RESEARCH AND DEVELOPMENT
At Medicover Genetics, we continuously strive to discover news ways to develop and improve the diagnostic journey of patients and people undergoing genetic testing. We have a growing R&D team with a strong publication track record in the field of in vitro genetic testing describing our innovative scientific work and cutting-edge technological advances.
We presented our work at several international scientific conferences demonstrating our leadership in the field of genetic testing.
Our work is supported by several research grants awarded to us for the development technologies for our genetic testing products.
● Fountzilas Elena et al. “Investigation of Clinically Significant Molecular Aberrations in Patients with Prostate Cancer: Implications for Personalized Treatment, Prognosis and Genetic Testing.” International Journal of Molecular Sciences vol. 24, 11834. 23 July 2023 Read the full article here
● Abul H. Elahi et al. “Targeted pharmacologic inhibition of S-phase kinase-associated protein 2 (SKP2) mediated cell cycle regulation in lung and other RB-Related cancers: A brief review of current status and future prospects.” Advancements in Biological Regulation vol. 88, 100964. 23 May 2023 Read the full article here
● Li, Y., Dinkel, H., Pakalniskyte, D., Busley, A. V., Cyganek, L., Zhong, R., Zhang, F., Xu, Q., Maywald, L., Aweimer, A., Huang, M., Liao, Z., Meng, Z., Yan, C., Prädel, T., Rose, L., Moscu-Gregor, A., Hohn, A., Yang, Z., Qiao, L., … El-Battrawy, I. “Novel insights in the pathomechanism of Brugada syndrome and fever-related type 1 ECG changes in a preclinical study using human-induced pluripotent stem cell-derived cardiomyocytes.” Clinical and Translational Medicine 13(3), e1130. March 2023 Read the full article here
● Kampmeier A, Leitão E, Parenti I, … , Heinrich U, Rost I, et al. “PHIP-associated Chung-Jansen syndrome: Report of 23 new individuals.” Frontiers in Cell and Developmental Biology vol. 10 1020609. 16 Jan. 2023, doi:10.3389/fcell.2022.1020609 Read the full article here
● Romanidou, Ourania et al. “Molecular profile and clinical features of patients with gliomas using a broad targeted next generation-sequencing panel.” Oncology letters vol. 25,1 38. 8 Dec. 2022 Read the full article here
● Souche E, Beltran S, Brosens E, … Dincer Y, Eck SH, et al. “Recommendations for whole genome sequencing in diagnostics for rare diseases.” European journal of human genetics EJHG vol. 30,9: 1017-1021, Sep. 2022, doi:10.1038/s41431-022-01113-x Read the full article here
● Kypri, Elena, Ioannides, Marios, Achilleos, Achilleas, Koumbaris, George, Patsalis, Philippos and Stumm, Markus. “Non-invasive prenatal screening tests – update 2022” Journal of Laboratory Medicine, vol. 46, no. 4, 2022, pp. 311-320. Read the full article here
● Himmelreich N, Dimitrov B, Zielonka M, Hüllen A, Hoffmann GF, Juenger H, Müller H, Lorenz I, Busse B, Marschall C, Schlüter G, Thiel C. “Missense variant c.1460 T > C (p.L487P) enhances protein degradation of ER mannosyltransferase ALG9 in two new ALG9-CDG patients presenting with West syndrome and review of the literature.” Molecular Genetics and Metabolism vol. 136,4 (2022): 274-281, doi:10.1016/j.ymgme.2022.06.005 Read the full article here
● Weber A, Liehr T, Al-Rikabi A, Bilgen S, Heinrich U, Schiller J, Stumm M. “The First Neocentric, Discontinuous, and Complex Small Supernumerary Marker Chromosome Composed of 7 Euchromatic Blocks Derived from 5 Different Chromosomes.”Biomedicines 10,5 1102. 10 May. 2022, doi:10.3390/biomedicines10051102 Read the full article here
● Kyrochristos, Ioannis D et al. “Proof-of-Concept Pilot Study on Comprehensive Spatiotemporal Intra-Patient Heterogeneity for Colorectal Cancer With Liver Metastasis.” Frontiers in oncology vol. 12 855463. 23 Mar. 2022 doi:10.3389/fonc.2022.855463 Read the full article here
