Department of Genetics,
Department of Neuroscience,
Department of Pediatrics
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A Novel Chd8 Mutant Mouse Displays Altered Ultrasonic Vocalizations and Enhanced Motor Coordination.
Autism research : official journal of the International Society for Autism Research Oct, 2020 | Pubmed ID: 32815320
High genetic burden in 163 Chinese children with status epilepticus.
Seizure Jan, 2021 | Pubmed ID: 33278787
Altered striatum centered brain structures in SHANK3 deficient Chinese children with genotype and phenotype profiling.
Progress in neurobiology May, 2021 | Pubmed ID: 33388374
Psychometric properties of the Chinese Parent Version of the Autism Spectrum Rating Scale: Rasch analysis.
Autism : the international journal of research and practice 10, 2021 | Pubmed ID: 33845648
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 Jan, 2022 | Pubmed ID: 34623748
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 May, 2022 | Pubmed ID: 34788807
Inhibition of Trpv4 rescues circuit and social deficits unmasked by acute inflammatory response in a Shank3 mouse model of Autism.
Molecular psychiatry Apr, 2022 | Pubmed ID: 35022531
Detecting regions of homozygosity improves the diagnosis of pathogenic variants and uniparental disomy in pediatric patients.
American journal of medical genetics. Part A Jun, 2022 | Pubmed ID: 35199448
Neural circuit pathology driven by Shank3 mutation disrupts social behaviors.
Cell reports Jun, 2022 | Pubmed ID: 35675770
Recommendations for the diagnosis and management of childhood Prader-Willi syndrome in China.
Orphanet journal of rare diseases 06, 2022 | Pubmed ID: 35698200
Comparative Proteome and Cis-Regulatory Element Analysis Reveals Specific Molecular Pathways Conserved in Dog and Human Brains.
Molecular & cellular proteomics : MCP Aug, 2022 | Pubmed ID: 35738554
A retrospective cohort analysis of the Yale pediatric genomics discovery program.
American journal of medical genetics. Part A Oct, 2022 | Pubmed ID: 35899841
Vitamin C epigenetically controls osteogenesis and bone mineralization.
Nature communications Oct, 2022 | Pubmed ID: 36202795
SHANK3 in vagal sensory neurons regulates body temperature, systemic inflammation, and sepsis.
Frontiers in immunology , 2023 | Pubmed ID: 36845137
CHD8 mutations increase gliogenesis to enlarge brain size in the nonhuman primate.
Cell discovery Mar, 2023 | Pubmed ID: 36878905
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 Aug, 2023 | Pubmed ID: 37013615
Shank3 deficits in the anteromedial bed nucleus of the stria terminalis trigger an anxiety phenotype in mice.
The European journal of neuroscience Jun, 2023 | Pubmed ID: 37165567
Novel epigenetic molecular therapies for imprinting disorders.
Molecular psychiatry Aug, 2023 | Pubmed ID: 37626134
Modeling SHANK3-associated autism spectrum disorder in Beagle dogs via CRISPR/Cas9 gene editing.
Molecular psychiatry Sep, 2023 | Pubmed ID: 37848710
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 Oct, 2023 | Pubmed ID: 37858139
Critical windows of greenness exposure during preconception and gestational periods in association with birthweight outcomes.
Environmental research, health : ERH Mar, 2024 | Pubmed ID: 38022394
Impaired synaptic function and hyperexcitability of the pyramidal neurons in the prefrontal cortex of autism-associated Shank3 mutant dogs.
Molecular autism Jan, 2024 | Pubmed ID: 38297387