Evidence map›Paper›PMID 32583268›Full record

ReviewPflugers Archiv : European journal of physiology2020

De novo CACNA1D Ca

Nadine J Ortner, Teresa Kaserer, J Nathan Copeland, Jörg Striessnig

Erratum issuedOpen access · hybridAbstract readReview
In one paragraph

Review in Pflugers Archiv : European journal of physiology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 41 papers.

0numbers the graph read from it
0cells of the map it votes in
41citing papers in PubMed
3.2field-weighted citation impact, top 7% 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

41 citing papers in PubMed, 66 citations in OpenAlex.

  1. Evaluation of Aldosterone Suppression by Cinnarizine, a Putative Cav1.3 Inhibitor.The Journal of clinical endocrinology and metabolism · 2025
    Trial
  2. Identification of novel functional sites in the CaProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  3. Article
  4. Article
  5. The genetics of hypertension.Nature reviews. Nephrology · 2026
    Review
  6. Article
  7. Article
  8. Deletion of the Voltage-Gated Calcium Channel Gene, CaCerebellum (London, England) · 2025
    Article
  9. Disease-modifying, multidimensional efficacy of putaminal CaMolecular therapy : the journal of the American Society of Gene Therapy · 2025
    Article
  10. Gating of hair cell CaScience advances · 2025
    Article
  11. Article
  12. Inactivation of CaV1 and CaV2 channels.The Journal of general physiology · 2025
    Review
  13. Article
  14. The L-type calcium channel CaV1.3: A potential target for cancer therapy.Journal of cellular and molecular medicine · 2024
    Review
  15. A Novel De Novo Gain-of-FunctionNeurology. Genetics · 2024
    Article
  16. A Review of theDiseases (Basel, Switzerland) · 2024
    Review
  17. Article
  18. Article
  19. Hypertension (Dallas, Tex. : 1979) · 2023
    Article
  20. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 2 institutions in 2 countries.

Nadine J OrtnerDepartment of Pharmacology and Toxicology, Institute of Pharmacy, Center for Molecular Biosciences Innsbruck, University of Innsbruck, Innsbruck, Austria. nadine.ortner@uibk.ac.at.ORCID 0000-0003-3882-3283
Teresa KasererDepartment of Pharmaceutical Chemistry, Institute of Pharmacy, Center for Molecular Biosciences Innsbruck, University of Innsbruck, Innsbruck, Austria.
J Nathan CopelandDuke Center for Autism and Brain Development, Duke Child and Family Mental Health and Developmental Neuroscience, Durham, USA.
Jörg StriessnigDepartment of Pharmacology and Toxicology, Institute of Pharmacy, Center for Molecular Biosciences Innsbruck, University of Innsbruck, Innsbruck, Austria. joerg.striessnig@uibk.ac.at.
Universität Innsbruck · ATCenter for Autism and Related Disorders · US

Funding

Austrian Science Fund FWF DOC 30Austrian Science Fund FWF DOC30/CavXAustrian Science Fund FWF P 27809Austrian Science Fund FWF P27809
6 · The paper itself

Abstract

The identification of rare disease-causing variants in humans by large-scale next-generation sequencing (NGS) studies has also provided us with new insights into the pathophysiological role of de novo missense variants in the CACNA1D gene that encodes the pore-forming α1-subunit of voltage-gated Cav1.3 L-type Ca

Indexed as

AnimalsCalciumCalcium Channels, L-TypeChannelopathiesHumansMutationPhenotypeCalciumCalcium Channels, L-TypeAutism spectrum disordersCACNA1DCalcium channel blockersNeurodevelopmental disordersVariantsVoltage-gated Ca2+ channels

Identifiers

PMID32583268
PMCPMC7351864
OpenAlexW3037305971

What Socratic 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 Socratic graph.