ArticleDisease models & mechanisms2017
Open access · goldAbstract read
In one paragraph
Article in Disease models & mechanisms, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.
0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
2.8field-weighted citation impact, top 9% of its field
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.
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.
Who cites it
18 citing papers in PubMed, 1 synthesis or guideline pooled it, 34 citations in OpenAlex.
- Putative Animal Models of Restless Legs Syndrome: A Systematic Review and Evaluation of Their Face and Construct Validity.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2023Pooled it
- TALE and Hox Transcription Factors Modulate Adult Behaviors in Zebrafish.Behavior genetics · 2026Article
- TALE and Hox Transcription Factors Control Adult Behaviors in Zebrafish.bioRxiv : the preprint server for biology · 2026Article
- Loss of Thy1 in Cortico-Striatal Pathways Alters Response to Dopamine and Gabapentin.ASN neuro · 2026Article
- Ephrin-B2 deletion in GABAergic neurons induces cognitive deficits associated with single-nucleus transcriptomic differences in the prefrontal cortex.BMC biology · 2025Article
- A patient-enriched MEIS1 coding variant causes a restless legs syndrome-like phenotype in mice.Sleep · 2024Article
- Deletion of SERF2 in mice delays embryonic development and alters amyloid deposit structure in the brain.Life science alliance · 2023Article
- Exploring the causes of augmentation in restless legs syndrome.Frontiers in neurology · 2023Review
- Restless legs syndrome: Over 50 years of European contribution.Journal of sleep research · 2022Review
- Consensus guidelines on the construct validity of rodent models of restless legs syndrome.Disease models & mechanisms · 2022Article
- In the pursuit of new social neurons. Neurogenesis and social behavior in mice: A systematic review.Frontiers in cell and developmental biology · 2022Review
- Consensus Guidelines on Rodent Models of Restless Legs Syndrome.Movement disorders : official journal of the Movement Disorder Society · 2021Review
- Cannabis for Restless Legs Syndrome.Advances in experimental medicine and biology · 2021Review
- Pharmacologic Treatment of Restless Legs Syndrome.Current neuropharmacology · 2021Review
- Deficiency of Meis1, a transcriptional regulator, in mice and worms: Neurochemical and behavioral characterizations with implications in the restless legs syndrome.Journal of neurochemistry · 2020Article
- PTPRD: neurobiology, genetics, and initial pharmacology of a pleiotropic contributor to brain phenotypes.Annals of the New York Academy of Sciences · 2019Review
- Review
- Differential Dopamine D1 and D3 Receptor Modulation and Expression in the Spinal Cord of Two Mouse Models of Restless Legs Syndrome.Frontiers in behavioral neuroscience · 2018Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
21 authors at 7 institutions in 2 countries.
Aaro V SalminenInstitute of Neurogenomics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.ORCID 0000-0002-6575-8336
Lillian GarrettInstitute of Developmental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.ORCID 0000-0003-4880-7076
Barbara SchormairInstitute of Neurogenomics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Jan RozmanGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.ORCID 0000-0002-8035-8904
Florian GiesertInstitute of Developmental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.ORCID 0000-0001-6825-8858
Kristina M NiedermeierInstitute of Developmental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Lore BeckerGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.ORCID 0000-0002-6890-4984
Birgit RathkolbGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Ildikó RáczGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
German Mouse Clinic Consortium
Martin KlingensporChair of Molecular Nutritional Medicine, Technical University Munich, EKFZ - Else Kröner Fresenius Center for Nutritional Medicine, Gregor-Mendel-Str. 2, 85350 Freising-Weihenstephan, Germany.ORCID 0000-0002-4502-6664
Thomas KlopstockDepartment of Neurology, Friedrich-Baur-Institute, Klinikum der Ludwig-Maximilians-Universität München, Ziemssenstr. 1a, 80336 Munich, Germany.
Eckhard WolfInstitute of Molecular Animal Breeding and Biotechnology, Gene Center, Ludwig-Maximilians-University München, 81377 Munich, Germany.
Andreas ZimmerInstitute of Molecular Psychiatry, Medical Faculty, University of Bonn, 53127 Bonn, Germany.
Valérie Gailus-DurnerGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Miguel TorresCentro Nacional de Investigaciones Cardiovasculares (CNIC), 28029 Madrid, Spain.ORCID 0000-0003-0906-4767
Helmut FuchsGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Martin Hrabě de AngelisGerman Mouse Clinic, Institute of Experimental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Wolfgang WurstInstitute of Developmental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.
Sabine M HölterInstitute of Developmental Genetics, Helmholtz Zentrum München, 85764 Neuherberg, Germany.ORCID 0000-0003-4878-5241
Juliane WinkelmannInstitute of Neurogenomics, Helmholtz Zentrum München, 85764 Neuherberg, Germany juliane.winkelmann@tum.de.ORCID 0000-0003-2667-9691
Helmholtz Zentrum München · DEGerman Center for Neurodegenerative Diseases · DEUniversity of Bonn · DEElse Kröner-Fresenius-Stiftung · DELudwig-Maximilians-Universität München · DESpanish National Centre for Cardiovascular Research · ESTUM Klinikum · DE
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
AgingAnimalsBehavior, AnimalDopamine AgonistsDopaminergic NeuronsFemaleFerritinsHaploinsufficiencyIronMaleMice, Inbred C57BLMotor ActivityMyeloid Ecotropic Viral Integration Site 1 ProteinNeurogenesisNociceptionPhenotypeDopamine AgonistsFerritinsIronMeis1 protein, mouseMyeloid Ecotropic Viral Integration Site 1 ProteinReceptors, DopamineTransferrinMeis1Mouse modelPramipexolePrepulse inhibitionRestless legs syndromeSensorimotor system
Identifiers
What OpenQuestion holds
Textmetadata
LicenceCC BY
Read underepoch 390
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.