Evidence map›Paper›PMID 35725899›Full record

SynthesisMolecular psychiatry2022

Transcriptomics analysis of human iPSC-derived dopaminergic neurons reveals a novel model for sporadic Parkinson's disease.

Julian Krauskopf, Kristel Eggermont, Rodrigo Furtado Madeiro Da Costa, Sacha Bohler, Duncan Hauser, Florian Caiment, Theo M de Kok, Catherine Verfaillie, Jos C Kleinjans

Abstract readMeta-Analysis
PubMed Publisher
In one paragraph

Synthesis in Molecular psychiatry, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

5 citing papers in PubMed.

  1. Article
  2. Review
  3. Proteomic insights into the biology of dopaminergic neurons.Frontiers in molecular neuroscience · 2025
    Review
  4. Article
  5. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Julian Krauskopf *Department of Toxicogenomics, Maastricht University, Maastricht, The Netherlands. j.krauskopf@maastrichtuniversity.nl.ORCID http://orcid.org/0000-0002-4349-9900
Kristel Eggermont *Stem Cell Institute, Department of Development and Regeneration, Katholieke Universiteit Leuven, Leuven, Belgium.
Rodrigo Furtado Madeiro Da CostaStem Cell Institute, Department of Development and Regeneration, Katholieke Universiteit Leuven, Leuven, Belgium.
Sacha BohlerDepartment of Toxicogenomics, Maastricht University, Maastricht, The Netherlands.
Duncan HauserDepartment of Toxicogenomics, Maastricht University, Maastricht, The Netherlands.
Florian CaimentDepartment of Toxicogenomics, Maastricht University, Maastricht, The Netherlands.
Theo M de KokDepartment of Toxicogenomics, Maastricht University, Maastricht, The Netherlands.
Catherine VerfaillieStem Cell Institute, Department of Development and Regeneration, Katholieke Universiteit Leuven, Leuven, Belgium.ORCID http://orcid.org/0000-0001-7564-4079
Jos C KleinjansDepartment of Toxicogenomics, Maastricht University, Maastricht, The Netherlands.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is a progressive, neurodegenerative disease affecting over 1% of the population beyond 65 years of age. Although some PD cases are inheritable, the majority of PD cases occur in a sporadic manner. Risk factors comprise next to heredity, age, and gender also exposure to neurotoxins from for instance pesticides and herbicides. As PD is characterized by a loss of dopaminergic neurons in the substantia nigra, it is nearly impossible to access and extract these cells from patients for investigating disease mechanisms. The emergence of induced pluripotent stem (iPSC) technology allows differentiating and growing human dopaminergic neurons, which can be used for in vitro disease modeling. Here, we differentiated human iPSCs into dopaminergic neurons, and subsequently exposed the cells to increasing concentrations of the neurotoxin MPP

Indexed as

Induced Pluripotent Stem CellsNeurodegenerative DiseasesParkinson DiseaseDopaminergic NeuronsHumansTranscriptome

Identifiers

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.