Evidence map›Paper›PMID 34335240›Full record

ArticleFrontiers in pharmacology2021

Mutational Characteristics of Causative Genes in Chinese Hereditary Spherocytosis Patients: a Report on Fourteen Cases and a Review of the Literature.

Dong Wang, Li Song, Li Shen, Kaihui Zhang, Yuqiang Lv, Min Gao, Jian Ma, Ya Wan, Zhongtao Gai, Yi Liu

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pharmacology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed
3.5field-weighted citation impact, top 6% 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

18 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Expanding the genetic landscape ofFrontiers in genetics · 2026
    Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Review
  8. Article
  9. Article
  10. Identification of a novelFrontiers in genetics · 2024
    Article
  11. Article
  12. Clinical and genetic diagnosis for 26 paitents with hereditary spherocytosis.Zhong nan da xue xue bao. Yi xue ban = Journal of Central South University. Medical sciences · 2023
    Article
  13. Article
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
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 2 institutions in 1 country.

Dong WangPediatric Research Institute, Qilu Children's Hospital of Shandong University, Jinan, China.
Li SongPediatric Hematology and Oncology, Qilu Children's Hospital of Shandong University, Jinan, China.
Li ShenClinical Laboratory, The Fourth Hospital of Jinan, Jinan, China.
Kaihui ZhangPediatric Research Institute, Qilu Children's Hospital of Shandong University, Jinan, China.
Yuqiang LvPediatric Research Institute, Qilu Children's Hospital of Shandong University, Jinan, China.
Min GaoPediatric Research Institute, Qilu Children's Hospital of Shandong University, Jinan, China.
Jian MaPediatric Research Institute, Qilu Children's Hospital of Shandong University, Jinan, China.
Ya WanPediatric Research Institute, Qilu Children's Hospital of Shandong University, Jinan, China.
Zhongtao GaiPediatric Research Institute, Qilu Children's Hospital of Shandong University, Jinan, China.
Yi LiuPediatric Research Institute, Qilu Children's Hospital of Shandong University, Jinan, China.
Qilu Hospital of Shandong University · CNFourth People’s Hospital of Jinan · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PubMed holds no abstract for this paper.

Indexed as

ANK1hereditary spherocytosismutationSPTBwhole exome sequencing

Identifiers

PMID34335240
PMCPMC8322660
OpenAlexW3184360644

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.