ITHANET: Information and database community portal for haemoglobinopathies
Petros KountourisiD, Coralea StephanouiD, Celeste BentoiD, Pavlos FanisiD, Jacques ÉlioniD, Raj RamesariD, Bin Alwi ZilfaliliD, Helen M RobinsoniD, Joanne Traeger‐SynodinosiD, Human Variome Project Global Globin 2020 Challenge, Carsten Werner LedereriD, Marina KleanthousiD
Abstract
Haemoglobinopathies are the commonest monogenic diseases, with millions of carriers and patients worldwide. Online resources for haemoglobinopathies are largely divided into specialised sites catering for patients, researchers and clinicians separately. However, the severity, ubiquity and surprising genetic complexity of the haemoglobinopathies call for an integrated website to serve as a free and comprehensive repository and tool for patients, scientists and health professionals alike. This paper presents the ITHANET community portal, an expanding resource for clinicians and researchers dealing with haemoglobinopathies. It integrates information on news, events, publications, clinical trials and haemoglobinopathy-related organisations and experts and, most importantly, databases of variations, epidemiology and diagnostic and clinical data. Specifically, ITHANET provides annotation for 2690 haemoglobinopathy-related variations, epidemiological data for more than 180 countries and information for more than 600 HPLC diagnostic reports. The ITHANET portal accepts and incorporates contributions to its content by local experts from any country in the world and is freely available for the public at http://www.ithanet.eu.
02 /Specification & Classification
Click any tag to browse matching papers- Citations
- 13
- Organism
- Research Focus
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Phenopolis: an open platform for harmonization and analysis of sequencing and phenotype data
Nikolas Pontikos, Jing Yu, … Vincent Plagnol·BioinformaticsPeer-reviewed·Mar 14, 2017
- Genetic variants of human platelet antigens in the Indian population from 1029 whole genomes
Mercy Rophina, Rahul C. Bhoyar, … Vinod Scaria·bioRxiv·Oct 29, 2022
- Analyzing globin gene variation in gnomAD: implications for variant interpretation in hemoglobinopathies
Mikaella Kontopoulou, Maria Xenophontos, … Petros Kountouris·bioRxiv·Sep 19, 2026
- The Polygenic and Monogenic Basis of Blood Traits and Diseases
Dragana Vuckovic, Erik L. Bao, … Εvangelos Εvangelou·CellPeer-reviewed·Sep 1, 2020
- Clustered regularly interspaced short palindromic repeats (CRISPR)-Diagnostics for differential detection of haemoglobin variant S, C, D and E
Patrick Adu, Prabhleen Kaur, … Debojyoti Chakraborty·medRxiv·Aug 26, 2025
- Molecular Screening of Hemoglobin S Variant in Anemia Patients of Eastern UP Population
Vandana Rai, Upendra Yadav, Pradeep Kumar·bioRxiv·Nov 4, 2019