Evidence map›Paper›PMID 36204321›Full record

ArticleFrontiers in genetics2022

Vici syndrome in Israel: Clinical and molecular insights.

Odelia Chorin, Yoel Hirsch, Rachel Rock, Liat Salzer Sheelo, Yael Goldberg, Hanna Mandel, Tova Hershkovitz, Nicole Fleischer, Lior Greenbaum, Uriel Katz and 8 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in genetics, 2022. 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
0.9field-weighted citation impact, top 25% 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. Article
  3. Article
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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

18 authors at 6 institutions in 1 country.

Odelia ChorinThe Institute for Rare Diseases, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Yoel HirschDor Yeshorim, Committee for Prevention of Jewish Genetic Diseases, New York, NY, United States.
Rachel RockThe Institute for Rare Diseases, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Liat Salzer SheeloSackler Faculty of Medicine, Tel-Aviv University, Tel Aviv-Yafo, Israel.
Yael GoldbergSackler Faculty of Medicine, Tel-Aviv University, Tel Aviv-Yafo, Israel.
Hanna MandelUnit of Inherited Metabolic Disorders, Ziv Medical Center, Safed, Israel.
Tova HershkovitzThe Genetics Institute, Rambam Health Care Campus, Haifa, Israel.
Nicole FleischerFDNA Inc, Boston, MA, United States.
Lior GreenbaumThe Danek Gertner Institute of Human Genetics, Sheba Medical Center, Ramat Gan, Israel.
Uriel KatzSackler Faculty of Medicine, Tel-Aviv University, Tel Aviv-Yafo, Israel.
Ortal BarelThe Genomic Unit, Sheba Cancer Research Center, Sheba Medical Center, Ramat Gan, Israel.
Nasrin HamedSackler Faculty of Medicine, Tel-Aviv University, Tel Aviv-Yafo, Israel.
Bruria Ben-ZeevSackler Faculty of Medicine, Tel-Aviv University, Tel Aviv-Yafo, Israel.
Shoshana GreenbergerSackler Faculty of Medicine, Tel-Aviv University, Tel Aviv-Yafo, Israel.
Nadra Nasser SamraInstitute of Human Genetics, Ziv Medical Center, Safed, Israel.
Michal Stern ZimmerSackler Faculty of Medicine, Tel-Aviv University, Tel Aviv-Yafo, Israel.
Annick Raas-RothschildThe Institute for Rare Diseases, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Ben Pode-ShakkedThe Institute for Rare Diseases, Edmond and Lily Safra Children's Hospital, Sheba Medical Center, Ramat Gan, Israel.
Edmond and Lily Safra Children's Hospital · ILSheba Medical Center · ILTel Aviv University · ILRebecca Sieff Hospital · ILRafael Advanced Defense Systems (Israel) · ILTechnion – Israel Institute of Technology · IL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

agenesis of corpus callosumautophagycardiomyopathycongenital cataractEPG5global developmental delayrecurrent Ashkenazi Jewish mutationVici syndrome

Identifiers

PMID36204321
PMCPMC9531146
OpenAlexW4297905652

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.