Evidence map›Paper›PMID 41807392›Full record

ArticleNature communications2026

Behavioral screening defines the molecular Parkinsonism-related subgroups in Drosophila.

Natalie Kaempf, Jorge S Valadas, Pieter Robberechts, Nils Schoovaerts, Roman Praschberger, Antonio Ortega, Eliana Nachman, Lorenzo Ghezzi, Ayse Kilic, Dries Chabot and 8 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
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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

18 authors.

Natalie KaempfVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium.ORCID http://orcid.org/0000-0002-5466-3972
Jorge S ValadasVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium.
Pieter RobberechtsKU Leuven, Department of Computer Science, Leuven, Belgium.ORCID http://orcid.org/0000-0002-3734-0047
Nils SchoovaertsVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium.
Roman PraschbergerVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium.ORCID http://orcid.org/0000-0001-7162-2403
Antonio OrtegaVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium.ORCID http://orcid.org/0000-0002-6617-341X
Eliana NachmanVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium.ORCID http://orcid.org/0000-0002-2069-6469
Lorenzo GhezziVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium.
Ayse KilicVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium.
Dries ChabotVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium.
Uli PechVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium.
Sabine KuenenVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium.ORCID http://orcid.org/0000-0001-9135-5293
Sven VilainVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium.ORCID http://orcid.org/0000-0002-9166-2792
El-Sayed BazVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium.ORCID http://orcid.org/0000-0003-1382-6090
Jeevanjot SinghVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium.
Jesse DavisKU Leuven, Department of Computer Science, Leuven, Belgium.
Sha LiuVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium.ORCID http://orcid.org/0000-0002-7168-330X
Patrik VerstrekenVIB-KU Leuven Center for Brain & Disease Research, Leuven, Belgium. patrik.verstreken@kuleuven.be.ORCID http://orcid.org/0000-0002-5073-5393

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) PE2759/1-1European Molecular Biology Organization (EMBO) 299-2019European Molecular Biology Organization (EMBO) 980-2019
6 · The paper itself

Abstract

Parkinson's disease (PD) and related familial Parkinsonism are defined by motor dysfunction, but the specific upstream molecular causes of these clinical symptoms can vary widely. We hypothesize that these causes converge onto a limited number of core cellular pathways. To investigate this, we created a collection of 24 genetically well-controlled Drosophila models of familial forms of PD and related mono-genic forms of Parkinsonism. Using unbiased behavioral screening and machine learning we identify clusters of mutants that converge on (1) mitochondrial function; (2) retromer/vesicle trafficking and proteostasis/autophagy. Genes within each cluster have a similar genetic interaction profile and compounds that target specific molecular pathways ameliorate dopaminergic neuron dysfunction in a cluster-specific manner. Together, our data indicate that familial PD and related forms of Parkinsonism may fall into two broad functional groups, and may inform further work toward targeted biomarker discovery and therapeutic development.

Indexed as

Behavior, AnimalDrosophila melanogasterParkinson DiseaseParkinsonian DisordersAnimalsAnimals, Genetically ModifiedDisease Models, AnimalDopaminergic NeuronsDrosophilaDrosophila ProteinsHumansMitochondriaMutationDrosophila Proteins

Identifiers

PMID41807392
PMCPMC13106710

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.