Evidence map›Paper›PMID 31113390›Full record

ArticleBMC medical genetics2019

Gene spectrum analysis of thalassemia for people residing in northern China.

Zhuo Yang, Wenzhe Zhou, Quexuan Cui, Ling Qiu, Bing Han

Open access · goldAbstract read
In one paragraph

Article in BMC medical genetics, 2019. 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
0.9field-weighted citation impact, top 25% 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.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Genotypes of thalassemia in children: an analysis of 30 417 cases.Zhongguo dang dai er ke za zhi = Chinese journal of contemporary pediatrics · 2021
    Article
  6. Review
  7. Review
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

5 authors at 1 institution in 1 country.

Zhuo YangDepartment of clinical laboratory, Peking Union Medical College Hospital, Chinese Academy of Medical Science, Beijing, China.
Wenzhe ZhouPeking Union Medical College, Chinese Academy of Medical Science, Beijing, China.
Quexuan CuiPeking Union Medical College, Chinese Academy of Medical Science, Beijing, China.
Ling QiuDepartment of clinical laboratory, Peking Union Medical College Hospital, Chinese Academy of Medical Science, Beijing, China.
Bing HanDepartment of hematology, Peking Union Medical College Hospital, Chinese Academy of Medical Science, Beijing, China. hanbing_li@sina.com.ORCID 0000-0003-3844-2608
Chinese Academy of Medical Sciences & Peking Union Medical College · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundSouthern China provinces have high incidence of thalassemia, however, sporadic cases can be found in northern China as well.

methodsPeople resided in north China who were suspected to have thalassemia were detected mutations by gap-polymerase chain reaction (Gap-PCR) and reverse dot blot (RDB) analyses. Those with positive findings from 2012 to 2017 were further analyzed for basic clinical data and ancestral information either by medical records or by telephone follow-up or both.

resultsMost people enrolled in our study had no or mild symptoms. For those with positive gene findings, people originated from the north had higher percentage of β-thalassemia gene mutations compared with those originated from the south (72.8% vs. 62.4%, χ

conclusionMost of people in north China with thalassemia mutation gene were thalassemia carriers. People originated from the north had higher frequency of β mutation than those originated from the south, but the north people had similar individual gene mutation profile compared with south people both for α and β mutations. People lived in different altitudes had different spectrum of β mutations.

Indexed as

AdolescentAdultChildChild, PreschoolChinaFemaleHumansIncidenceInfantInfant, NewbornMaleMiddle AgedMutationPolymerase Chain ReactionThalassemiaYoung AdultAltitudeChinaGene mutationSpectrumThalassemia

Identifiers

PMID31113390
PMCPMC6530100
OpenAlexW2947272258

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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.