Evidence map›Paper›PMID 28855716›Full record

ArticleJournal of human genetics2017

A genome-wide association analysis identifies NMNAT2 and HCP5 as susceptibility loci for Kawasaki disease.

Jae-Jung Kim, Sin Weon Yun, Jeong Jin Yu, Kyung Lim Yoon, Kyung-Yil Lee, Hong-Ryang Kil, Gi Beom Kim, Myung-Ki Han, Min Seob Song, Hyoung Doo Lee and 12 more

Abstract read
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In one paragraph

Article in Journal of human genetics, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 29 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
29citing papers in PubMed, 1 pooled it
5.5field-weighted citation impact, top 4% 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

29 citing papers in PubMed, 1 synthesis or guideline pooled it, 46 citations in OpenAlex.

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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

22 authors at 19 institutions in 2 countries.

Jae-Jung KimAsan Institute for Life Sciences, University of Ulsan College of Medicine, Seoul, Korea.
Sin Weon YunDepartment of Pediatrics, Chung-Ang University Hospital, Seoul, Korea.
Jeong Jin YuDepartment of Pediatrics, University of Ulsan College of Medicine, Asan Medical Center, Seoul, Korea.
Kyung Lim YoonDepartment of Pediatrics, Kyung Hee University Hospital at Gangdong, Seoul, Korea.
Kyung-Yil LeeDepartment of Pediatrics, The Catholic University of Korea, Daejeon St Mary's Hospital, Daejeon, Korea.
Hong-Ryang KilDepartment of Pediatrics, Chungnam National University Hospital, Daejeon, Korea.
Gi Beom KimDepartment of Pediatrics, Seoul National University Children's Hospital, Seoul, Korea.
Myung-Ki HanDepartment of Pediatrics, University of Ulsan, Gangneung Asan Hospital, Gangneung, Korea.
Min Seob SongDepartment of Pediatrics, Inje University Paik Hospital, Busan, Korea.
Hyoung Doo LeeDepartment of Pediatrics, Pusan National University Hospital, Busan, Korea.
Kee Soo HaDepartment of Pediatrics, Korea University Hospital, Seoul, Korea.
Sejung SohnDepartment of Pediatrics, Ewha Womans University Hospital, Seoul, Korea.
Todd A JohnsonLaboratory for Medical Science Mathematics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Atsushi TakahashiLaboratory for Statistical Analysis, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Michiaki KuboLaboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Tatsuhiko TsunodaLaboratory for Medical Science Mathematics, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Kaoru ItoLaboratory for Cardiovascular diseases, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Yoshihiro OnouchiLaboratory for Cardiovascular diseases, RIKEN Center for Integrative Medical Sciences, Yokohama, Japan.
Young Mi HongDepartment of Pediatrics, Ewha Womans University Hospital, Seoul, Korea.
Gi Young JangDepartment of Pediatrics, Korea University Hospital, Seoul, Korea.
Jong-Keuk LeeAsan Institute for Life Sciences, University of Ulsan College of Medicine, Seoul, Korea.
Korean Kawasaki Disease Genetics Consortium
Korea University Medical Center · KRUniversity of Ulsan · KRAsan Medical Center · KREwha Womans University · KRThe Catholic University of Korea Daejeon St. Mary's Hospital · KRRIKEN Center for Integrative Medical Sciences · JPChung-Ang University Hospital · KRChungnam National University Hospital · KRInje University Busan Paik Hospital · KRKyung Hee University Hospital at Gangdong · KRPusan National University Hospital · KRSeoul National University Children's Hospital · KRUlsan College · KRChiba University · JPGangneung Asan Hospital · KRNational Cerebral and Cardiovascular Center · JPSeoul Medical Center · KRTokyo Medical and Dental University · JPYonsei University · KR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kawasaki disease (KD), a systemic vasculitis of infants and children, manifests as fever and mucocutaneous inflammation. Although its etiology is largely unknown, the epidemiological data suggest that genetic factors are important in KD susceptibility. To identify genetic variants influencing KD susceptibility, we performed a genome-wide association study (GWAS) and replication study using a total of 915 children with KD and 4553 controls in the Korean population. Six single-nucleotide polymorphisms (SNPs) in three loci were associated significantly with KD susceptibility (P<1.0 × 10

Indexed as

ChildGenetic LociGenetic Predisposition to DiseaseGenome-Wide Association StudyGenotypeHistocompatibility Antigens Class IHumansMucocutaneous Lymph Node SyndromeNicotinamide-Nucleotide AdenylyltransferaseNucleoside-TriphosphataseOdds RatioPolymorphism, Single NucleotideRepublic of KoreaRNA, Long NoncodingHCP5 long noncoding RNA, humanHistocompatibility Antigens Class INicotinamide-Nucleotide AdenylyltransferaseNLRP14 protein, humanNMNAT2 protein, humanNucleoside-TriphosphataseRNA, Long Noncoding

Identifiers

PMID28855716
OpenAlexW2752415120

What OpenQuestion holds

Textmetadata
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.