Qiao JD - Search Results

1

UNC13B variants associated with partial epilepsy with favourable outcome.

Wang J, Qiao JD, Liu XR, Liu DT, Chen YH, Wu Y, Sun Y, Yu J, Ren RN, Mei Z, Liu YX, Shi YW, Jiang M, Lin SM, He N, Li B, Bian WJ, Li BM, Yi YH, Su T, Liu HK, Gu WY, Liao WP. Wang J, et al. Among authors: qiao jd. Brain. 2021 Nov 29;144(10):3050-3060. doi: 10.1093/brain/awab164. Brain. 2021. PMID: 33876820 Free PMC article.

2

CELSR3 variants are associated with febrile seizures and epilepsy with antecedent febrile seizures.

Li J, Lin SM, Qiao JD, Liu XR, Wang J, Jiang M, Zhang J, Zhong M, Chen XQ, Zhu J, He N, Su T, Shi YW, Yi YH, Liao WP; China Epilepsy Gene 1.0 Project. Li J, et al. Among authors: qiao jd. CNS Neurosci Ther. 2022 Mar;28(3):382-389. doi: 10.1111/cns.13781. Epub 2021 Dec 23. CNS Neurosci Ther. 2022. PMID: 34951123 Free PMC article.

3

Reply: UNC13B and focal epilepsy.

Qiao JD, Li X, Li J, Guo QH, Tang XQ, Chen LZ, Su T, Yi YH, Wang J, Liao WP. Qiao JD, et al. Brain. 2022 Apr 29;145(3):e13-e16. doi: 10.1093/brain/awab486. Brain. 2022. PMID: 35380625 No abstract available.

4

YWHAZ variation causes intellectual disability and global developmental delay with brain malformation.

Wan RP, Liu ZG, Huang XF, Kwan P, Li YP, Qu XC, Ye XG, Chen FY, Zhang DW, He MF, Wang J, Mao YL, Qiao JD. Wan RP, et al. Among authors: qiao jd. Hum Mol Genet. 2023 Jan 13;32(3):462-472. doi: 10.1093/hmg/ddac210. Hum Mol Genet. 2023. PMID: 36001342 Free PMC article.

5

MED12 variants associated with X-linked recessive partial epilepsy without intellectual disability.

Yang JH, Liu ZG, Liu CL, Zhang MR, Jia YL, Zhai QX, He MF, He N, Qiao JD. Yang JH, et al. Among authors: qiao jd. Seizure. 2024 Mar;116:30-36. doi: 10.1016/j.seizure.2023.02.018. Epub 2023 Feb 27. Seizure. 2024. PMID: 36894399

6

Heterozygous Variants in KCNJ10 Cause Paroxysmal Kinesigenic Dyskinesia Via Haploinsufficiency.

Li YL, Lin J, Huang X, Zeng RH, Zhang G, Xu JN, Lin KJ, Chen XS, He MF, Qiao JD, Cheng X, Zhu D, Xiong ZQ, Chen WJ. Li YL, et al. Among authors: qiao jd. Ann Neurol. 2024 Oct;96(4):758-773. doi: 10.1002/ana.27018. Epub 2024 Jul 9. Ann Neurol. 2024. PMID: 38979912

7

Investigation of epilepsy-related genes in a Drosophila model.

Qu X, Lai X, He M, Zhang J, Xiang B, Liu C, Huang R, Shi Y, Qiao J. Qu X, et al. Neural Regen Res. 2024 Dec 16. doi: 10.4103/NRR.NRR-D-24-00877. Online ahead of print. Neural Regen Res. 2024. PMID: 39688550 Free article.

8

Knockout of PINK1 altered the neural connectivity of Drosophila dopamine PPM3 neurons at input and output sites.

Qiao JD, Mao YL. Qiao JD, et al. Invert Neurosci. 2020 Aug 6;20(3):11. doi: 10.1007/s10158-020-00244-4. Invert Neurosci. 2020. PMID: 32766952

9

Ketone Body Rescued Seizure Behavior of LRP1 Deficiency in Drosophila by Modulating Glutamate Transport.

Zhang JM, Chen MJ, He JH, Li YP, Li ZC, Ye ZJ, Bao YH, Huang BJ, Zhang WJ, Kwan P, Mao YL, Qiao JD. Zhang JM, et al. Among authors: qiao jd. J Mol Neurosci. 2022 Aug;72(8):1706-1714. doi: 10.1007/s12031-022-02026-6. Epub 2022 Jun 7. J Mol Neurosci. 2022. PMID: 35668313

10

Efficient strategies based on behavioral and electrophysiological methods for epilepsy-related gene screening in the Drosophila model.

Liu CQ, Qu XC, He MF, Liang DH, Xie SM, Zhang XX, Lin YM, Zhang WJ, Wu KC, Qiao JD. Liu CQ, et al. Among authors: qiao jd. Front Mol Neurosci. 2023 Apr 20;16:1121877. doi: 10.3389/fnmol.2023.1121877. eCollection 2023. Front Mol Neurosci. 2023. PMID: 37152436 Free PMC article.

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