Evidence map›Paper›PMID 35272499›Full record

ArticleThyroid : official journal of the American Thyroid Association2022

Whole-Exome Sequencing in Congenital Hypothyroidism Due to Thyroid Dysgenesis.

Stéphanie Larrivée-Vanier, Martineau Jean-Louis, Fabien Magne, Helen Bui, Guy A Rouleau, Dan Spiegelman, Mark E Samuels, Zoha Kibar, Guy Van Vliet, Johnny Deladoëy

Open access · hybridAbstract read
In one paragraph

Article in Thyroid : official journal of the American Thyroid Association, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed, 11 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
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

10 authors at 3 institutions in 2 countries.

Stéphanie Larrivée-VanierResearch Center of Centre Hospitalier Universitaire Sainte-Justine, Université de Montréal, Montréal, Canada.
Martineau Jean-LouisResearch Center of Centre Hospitalier Universitaire Sainte-Justine, Université de Montréal, Montréal, Canada.
Fabien MagneResearch Center of Centre Hospitalier Universitaire Sainte-Justine, Université de Montréal, Montréal, Canada.
Helen BuiDepartment of Endocrinology, McGill University Health Center, Montréal, Canada.
Guy A RouleauMontreal Neurological Institute, McGill University, Montréal, Canada.
Dan SpiegelmanMontreal Neurological Institute, McGill University, Montréal, Canada.
Mark E SamuelsResearch Center of Centre Hospitalier Universitaire Sainte-Justine, Université de Montréal, Montréal, Canada.
Zoha KibarResearch Center of Centre Hospitalier Universitaire Sainte-Justine, Université de Montréal, Montréal, Canada.
Guy Van VlietResearch Center of Centre Hospitalier Universitaire Sainte-Justine, Université de Montréal, Montréal, Canada.
Johnny DeladoëyResearch Center of Centre Hospitalier Universitaire Sainte-Justine, Université de Montréal, Montréal, Canada.ORCID 0000-0002-2060-1730
Centre Hospitalier Universitaire Sainte-Justine · CAMontreal Neurological Institute and Hospital · CAMcGill University Health Centre · CA

Funding

CIHR
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Congenital HypothyroidismThyroid DysgenesisCase-Control StudiesExomeExome SequencingHumansMutationathyreosisbirth defectsnonsyndromic congenital hypothyroidismthyroid dysgenesisthyroid ectopy

Identifiers

PMID35272499
PMCPMC9145262
OpenAlexW4220893801

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.