Evidence map›Paper›PMID 28748147›Full record

ArticleMolecular genetics and metabolism reports2017

Confirmation that

Michael J Muriello, Sarah Viall, Teodoro Bottiglieri, Kristina Cusmano-Ozog, Carlos R Ferreira

Open access · goldAbstract readCase Reports
PubMed Full text at PMC Publisher
In one paragraph

Article in Molecular genetics and metabolism reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

5 citing papers in PubMed, 11 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

5 authors at 3 institutions in 1 country.

Michael J MurielloMcKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University School of Medicine, Baltimore, MD, USA.
Sarah ViallDivision of Genetics and Metabolism, Children's National Health System, Washington, DC, USA.
Teodoro BottiglieriCenter of Metabolomics, Institute of Metabolic Disease, Baylor Research Institute, Dallas, TX, USA.
Kristina Cusmano-OzogDivision of Genetics and Metabolism, Children's National Health System, Washington, DC, USA.
Carlos R FerreiraDivision of Genetics and Metabolism, Children's National Health System, Washington, DC, USA.
Children's National · USJohns Hopkins Medicine · USNational Human Genome Research Institute · US

Funding

Postdoctoral Medical Genetics Training GrantT32GM007471 · NIGMS · JOHNS HOPKINS UNIVERSITY · PI TAO WANG · 1985 to 2026
$8.0M
NIGMS NIH HHS T32 GM007471
6 · The paper itself

Abstract

Methionine adenosyltransferase (MAT) I/III deficiency is an inborn error of metabolism caused by mutations in

Indexed as

AdoHcy, S-adenosyl-homocysteineAdoMet, S-adenosyl-methionineHypermethioninemiaMAT1AMAT, methionine adenosyltransferaseMethionine adenosyltransferase I/III deficiencyMudd's diseasePPPase, tripolyphosphataseWT, wild-type

Identifiers

PMID28748147
PMCPMC5512230
OpenAlexW2736136812

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.