81330027/National Natural Science Foundation of China[Grants and Funding] - Search Results

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2017	1
2018	1
2020	1
2024	0

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Genotype and Phenotype Correlations for TBL1XR1 in Neurodevelopmental Disorders.

Quan Y, Zhang Q, Chen M, Wu H, Ou J, Shen Y, Li K, Xun G, Zhao J, Hu Z, Xia K, Guo H. Quan Y, et al. J Mol Neurosci. 2020 Dec;70(12):2085-2092. doi: 10.1007/s12031-020-01615-7. Epub 2020 Jun 10. J Mol Neurosci. 2020. PMID: 32524419 Review.

Genotype and phenotype correlations for SHANK3 de novo mutations in neurodevelopmental disorders.

Li Y, Jia X, Wu H, Xun G, Ou J, Zhang Q, Li H, Bai T, Hu Z, Zou X, Xia K, Guo H. Li Y, et al. Am J Med Genet A. 2018 Dec;176(12):2668-2676. doi: 10.1002/ajmg.a.40666. Epub 2018 Dec 9. Am J Med Genet A. 2018. PMID: 30537371 Review.

Vitamin D-related genes are subjected to significant de novo mutation burdens in autism spectrum disorder.

Li J, Wang L, Yu P, Shi L, Zhang K, Sun ZS, Xia K. Li J, et al. Am J Med Genet B Neuropsychiatr Genet. 2017 Jul;174(5):568-577. doi: 10.1002/ajmg.b.32543. Epub 2017 Apr 13. Am J Med Genet B Neuropsychiatr Genet. 2017. PMID: 28407358

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