Qin Y - Search Results

1

Associations between polygenic risk scores and amplitude of low-frequency fluctuation of inferior frontal gyrus in schizophrenia.

Kang J, Jiao Z, Qin Y, Wang Y, Wang J, Jin L, Feng J, Wang F, Tang Y, Gong X. Kang J, et al. Among authors: qin y. J Psychiatr Res. 2022 Mar;147:4-12. doi: 10.1016/j.jpsychires.2021.12.043. Epub 2022 Jan 3. J Psychiatr Res. 2022. PMID: 34999338

2

A promoter variant in ZNF804A decreasing its expression increases the risk of autism spectrum disorder in the Han Chinese population.

Zhang L, Qin Y, Gong X, Peng R, Cai C, Zheng Y, Du Y, Wang H. Zhang L, et al. Among authors: qin y. Transl Psychiatry. 2019 Jan 22;9(1):31. doi: 10.1038/s41398-019-0369-x. Transl Psychiatry. 2019. PMID: 30670685 Free PMC article.

3

Polygenic risk for autism spectrum disorder affects left amygdala activity and negative emotion in schizophrenia.

Qin Y, Kang J, Jiao Z, Wang Y, Wang J, Wang H, Feng J, Jin L, Wang F, Gong X. Qin Y, et al. Transl Psychiatry. 2020 Sep 21;10(1):322. doi: 10.1038/s41398-020-01001-2. Transl Psychiatry. 2020. PMID: 32958750 Free PMC article.

4

Associations between hemispheric asymmetry and schizophrenia-related risk genes in people with schizophrenia and people at a genetic high risk of schizophrenia.

Zhu Y, Wang S, Gong X, Edmiston EK, Zhong S, Li C, Zhao P, Wei S, Jiang X, Qin Y, Kang J, Wang Y, Sun Q, Gong G, Wang F, Tang Y. Zhu Y, et al. Among authors: qin y. Br J Psychiatry. 2021 Jul;219(1):392-400. doi: 10.1192/bjp.2021.47. Br J Psychiatry. 2021. PMID: 35048853 Free PMC article.

5

A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling.

Qin Y, Du Y, Chen L, Liu Y, Xu W, Liu Y, Li Y, Leng J, Wang Y, Zhang XY, Feng J, Zhang F, Jin L, Qiu Z, Gong X, Wang H. Qin Y, et al. Mol Psychiatry. 2022 Jul;27(7):2985-2998. doi: 10.1038/s41380-022-01539-1. Epub 2022 Apr 6. Mol Psychiatry. 2022. PMID: 35388181 Free PMC article.

6

Correction: A recurrent SHANK1 mutation implicated in autism spectrum disorder causes autistic-like core behaviors in mice via downregulation of mGluR1-IP3R1-calcium signaling.

Qin Y, Du Y, Chen L, Liu Y, Xu W, Liu Y, Li Y, Leng J, Wang Y, Zhang XY, Feng J, Zhang F, Jin L, Qiu Z, Gong X, Wang H. Qin Y, et al. Mol Psychiatry. 2022 Sep;27(9):3922. doi: 10.1038/s41380-022-01605-8. Mol Psychiatry. 2022. PMID: 35538194 Free PMC article. No abstract available.

7

Downregulation of mGluR1-mediated signaling underlying autistic-like core symptoms in Shank1 P1812L-knock-in mice.

Qin Y, Zhang XY, Liu Y, Ma Z, Tao S, Li Y, Peng R, Wang F, Wang J, Feng J, Qiu Z, Jin L, Wang H, Gong X. Qin Y, et al. Transl Psychiatry. 2023 Oct 25;13(1):329. doi: 10.1038/s41398-023-02626-9. Transl Psychiatry. 2023. PMID: 37880287 Free PMC article.

8

Loss-of-function or gain-of-function variations in VINCULIN (VCL) are risk factors of human neural tube defects.

Wang Y, Qin Y, Peng R, Wang H. Wang Y, et al. Among authors: qin y. Mol Genet Genomic Med. 2021 Feb;9(2):e1563. doi: 10.1002/mgg3.1563. Epub 2021 Jan 24. Mol Genet Genomic Med. 2021. PMID: 33491343 Free PMC article.

9

'Virtual experience' as an intervention before a positron emission tomography/CT scan may ease patients' anxiety and improve image quality.

Sun Y, Sun Y, Qin Y, Zhang Y, Yuan H, Yang Z. Sun Y, et al. Among authors: qin y. J Med Imaging Radiat Oncol. 2020 Oct;64(5):641-648. doi: 10.1111/1754-9485.13078. Epub 2020 Jun 30. J Med Imaging Radiat Oncol. 2020. PMID: 32608179 Clinical Trial.

10

Novel compound heterozygous mutations in the LARS2 gene in a Chinese family with hearing loss.

Lu M, Zhou K, Yang X, Lin L, Lu L, Qin Y, Zhou N, Li L. Lu M, et al. Among authors: qin y. Neurogenetics. 2025 Jan 7;26(1):17. doi: 10.1007/s10048-024-00797-1. Neurogenetics. 2025. PMID: 39762667

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