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Gonzalo Sanchez Nidos bilde

Gonzalo Sanchez Nido

Postdoktor
  • E-postGonzalo.Nido@uib.no
  • Besøksadresse
    Haukeland Universitetssykehus Laboratoriebygget, 7. etg. Heis øst
  • Postadresse
    Postboks 7804
    5020 Bergen
Vitenskapelig artikkel
  • Vis forfatter(e) 2020. Using urine to diagnose large-scale mtDNA deletions in adult patients. Annals of clinical and translational neurology. 1318-1326.
  • Vis forfatter(e) 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.
  • Vis forfatter(e) 2020. Differential transcript usage in the Parkinson’s disease brain. PLoS Genetics. 1-24.
  • Vis forfatter(e) 2020. Common gene expression signatures in Parkinson’s disease are driven by changes in cell composition. Acta neuropathologica communications. 1-14.
  • Vis forfatter(e) 2018. Ultradeep mapping of neuronal mitochondrial deletions in Parkinson's disease. Neurobiology of Aging. 120-127.
  • Vis forfatter(e) 2018. Rare genetic variation in mitochondrial pathways influences the risk for parkinson's disease. Movement Disorders. 1591-1600.
  • Vis forfatter(e) 2016. Learning structural bioinformatics and evolution with a snake puzzle. PeerJ. 1-38.
  • Vis forfatter(e) 2016. Defective mitochondrial DNA homeostasis in the substantia nigra in Parkinson disease. Nature Communications. 11 sider.
Brev til redaktøren
  • Vis forfatter(e) 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

  1. Toker L, Nido GS, Tzoulis C. Not every estimate counts. (Under review Nature Neuroscience) 
  2. 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)
  3. 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)
  4. 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

  1. 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)
  2. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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
  8. 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
  9. 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
  10. Nido GS, Williams J, Benuskova L. Bistable properties of a memory-related gene regulatory network. Neural Networks (IJCNN), IEEE 2012
  11. 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
  12. 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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