Evidence map›Paper›PMID 21792231›Full record

ArticleEuropean journal of human genetics : EJHG2012

Natural positive selection and north-south genetic diversity in East Asia.

Chen Suo, Haiyan Xu, Chiea-Chuen Khor, Rick Th Ong, Xueling Sim, Jieming Chen, Wan-Ting Tay, Kar-Seng Sim, Yi-Xin Zeng, Xuejun Zhang and 5 more

Abstract read
In one paragraph

Article in European journal of human genetics : EJHG, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 2 pooled it
–field-weighted citation impact
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

27 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Efficiency of trans-ethnic genome-wide meta-analysis and fine-mapping.European journal of human genetics : EJHG · 2012
    Pooled it
  3. Global patterns of natural selection inferred using ancient DNA.bioRxiv : the preprint server for biology · 2026
    Article
  4. Article
  5. HLA-Cw1 and Psoriasis.American journal of clinical dermatology · 2021
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Whole Mitochondrial DNA Sequencing Analysis in 47 Han Populations in Southwest China.Medical science monitor : international medical journal of experimental and clinical research · 2019
    Article
  11. Article
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  13. Article
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  15. Article
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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

15 authors.

Chen SuoCentre for Molecular Epidemiology, National University of Singapore, Singapore, Singapore.
Haiyan Xu
Chiea-Chuen Khor
Rick Th Ong
Xueling Sim
Jieming Chen
Wan-Ting Tay
Kar-Seng Sim
Yi-Xin Zeng
Xuejun Zhang
Jianjun Liu
E-Shyong Tai
Tien-Yin Wong
Kee-Seng Chia
Yik-Ying Teo

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent reports have identified a north-south cline in genetic variation in East and South-East Asia, but these studies have not formally explored the basis of these clinical differences. Understanding the origins of these variations may provide valuable insights in tracking down the functional variants in genomic regions identified by genetic association studies. Here we investigate the genetic basis of these differences with genome-wide data from the HapMap, the Human Genome Diversity Project and the Singapore Genome Variation Project. We implemented four bioinformatic measures to discover genomic regions that are considerably differentiated either between two Han Chinese populations in the north and south of China, or across 22 populations in East and South-East Asia. These measures prioritized genomic stretches with: (i) regional differences in the allelic spectrum for SNPs common to the two Han Chinese populations; (ii) differential evidence of positive selection between the two populations as quantified by integrated haplotype score (iHS) and cross-population extended haplotype homozygosity (XP-EHH); (iii) significant correlation between allele frequencies and geographical latitudes of the 22 populations. We also explored the extent of linkage disequilibrium variations in these regions, which is important in combining genetic association studies from North and South Chinese. Two of the regions that emerged are found in HLA class I and II, suggesting that the HLA imputation panel from the HapMap may not be directly applicable to every Chinese sample. This has important implications to autoimmune studies that plan to impute the classical HLA alleles to fine map the SNP association signals.

Indexed as

Genetic VariationPolymorphism, Single NucleotideSelection, GeneticAltitudeAsia, EasternComputational BiologyEthnicityGene FrequencyGenes, MHC Class IGenetics, PopulationGenome, HumanHaplotypesHapMap ProjectHomozygoteHumansLinkage Disequilibrium

Identifiers

PMID21792231
PMCPMC3234507

What OpenQuestion holds

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Registered trials

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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.