Author

Maria Xenophontos

Observed names: M Xenophontos, Xenophontos Maria, Xenophontos, Maria

Institution: Cyprus Institute of Neurology and Genetics

Observed institutions: European Bioinformatics Institute, Wellcome/MRC Cambridge Stem Cell Institute, University of Cambridge, Wellcome Centre for Cell Biology, The Cyprus Institute of Neurology & Genetics - Postgraduate Education, Cyprus Institute of Neurology and Genetics, Wellcome Trust, University of Edinburgh

ORCID: 0000-0001-5978-0193

Observed ORCID: 0000-0001-5978-0193

OpenAlex ID: A5013935648

The Nucleosome Remodeling and Deacetylation Complex Modulates Chromatin Structure at Sites of Active Transcription to Fine-Tune Gene Expression

2018 · Susanne Bornelöv, Nicola Reynolds, et al. · Molecular Cell · 185

Immortality, but not oncogenic transformation, of primary human cells leads to epigenetic reprogramming of DNA methylation and gene expression

2013 · Katrina Gordon, Thomas Clouaire, et al. · Nucleic Acids Research · 43

Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2, and HBB associated with haemoglobinopathies

2022 · Stella Tamana, Maria Xenophontos, et al. · eLife · 15

A Novel Tool for the Analysis and Detection of Copy Number Variants Associated with Haemoglobinopathies

2022 · Anna Minaidou, Stella Tamana, et al. · International Journal of Molecular Sciences · 7

IthaPhen: An Interactive Database of Genotype-Phenotype Data for Hemoglobinopathies

2023 · Maria Xenophontos, Anna Minaidou, et al. · HemaSphere · 6

Pilot of the International Hemoglobinopathy Research Network for a multiethnic genome-wide association study

2026 · Petros Kountouris, Coralea Stephanou, et al. · Blood Global Hematology · 2

P128: Ithanet: an Information and Database Community Portal for Haemoglobinopathies

2022 · A Minaidou, C Stephanou, et al. · HemaSphere · 2

The ITHANET-Human Variome Project: Moving Functional Annotation Forward

2019 · Petros Kountouris, Coralea Stephanou, et al. · Hemoglobin · 2

Author response: Evaluation of in silico predictors on short nucleotide variants in HBA1, HBA2, and HBB associated with haemoglobinopathies

2022 · Stella Tamana, Maria Xenophontos, et al. · 1

The Nucleosome Remodelling and Deacetylation complex restricts Mediator access to enhancers to control transcription

2017 · Maria Xenophontos, Nicola Reynolds, et al. · bioRxiv (Cold Spring Harbor Laboratory) · 1

Large-scale modelling of β-thalassaemia carrier prevalence: geostatistical predictions and population estimates from a global evidence base

2026 · Mikaella Kontopoulou, Chigozie Edson Utazi, et al. · medRxiv

Analyzing globin gene variation in gnomAD: implications for variant interpretation in hemoglobinopathies

2026 · Kontopoulou Mikaella, Xenophontos Maria, et al. · bioRxiv (Cold Spring Harbor Laboratory)

A FAIR layer for the INHERENT haemoglobinopathy patient registry

2026 · Stella Tamana, Christina Yiangou, et al. · medRxiv

The JARDIN Hackathon to Seek Solutions to Overcome Technical Barriers in Health Data Exchange: From the Point of Care to European Registry Networks

2026 · César Bernabé, Daphne Wijnbergen, et al. · Data Science Journal

Analysis of the pilot study of the International Hemoglobinopathy Research Network (INHERENT)

2025 · Kountouris, Petros, Stephanou, Coralea, et al. · Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT)

Analysis of the Pilot Study of the International Hemoglobinopathy Research Network (INHERENT)

2024 · Natasha Archer, Coralea Stephanou, et al. · Blood

Educating the whole person : the case of a private university in Cyprus

2019 · Maria Xenophontos

Works count: 17

Citation count: 264

H-index: 5

I10-index: 3