● Westphal DS, Pollmann K, Marschall C, Wacker-Gussmann A, Oberhoffer-Fritz R, Laugwitz KL, Ewert P, Wolf CM. “It Is Not Carved in Stone-The Need for a Genetic Reevaluation of Variants in Pediatric Cardiomyopathies.” Journal of Cardiovascular Development and Disease 9(2):41. 25 Jan. 2022, doi:10.3390/jcdd9020041 Read the full article here
● Wimmer R, Neumann U, Weber A, Isau M, Renner-Luetzkendorf H, Zschieschang P, Wachter O, Hirv K, Stumm M. “Intersexual Twins due to Tetragametic Chimerism.” Cytogenetic and Genome Research vol. 162,7 (2022): 378-385. doi:10.1159/000528737 Read the full article here
● Maier F, Frühwald M, Heinrich U, Schimmel M, Wahl D, Eggermann T. “Overgrowth-associated partial trisomy 15q24.3-qter and mosaic 11p15.5 duplication involving Silver-Russell region in a patient with lateralized asymmetry and developmental delay.” Clinical Dysmorphology vol. 30,4: 189-193, 01 Oct. 2021, doi:10.1097/MCD.0000000000000378 Read the full article here
● Mentzel J, Wetzig T, Rütten A, Hörtnagel K, Tischkowitz M, Ziemer M. “Sweat duct proliferation associated with aggregation of elastic tissue and atrophodermia vermiculata: a simulator of microcystic adnexal carcinoma – a family with MALTA-syndrome.” Journal der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG vol. 19,7 (2021): 1052-1056, doi:10.1111/ddg.14416 Read the full article here
● Neuser S, Brechmann B, Heimer G, Brösse I, Schubert S, O’Grady L, Zech M, Srivastava S, Sweetser DA, Dincer Y, et al. “Clinical, neuroimaging, and molecular spectrum of TECPR2-associated hereditary sensory and autonomic neuropathy with intellectual disability.” Human Mutation vol. 42,6 (2021): 762-776. doi:10.1002/humu.24206 Read the full article here
● Chrysostomou, Andreas C et al. “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.” Viruses vol. 13,6 1098. 9 Jun. 2021, doi:10.3390/v13061098 Read the full article here
● Zech M, Boesch S, Škorvánek M, Necpál J, Švantnerová J, Wagner M, Dincer Y, et al. “Clinically relevant copy-number variants in exome sequencing data of patients with dystonia.” Parkinsonism & Related Disorders vol. 84 (2021): 129-134. doi:10.1016/j.parkreldis.2021.02.013 Read the full article here
● Fountzilas, Elena et al. “Clinical Significance of Germline Cancer Predisposing Variants in Unselected Patients with Pancreatic Adenocarcinoma.” Cancers vol. 13,2 198. 8 Jan. 2021, doi:10.3390/cancers13020198 Read the full article here
● Ioannides, Marios et al. “Development of a new methylation-based fetal fraction estimation assay using multiplex ddPCR.” Molecular genetics & genomic medicine vol. 8,2 (2020): e1094. doi:10.1002/mgg3.1094 Read the full article here
● Koumbaris, George et al. “Targeted capture enrichment followed by NGS: development and validation of a single comprehensive NIPT for chromosomal aneuploidies, microdeletion syndromes and monogenic diseases.” Molecular cytogenetics vol. 12 48. 21 Nov. 2019, doi:10.1186/s13039-019-0459-8 Read the full article here
● Kypri, Elena et al. “Non-invasive prenatal testing of fetal chromosomal aneuploidies: validation and clinical performance of the veracity test.” Molecular cytogenetics vol. 12 34. 15 Jul. 2019, doi:10.1186/s13039-019-0446-0 Read the full article here
● Keravnou, Anna et al. “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.” PloS one vol. 13,6 e0199010. 11 Jun. 2018, doi:10.1371/journal.pone.0199010 Read the full article here
● Neofytou, Maria C et al. “Targeted capture enrichment assay for non-invasive prenatal testing of large and small size sub-chromosomal deletions and duplications.” PloS one vol. 12,2 e0171319. 3 Feb. 2017, doi:10.1371/journal.pone.0171319 Read the full article here
● Keravnou, Anna et al. “Whole-genome fetal and maternal DNA methylation analysis using MeDIP-NGS for the identification of differentially methylated regions.” Genetics research vol. 98 e15. 11 Nov. 2016, doi:10.1017/S0016672316000136 Read the full article here
● Koumbaris, George et al. “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.” Clinical chemistry vol. 62,6 (2016): 848-55. doi:10.1373/clinchem.2015.252502 Read the full article here
