Nido GS - Search Results

1

Ultra-deep whole genome bisulfite sequencing reveals a single methylation hotspot in human brain mitochondrial DNA.

Guitton R, Dölle C, Alves G, Ole-Bjørn T, Nido GS, Tzoulis C. Guitton R, et al. Among authors: nido gs. Epigenetics. 2022 Aug;17(8):906-921. doi: 10.1080/15592294.2022.2045754. Epub 2022 Mar 7. Epigenetics. 2022. PMID: 35253628 Free PMC article.

2

Defective mitochondrial DNA homeostasis in the substantia nigra in Parkinson disease.

Dölle C, Flønes I, Nido GS, Miletic H, Osuagwu N, Kristoffersen S, Lilleng PK, Larsen JP, Tysnes OB, Haugarvoll K, Bindoff LA, Tzoulis C. Dölle C, et al. Among authors: nido gs. Nat Commun. 2016 Nov 22;7:13548. doi: 10.1038/ncomms13548. Nat Commun. 2016. PMID: 27874000 Free PMC article.

3

Ultradeep mapping of neuronal mitochondrial deletions in Parkinson's disease.

Nido GS, Dölle C, Flønes I, Tuppen HA, Alves G, Tysnes OB, Haugarvoll K, Tzoulis C. Nido GS, et al. Neurobiol Aging. 2018 Mar;63:120-127. doi: 10.1016/j.neurobiolaging.2017.10.024. Epub 2017 Dec 8. Neurobiol Aging. 2018. PMID: 29257976 Free article.

4

No evidence for rare TRAP1 mutations influencing the risk of idiopathic Parkinson's disease.

Gaare JJ, Nido GS, Sztromwasser P, Knappskog PM, Dahl O, Lund-Johansen M, Alves G, Tysnes OB, Johansson S, Haugarvoll K, Tzoulis C. Gaare JJ, et al. Among authors: nido gs. Brain. 2018 Mar 1;141(3):e16. doi: 10.1093/brain/awx378. Brain. 2018. PMID: 29373637 Free PMC article. No abstract available.

5

Rare genetic variation in mitochondrial pathways influences the risk for Parkinson's disease.

Gaare JJ, Nido GS, Sztromwasser P, Knappskog PM, Dahl O, Lund-Johansen M, Maple-Grødem J, Alves G, Tysnes OB, Johansson S, Haugarvoll K, Tzoulis C. Gaare JJ, et al. Among authors: nido gs. Mov Disord. 2018 Oct;33(10):1591-1600. doi: 10.1002/mds.64. Epub 2018 Sep 5. Mov Disord. 2018. PMID: 30256453 Free PMC article.

6

Common gene expression signatures in Parkinson's disease are driven by changes in cell composition.

Nido GS, Dick F, Toker L, Petersen K, Alves G, Tysnes OB, Jonassen I, Haugarvoll K, Tzoulis C. Nido GS, et al. Acta Neuropathol Commun. 2020 Apr 21;8(1):55. doi: 10.1186/s40478-020-00932-7. Acta Neuropathol Commun. 2020. PMID: 32317022 Free PMC article.

7

Using urine to diagnose large-scale mtDNA deletions in adult patients.

Varhaug KN, Nido GS, de Coo I, Isohanni P, Suomalainen A, Tzoulis C, Knappskog P, Bindoff LA. Varhaug KN, et al. Among authors: nido gs. Ann Clin Transl Neurol. 2020 Aug;7(8):1318-1326. doi: 10.1002/acn3.51119. Epub 2020 Jul 7. Ann Clin Transl Neurol. 2020. PMID: 32634300 Free PMC article.

8

Meta-analysis of whole-exome sequencing data from two independent cohorts finds no evidence for rare variant enrichment in Parkinson disease associated loci.

Gaare JJ, Nido G, Dölle C, Sztromwasser P, Alves G, Tysnes OB, Haugarvoll K, Tzoulis C. Gaare JJ, et al. PLoS One. 2020 Oct 1;15(10):e0239824. doi: 10.1371/journal.pone.0239824. eCollection 2020. PLoS One. 2020. PMID: 33002040 Free PMC article.

9

Differential transcript usage in the Parkinson's disease brain.

Dick F, Nido GS, Alves GW, Tysnes OB, Nilsen GH, Dölle C, Tzoulis C. Dick F, et al. Among authors: nido gs. PLoS Genet. 2020 Nov 2;16(11):e1009182. doi: 10.1371/journal.pgen.1009182. eCollection 2020 Nov. PLoS Genet. 2020. PMID: 33137089 Free PMC article.

10

Genome-wide histone acetylation analysis reveals altered transcriptional regulation in the Parkinson's disease brain.

Toker L, Tran GT, Sundaresan J, Tysnes OB, Alves G, Haugarvoll K, Nido GS, Dölle C, Tzoulis C. Toker L, et al. Among authors: nido gs. Mol Neurodegener. 2021 May 5;16(1):31. doi: 10.1186/s13024-021-00450-7. Mol Neurodegener. 2021. PMID: 33947435 Free PMC article.

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