Evidence map›Paper›PMID 31852448›Full record

ArticleBMC genetics2019

Genome-wide association study of morbid obesity in Han Chinese.

Kuang-Mao Chiang, Heng-Cheng Chang, Hsin-Chou Yang, Chien-Hsiun Chen, Hsin-Hung Chen, Wei-Jei Lee, Wen-Harn Pan

Open access · diamondAbstract read
In one paragraph

Article in BMC genetics, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.8field-weighted citation impact, top 6% 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

25 citing papers in PubMed, 37 citations in OpenAlex.

  1. Association of theInternational journal of molecular sciences · 2026
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  9. Genetic Variations inJournal of obesity · 2024
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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

7 authors at 6 institutions in 1 country.

Kuang-Mao ChiangInstitute of Biomedical Sciences, Academia Sinica, Taipei City, Taiwan.
Heng-Cheng ChangDepartment of Gynecology and Obstetrics, School of Medicine, Taipei Medical University, Taipei City, Taiwan.
Hsin-Chou YangInstitute of Statistical Science, Academia Sinica, Taipei City, Taiwan.
Chien-Hsiun ChenInstitute of Biomedical Sciences, Academia Sinica, Taipei City, Taiwan.
Hsin-Hung ChenDepartment of Nutrition and Health Science, Chang Jung Christian University, Tainan City, Taiwan.
Wei-Jei LeeDepartment of Surgery, Min-Sheng General Hospital, Taoyuan City, Taiwan. wjlee_obessurg_tw@yahoo.com.tw.
Wen-Harn PanInstitute of Biomedical Sciences, Academia Sinica, Taipei City, Taiwan. pan@ibms.sinica.edu.tw.ORCID 0000-0001-9136-0658
Institute of Biomedical Sciences, Academia Sinica · TWChang Jung Christian University · TWInstitute of Statistical Science, Academia Sinica · TWMin Sheng General Hospital · TWNational Health Research Institutes · TWTaipei Medical University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundAs obesity is becoming pandemic, morbid obesity (MO), an extreme type of obesity, is an emerging issue worldwide. It is imperative to understand the factors responsible for huge weight gain in certain populations in the modern society. Very few genome-wide association studies (GWAS) have been conducted on MO patients. This study is the first MO-GWAS study in the Han-Chinese population in Asia.

methodsWe conducted a two-stage GWAS with 1110 MO bariatric patients (body mass index [BMI] ≥ 35 kg/m

resultsThe results of the joint analysis for the second stage revealed six top ranking SNPs, including rs8050136 (p-value = 7.80 × 10

conclusionThe most significantly associated locus of MO in the Han-Chinese population was the well-known FTO gene. These SNPs located in intron 1, may include the leptin receptor modulator. Other significant loci, showing weak associations with MO, also suggested the potential mechanism underlying the disorders with eating behaviors or brain/neural development.

Indexed as

Polymorphism, Single NucleotideAdultAlpha-Ketoglutarate-Dependent Dioxygenase FTOAsian PeopleCarrier ProteinsCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleMembrane ProteinsMiddle AgedObesity, MorbidReceptor, ErbB-4RNA Splicing FactorsAlpha-Ketoglutarate-Dependent Dioxygenase FTOCarrier ProteinsCSMD3 protein, humanERBB4 protein, humanFTO protein, humanMembrane ProteinsRBFOX1 protein, humanReceptor, ErbB-4RNA Splicing FactorsTMTC1 protein, humanBody mass indexFTOGenome-wide association studyMorbid obesity

Identifiers

PMID31852448
PMCPMC6921553
OpenAlexW2995008109

What OpenQuestion holds

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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.