● Ioannides, Marios et al. “Inter-individual methylation variability in differentially methylated regions between maternal whole blood and first trimester CVS.” Molecular cytogenetics vol. 7,1 73. 1 Nov. 2014, doi:10.1186/s13039-014-0073-8 Read the full article here
● Papageorgiou, Elisavet A et al. “The Epigenome View: An Effort towards Non-Invasive Prenatal Diagnosis.” Genes vol. 5,2 310-29. 9 Apr. 2014, doi:10.3390/genes5020310 Read the full article here
● Antoniou, Pavlos et al. “Identifying differentially methylated regions by efficient bit-masking of DNA microarrays to use as markers for non invasive prenatal diagnosis.” Engineering Intelligent Systems. 22. 109-117. 2014. Read the full article here
● Kyriakou, Skevi et al. “Variability of ffDNA in maternal plasma does not prevent correct classification of trisomy 21 using MeDIP-qPCR methodology.” Prenatal diagnosis vol. 33,7 (2013): 650-5. doi:10.1002/pd.4140 Read the full article here
● Papageorgiou, Elisavet A et al. “Author’s response regarding “MeDIP-qPCR approach for non-invasive prenatal diagnosis of Down syndrome: accuracy and reproducibility”.” Prenatal diagnosis vol. 33,4 (2013): 404-5. doi:10.1002/pd.4048 Read the full article here
● Papageorgiou, Elisavet A, and Patsalis, Philippos C. “Maternal plasma sequencing: a powerful tool towards fetal whole genome recovery.” BMC medicine vol. 11 56. 27 Feb. 2013, doi:10.1186/1741-7015-11-56 Read the full article here
● Patsalis, Philippos C. “Reply to: Technical concerns about immunoprecipitation of methylated fetal DNA for noninvasive trisomy 21 diagnosis”. Nat Med 18, 1328–1329 (2012). https://doi.org/10.1038/nm.2914 Read the full article here
● Patsalis, Philippos C and Papageorgiou, Elisavet A. “Non-Invasive Prenatal Diagnosis (NIPD) of Down Syndrome using real time qPCR.” ECA Newsletter, July 2012.
● Velissariou, Voula and Patsalis, Philippos C. “The Future of Prenatal Diagnosis of Genetic Diseases of the Embryo: Non-Invasive Prenatal Diagnosis in free DNA of the Pregnant Woman.” Medical Analects, July-September 15:713-717, 2012.
● Patsalis, Philippos C. “A new method for non-invasive prenatal diagnosis of Down syndrome using MeDIP real time qPCR.” Applied & translational genomics vol. 1 3-8. 26 May. 2012, doi:10.1016/j.atg.2012.04.001 Read the full article here
● Tsaliki, Evdokia et al. “MeDIP real-time qPCR of maternal peripheral blood reliably identifies trisomy 21.” Prenatal diagnosis vol. 32,10 (2012): 996-1001. doi:10.1002/pd.3947 Read the full article here
● Papageorgiou, Elisavet A, and Philippos C Patsalis. “Non-invasive prenatal diagnosis of aneuploidies: new technologies and clinical applications.” Genome medicine vol. 4,5 46. 28 May. 2012, doi:10.1186/gm345 Read the full article here
● Patsalis, Philippos C et al. “A new non-invasive prenatal diagnosis of Down syndrome through epigenetic markers and real-time qPCR.” Expert opinion on biological therapy vol. 12 Suppl 1 (2012): S155-61. doi:10.1517/14712598.2012.674108 Read the full article here
● Koumbaris, George et al. “FoSTeS, MMBIR and NAHR at the human proximal Xp region and the mechanisms of human Xq isochromosome formation.” Human molecular genetics vol. 20,10 (2011): 1925-36. doi:10.1093/hmg/ddr074 Read the full article here
● Papageorgiou, Elisavet A et al. “Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21.” Nature medicine vol. 17,4 (2011): 510-3. doi:10.1038/nm.2312 Read the full article here
● Development of a novel, Preimplantation Genetic Testing (PGT) Kit. Competitive grant by Research Promotion Foundation, Cyprus.
● Accelerating the commercialization of non-invasive tests for liquid biopsy of solid tumor cancers (LIQ-BIOPSY). Competitive grant by Research Promotion Foundation, Cyprus.
● Proof of Concept study for ERC NIPD discovered biomarkers (mR-NIPD). Competitive grant by European Research Council (ERC) Proof of Concept Grant, European Union.
● A novel non-invasive prenatal diagnosis of genetic disorders (NIPD). Competitive grant by European Research Council (ERC) Advanced Investigator Grant, European Union.
