- E-postgonzalo.nido@uib.no
- BesøksadresseHaukeland Universitetssykehus Laboratoriebygget, 7. etg. Heis øst5009 Bergen
- PostadressePostboks 78045020 Bergen
Vitenskapelig artikkel
- (2023). POLG genotype influences degree of mitochondrial dysfunction in iPSC derived neural progenitors, but not the parent iPSC or derived glia. Experimental Neurology. 16 sider.
- (2023). Not every estimate counts – evaluation of cell composition estimation approaches in brain bulk tissue data. Genome Medicine.
- (2023). Nicotinamide riboside supplementation is not associated with altered methylation homeostasis in Parkinson's disease. iScience.
- (2023). DNA Methylation Age Acceleration Is Not Associated with Age of Onset in Parkinson's Disease. Movement Disorders.
- (2023). Altered transcriptome-proteome coupling indicates aberrant proteostasis in Parkinson's disease. iScience. 21 sider.
- (2022). Ultra-deep whole genome bisulfite sequencing reveals a single methylation hotspot in human brain mitochondrial DNA. Epigenetics. 16 sider.
- (2022). The NADPARK study: A randomized phase I trial of nicotinamide riboside supplementation in Parkinson's disease. Cell Metabolism. 396-407.e6.
- (2022). No evidence of extensive non-CpG methylation in mtDNA. Nucleic Acids Research (NAR). 9190-9194.
- (2021). Genome-wide histone acetylation analysis reveals altered transcriptional regulation in the Parkinson’s disease brain. Molecular Neurodegeneration. 1-20.
- (2021). Distinct Mitochondrial Remodeling During Mesoderm Differentiation in a Human-Based Stem Cell Model. Frontiers in Cell and Developmental Biology. 1-12.
- (2020). Using urine to diagnose large-scale mtDNA deletions in adult patients. Annals of clinical and translational neurology. 1318-1326.
- (2020). Meta-analysis of whole-exome sequencing data from two independent cohorts finds no evidence for rare variant enrichment in Parkinson disease associated loci. PLOS ONE. 1-9.
- (2020). Differential transcript usage in the Parkinson’s disease brain. PLoS Genetics. 1-24.
- (2020). Common gene expression signatures in Parkinson’s disease are driven by changes in cell composition. Acta neuropathologica communications. 1-14.
- (2018). Ultradeep mapping of neuronal mitochondrial deletions in Parkinson's disease. Neurobiology of Aging. 120-127.
- (2018). Rare genetic variation in mitochondrial pathways influences the risk for parkinson's disease. Movement Disorders. 1591-1600.
- (2016). Learning structural bioinformatics and evolution with a snake puzzle. PeerJ. 1-38.
- (2016). Defective mitochondrial DNA homeostasis in the substantia nigra in Parkinson disease. Nature Communications. 11 sider.
Brev til redaktøren
- (2018). No evidence for rare TRAP1 mutations influencing the risk of idiopathic Parkinson's disease. Brain. e16-e16.
Se fullstendig oversikt over publikasjoner i CRIStin.
Submitted
- Toker L, Nido GS, Tzoulis C. Not every estimate counts. (Under review Nature Neuroscience)
- Toker L, Tran GT, Sundaresan J, Tysnes OB, Alves G, Haugarvoll K, Nido GS, Dölle C, Tzoulis C. Genome-wide histone acetylation analysis reveals altered transcriptional regulation in the Parkinson's disease brain. (Under review - Molecular Neurodegeneration)
- Gaare JJ, Nido GS, Dolle C, Sztromwasser P, Alves G, Tysnes OB, Haugarvoll K, Tzoulis C. No evidence for rare variant enrichment in Parkinson disease associated loci. (Under review - PLoS One)
- Dick F, Nido GS, Alves G, Tysnes OB, Nilsen GH, Dölle C, Tzoulis C. Differential transcript usage in the Parkinson’s disease brain. (Accepted for publication - PLoS Genetics)
Published
- Nido GS, Dick F, Toker L, Petersen K, Alves G, Tysnes OB, Jonassen I, Haugarvoll K, Tzoulis C. Common gene expression signatures in Parkinson’s disease are driven by changes in cell composition. Acta Neuropathologica Communications 2020; 8(55)
- Varhaug KN, Nido GS, de Coo R, Isohanni P, Suomalainen A, Tzoulis C, Knappskog P, Bindoff LA. Using urine to diagnose large-scale mtDNA deletions in adult patients. Annals of Clinical and Translational Neurology 2020; 7(8):1318-1326
- Gaare JJ, Nido GS, Sztromwasser P, Knappskog P, Dahl O, Johansen ML, Grødem JM, Alves G, Tysnes OB, Johansson S, Haugarvoll H and Tzoulis C. Rare variation in biological pathways and their impact on development and progression of Parkinson’s disease. European Journal of Neurology 2019; 26:37-37
- Gaare JJ, Nido GS, Sztromwasser P, Knappskog P, Dahl O, Johansen ML, Alves G, Tysnes OB, Johansson S, Haugarvoll H and Tzoulis C. No evidence for rare TRAP1 mutations influencing the risk of idiopathic Parkinson disease. Brain 2018; 141(3), e16-e19
- Gaare JJ, Nido GS, Sztromwasser P, Knappskog P, Dahl O, Johansen ML, Grødem JM, Alves G, Tysnes OB, Johansson S, Haugarvoll H and Tzoulis C. Rare genetic variation in mitochondrial pathways influences the risk for Parkinson disease. Movement Disorders 2018; 33(10):1591-1600
- Nido GS, Dölle C, Flønes I, Tuppen HA, Alves G, Tysnes OB, Haugarvoll K and Tzoulis C. Ultra-deep mapping of neuronal mitochondrial deletions in Parkinson’s disease. Neurobiology of Aging 2018; 63:120-127
- Dölle C, Flønes I, Nido GS, Miletic H, Kristoffersen S, Lilleng KP, Larsen JP, Tysness OB, Haugarvoll K, Bindoff LA, and Tzoulis C. Defective mitochondrial DNA homeostasis in the dopaminergic substantia nigra of patients with Parkinson’s disease. Nature Communications 2016; 7:13548
- Nido GS, Bachschmid-Romano L, Bastolla U, Pascual-García A. Learning structural bioinformatics and evolution with a snake puzzle. PeerJ Computer Science, 2016;2:e100
- Nido GS, Ryan MM, Benuskova L, and Williams J. Dynamical properties of gene regulatory networks involved in long-term potentiation. Frontiers in Molecular Neuroscience 2015;8
- Nido GS, Williams J, Benuskova L. Bistable properties of a memory-related gene regulatory network. Neural Networks (IJCNN), IEEE 2012
- Nido GS, Méndez R, Pascual-García A, Abia D, Bastolla U. Protein disorder in the centrosome correlates with complexity in cell types number. Molecular BioSystems 2012; 8(1):353-67
- Pascual‐García, A., Abia, D., Méndez, R., Nido, G. S., & Bastolla, U. Quantifying the evolutionary divergence of protein structures: the role of function change and function conservation. Proteins: Structure, Function, and Bioinformatics 2010; 78(1):181-196
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