Gonzalo Sanchez Nido

Academic article

Show author(s) (2023). POLG genotype influences degree of mitochondrial dysfunction in iPSC derived neural progenitors, but not the parent iPSC or derived glia. Experimental Neurology.
Show author(s) (2023). Not every estimate counts – evaluation of cell composition estimation approaches in brain bulk tissue data. Genome Medicine.
Show author(s) (2023). Nicotinamide riboside supplementation is not associated with altered methylation homeostasis in Parkinson's disease. iScience.
Show author(s) (2023). Altered transcriptome-proteome coupling indicates aberrant proteostasis in Parkinson's disease. iScience. 21 pages.

Show author(s) (2022). Ultra-deep whole genome bisulfite sequencing reveals a single methylation hotspot in human brain mitochondrial DNA. Epigenetics. 16 pages.
Show author(s) (2022). The NADPARK study: A randomized phase I trial of nicotinamide riboside supplementation in Parkinson's disease. Cell Metabolism. 396-407.e6.
Show author(s) (2022). No evidence of extensive non-CpG methylation in mtDNA. Nucleic Acids Research (NAR). 9190-9194.

Show author(s) (2021). Genome-wide histone acetylation analysis reveals altered transcriptional regulation in the Parkinson’s disease brain. Molecular Neurodegeneration. 1-20.
Show author(s) (2021). Distinct Mitochondrial Remodeling During Mesoderm Differentiation in a Human-Based Stem Cell Model. Frontiers in Cell and Developmental Biology. 1-12.

Show author(s) (2020). Using urine to diagnose large-scale mtDNA deletions in adult patients. Annals of clinical and translational neurology. 1318-1326.
Show author(s) (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.
Show author(s) (2020). Differential transcript usage in the Parkinson’s disease brain. PLoS Genetics. 1-24.
Show author(s) (2020). Common gene expression signatures in Parkinson’s disease are driven by changes in cell composition. Acta neuropathologica communications. 1-14.

Show author(s) (2018). Ultradeep mapping of neuronal mitochondrial deletions in Parkinson's disease. Neurobiology of Aging. 120-127.
Show author(s) (2018). Rare genetic variation in mitochondrial pathways influences the risk for parkinson's disease. Movement Disorders. 1591-1600.

Show author(s) (2016). Learning structural bioinformatics and evolution with a snake puzzle. PeerJ. 1-38.
Show author(s) (2016). Defective mitochondrial DNA homeostasis in the substantia nigra in Parkinson disease. Nature Communications. 11 pages.

Letter to the editor

Show author(s) (2018). No evidence for rare TRAP1 mutations influencing the risk of idiopathic Parkinson's disease. Brain. e16-e16.

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