ArticleZhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi2018
[The characteristic of hereditary spherocytosis related gene mutation in 37 Chinese hereditary spherocytisis patients].
Article in Zhonghua xue ye xue za zhi = Zhonghua xueyexue zazhi, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers, 1 of them a synthesis that pooled 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.
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.
Who cites it
12 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.
- A novel variant of SLC4A1 for hereditary spherocytosis in a Chinese family: a case report and systematic review.BMC medical genomics · 2022Pooled it
- Case Report: Abnormally low hemoglobin A1c in a diabetic patient withFrontiers in endocrinology · 2026Article
- A novelFrontiers in pediatrics · 2026Article
- Multigene Panel Testing Reveals Novel Variants in Hereditary Spherocytosis Patients in TürkiyeTurkish journal of haematology : official journal of Turkish Society of Haematology · 2025Article
- Clinical characteristics of hereditary spherocytosis with red blood cell membrane protein gene variants.Frontiers in pediatrics · 2025Article
- Clinical and genetic characteristics of Chinese pediatric and adult patients with hereditary spherocytosis.Orphanet journal of rare diseases · 2024Article
- Severe Microcytic Anemia Caused by Complex Hereditary Spherocytosis and X-Linked Sideroblastic Anemia with Mutations inJournal of clinical medicine · 2023Article
- The updated beta-spectrin mutations in patients with hereditary spherocytosis by targeted next-generation sequencing.Journal of human genetics · 2021Article
- Facilitating EMA binding test performance using fluorescent beads combined with next-generation sequencing.EJHaem · 2021Article
- A clinical and experimental study of adult hereditary spherocytosis in the Chinese population.The Kaohsiung journal of medical sciences · 2020Article
- How will next generation sequencing (NGS) improve the diagnosis of congenital hemolytic anemia?Annals of translational medicine · 2020Article
- Clinical utility of targeted gene enrichment and sequencing technique in the diagnosis of adult hereditary spherocytosis.Annals of translational medicine · 2019Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
17 authors at 1 institution in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
PubMed holds no abstract for this paper.
Indexed as
Identifiers
What OpenQuestion holds
Registered trials
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.