Evidence map›Paper›PMID 31067829›Full record

ArticleMedicina (Kaunas, Lithuania)2019

Genotype⁻Phenotype Correlation in a New Fabry-Disease-Causing Mutation.

Agnė Čerkauskaitė, Rimantė Čerkauskienė, Marius Miglinas, Arvydas Laurinavičius, Can Ding, Arndt Rolfs, Lina Vencevičienė, Jūratė Barysienė, Edita Kazėnaitė, Eglė Sadauskienė

Open access · goldAbstract readCase Reports
In one paragraph

Article in Medicina (Kaunas, Lithuania), 2019. 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
0.7field-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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Review
  2. Review
  3. Article
  4. Review
  5. 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

10 authors at 3 institutions in 2 countries.

Agnė ČerkauskaitėInstitute of Biomedical Sciences, Faculty of medicine, Vilnius University, Santariškių 2, 08406 Vilnius, Lithuania. a.cerkauskaite@gmail.com.
Rimantė ČerkauskienėInstitute of Clinical Medicine, Faculty of medicine, Vilnius University, Santariškių 2, 08406 Vilnius, Lithuania. rimante.cerkauskiene@gmail.com.
Marius MiglinasInstitute of Clinical Medicine, Faculty of medicine, Vilnius University, Santariškių 2, 08406 Vilnius, Lithuania. Marius.Miglinas@santa.lt.
Arvydas LaurinavičiusInstitute of Biomedical Sciences, Faculty of medicine, Vilnius University, Santariškių 2, 08406 Vilnius, Lithuania. Arvydas.Laurinavicius@vpc.lt.
Can DingInstitute of Human Genetics, University Medical Center of the Johannes Gutenberg University Mainz, Langenbeckstraße 1, 55131 Mainz, Germany. dingcangut@gmail.com.
Arndt RolfsUniversity of Rostock, Gehlsheimerstrasse 20, 18147 Rostock, Germany. arndt.rolfs@med.uni-rostock.de.
Lina VencevičienėInstitute of Clinical Medicine, Faculty of medicine, Vilnius University, Santariškių 2, 08406 Vilnius, Lithuania. Jurate.Barysiene@santa.lt.
Jūratė BarysienėInstitute of Clinical Medicine, Faculty of medicine, Vilnius University, Santariškių 2, 08406 Vilnius, Lithuania. urate.Barysiene@santa.lt.
Edita KazėnaitėInstitute of Biomedical Sciences, Faculty of medicine, Vilnius University, Santariškių 2, 08406 Vilnius, Lithuania. Edita.Kazenaite@santa.lt.
Eglė SadauskienėInstitute of Clinical Medicine, Faculty of medicine, Vilnius University, Santariškių 2, 08406 Vilnius, Lithuania. Egle.Sadauskiene@santa.lt.
Vilnius University · LTCentogene (Germany) · DEJohannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

alpha-GalactosidaseDyspneaElectrocardiographyFabry DiseaseFemaleGlycolipidsHumansLithuaniaMiddle AgedMutationSphingolipidsalpha-GalactosidaseGLA protein, humanglobotriaosyl lysosphingolipidGlycolipidsSphingolipidsclassical manifestationFabry diseaseGLA genenovel mutationα-galactosidase A

Identifiers

PMID31067829
PMCPMC6571633
OpenAlexW2945133115

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.