Evidence map›Paper›PMID 38275609›Full record

ArticleGenes2024

Gollop-Wolfgang Complex Is Associated with a Monoallelic Variation in

Adrian Odrzywolski, Beyhan Tüysüz, Philippe Debeer, Erika Souche, Arnout Voet, Boyan Dimitrov, Paulina Krzesińska, Joris Robert Vermeesch, Przemko Tylzanowski

Open access · goldAbstract read
In one paragraph

Article in Genes, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.7field-weighted citation impact, top 33% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Article
  3. 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

9 authors at 4 institutions in 3 countries.

Adrian OdrzywolskiLaboratory for Cytogenetics and Genome Research, Department of Human Genetics, KU Leuven, B-3000 Leuven, Belgium.ORCID 0000-0002-3370-8801
Beyhan TüysüzDepartment of Pediatric Genetics, Cerrahpasa Faculty of Medicine, Istanbul University-Cerrahpasa, 34098 Istanbul, Turkey.
Philippe DebeerLocomotor and Neurological Disorders, Department of Development and Regeneration, KU Leuven, B-3000 Leuven, Belgium.
Erika SoucheLaboratory for Cytogenetics and Genome Research, Department of Human Genetics, KU Leuven, B-3000 Leuven, Belgium.
Arnout VoetLaboratory of Biomolecular Modelling and Design, Department of Chemistry, KU Leuven, 3001 Heverlee, Belgium.
Boyan DimitrovClinical Sciences, Research Group Reproduction and Genetics, Centre for Medical Genetics, Centre for Medical Genetics, Universitair Ziekenhuis Brussel (UZ Brussel), Vrije Universiteit Brussel (VUB), 1090 Brussels, Belgium.
Paulina KrzesińskaLaboratory of Molecular Genetics, Medical University of Lublin, 20-093 Lublin, Poland.
Joris Robert VermeeschLaboratory for Cytogenetics and Genome Research, Department of Human Genetics, KU Leuven, B-3000 Leuven, Belgium.ORCID 0000-0002-3071-1191
Przemko TylzanowskiLaboratory of Molecular Genetics, Medical University of Lublin, 20-093 Lublin, Poland.
KU Leuven · BEMedical University of Lublin · PLIstanbul University-Cerrahpaşa · TRVrije Universiteit Brussel · BE

Funding

National Science Center 2013/11/B/NZ4/03660
6 · The paper itself

Abstract

Gollop-Wolfgang complex (GWC) is a rare congenital limb anomaly characterized by tibial aplasia with femur bifurcation, ipsilateral bifurcation of the thigh bone, and split hand and monodactyly of the feet, resulting in severe and complex limb deformities. The genetic basis of GWC, however, has remained elusive. We studied a three-generation family with four GWC-affected family members. An analysis of whole-genome sequencing results using a custom pipeline identified the

Indexed as

Abnormalities, MultipleHand Deformities, CongenitalFemurHumansTibiaWnt ProteinsWnt11 protein, humanWnt ProteinsGollop–Wolfgang complexsplit-hand/foot malformationwhole genome sequencingWNT11

Identifiers

PMID38275609
PMCPMC10815061
OpenAlexW4391088781

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.