Evidence map›Paper›PMID 29160859›Full record

ArticleInternational journal of molecular sciences2017

The Role of RNF213 4810G>A and 4950G>A Variants in Patients with Moyamoya Disease in Korea.

Young Seok Park, Hui Jeong An, Jung Oh Kim, Won Seop Kim, In Bo Han, Ok Joon Kim, Nam Keun Kim, Dong-Seok Kim

Open access · goldAbstract read
In one paragraph

Article in International journal of molecular sciences, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
  4. The Genetic Basis of Moyamoya Disease.Translational stroke research · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. Progress in moyamoya disease.Neurosurgical review · 2020
    Review
  9. Article
  10. Moyamoya angiopathy in PHACE syndrome not associated with RNF213 variants.Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery · 2019
    Article
  11. 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

8 authors at 4 institutions in 1 country.

Young Seok ParkDepartment of Neurosurgery, College of Medicine, Chungbuk National University, Cheongju 28644, Korea. youngseokparkmd@gmail.com.
Hui Jeong AnDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea. tody2209@naver.com.
Jung Oh KimDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea. jokim8505@gmail.com.
Won Seop KimDepartment of Pediatrics, College of Medicine, Chungbuk National University, Cheongju 28644, Korea. wskim@chungbuk.ac.kr.
In Bo HanDepartment of Neurology, CHA Bundang Medical Center, School of Medicine, CHA University, Seongnam 13496, Korea. haninbo@gmail.com.
Ok Joon KimDepartment of Neurology, CHA Bundang Medical Center, School of Medicine, CHA University, Seongnam 13496, Korea. okjun77@cha.ac.kr.
Nam Keun KimDepartment of Biomedical Science, College of Life Science, CHA University, Seongnam 13488, Korea. nkkim@cha.ac.kr.ORCID 0000-0003-0541-3528
Dong-Seok KimDepartment of Pediatric Neurosurgery, Severance Hospital, Seoul 03722, Korea. dskim@yuhs.ac.
CHA University · KRCHA University Bundang Medical Center · KRChungbuk National University · KRSeverance Hospital · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although a founder variant of

Indexed as

AllelesGenetic Predisposition to DiseasePolymorphism, Single NucleotideAdenosine TriphosphatasesAdolescentAdultCase-Control StudiesFemaleGene FrequencyGenotypeHaplotypesHumansMaleMoyamoya DiseasePopulation GroupsRepublic of KoreaAdenosine TriphosphatasesRNF213 protein, humanUbiquitin-Protein Ligasescerebrovascular diseasegeneticmoyamoya diseaseRNF213single nucleotide polymorphismstroke

Identifiers

PMID29160859
PMCPMC5713443
OpenAlexW2770553334

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.