Marios Ioannides

756 total citations
25 papers, 443 citations indexed

About

Marios Ioannides is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Marios Ioannides has authored 25 papers receiving a total of 443 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 14 papers in Genetics and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Marios Ioannides's work include Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (11 papers) and Fetal and Pediatric Neurological Disorders (7 papers). Marios Ioannides is often cited by papers focused on Prenatal Screening and Diagnostics (12 papers), Genomic variations and chromosomal abnormalities (11 papers) and Fetal and Pediatric Neurological Disorders (7 papers). Marios Ioannides collaborates with scholars based in Cyprus, Greece and Belgium. Marios Ioannides's co-authors include Philippos C. Patsalis, Carolina Sismani, George Koumbaris, Pavlos Antoniou, Michael D. Hadjidaniel, Christodoulos Christodoulou, Chrysanthia A. Leontiou, Achilleas Achilleos, Voula Velissariou and Kyriakos Tsangaras and has published in prestigious journals such as PLoS ONE, Human Molecular Genetics and Clinical Chemistry.

In The Last Decade

Marios Ioannides

24 papers receiving 428 citations

Peers

Countries citing papers authored by Marios Ioannides

Since Specialization

Citations

This map shows the geographic impact of Marios Ioannides's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Marios Ioannides with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Marios Ioannides more than expected).

Fields of papers citing papers by Marios Ioannides

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Marios Ioannides. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Marios Ioannides. The network helps show where Marios Ioannides may publish in the future.

