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