Li H - Search Results

1

Novel compound heterozygous mutation in STAMBP causes a neurodevelopmental disorder by disrupting cortical proliferation.

Hu M, Li H, Huang Z, Li D, Xu Y, Xu Q, Chen B, Wang Y, Deng J, Zhu M, Feng W, Xu X. Hu M, et al. Among authors: li d, li h. Front Neurosci. 2022 Aug 10;16:963813. doi: 10.3389/fnins.2022.963813. eCollection 2022. Front Neurosci. 2022. PMID: 36033615 Free PMC article.

2

Li H, Zhao P, Xu Q, Shan S, Hu C, Qiu Z, Xu X. Li H, et al. Sci Rep. 2016 Jul 19;6:29878. doi: 10.1038/srep29878. Sci Rep. 2016. PMID: 27430727 Free PMC article.

3

Distinct Defects in Spine Formation or Pruning in Two Gene Duplication Mouse Models of Autism.

Wang M, Li H, Takumi T, Qiu Z, Xu X, Yu X, Bian WJ. Wang M, et al. Among authors: li h. Neurosci Bull. 2017 Apr;33(2):143-152. doi: 10.1007/s12264-017-0111-8. Epub 2017 Mar 3. Neurosci Bull. 2017. PMID: 28258509 Free PMC article.

4

Effects of Parent-Implemented Early Start Denver Model Intervention on Chinese Toddlers with Autism Spectrum Disorder: A Non-Randomized Controlled Trial.

Zhou B, Xu Q, Li H, Zhang Y, Wang Y, Rogers SJ, Xu X. Zhou B, et al. Among authors: li h. Autism Res. 2018 Apr;11(4):654-666. doi: 10.1002/aur.1917. Epub 2018 Feb 7. Autism Res. 2018. PMID: 29412514 Clinical Trial.

5

Alterations in plasma cytokine levels in chinese children with autism spectrum disorder.

Hu CC, Xu X, Xiong GL, Xu Q, Zhou BR, Li CY, Qin Q, Liu CX, Li HP, Sun YJ, Yu X. Hu CC, et al. Autism Res. 2018 Jul;11(7):989-999. doi: 10.1002/aur.1940. Epub 2018 Mar 9. Autism Res. 2018. PMID: 29522267

6

Improving the early screening procedure for autism spectrum disorder in young children: Experience from a community-based model in shanghai.

Li C, Zhu G, Feng J, Xu Q, Zhou Z, Zhou B, Hu C, Liu C, Li H, Wang Y, Yan W, Ge X, Xu X. Li C, et al. Among authors: li h. Autism Res. 2018 Sep;11(9):1206-1217. doi: 10.1002/aur.1984. Epub 2018 Sep 19. Autism Res. 2018. PMID: 30230702

7

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.

Xu Q, Li CY, Wang Y, Li HP, Wu BB, Jiang YH, Xu X. Xu Q, et al. BMC Med Genomics. 2018 Oct 23;11(1):92. doi: 10.1186/s12920-018-0421-3. BMC Med Genomics. 2018. PMID: 30352594 Free PMC article.

8

Autism-associated CHD8 deficiency impairs axon development and migration of cortical neurons.

Xu Q, Liu YY, Wang X, Tan GH, Li HP, Hulbert SW, Li CY, Hu CC, Xiong ZQ, Xu X, Jiang YH. Xu Q, et al. Mol Autism. 2018 Dec 19;9:65. doi: 10.1186/s13229-018-0244-2. eCollection 2018. Mol Autism. 2018. PMID: 30574290 Free PMC article.

9

Altered striatum centered brain structures in SHANK3 deficient Chinese children with genotype and phenotype profiling.

Liu C, Li D, Yang H, Li H, Xu Q, Zhou B, Hu C, Li C, Wang Y, Qiao Z, Jiang YH, Xu X. Liu C, et al. Among authors: li c, li d, li h. Prog Neurobiol. 2021 May;200:101985. doi: 10.1016/j.pneurobio.2020.101985. Epub 2020 Dec 31. Prog Neurobiol. 2021. PMID: 33388374 Free PMC article.

10

Common and Distinct Disruptions of Cortical Surface Morphology Between Autism Spectrum Disorder Children With and Without SHANK3 Deficiency.

Li D, Liu C, Huang Z, Li H, Xu Q, Zhou B, Hu C, Zhang Y, Wang Y, Nie J, Qiao Z, Yin D, Xu X. Li D, et al. Among authors: li h. Front Neurosci. 2021 Oct 28;15:751364. doi: 10.3389/fnins.2021.751364. eCollection 2021. Front Neurosci. 2021. PMID: 34776852 Free PMC article.

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