Evidence map›Paper›PMID 35269902›Full record

ReviewInternational journal of molecular sciences2022

The Molecular Basis of FIX Deficiency in Hemophilia B.

Guomin Shen, Meng Gao, Qing Cao, Weikai Li

Open access · goldAbstract readReview
In one paragraph

Review in International journal of molecular sciences, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
8.2field-weighted citation impact, top 2% 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

19 citing papers in PubMed, 52 citations in OpenAlex.

  1. Article
  2. Review
  3. Review
  4. Article
  5. Haemophilia B: an illustrative review of current challenges and opportunities.Research and practice in thrombosis and haemostasis · 2025
    Article
  6. CRISPR/Cas9 mediated generation of zebrafish f9a mutant as a model for hemophilia B.Blood coagulation & fibrinolysis : an international journal in haemostasis and thrombosis · 2025
    Article
  7. Article
  8. Review
  9. Identification of NovelJournal of blood medicine · 2025
    Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Article
  15. Article
  16. Comparative analysis of codon usage patterns ofFrontiers in microbiology · 2023
    Article
  17. Article
  18. Article
  19. Study on the Mutation of FⅨ Gene in 31 Patients with Type B Hemophilia.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    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

4 authors at 2 institutions in 2 countries.

Guomin ShenHenan International Joint Laboratory of Thrombosis and Hemostasis, Henan University of Science and Technology, Luoyang 471023, China.ORCID 0000-0002-5006-2790
Meng GaoHenan International Joint Laboratory of Thrombosis and Hemostasis, Henan University of Science and Technology, Luoyang 471023, China.ORCID 0000-0002-8792-1093
Qing CaoHenan International Joint Laboratory of Thrombosis and Hemostasis, Henan University of Science and Technology, Luoyang 471023, China.ORCID 0000-0003-2517-2231
Weikai LiDepartment of Biochemistry and Molecular Biophysics, Washington University in St. Louis School of Medicine, St. Louis, MO 63110, USA.
Henan University of Science and Technology · CNWashington University in St. Louis · US

Funding

STRUCTURAL AND FUNCTIONAL BASIS OF THE VITAMIN K CYCLER01HL121718 · NHLBI · WASHINGTON UNIVERSITY · PI Weikai Li · 2014 to 2026
$5.2M
STRUCTURAL BASIS OF SCHNYDER CORNEAL DYSTROPHYR21EY028705 · NEI · WASHINGTON UNIVERSITY · PI LI, WEIKAI, WEISS, JAYNE S · 2018 to 2019
$424k
National Natural Science Foundation of China 82170133, 81770140, 31900412NEI NIH HHS R21 EY028705NHLBI NIH HHS R01 HL121718
6 · The paper itself

Abstract

Coagulation factor IX (FIX) is a vitamin K dependent protein and its deficiency causes hemophilia B, an X-linked recessive bleeding disorder. More than 1000 mutations in the

Indexed as

Hemophilia AHemophilia BCodon, NonsenseFactor IXHumansMutationPhenotypeCodon, NonsenseFactor IXaberrant splicingcoagulation factor IXcoagulation factor VIIIhemophilia Bmissense mutationmolecular mechanismpoint mutationvitamin Kvitamin K-dependent proteinsγ-carboxylation

Identifiers

PMID35269902
PMCPMC8911121
OpenAlexW4214911736

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.