Evidence map›Paper›PMID 34828275›Full record

ArticleGenes2021

Beyond Trinucleotide Repeat Expansion in Fragile X Syndrome: Rare Coding and Noncoding Variants in

Cedrik Tekendo-Ngongang, Angela Grochowsky, Benjamin D Solomon, Sho T Yano

Open access · goldAbstract read
In one paragraph

Article in Genes, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
2.1field-weighted citation impact, top 12% 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

10 citing papers in PubMed, 17 citations in OpenAlex.

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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

4 authors at 2 institutions in 1 country.

Cedrik Tekendo-NgongangNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.ORCID 0000-0002-2709-4807
Angela GrochowskyDepartment of Pediatrics, Vanderbilt University Medical Center, Nashville, TN 37232, USA.
Benjamin D SolomonNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
Sho T YanoNational Human Genome Research Institute, National Institutes of Health, Bethesda, MD 20892, USA.
National Institutes of Health · USVanderbilt University Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

5' Untranslated RegionsAdultFemaleFragile X Messenger Ribonucleoprotein 1Fragile X SyndromeGene FrequencyGenetic Association StudiesHumansInfantInfant, NewbornMaleMutationOpen Reading FramesPregnancyRNA, MessengerSequence Deletion5' Untranslated RegionsFMR1 protein, humanFragile X Messenger Ribonucleoprotein 1RNA, Messengercopy number variantsFMR1FMRPfragile Xvariant classification

Identifiers

PMID34828275
PMCPMC8623550
OpenAlexW3208194897

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.