Evidence map›Paper›PMID 34721296›Full record

ArticleFrontiers in endocrinology2021

Overlapping Phenotypes Associated With

Arnaud Molin, Sandrine Lemoine, Martin Kaufmann, Pierre Breton, Marie Nowoczyn, Céline Ballandonne, Nadia Coudray, Hervé Mittre, Nicolas Richard, Amélie Ryckwaert and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 30 citations in OpenAlex.

  1. Review
  2. Observational
  3. The Significance of Fibroblast Growth Factor 23 and 24,25-Dihydroxyvitamin D in Dent Disease Type 1.Clinical journal of the American Society of Nephrology : CJASN · 2026
    Article
  4. Article
  5. Article
  6. Identification of a Novel HomozygousInternational journal of molecular sciences · 2025
    Article
  7. Article
  8. Article
  9. Article
  10. Animals : an open access journal from MDPI · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Mineral Metabolism in Children: Interrelation between Vitamin D and FGF23.International journal of molecular sciences · 2023
    Review
  16. Article
  17. Article
  18. Review
  19. 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

14 authors at 6 institutions in 2 countries.

Arnaud MolinCaen University Hospital, Department of Genetics, Molecular Genetics Laboratory and Reference Center for Rare Diseases of Calcium and Phosphorus Metabolism (OSCAR), Caen, France.
Sandrine LemoineDepartment of Nephrology and Renal Functional Explorations, Edouard Herriot Hospital, Lyon, France.
Martin KaufmannQueen's University, Department of Biomedical and Molecular Sciences, Kingston, ON, Canada.
Pierre BretonCaen University Hospital, Department of Genetics, Molecular Genetics Laboratory and Reference Center for Rare Diseases of Calcium and Phosphorus Metabolism (OSCAR), Caen, France.
Marie NowoczynCaen University Hospital, Department of Biochemistry, Caen, France.
Céline BallandonneBioTARGEN, Caen Normandy University, Caen, France.
Nadia CoudrayCaen University Hospital, Department of Genetics, Molecular Genetics Laboratory and Reference Center for Rare Diseases of Calcium and Phosphorus Metabolism (OSCAR), Caen, France.
Hervé MittreCaen University Hospital, Department of Genetics, Molecular Genetics Laboratory and Reference Center for Rare Diseases of Calcium and Phosphorus Metabolism (OSCAR), Caen, France.
Nicolas RichardCaen University Hospital, Department of Genetics, Molecular Genetics Laboratory and Reference Center for Rare Diseases of Calcium and Phosphorus Metabolism (OSCAR), Caen, France.
Amélie RyckwaertDepartment of Pediatrics, Rennes University Hospital, Rennes, France.
Alinoe LavillaureixDepartment of Genetics, Rennes University Hospital, Rennes, France.
Glenville JonesQueen's University, Department of Biomedical and Molecular Sciences, Kingston, ON, Canada.
Justine BacchettaUniversity of Lyon, University of Lyon 1, Villeurbanne, France.
Marie-Laure KottlerCaen University Hospital, Department of Genetics, Molecular Genetics Laboratory and Reference Center for Rare Diseases of Calcium and Phosphorus Metabolism (OSCAR), Caen, France.
Université de Caen Normandie · FRQueen's University · CACentre Hospitalier Universitaire de Rennes · FRHôpital Edouard Herriot · FRInserm · FRInstitut de génétique et de développement de Rennes · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mutations in

Indexed as

MutationPhenotypeAdolescentAdultAgedAged, 80 and overChildChild, PreschoolFemaleHumansHypercalcemiaInfantInfant, NewbornMaleMiddle AgedSodium-Phosphate Cotransporter Proteins, Type IIaSLC34A1 protein, humanSLC34A3 protein, humanSodium-Phosphate Cotransporter Proteins, Type IIaSodium-Phosphate Cotransporter Proteins, Type IIcVitamin D3 24-Hydroxylasecalcitriol induced hypercalcemiaCYP24A1- hydroxylasehypersensitivity to vitamin Dphosphate wasting diseasesSLC34A1 geneSLC34A3 genevitamin D

Identifiers

PMID34721296
PMCPMC8548709
OpenAlexW3204975840

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.