Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
0numbers the graph read from it
0cells of the map it votes in
2citing 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.
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
17 authors.
Alba PascualLaboratory of Neurogenetics and Molecular Medicine, Center for Genomic Sciences in Medicine, Institut de Recerca Sant Joan de Déu, 08950 Barcelona, Spain.
Thaleia MoulkaLaboratory of Neurogenetics and Molecular Medicine, Center for Genomic Sciences in Medicine, Institut de Recerca Sant Joan de Déu, 08950 Barcelona, Spain.ORCID 0009-0002-3349-9517
Oriol de FàbreguesNeurodegenerative Diseases Research Group, Vall d'Hebron Research Institute, Center for Networked Biomedical Research on Neurodegenerative Diseases (CIBERNED), 08035 Barcelona, Spain.
Roberta RepossiLaboratory of Neurogenetics and Molecular Medicine, Center for Genomic Sciences in Medicine, Institut de Recerca Sant Joan de Déu, 08950 Barcelona, Spain.ORCID 0009-0004-8604-6778
Pedro J García-RuizUnit of Movement Disorders, Department of Neurology, Fundación Jimenez Díaz, 28040 Madrid, Spain.
Saida OrtolanoRare Diseases & Pediatric Medicine Research Group, Galicia Sur Health Research Institute (IIS Galicia Sur), Servicio Gallego de Salud-Universidad de Vigo (SERGAS-UVIGO), 36213 Vigo, Spain.ORCID 0000-0002-1098-3376
Marisel De LuccaDepartment of Biological Sciences, Faculty of Health Sciences, Universidad Técnica de Manabí, Portoviejo 130105, Ecuador.ORCID 0000-0002-1557-2955
Lydia Vela-DesojoMovement Disorders Unit, Department of Neurology, Hospital Universitario Fundación Alcorcón, 28922 Madrid, Spain.
Marta Alves-VillarRare Diseases & Pediatric Medicine Research Group, Galicia Sur Health Research Institute (IIS Galicia Sur), Servicio Gallego de Salud-Universidad de Vigo (SERGAS-UVIGO), 36213 Vigo, Spain.ORCID 0009-0005-9244-6513
Marcos FríasConfocal Microscopy and Cellular Imaging Unit, Hospital Sant Joan de Déu, 08950 Barcelona, Spain.
Cici Feliz-FelizUnit of Movement Disorders, Department of Neurology, Fundación Jimenez Díaz, 28040 Madrid, Spain.
Mònica RoldánConfocal Microscopy and Cellular Imaging Unit, Hospital Sant Joan de Déu, 08950 Barcelona, Spain.ORCID 0000-0002-9530-6234
Jonathan OlivalLaboratory of Neurogenetics and Molecular Medicine, Center for Genomic Sciences in Medicine, Institut de Recerca Sant Joan de Déu, 08950 Barcelona, Spain.
Guerau FernàndezLaboratory of Neurogenetics and Molecular Medicine, Center for Genomic Sciences in Medicine, Institut de Recerca Sant Joan de Déu, 08950 Barcelona, Spain.
Francesc PalauLaboratory of Neurogenetics and Molecular Medicine, Center for Genomic Sciences in Medicine, Institut de Recerca Sant Joan de Déu, 08950 Barcelona, Spain.ORCID 0000-0002-8635-5421
Jordi PijuanLaboratory of Neurogenetics and Molecular Medicine, Center for Genomic Sciences in Medicine, Institut de Recerca Sant Joan de Déu, 08950 Barcelona, Spain.ORCID 0000-0003-0350-6376
Janet HoenickaLaboratory of Neurogenetics and Molecular Medicine, Center for Genomic Sciences in Medicine, Institut de Recerca Sant Joan de Déu, 08950 Barcelona, Spain.ORCID 0000-0002-6790-6988
Funding
AGAUR/Generalitat de Catalunya and European Regional Development Fund (FEDER) SLT002/16/0030, 2021-SGR-01610Fondo de Investigación Sanitaria, Instituto Salud Carlos III PI022/00168
6 · The paper itself
Abstract
Despite significant advances in understanding the genetics of Parkinson's disease (PD) and Parkinsonism, the diagnostic yield remains low. Pathogenic variants of
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.
Lysosomal Network Defects in Early-Onset Parkinson's Disease Patients Carrying Rare Variants in Lysosomal Hydrolytic Enzyme Genes. · full record | OpenQuestion