Evidence map›Paper›PMID 33747056›Full record

ArticleFrontiers in genetics2021

Corrigendum: Characteristics of Genetic Variations Associated With Lennox-Gastaut Syndrome in Korean Families.

Jin Ok Yang, Min-Hyuk Choi, Ji-Yong Yoon, Jeong-Ju Lee, Sang Ook Nam, Soo Young Jun, Hyeok Hee Kwon, Sohyun Yun, Su-Jin Jeon, Iksu Byeon and 6 more

Open access · goldAbstract readPublished Erratum
PubMed Full text at PMC Publisher
In one paragraph

Article in Frontiers in genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.2field-weighted citation impact, top 58% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors at 8 institutions in 1 country.

Jin Ok YangKorea BioInformation Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Min-Hyuk ChoiRare-Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Ji-Yong YoonRare-Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Jeong-Ju LeeRare-Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Sang Ook NamDepartment of Pediatrics, Pusan National University Children's Hospital, Pusan National University School of Medicine, Yangsan, South Korea.
Soo Young JunRare-Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Hyeok Hee KwonDepartment of Medical Science and Anatomy, Chungnam National University, Daejeon, South Korea.
Sohyun YunRare-Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Su-Jin JeonRare-Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Iksu ByeonKorea BioInformation Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Debasish HalderRare-Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Juhyun KongDepartment of Pediatrics, Pusan National University Children's Hospital, Pusan National University School of Medicine, Yangsan, South Korea.
Byungwook LeeKorea BioInformation Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Jeehun LeeDepartment of Pediatrics, Samsung Medical Center, Sungkyunkwan University School of Medicine, Seoul, South Korea.
Joon-Won KangDepartment of Pediatrics and Medical Science, Chungnam National University Hospital, College of Medicine, Chungnam National University, Daejeon, South Korea.
Nam-Soon KimRare-Disease Research Center, Korea Research Institute of Bioscience and Biotechnology, Daejeon, South Korea.
Korea Research Institute of Bioscience and Biotechnology · KRKorea University of Science and Technology · KRPusan National University Yangsan Hospital · KRChungnam National University · KRChungnam National University Hospital · KRKorea Institute of Brain Science · KRSamsung Medical Center · KRSungkyunkwan University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

[This corrects the article DOI: 10.3389/fgene.2020.590924.].

Indexed as

epilepsygenetic variationLennox-Gastaut syndromeRare-diseaseswhole-exome sequencing

Identifiers

PMID33747056
PMCPMC7978109
OpenAlexW3135623046

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.