Evidence map›Paper›PMID 34828390›Full record

ArticleGenes2021

Evidence for a Genotype-Phenotype Correlation in Patients with Pathogenic

Sarah C Grünert, Anke Schumann, Federico Baronio, Konstantinos Tsiakas, Simona Murko, Ute Spiekerkoetter, René Santer

Open access · goldAbstract readCase Reports
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 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
1.2field-weighted citation impact, top 21% 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

4 citing papers in PubMed, 8 citations in OpenAlex.

  1. Genes · 2024
    Article
  2. Article
  3. Article
  4. Exome Sequencing in Monogenic Forms of Rickets.Indian journal of pediatrics · 2023
    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

7 authors at 3 institutions in 2 countries.

Sarah C GrünertDepartment of General Pediatrics, Adolescent Medicine and Neonatology, Medical Center-University of Freiburg, 79106 Freiburg, Germany.ORCID 0000-0001-5986-0468
Anke SchumannDepartment of General Pediatrics, Adolescent Medicine and Neonatology, Medical Center-University of Freiburg, 79106 Freiburg, Germany.
Federico BaronioPediatric Unit, Department of Medical and Surgical Sciences, Regional Center for Expanded Newborn Screening, S. Orsola-Malpighi University Hospital, 40138 Bologna, Italy.ORCID 0000-0003-3470-6880
Konstantinos TsiakasDepartment of Pediatrics, University Medical Center Eppendorf, 20246 Hamburg, Germany.
Simona MurkoDepartment of Pediatrics, University Medical Center Eppendorf, 20246 Hamburg, Germany.
Ute SpiekerkoetterDepartment of General Pediatrics, Adolescent Medicine and Neonatology, Medical Center-University of Freiburg, 79106 Freiburg, Germany.
René SanterDepartment of Pediatrics, University Medical Center Eppendorf, 20246 Hamburg, Germany.
Universität Hamburg · DEUniversity of Freiburg · DEIRCCS Azienda Ospedliero-Universitaria di Bologna Policlinico di Sant'Orsola · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Fanconi-Bickel syndrome (FBS) is a very rare but distinct clinical entity with the combined features of hepatic glycogen storage disease, generalized proximal renal tubular dysfunction with disproportionately severe glucosuria, and impaired galactose tolerance. Here, we report five cases (out of 93 diagnosed in our lab) with pathogenic variants on both

Indexed as

MutationPhenotypeAdolescentAdultAnimalsFanconi SyndromeFemaleGenotypeGlucoseGlucose Transporter Type 2HomozygoteHumansInfantMalePedigreeXenopusGlucoseGlucose Transporter Type 2SLC2A2 protein, humanFanconi-Bickel syndromegenotype-phenotype correlationglucosuriaGLUT2glycogen storage diseaseSLC2A2

Identifiers

PMID34828390
PMCPMC8622088
OpenAlexW3212200173

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.