Evidence map›Paper›PMID 35216353›Full record

ArticleInternational journal of molecular sciences2022

Transcriptional Alterations in X-Linked Dystonia-Parkinsonism Caused by the SVA Retrotransposon.

Jelena Pozojevic, Shela Marie Algodon, Joseph Neos Cruz, Joanne Trinh, Norbert Brüggemann, Joshua Laß, Karen Grütz, Susen Schaake, Ronnie Tse, Veronica Yumiceba and 16 more

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.9field-weighted citation impact, top 30% of its field
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

13 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
  2. Research progress on lysine acetylation (Review).International journal of molecular medicine · 2026
    Review
  3. Long-read sequencing reveals SVA insertion in AP3B1 causing Hermansky-Pudlak syndrome 2.Pediatric allergy and immunology : official publication of the European Society of Pediatric Allergy and Immunology · 2026
    Article
  4. Article
  5. Article
  6. Review
  7. Article
  8. The roles of TAF1 in neuroscience and beyond.Royal Society open science · 2024
    Review
  9. Article
  10. Article
  11. Transcriptional Regulation and Its Misregulation in Human Diseases.International journal of molecular sciences · 2023
    Article
  12. CRISPR deletion of a SINE-VNTR-Frontiers in neurology · 2023
    Article
  13. The Effect of Glucocorticoids onJournal of the ASEAN Federation of Endocrine Societies · 2023
    Article
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

26 authors at 8 institutions in 2 countries.

Jelena PozojevicInstitute of Neurogenetics, University of Lübeck, 23538 Lübeck, Germany.
Shela Marie AlgodonInstitute of Neurogenetics, University of Lübeck, 23538 Lübeck, Germany.
Joseph Neos CruzInstitute of Neurogenetics, University of Lübeck, 23538 Lübeck, Germany.
Joanne TrinhInstitute of Neurogenetics, University of Lübeck, 23538 Lübeck, Germany.
Norbert BrüggemannInstitute of Neurogenetics, University of Lübeck, 23538 Lübeck, Germany.
Joshua LaßInstitute of Neurogenetics, University of Lübeck, 23538 Lübeck, Germany.
Karen GrützInstitute of Neurogenetics, University of Lübeck, 23538 Lübeck, Germany.ORCID 0000-0001-8409-3918
Susen SchaakeInstitute of Neurogenetics, University of Lübeck, 23538 Lübeck, Germany.
Ronnie TseInstitute of Neurogenetics, University of Lübeck, 23538 Lübeck, Germany.
Veronica YumicebaInstitute of Human Genetics, University of Lübeck, 23538 Lübeck, Germany.ORCID 0000-0001-6998-7913
Nathalie KruseInstitute of Human Genetics, University of Lübeck, 23538 Lübeck, Germany.
Kristin SchulzInstitute of Human Genetics, University of Lübeck, 23538 Lübeck, Germany.
Varun K A SreenivasanInstitute of Human Genetics, University of Lübeck, 23538 Lübeck, Germany.
Raymond L RosalesThe Hospital Neuroscience Institute, Department of Neurology and Psychiatry and The FMS-Research Center for Health Sciences, University of Santo Tomas, Manila 1008, Philippines.ORCID 0000-0001-6387-1389
Roland Dominic G JamoraDepartment of Neurosciences, College of Medicine-Philippine General Hospital, University of the Philippines Manila, Manila 1000, Philippines.ORCID 0000-0001-5317-7369
Cid Czarina E DiestaDepartment of Neurosciences, Movement Disorders Clinic, Makati Medical Center, Makati City 1229, Philippines.
Jakob MatschkeInstitute of Neuropathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Markus GlatzelInstitute of Neuropathology, University Medical Center Hamburg-Eppendorf, 20246 Hamburg, Germany.
Philip SeiblerInstitute of Neurogenetics, University of Lübeck, 23538 Lübeck, Germany.
Kristian HändlerInstitute of Human Genetics, University of Lübeck, 23538 Lübeck, Germany.
Aleksandar RakovicInstitute of Neurogenetics, University of Lübeck, 23538 Lübeck, Germany.
Henriette KirchnerInstitute of Human Genetics, University of Lübeck, 23538 Lübeck, Germany.
Malte SpielmannInstitute of Human Genetics, University of Lübeck, 23538 Lübeck, Germany.
Frank J KaiserInstitut für Humangenetik, Universitätsklinikum Essen, Universität Duisburg-Essen, 45147 Essen, Germany.
Christine KleinInstitute of Neurogenetics, University of Lübeck, 23538 Lübeck, Germany.ORCID 0000-0003-2102-3431
Ana WestenbergerInstitute of Neurogenetics, University of Lübeck, 23538 Lübeck, Germany.
University of Lübeck · DEUniversität Hamburg · DEEssen University Hospital · DEGerman Centre for Cardiovascular Research · DEMakati Medical Center · PHPhilippine General Hospital · PHUniversity Hospital Schleswig-Holstein · DEUniversity of Santo Tomas · PH

Funding

Deutsche Forschungsgemeinschaft FOR2488Deutsche Forschungsgemeinschaft KI-1887/2-1University of Lübeck J14-2021
6 · The paper itself

Abstract

X-linked dystonia-parkinsonism (XDP) is a severe neurodegenerative disorder that manifests as adult-onset dystonia combined with parkinsonism. A SINE-VNTR-Alu (SVA) retrotransposon inserted in an intron of the

Indexed as

AdolescentAdultDNA MethylationDystonic DisordersFemaleGenetic Diseases, X-LinkedHistone AcetyltransferasesHumansIntronsMaleMiddle AgedParkinsonian DisordersPromoter Regions, GeneticRetroelementsShort Interspersed Nucleotide ElementsTATA-Binding Protein Associated FactorsHistone AcetyltransferasesRetroelementsTATA-binding protein associated factor 250 kDaTATA-Binding Protein Associated FactorsTranscription Factor TFIIDepigeneticsretrotransposonsplicingSVAtranscriptionXDP

Identifiers

PMID35216353
PMCPMC8875906
OpenAlexW4213352368

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.