Co-authorship network of co-authors of Marios Ioannides

This figure shows the co-authorship network connecting the top 25 collaborators of Marios Ioannides. A scholar is included among the top collaborators of Marios Ioannides based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Marios Ioannides. Marios Ioannides is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Comparison of targeted next generation sequencing assays in non-small cell lung cancer patients 2024 ·Discover Oncology ·(unknown), (unknown), Saulius Cicėnas, (unknown), Alexia Eliades, Achilleas Achilleos, (unknown), Kyriakos Tsangaras, Marios Ioannides, George Koumbaris, (unknown), (unknown), Philippos C. Patsalis	0
2	Investigating TNNC1 gene inheritance and clinical outcomes through a comprehensive familial study 2024 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Carolina Sismani, (unknown), Marios Ioannides, George Koumbaris	1
3	Proof-of-Concept Pilot Study on Comprehensive Spatiotemporal Intra-Patient Heterogeneity for Colorectal Cancer With Liver Metastasis 2022 ·Frontiers in Oncology ·(unknown), Georgios K. Glantzounis, Anna Goussia, Alexia Eliades, Achilleas Achilleos, Kyriakos Tsangaras, Irene Hadjidemetriou, (unknown), Marios Ioannides, George Koumbaris, Michail Mitsis, Philippos C. Patsalis, Dimitrios H Roukos	2
4	A Comprehensive Molecular Epidemiological Analysis of SARS-CoV-2 Infection in Cyprus from April 2020 to January 2021: Evidence of a Highly Polyphyletic and Evolving Epidemic 2021 ·Viruses ·(unknown), Bram Vrancken, George Koumbaris, (unknown), (unknown), (unknown), (unknown), (unknown), Dora C. Stylianou, Marios Ioannides, (unknown), (unknown), (unknown), Philippe Lemey, Anne–Mieke Vandamme, (unknown), Leondios G. Kostrikis	12
5	Development of a new methylation‐based fetal fraction estimation assay using multiplex ddPCR 2019 ·Molecular Genetics & Genomic Medicine ·Marios Ioannides, Achilleas Achilleos, (unknown), (unknown), (unknown), Kyriakos Tsangaras, (unknown), George Koumbaris, Philippos C. Patsalis	13
6	Targeted capture enrichment followed by NGS: development and validation of a single comprehensive NIPT for chromosomal aneuploidies, microdeletion syndromes and monogenic diseases 2019 ·Molecular Cytogenetics ·George Koumbaris, Achilleas Achilleos, (unknown), (unknown), Kyriakos Tsangaras, (unknown), (unknown), Carolina Sismani, Voula Velissariou, Georgia Christopoulou, Pantelis Constantoulakis, Emmanouil Manolakos, Ioannis Papoulidis, (unknown), Marios Ioannides, Philippos C. Patsalis	20
7	Non-invasive prenatal testing of fetal chromosomal aneuploidies: validation and clinical performance of the veracity test 2019 ·Molecular Cytogenetics ·(unknown), Marios Ioannides, (unknown), (unknown), (unknown), Voula Velissariou, (unknown), Alfredo Santana, (unknown), Kyriakos Tsangaras, Achilleas Achilleos, Philippos C. Patsalis, George Koumbaris	9
8	MeDIP combined with in-solution targeted enrichment followed by NGS: Inter-individual methylation variability of fetal-specific biomarkers and their implementation in a proof of concept study for NIPT 2018 ·PLoS ONE ·(unknown), Marios Ioannides, (unknown), Kyriakos Tsangaras, Achilleas Achilleos, (unknown), (unknown), Michael D. Hadjidaniel, (unknown), (unknown), Carolina Sismani, George Koumbaris, Philippos C. Patsalis	9
9	Targeted capture enrichment assay for non-invasive prenatal testing of large and small size sub-chromosomal deletions and duplications 2017 ·PLoS ONE ·(unknown), Kyriakos Tsangaras, (unknown), (unknown), Marios Ioannides, Achilleas Achilleos, (unknown), (unknown), Carolina Sismani, George Koumbaris, Philippos C. Patsalis	31
10	Whole-genome fetal and maternal DNA methylation analysis using MeDIP-NGS for the identification of differentially methylated regions 2016 ·Genetics Research ·(unknown), Marios Ioannides, Kyriakos Tsangaras, (unknown), Michael D. Hadjidaniel, Elisavet A. Papageorgiou, (unknown), Pavlos Antoniou, (unknown), Achilleas Achilleos, (unknown), (unknown), Carolina Sismani, George Koumbaris, Philippos C. Patsalis	11
11	Cell-Free DNA Analysis of Targeted Genomic Regions in Maternal Plasma for Non-Invasive Prenatal Testing of Trisomy 21, Trisomy 18, Trisomy 13, and Fetal Sex 2016 ·Clinical Chemistry ·George Koumbaris, (unknown), Kyriakos Tsangaras, Achilleas Achilleos, (unknown), (unknown), Voula Velissariou, Georgia Christopoulou, (unknown), (unknown), (unknown), Anna Latos‐Bieleńska, Marek Pietryga, Alfredo Santana, Nikoletta Nagy, Márta Széll, Piotr Laudański, Elisavet A. Papageorgiou, Marios Ioannides, Philippos C. Patsalis	41
12	Bisulfite Conversion of DNA: Performance Comparison of Different Kits and Methylation Quantitation of Epigenetic Biomarkers that Have the Potential to Be Used in Non-Invasive Prenatal Testing 2015 ·PLoS ONE ·Chrysanthia A. Leontiou, Michael D. Hadjidaniel, (unknown), Pavlos Antoniou, Marios Ioannides, Philippos C. Patsalis	63
13	Inter-individual methylation variability in differentially methylated regions between maternal whole blood and first trimester CVS 2014 ·Molecular Cytogenetics ·Marios Ioannides, Elisavet A. Papageorgiou, (unknown), Evdokia Tsaliki, Christiana Spyrou, Michael D. Hadjidaniel, Carolina Sismani, George Koumbaris, Philippos C. Patsalis	11
14	Duplication of exons 3–10 of the HSD17B3 gene: A novel type of genetic defect underlying 17β-HSD-3 deficiency 2012 ·Gene ·Vassos Neocleous, Carolina Sismani, Christos Shammas, Elisavet Efstathiou, (unknown), Marios Ioannides, (unknown), Philippos C. Patsalis, Leonidas A. Phylactou, Nicos Skordis	12
15	21 Mb deletion in chromosome band 13q22.2q32.1 associated with mild/moderate psychomotor retardation, growth hormone insufficiency, short neck, micrognathia, hypotonia, dysplastic ears and other dysmorphic features 2011 ·European Journal of Medical Genetics ·(unknown), Elena Panayiotou, Carolina Sismani, George Koumbaris, Marios Ioannides, Christos Costalos, (unknown), (unknown), Philippos C. Patsalis	2
16	Phenotype–genotype correlation of a patient with a “balanced” translocation 9;15 and cryptic 9q34 duplication and 15q21q25 deletion 2010 ·American Journal of Medical Genetics Part A ·(unknown), Carolina Sismani, Christodoulos Christodoulou, Marios Ioannides, Maria Kalmanti, Philippos C. Patsalis	11
17	Clinical application of whole-genome array CGH during prenatal diagnosis: Study of 25 selected pregnancies with abnormal ultrasound findings or apparently balanced structural aberrations 2010 ·Molecular Cytogenetics ·(unknown), Carolina Sismani, Marios Ioannides, Christodoulos Christodoulou, George Koumbaris, (unknown), Ioannis Georgiou, Voula Velissariou, Philippos C. Patsalis	37
18	Cryptic genomic imbalances in patients with de novo or familial apparently balanced translocations and abnormal phenotype 2008 ·Molecular Cytogenetics ·Carolina Sismani, Sofia Kitsiou‐Tzeli, Marios Ioannides, Christodoulos Christodoulou, Violetta Anastasiadou, (unknown), (unknown), (unknown), (unknown), Philippos C. Patsalis	53
19	Distal del(4) (q33) syndrome: Detailed clinical presentation and molecular description with array-CGH 2007 ·European Journal of Medical Genetics ·Sofia Kitsiou‐Tzeli, Carolina Sismani, George Koumbaris, Marios Ioannides, Emmanuel Kanavakis, A Kolialexi, Ariadni Mavrou, (unknown), Philippos C. Patsalis	14
20	Array-CGH analysis and clinical description of 2q37.3 de novo subtelomeric deletion 2006 ·European Journal of Medical Genetics ·Sofia Kitsiou‐Tzeli, Carolina Sismani, Marios Ioannides, Stavros Bashiardes, (unknown), (unknown), Aggeliki Kοlialexi, Ariadni Mavrou, (unknown), Philippos C. Patsalis	18

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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