Evidence map›Paper›PMID 18043865›Full record

ArticleJournal of human genetics2008

Evaluation of resequencing on number of tag SNPs of 13 atherosclerosis-related genes in Thai population.

Chintana Tocharoentanaphol, Somying Promso, Dianna Zelenika, Tassanee Lowhnoo, Sissades Tongsima, Thanyachai Sura, Wasun Chantratita, Fumihiko Matsuda, Sean Mooney, Anavaj Sakuntabhai

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Article in Journal of human genetics, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.1field-weighted citation impact, top 21% 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

7 citing papers in PubMed, 10 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

10 authors at 5 institutions in 3 countries.

Chintana TocharoentanapholCentre National de Génotypage, 2 rue Gaston Crémieux, CP 5721, 91057, Evry Cedex, France. chintaphol@hotmail.com.
Somying PromsoDepartment of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, 10400, Thailand.
Dianna ZelenikaCentre National de Génotypage, 2 rue Gaston Crémieux, CP 5721, 91057, Evry Cedex, France.
Tassanee LowhnooCentre National de Génotypage, 2 rue Gaston Crémieux, CP 5721, 91057, Evry Cedex, France.
Sissades TongsimaNational Center for Genetic Engineering and Biotechnology, Pathumthani, Thailand.
Thanyachai SuraDepartment of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, 10400, Thailand.
Wasun ChantratitaDepartment of Pathology, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, 10400, Thailand.
Fumihiko MatsudaCentre National de Génotypage, 2 rue Gaston Crémieux, CP 5721, 91057, Evry Cedex, France.
Sean MooneyCenter for Computational Biology and Bioinformatics, Department of Medical and Molecular Genetics, Indiana University School of Medicine, Indianapolis, IN, 46202, USA.
Anavaj SakuntabhaiDepartment of Medicine, Faculty of Medicine Ramathibodi Hospital, Mahidol University, Bangkok, 10400, Thailand.
Centre National de Recherche en Génomique Humaine · FRRamathibodi Hospital · THIndiana University School of MedicineMahidol University · THNational Center for Genetic Engineering and Biotechnology · TH

Funding

Bioinformatics approaches to characterizing amino acid function.K22LM009135 · NLM · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI MOONEY, SEAN DAVID · 2006 to 2008
$465k
NLM NIH HHS K22LM009135
6 · The paper itself

Abstract

In the candidate gene approach, information about the distribution of single nucleotide polymorphisms (SNPs) is a crucial requirement for choosing efficient markers necessary for a case-control association study. To obtain such information, we discovered SNPs in 13 genes related to atherosclerosis by resequencing exon-flanking regions of 32 healthy Thai individuals. In total, 194 polymorphisms were identified, 184 of them SNPs, four insertions, and the rest deletions. Fifty-nine of the SNPs were characterized as novel polymorphisms, and these accounted for 30% of the identified SNPs. Comparing allele frequency distributions of the Thai population with other Asian populations shows similar patterns. In contrast, a low correlation pattern (r = 0.521) was found when comparing with either Caucasian or African populations. However, some rare alleles (rs11574541 and rs10874913) are found in the Thai population but not in other Asian populations. Most of the novel SNPs found were located outside the haplotype blocks generated by known SNPs in the Thai population. Only 5.77% of the novel SNPs lies in these defined haplotype blocks. The selection of haplotype-tagging SNPs shows that 8 of 13 genes benefited from the ethnic-specific genotype information. That is, when at least one novel SNP was present, the tagging SNPs chosen were altered. Functional prediction of 16 nonsynonymous SNPs (nsSNPs) by three different algorithm tools demonstrated that five nsSNPs possibly alter their corresponding protein functions. These results provide necessary information for conducting further genetic association studies involving the Thai population and demonstrate that resequencing of candidate genes provides more complete information for full genetic studies.

Indexed as

Polymorphism, Single NucleotideSequence Tagged SitesAtherosclerosisBlack PeopleGene FrequencyGenetics, PopulationGenetic VariationHumansLinkage DisequilibriumModels, GeneticSequence Analysis, DNAThailand

Identifiers

PMID18043865
OpenAlexW2003858996

What OpenQuestion holds

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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.