Yong-hui Jiang

Department of Genetics, Yale University School of Medicine

Affiliated withYale University School of Medicine

Research Area

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JoVE Journal Publications

ArticleTotal : 1	Year
Publication title Cited by 3	2024

Other Publications

Article	Year
A Novel Chd8 Mutant Mouse Displays Altered Ultrasonic Vocalizations and Enhanced Motor Coordination. Autism research : official journal of the International Society for Autism Research\| PubMed ID: 32815320	2020
High genetic burden in 163 Chinese children with status epilepticus. Seizure\| PubMed ID: 33278787	2021
Altered striatum centered brain structures in SHANK3 deficient Chinese children with genotype and phenotype profiling. Progress in neurobiology\| PubMed ID: 33388374	2021
Psychometric properties of the Chinese Parent Version of the Autism Spectrum Rating Scale: Rasch analysis. Autism : the international journal of research and practice\| PubMed ID: 33845648	2021
D-bifunctional protein deficiency caused by splicing variants in a neonate with severe peroxisomal dysfunction and persistent hypoglycemia. American journal of medical genetics. Part A\| PubMed ID: 34623748	2022
Mutations of the histone linker H1-4 in neurodevelopmental disorders and functional characterization of neurons expressing C-terminus frameshift mutant H1.4. Human molecular genetics\| PubMed ID: 34788807	2022
Inhibition of Trpv4 rescues circuit and social deficits unmasked by acute inflammatory response in a Shank3 mouse model of Autism. Molecular psychiatry\| PubMed ID: 35022531	2022
Detecting regions of homozygosity improves the diagnosis of pathogenic variants and uniparental disomy in pediatric patients. American journal of medical genetics. Part A\| PubMed ID: 35199448	2022
Neural circuit pathology driven by Shank3 mutation disrupts social behaviors. Cell reports\| PubMed ID: 35675770	2022
Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China. Orphanet journal of rare diseases\| PubMed ID: 35698200	2022
Comparative Proteome and Cis-Regulatory Element Analysis Reveals Specific Molecular Pathways Conserved in Dog and Human Brains. Molecular & cellular proteomics : MCP\| PubMed ID: 35738554	2022
A retrospective cohort analysis of the Yale pediatric genomics discovery program. American journal of medical genetics. Part A\| PubMed ID: 35899841	2022
Vitamin C epigenetically controls osteogenesis and bone mineralization. Nature communications\| PubMed ID: 36202795	2022
SHANK3 in vagal sensory neurons regulates body temperature, systemic inflammation, and sepsis. Frontiers in immunology\| PubMed ID: 36845137	2023
CHD8 mutations increase gliogenesis to enlarge brain size in the nonhuman primate. Cell discovery\| PubMed ID: 36878905	2023
Estimation on risk of spontaneous abortions by genomic disorders from a meta-analysis of microarray results on large case series of pregnancy losses. Molecular genetics & genomic medicine\| PubMed ID: 37013615	2023
Shank3 deficits in the anteromedial bed nucleus of the stria terminalis trigger an anxiety phenotype in mice. The European journal of neuroscience\| PubMed ID: 37165567	2023
Novel epigenetic molecular therapies for imprinting disorders. Molecular psychiatry\| PubMed ID: 37626134	2023
Modeling SHANK3-associated autism spectrum disorder in Beagle dogs via CRISPR/Cas9 gene editing. Molecular psychiatry\| PubMed ID: 37848710	2023
Identifying critical windows of air pollution exposure during preconception and gestational period on birthweight: a prospective cohort study. Environmental health : a global access science source\| PubMed ID: 37858139	2023
Critical windows of greenness exposure during preconception and gestational periods in association with birthweight outcomes. Environmental research, health : ERH\| PubMed ID: 38022394	2024
Impaired synaptic function and hyperexcitability of the pyramidal neurons in the prefrontal cortex of autism-associated Shank3 mutant dogs. Molecular autism\| PubMed ID: 38297387	2024