Evidence map›Paper›PMID 36721228›Full record

ArticleHuman genomics2023

Genome-wide allele and haplotype-sharing patterns suggested one unique Hmong-Mein-related lineage and biological adaptation history in Southwest China.

Guanglin He, Jiawen Wang, Lin Yang, Shuhan Duan, Qiuxia Sun, Youjing Li, Jun Wu, Wenxin Wu, Zheng Wang, Yan Liu and 7 more

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Human genomics, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
9.4field-weighted citation impact, top 2% 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. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

17 authors at 7 institutions in 1 country.

Guanglin He *Institute of Rare Diseases, West China Hospital of Sichuan University, Sichuan University, Chengdu, 610041, China. guanglinhescu@163.com.
Jiawen Wang *College of Forensic Medicine, Guizhou Medical University, Guiyang, 550004, China.
Lin Yang *College of Forensic Medicine, Guizhou Medical University, Guiyang, 550004, China.
Shuhan Duan *School of Basic Medical Sciences, North Sichuan Medical College, Nanchong, 637000, China.
Qiuxia SunDepartment of Forensic Medicine, College of Basic Medicine, Chongqing Medical University, Chongqing, 400331, China.
Youjing LiCongjiang People's Hospital, Congjiang, 557499, China.
Jun WuCollege of Forensic Medicine, Guizhou Medical University, Guiyang, 550004, China.
Wenxin WuCollege of Forensic Medicine, Guizhou Medical University, Guiyang, 550004, China.
Zheng WangInstitute of Forensic Medicine, West China School of Basic Medical Sciences and Forensic Medicine, Sichuan University, Chengdu, 610000, China.
Yan LiuInstitute of Rare Diseases, West China Hospital of Sichuan University, Sichuan University, Chengdu, 610041, China.
Renkuan TangDepartment of Forensic Medicine, College of Basic Medicine, Chongqing Medical University, Chongqing, 400331, China.
Junbao YangSchool of Basic Medical Sciences, North Sichuan Medical College, Nanchong, 637000, China.
Chao LiuFaculty of Forensic Medicine, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, 510275, China.
Buhong YuanLongli People's Hospital, Longli, 551299, China.
Daoyong WangNayong Guohua Yixin Hospital, Nayong, 553306, China.
Jianwei XuDepartment of Pharmacology, School of Basic Medicine, Guizhou Medical University, Guiyang, 550004, China. 363912577@qq.com.
Mengge Wang *Faculty of Forensic Medicine, Zhongshan School of Medicine, Sun Yat-Sen University, Guangzhou, 510275, China. menggewang2021@163.com.
Guiyang Medical University · CNNorth Sichuan Medical University · CNChongqing Medical University · CNSun Yat-sen University · CNQujiang People's Hospital · CNSichuan University · CNWest China Medical Center of Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundFine-scale genetic structure of ethnolinguistically diverse Chinese populations can fill the gap in the missing diversity and evolutionary landscape of East Asians, particularly for anthropologically informed Chinese minorities. Hmong-Mien (HM) people were one of the most significant indigenous populations in South China and Southeast Asia, which were suggested to be the descendants of the ancient Yangtze rice farmers based on linguistic and archeological evidence. However, their deep population history and biological adaptative features remained to be fully characterized.

objectivesTo explore the evolutionary and adaptive characteristics of the Miao people, we genotyped genome-wide SNP data in Guizhou HM-speaking populations and merged it with modern and ancient reference populations via a comprehensive population genetic analysis and evolutionary admixture modeling.

resultsThe overall genetic admixture landscape of Guizhou Miao showed genetic differentiation between them and other linguistically diverse Guizhou populations. Admixture models further confirmed that Miao people derived their primary ancestry from geographically close Guangxi Gaohuahua people. The estimated identity by descent and effective population size confirmed a plausible population bottleneck, contributing to their unique genetic diversity and population structure patterns. We finally identified several natural selection candidate genes associated with several biological pathways.

conclusionsGuizhou Miao possessed a specific genetic structure and harbored a close genetic relationship with geographically close southern Chinese indigenous populations and Guangxi historical people. Miao people derived their major ancestry from geographically close Guangxi Gaohuahua people and experienced a plausible population bottleneck which contributed to the unique pattern of their genetic diversity and structure. Future ancient DNA from Shijiahe and Qujialing will provide new insights into the origin of the Miao people.

Indexed as

Adaptation, BiologicalAsian PeopleAllelesChinaHaplotypesHumansAdmixture modelBiological adaptationEvolutionary historyGenetic structureMiao

Identifiers

PMID36721228
PMCPMC9887792
OpenAlexW4318617576

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.