovering how Gene, Molecular biology are connected with Gene expression, Methylation, Pathology, Neurodegeneration and Ubiquitin ligase and other disciplines.
His scientific interests lie mostly in Genetics, Autism, Neuroscience, Gene and Autism spectrum disorder. Phenotype, Epigenetics, Exome sequencing, Angelman syndrome and UBE3A are the subjects of his Genetics studies. His work in Angelman syndrome addresses issues such as Epilepsy, which are connected to fields such as Quinidine.
His Autism study combines topics from a wide range of disciplines, such as Synaptic plasticity, Schizophrenia, Intellectual disability and Clinical psychology. His Neuroscience research incorporates elements of Mutation, Long-term potentiation and Mutant. His work carried out in the field of Mutation brings together such families of science as Ankyrin and Cell biology.
Yong-hui Jiang mainly investigates Gene, Neuroscience, Genetics, Autism spectrum disorder and Autism. Yong-hui Jiang has researched Gene in several fields, including CHARGE syndrome and Cell biology. Yong-hui Jiang focuses mostly in the field of Cell biology, narrowing it down to matters related to Conformational change and, in some cases, Mutation and Missense mutation.
The Neuroscience study combines topics in areas such as Angelman syndrome, Ubiquitin, Potassium channel, Intellectual disability and Ubiquitin-Protein Ligase E3A. The study of Genetics is intertwined with the study of Synaptogenesis in a number of ways. His Autism study incorporates themes from Psychosocial, Genetic testing and Public health.
His primary areas of investigation include Genetics, Epigenetics, Gene, Autism spectrum disorder and Angelman syndrome. His work on Genetics is being expanded to include thematically relevant topics such as Hypertrichosis. His studies in Epigenetics integrate themes in fields like DNA methylation, Reprogramming, DNA, Synaptogenesis and Transcription.
Yong-hui Jiang interconnects Social behavior, Internal medicine, Hippocampus and SHANK2 in the investigation of issues within Autism spectrum disorder. His research in Angelman syndrome intersects with topics in Ubiquitin, Potassium channel, Ubiquitin-Protein Ligase E3A, Channelopathy and UBE3A. Yong-hui Jiang combines subjects such as Neuroscience and Epilepsy with his study of Ubiquitin.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Molecular classification of cutaneous malignant melanoma by gene expression profiling
M. Bittner;P.S.J. Meltzer;Y.D. Chen;Y. Jiang.
De novo truncating mutations in E6-AP ubiquitin-protein ligase gene (UBE3A) in Angelman syndrome.
Toshinobu Matsuura;James S. Sutcliffe;Ping Fang;Robert-Jan Galjaard.
Nature Genetics (1997)
MUTATION OF THE ANGELMAN UBIQUITIN LIGASE IN MICE CAUSES INCREASED CYTOPLASMIC P53 AND DEFICITS OF CONTEXTUAL LEARNING AND LONG-TERM POTENTIATION
Y. H. Jiang;D. Armstrong;U. Albrecht;C. M. Atkins.
Mutation of the E6-AP Ubiquitin Ligase Reduces Nuclear Inclusion Frequency While Accelerating Polyglutamine-Induced Pathology in SCA1 Mice
Christopher J Cummings;Eyal Reinstein;Yaling Sun;Barbara Antalffy.
Autism as a disorder of neural information processing: directions for research and targets for therapy
M K Belmonte;E H Cook;G M Anderson;J L R Rubenstein.
Molecular Psychiatry (2004)
EPIGENETICS AND HUMAN DISEASE
Yong Hui Jiang;Jan Bressler;Arthur L. Beaudet.
Annual Review of Genomics and Human Genetics (2004)
Modeling autism by SHANK gene mutations in mice.
Yong-hui Jiang;Michael D. Ehlers.
Synaptic dysfunction and abnormal behaviors in mice lacking major isoforms of Shank3
Xiaoming Wang;Portia A. McCoy;Ramona M. Rodriguiz;Yanzhen Pan.
Human Molecular Genetics (2011)
Detection of Clinically Relevant Genetic Variants in Autism Spectrum Disorder by Whole-Genome Sequencing
Yong-hui Jiang;Ryan K.C. Yuen;Xin Jin;Xin Jin;Mingbang Wang.
American Journal of Human Genetics (2013)
Correction: Corrigendum: Genetic Variants Identified from Epilepsy of Unknown Etiology in Chinese Children by Targeted Exome Sequencing
Yimin Wang;Xiaonan Du;Rao Bin;Shanshan Yu.
Scientific Reports (2017)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: