Academic article
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Kverneng, Simon Ulvenes; Stige, Kjersti Eline; Berven, Haakon
et al. (2025). Mitochondrial complex I deficiency occurs in skeletal muscle of a subgroup of individuals with Parkinson’s disease. (external link)
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Flønes, Irene; Toker, Lilah; Sandnes, Dagny Ann
et al. (2024). Mitochondrial complex I deficiency stratifies idiopathic Parkinson’s disease. (external link)
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Nido, Gonzalo Sanchez; Castelli, Martina Galatea; Mostafavi, Sepideh
et al. (2024). Single-nucleus transcriptomics reveals disease- and
pathology-specific signatures in α-synucleinopathies. (external link)
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Toker, Lilah; Nido, Gonzalo Sanchez; Tzoulis, Charalampos
(2023). Not every estimate counts – evaluation of cell composition estimation approaches in brain bulk tissue data. (external link)
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Dick, Fiona; Tysnes, Ole-Bjørn; Alves, Guido Werner
et al. (2023). Altered transcriptome-proteome coupling indicates aberrant proteostasis in Parkinson's disease. (external link)
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Hong, Yu; Kristiansen, Cecilie Katrin; Chen, Anbin
et al. (2023). POLG genotype influences degree of mitochondrial dysfunction in iPSC derived neural progenitors, but not the parent iPSC or derived glia. (external link)
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Gaare, Johannes Jernqvist; Dölle, Christian; Brakedal, Brage
et al. (2023). Nicotinamide riboside supplementation is not associated with altered methylation homeostasis in Parkinson's disease. (external link)
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Gaare, Johannes Jernqvist; Brügger, Kim; Nido, Gonzalo Sanchez
et al. (2023). DNA Methylation Age Acceleration Is Not Associated with Age of Onset in Parkinson's Disease. (external link)
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Brakedal, Brage; Dölle, Christian; Riemer, Frank
et al. (2022). The NADPARK study: A randomized phase I trial of nicotinamide riboside supplementation in Parkinson's disease. (external link)
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Guitton, Romain Guillaume Bernard; Nido, Gonzalo Sanchez; Tzoulis, Charalampos
(2022). No evidence of extensive non-CpG methylation in mtDNA. (external link)
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Guitton, Romain Guillaume Bernard; Dölle, Christian; Alves, Guido Werner
et al. (2022). Ultra-deep whole genome bisulfite sequencing reveals a single methylation hotspot in human brain mitochondrial DNA. (external link)
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Toker, Lilah; Tran, Gia T.; Sundaresan, Janani
et al. (2021). Genome-wide histone acetylation analysis reveals altered transcriptional regulation in the Parkinson’s disease brain. (external link)
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Mostafavi, Sepideh; Balafkan, Novin; Pettersen, Ina Katrine Nitschke
et al. (2021). Distinct Mitochondrial Remodeling During Mesoderm Differentiation in a Human-Based Stem Cell Model. (external link)
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Dick, Fiona; Nido, Gonzalo Sanchez; Alves, Guido Werner
et al. (2020). Differential transcript usage in the Parkinson’s disease brain. (external link)
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Gaare, Johannes Jernqvist; Nido, Gonzalo Sanchez; Dölle, Christian
et al. (2020). Meta-analysis of whole-exome sequencing data from two independent cohorts finds no evidence for rare variant enrichment in Parkinson disease associated loci. (external link)
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Varhaug, Kristin Nielsen; Nido, Gonzalo Sanchez; Coo, Irenaeus de
et al. (2020). Using urine to diagnose large-scale mtDNA deletions in adult patients. (external link)
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Nido, Gonzalo Sanchez; Dick, Fiona; Toker, Lilah
et al. (2020). Common gene expression signatures in Parkinson’s disease are driven by changes in cell composition. (external link)
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Gaare, Johannes Jernqvist; Nido, Gonzalo Sanchez; Sztromwasser, Pawel Szymon
et al. (2018). Rare genetic variation in mitochondrial pathways influences the risk for parkinson's disease. (external link)
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Nido, Gonzalo Sanchez; Dölle, Christian; Flønes, Irene Hana
et al. (2018). Ultradeep mapping of neuronal mitochondrial deletions in Parkinson's disease. (external link)
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Nido, Gonzalo Sanchez; Bachschmid-Romano, Ludovica; Bastolla, Ugo
et al. (2016). Learning structural bioinformatics and evolution with a snake puzzle. (external link)
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Dölle, Christian; Flønes, Irene Hana; Nido, Gonzalo Sanchez
et al. (2016). Defective mitochondrial DNA homeostasis in the substantia nigra in Parkinson disease. (external link)
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