Evidence map›Paper›PMID 37424725›Full record

ArticleFrontiers in genetics2023

Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome.

Alexandra Garza Flores, Ida Nordgren, Maria Pettersson, Dora Dias-Santagata, Daniel Nilsson, Anna Hammarsjö, Anna Lindstrand, Dominyka Batkovskyte, Janey Wiggs, David S Walton and 6 more

Open access · goldAbstract readCase Reports
In one paragraph

Article in Frontiers in genetics, 2023. 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
2.2field-weighted citation impact, top 11% 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, 7 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. 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

16 authors at 6 institutions in 2 countries.

Alexandra Garza FloresMedical Genetics, Mass General for Children, Boston, MA, United States.
Ida NordgrenDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Maria PetterssonDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Dora Dias-SantagataDepartment of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, MA, United States.
Daniel NilssonDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Anna HammarsjöDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Anna LindstrandDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Dominyka BatkovskyteDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Janey WiggsDepartment of Ophthalmology, Ocular Genomics Institute, Mass Eye and Ear Infirmary, Harvard Medical School, Boston, MA, United States.
David S WaltonDepartment of Ophthalmology, Harvard Medical School, Boston, MA, United States.
Paula GoldenbergMedical Genetics, Mass General for Children, Boston, MA, United States.
Jesper EisfeldtDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Angela E LinMedical Genetics, Mass General for Children, Boston, MA, United States.
Ralph S LachmanDepartment of Radiological Sciences and Pediatrics, UCLA School of Medicine, Los Angeles, CA, United States.
Gen NishimuraDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Giedre GrigelionieneDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
Karolinska University Hospital · SEKarolinska Institutet · SEMassachusetts General Hospital · USHarvard University · USMassachusetts Eye and Ear Infirmary · USUniversity of California, Los Angeles · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

Axenfeld-Rieger Syndromecase reportDe Hauwere SyndromeFOXC1genome sequencingskeletal anomalies

Identifiers

PMID37424725
PMCPMC10326848
OpenAlexW4381930047

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.