PubMed for id: 816141

Year	Number of Results
1993	1
2012	1
2013	1
2014	1
2016	1
2017	1
2019	1
2020	1
2021	2
2022	1
2023	2
2024	0

1

Impaired pre-synaptic plasticity and visual responses in auxilin-knockout mice.

Cheng X, Tang Y, Vidyadhara DJ, Li BZ, Zimmerman M, Pak A, Nareddula S, Edens PA, Chandra SS, Chubykin AA. Cheng X, et al. iScience. 2023 Sep 6;26(10):107842. doi: 10.1016/j.isci.2023.107842. eCollection 2023 Oct 20. iScience. 2023. PMID: 37766983 Free PMC article.

2

Dopamine transporter and synaptic vesicle sorting defects underlie auxilin-associated Parkinson's disease.

Vidyadhara DJ, Somayaji M, Wade N, Yücel B, Zhao H, Shashaank N, Ribaudo J, Gupta J, Lam TT, Sames D, Greene LE, Sulzer DL, Chandra SS. Vidyadhara DJ, et al. Cell Rep. 2023 Mar 28;42(3):112231. doi: 10.1016/j.celrep.2023.112231. Epub 2023 Mar 14. Cell Rep. 2023. PMID: 36920906 Free PMC article.

3

Monogenic Parkinson's Disease: Genotype, Phenotype, Pathophysiology, and Genetic Testing.

Jia F, Fellner A, Kumar KR. Jia F, et al. Genes (Basel). 2022 Mar 7;13(3):471. doi: 10.3390/genes13030471. Genes (Basel). 2022. PMID: 35328025 Free PMC article. Review.

4

DNAJC6 Parkinson Disease.

Kurian MA, Abela L. Kurian MA, et al. 2021 May 13. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. 2021 May 13. In: Adam MP, Feldman J, Mirzaa GM, Pagon RA, Wallace SE, Bean LJH, Gripp KW, Amemiya A, editors. GeneReviews^® [Internet]. Seattle (WA): University of Washington, Seattle; 1993–2024. PMID: 33983693 Free Books & Documents. Review.

5

Neurodevelopmental defects and neurodegenerative phenotypes in human brain organoids carrying Parkinson's disease-linked DNAJC6 mutations.

Wulansari N, Darsono WHW, Woo HJ, Chang MY, Kim J, Bae EJ, Sun W, Lee JH, Cho IJ, Shin H, Lee SJ, Lee SH. Wulansari N, et al. Sci Adv. 2021 Feb 17;7(8):eabb1540. doi: 10.1126/sciadv.abb1540. Print 2021 Feb. Sci Adv. 2021. PMID: 33597231 Free PMC article.

6

Genetics of Parkinson's disease.

Cherian A, Divya KP. Cherian A, et al. Acta Neurol Belg. 2020 Dec;120(6):1297-1305. doi: 10.1007/s13760-020-01473-5. Epub 2020 Aug 19. Acta Neurol Belg. 2020. PMID: 32813147 Review.

7

'Atypical' Parkinson's disease - genetic.

Weissbach A, Wittke C, Kasten M, Klein C. Weissbach A, et al. Int Rev Neurobiol. 2019;149:207-235. doi: 10.1016/bs.irn.2019.10.011. Epub 2019 Nov 25. Int Rev Neurobiol. 2019. PMID: 31779813 Review.

8

Parkinson Sac Domain Mutation in Synaptojanin 1 Impairs Clathrin Uncoating at Synapses and Triggers Dystrophic Changes in Dopaminergic Axons.

Cao M, Wu Y, Ashrafi G, McCartney AJ, Wheeler H, Bushong EA, Boassa D, Ellisman MH, Ryan TA, De Camilli P. Cao M, et al. Neuron. 2017 Feb 22;93(4):882-896.e5. doi: 10.1016/j.neuron.2017.01.019. Neuron. 2017. PMID: 28231468 Free PMC article.

9

Genetics of Parkinson's disease.

Lill CM. Lill CM. Mol Cell Probes. 2016 Dec;30(6):386-396. doi: 10.1016/j.mcp.2016.11.001. Epub 2016 Nov 4. Mol Cell Probes. 2016. PMID: 27818248 Review.

10

Genetics of Parkinson's disease--state of the art, 2013.

Bonifati V. Bonifati V. Parkinsonism Relat Disord. 2014 Jan;20 Suppl 1:S23-8. doi: 10.1016/S1353-8020(13)70009-9. Parkinsonism Relat Disord. 2014. PMID: 24262182 Review.

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