ReviewInternational journal of hematology-oncology and stem cell research2020
Hemoglobinopathies in Iran: An Updated Review.
Review in International journal of hematology-oncology and stem cell research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.
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
15 citing papers in PubMed.
- Appreciating diversity: a review of the Iranian genomic landscape.European journal of human genetics : EJHG · 2026Review
- Investigating the Efficacy of the CRISPR/Cas9 Gene-Editing System for Targeting the HBB FSC 36-37 (-T) Mutation Locus in Hematopoietic Stem Cells.Molecular biotechnology · 2026Article
- Machine learning improves detection of alpha thalassemia carriers compared to clinical features.Scientific reports · 2025Article
- Application of the health belief model to explain pre-conception care among women with sickle cell disease: a cross-sectional study.BMC pregnancy and childbirth · 2025Article
- Experiences of Iranian Patients with Thalassemia Major Regarding Their Palliative and Supportive Care Needs: A Qualitative Content Analysis.International journal of community based nursing and midwifery · 2025Article
- Assessing knowledge on thalassemia for prevention and management practices among the tribal population of Sitteri Panchayat, Dharmapuri District, Tamil Nadu, India.Journal of family medicine and primary care · 2025Article
- Article
- Hematologic Parameters Cut-off Assessment of Adult Alpha-Thalassemia Patients in Iran.International journal of hematology-oncology and stem cell research · 2024Article
- Spectrum of Beta-Thalassemia Mutations in Potential Carriers with Microcytic Hypochromic Anemia from Mazandaran and Golestan, Northern Provinces of Iran.BioMed research international · 2024Article
- Routine antenatal molecular testing for α-thalassemia at a tertiary referral hospital in China: ten years of experience.Frontiers in genetics · 2024Article
- Correlation of Magnesium Level with Cardiac and Hepatic Hemosiderosis Measured by T2*MRI Technique and Age in Patients with Thalassemia Major.International journal of hematology-oncology and stem cell research · 2023Article
- A novel compound heterozygous of β-thalassemia with HbG-Coushatta: case report of Iran.Human genome variation · 2023Article
- Quality of Life and Related Paraclinical Factors in Iranian Patients with Transfusion-Dependent Thalassemia.Journal of environmental and public health · 2021Article
- Ocular Biometric Findings in Thalassemia Major: A Systematic Review and Meta-Analysis.Journal of current ophthalmologyReview
- Prevalence and assessment of the impact of iron-deficiency anemia in beta-thalassemia trait subjects: A study from a tertiary care center of Western India.Asian journal of transfusion scienceArticle
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
3 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
Hemoglobinopathies are the most common single gene disorders (monogenic disorders) in the world population. Due to specific position of Iran and the presence of multi-ethnic groups in the country, there are many varieties in the molecular genetics and clinical features of hemoglobinopathies in Iran. Hemoglobinopathies include structural variants, thalassemias, and hereditary persistence of fetal hemoglobin. In this review, we look at the common structural variants in various parts of the country along with their hematological and clinical characteristics. Also, we discuss about the burden of the thalassemias in the country, different types, complications, molecular defects and therapy.
Indexed as
Identifiers
32461799PMC7231794What 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.