Evidence map›Paper›PMID 35783323›Full record

ArticleFrontiers in pediatrics2022

Molecular Spectrum, Ethnic and Geographical Distribution of Thalassemia in the Southern Area of Hainan, China.

Ying Yu, Chunjiao Lu, Ying Gao, Cuiyun Li, Dongxue Li, Jie Wang, Hui Wei, Zhaohui Lu, Guoling You

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.7field-weighted citation impact, top 15% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 11 citations in OpenAlex.

  1. Pooled it
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  3. Review
  4. Article
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  7. Article
  8. Genotype analysis of 55,281 cases of thalassemia in northern Guangxi.American journal of translational research · 2024
    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

9 authors at 1 institution in 1 country.

Ying YuAntenatal Diagnostic Center, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Chunjiao LuAntenatal Diagnostic Center, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Ying GaoDepartment of Public Health, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Cuiyun LiAntenatal Diagnostic Center, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Dongxue LiAntenatal Diagnostic Center, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Jie WangAntenatal Diagnostic Center, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Hui WeiDepartment of Public Health, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Zhaohui LuDepartment of Pediatric Surgery, Sanya Women and Children's Hospital Managed by Shanghai Children's Medical Center, Sanya, China.
Guoling YouDepartment of Laboratory Medicine, Shanghai Children's Medical Center, School of Medicine, Shanghai Jiao Tong University, Shanghai, China.
Shanghai Children's Medical Center · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Thalassemia is one of the most common genetic diseases in southern China. Accurate population frequency data regarding the occurrence and distribution of thalassemia are important for designing appropriate prevention strategies for thalassemia. This study aims to reveal the molecular spectrum, ethnic and geographical distribution of thalassemia in the southern area of Hainan Province, China. Methods: A total of 9813 suspected carriers of thalassemia were screened for genetic analysis by using the PCR-reverse dot blot hybridization method targeting three known deletions of α-thalassemias (-- Results: Approximately 6,924 subjects were genetically diagnosed as thalassemia carriers or patients, including 5812 cases of α-thalassemia (83.9%), 369 cases of β-thalassemia (5.3%), and 743 cases of α-composite β-thalassemia (10.7%). A total of 21 distinct genotypes were identified among the 5,812 α-thalassemia carriers, -α Conclusions: Our study indicates that there is high genetic heterogeneity, geographical and ethnic differences in thalassemia in populations in the southern area of Hainan Province. These findings will be helpful in guiding genetic counseling and prenatal diagnosis of thalassemia in Hainan Province.

Indexed as

Chinagenetic diagnosisHainan Provincemolecular spectrumthalassemia

Identifiers

PMID35783323
PMCPMC9245522
OpenAlexW4281953906

What OpenQuestion holds

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LicenceCC BY
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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.