Evidence mapPaperPMID 41897354Full record

ReviewBiomolecules2026

Expanded Clinical Spectrum of Autosomal-Dominant STT3A-CDG.

Hamdan Al-Shahrani, Evelin Szabó, Caroline Staccone, Georgia MacDonald, Yutaka Furuta, Daniel Schecter, Andrew C Edmondson, Anne McRae, Josh Baker, Eva Morava and 1 more

Abstract readReview
In one paragraph

Review in Biomolecules, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

Hamdan Al-ShahraniDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Evelin SzabóDepartment of Human Anatomy, University of Pécs Medical School, 7624 Pécs, Hungary.ORCID 0000-0001-5832-8832
Caroline StacconeDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Georgia MacDonaldDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.ORCID 0000-0003-2114-0494
Yutaka FurutaDepartment of Human Genetics, School of Medicine, Emory University, Atlanta, GA 30332, USA.ORCID 0009-0001-7278-8242
Daniel SchecterDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.
Andrew C EdmondsonDepartment of Pediatrics, Division of Human Genetics, Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
Anne McRaeDivision of Genetics, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.
Josh BakerDivision of Genetics, Ann & Robert H. Lurie Children's Hospital of Chicago, Chicago, IL 60611, USA.ORCID 0000-0002-3178-2848
Eva MoravaDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.ORCID 0000-0001-7441-700X
Rory J TinkerDepartment of Genetics and Genomic Sciences, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.ORCID 0000-0001-7093-8844

Funding

NCATS NIH HHS 1U54NS115198-05NIGMS NIH HHS 2T32GM082773-16
6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Congenital Disorders of GlycosylationHexosyltransferasesMembrane ProteinsChild, PreschoolFemaleGenes, DominantGlycosylationHumansMutationPhenotypeHexosyltransferasesMembrane ProteinsSTT3A protein, humancongenital disorder of glycosylationdominant-negativegenotype–phenotype correlationoligosaccharyltransferaseSTT3A

Identifiers

PMID41897354
PMCPMC13024167

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.