Evidence map›Paper›PMID 35055433›Full record

ArticleJournal of personalized medicine2022

Clinical, Genetic and Functional Characterization of a Novel

Senthil Selvaraj, Dírcea Rodrigues, Navaneethakrishnan Krishnamoorthy, Khalid A Fakhro, Luís R Saraiva, Manuel C Lemos

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.8field-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

1 citing paper in PubMed, 5 citations in OpenAlex.

  1. 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

6 authors at 4 institutions in 3 countries.

Senthil SelvarajDepartment of Genetics, Sidra Medicine, Doha P.O. Box 26999, Qatar.
Dírcea RodriguesServiço de Endocrinologia, Diabetes e Metabolismo, Centro Hospitalar Universitário de Coimbra, 3000-075 Coimbra, Portugal.
Navaneethakrishnan KrishnamoorthyDepartment of Genetics, Sidra Medicine, Doha P.O. Box 26999, Qatar.ORCID 0000-0002-5096-4612
Khalid A FakhroDepartment of Genetics, Sidra Medicine, Doha P.O. Box 26999, Qatar.ORCID 0000-0002-3150-1276
Luís R SaraivaDepartment of Genetics, Sidra Medicine, Doha P.O. Box 26999, Qatar.ORCID 0000-0003-4079-0396
Manuel C LemosCICS-UBI, Health Sciences Research Centre, University of Beira Interior, 6200-506 Covilhã, Portugal.ORCID 0000-0001-9326-8900
Hamad bin Khalifa University · QAHospitais da Universidade de Coimbra · PTMonell Chemical Senses Center · USUniversity of Beira Interior · PT

Funding

Fundação para a Ciência e Tecnologia UIDB/00709/2020Qatar Foundation Sidra Medicine #SDR400038
6 · The paper itself

Abstract

Nephrogenic diabetes insipidus (NDI) is a rare disorder characterized by renal unresponsiveness to the hormone vasopressin, leading to excretion of large volumes of diluted urine. Mutations in the arginine vasopressin receptor-2 (

Indexed as

AVPR2case reportgeneticsnephrogenic diabetes insipidusvasopressin

Identifiers

PMID35055433
PMCPMC8779739
OpenAlexW4205511841

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.