Evidence map›Paper›PMID 36347915›Full record

ArticleScientific reports2022

Two independent variants of epidermal growth factor receptor associated with risk of glioma in a Korean population.

In Ki Baek, Hyun Sub Cheong, Seok Namgoong, Jeong-Hyun Kim, Seok-Gu Kang, Seon-Jin Yoon, Se Hoon Kim, Jong Hee Chang, Lyoung Hyo Kim, Hyoung Doo Shin

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.3field-weighted citation impact, top 39% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

10 authors at 3 institutions in 1 country.

In Ki BaekDepartment of Life Science, Sogang University, Seoul, 04107, Republic of Korea.
Hyun Sub CheongResearch Institute for Life Science, GW Vitek, Inc., Seoul, Republic of Korea.
Seok NamgoongResearch Institute for Life Science, GW Vitek, Inc., Seoul, Republic of Korea.
Jeong-Hyun KimDepartment of Medicine, University of Ulsan College of Medicine, Seoul, Republic of Korea.
Seok-Gu KangDepartment of Neurosurgery, Yonsei University College of Medicine, Seoul, Republic of Korea.
Seon-Jin YoonDepartment of Neurosurgery, Yonsei University College of Medicine, Seoul, Republic of Korea.
Se Hoon KimDepartment of Pathology, Yonsei University College of Medicine, Seoul, Republic of Korea.
Jong Hee ChangDepartment of Neurosurgery, Yonsei University College of Medicine, Seoul, Republic of Korea. CHANGJH@yuhs.ac.
Lyoung Hyo KimResearch Institute for Life Science, GW Vitek, Inc., Seoul, Republic of Korea. lyoung@gwvitek.com.
Hyoung Doo ShinDepartment of Life Science, Sogang University, Seoul, 04107, Republic of Korea. hdshin@sogang.ac.kr.
Yonsei University · KRSogang University · KRUniversity of Ulsan · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gliomas are the most common primary tumors in the brain and spinal cord. In previous GWASs, SNPs in epidermal growth factor receptor (EGFR) have been reported as risk loci for gliomas. However, EGFR variants associated with gliomas in the Korean population remain unstudied. This study explored the association of EGFR SNPs with the risk of glioma. We genotyped 13 EGFR exon SNPs in a case-control study that included 324 Korean patients diagnosed with glioma and 480 population-based controls. Statistical analyses of the association between EGFR SNPs and glioma risk were conducted using logistic regression. Both stepwise analysis and conditional logistic analysis were performed to identify independent associations among genotyped variants. We confirmed that two SNPs (rs2227983, rs1050171) were significantly associated with glioma (rs2227983: odds ratio = 1.42, P

Indexed as

Brain NeoplasmsGliomaCase-Control StudiesErbB ReceptorsGenetic Predisposition to DiseaseHumansPolymorphism, Single NucleotideRepublic of KoreaRisk FactorsErbB Receptors

Identifiers

PMID36347915
PMCPMC9643523
OpenAlexW4308573811

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.