● A new genetic laboratory for non-invasive prenatal diagnosis (ANGELAB). Competitive grant by 7th Framework Programme (ICT), European Union.
● Development and validation of a non-invasive prenatal diagnostic (NIPD) kit for aneuploidy detection (NIPD-KIT). Competitive grant by Eurostars Program, European Union and Cyprus Research Promotion Foundation.
● Development of an innovative non-invasive prenatal diagnostic test (NIPD21). Competitive grant by Ministry of Energy, Commerce, Industry and Tourism, Cyprus.
● Using fetal specific methylated markers for the development of non-invasive prenatal diagnosis for Down Syndrome. Competitive grant by Research Promotion Foundation (RPF) Young Researcher Award, Cyprus.
● Methods and compositions for non-invasive prenatal diagnosis of fetal aneuploidies. Competitive grant by Research Promotion Foundation Innovation, Cyprus.
● New Minimal Residual Disease Detection Liquid Biopsy Test (NeoMRD). Competitive grant by Research and Innovation Foundation, Cyprus (2022-2024).
● Development of Non-Invasive Prenatal Testing (NIPT) for Fetal Whole Competitive grant by Research and Innovation Foundation, Cyprus (2021-2023).
● Proof of Concept study for the development of methylation based NIPT for trisomy 21 using droplet digital PCR Competitive grant by European Research Council (ERC) Proof of Concept, European Union (2021-2022).
● “Medicover Healthcare”, 1st Hospital Services Conference, Medicover, 14-15 October 2022, Torun, Poland.
● “A new generation genetic testing technology platform for NIPT, Liquid biopsy and beyond”, Genetics 2022. Developments and applications in Medicine, 21st May 2022, Athens, Greece.
● “Vision for Life Sciences and Biotechnology for a Healthy and Sustainable EU”, The 2nd Hellenic Biocluster Forum, 4 – 5 November 2021, Athens, Greece.
● “Prenatal Testing: More, Better, Safe, Effective, For All”, 19th Annual Laboratory Management and Medicine Congress, 3-6 February 2020, Dubai, United Arab Emirates.
● “New Advancements in NIPT for Prenatal Screening of Genetic Diseases”, 2nd Arab Association of Genetic Research Conference, 26-27 November 2019, Cairo, Egypt.
● “A new generation technology for genetic testing in preconception, prenatal, postnatal and oncology”, The 1st Congress on Women’s Health Innovations & Inventions, 9 – 11 July 2019, Tel Aviv, Israel.
● “A single comprehensive NIPT for aneuploidies, microdeletions and point mutations”, 3rd Symposium on Clinical Genetics & Genomics & 19th Educational Seminar in Genetics, 31 May-1 June 2019, Athens, Greece.
● “New Advancements in NIPT for prenatal screening of genetic diseases”, The 10th International Symposium on Diabetes, Hypertension, Metabolic Syndrome and Pregnancy, 29 May – 1 June 2019, Florence, Italy.
● “New Generation Non-Invasive Genetic Testing for the Detection of Chromosomal Syndromes, Microdetion and Single Gene Diseases”, 4th Scientific Conference: “Prenatal Diagnosis and Treatment of Fetus”, 18 May 2019, Athens, Greece.
● “Clinical utility of tissue and plasma DNA profiling of solid tumor cancer patients”, 2nd Conference “Genetic Innovations in 2019”, 7 February 2019, Kaunas, Lithuania.
● “Liquid Biobsy”, Annual Conference of ISMPO (India Society of Medical & Paediatric Oncology) – ISMPOCON JAIPUR 2018, 16-18 November 2018.
● ’Genomics’, The omics & maternal-fetal – neonatal medicine from top research to the bed side; can we predict pregnancy complications? XXVI European Congress of the European Association of Perinatal Medicine, 5-8 September 2018, St. Petersburg, Russia.
● “cfDNA: Single gene disorders”, 17th World Congress in Fetal Medicine, 24-28 June 2018, Athens, Greece.
● “NIPT Beyond Aneuploidies”, Corporate Satellite Session during ESHG 2018 Conference, 17 June 2018, Milan, Italy.
● “The Genome”. The 9th International Symposium on Diabetes, Hypertention, Metabolic Syndrome and Pregnancy, DIPAP2017, Barchelona, Spain, 8 March 2017, Invited Lecturer.
● “Genetics, Material Fetal Medicine and the Great Obstretrical Syndromes”. The 9th International Symposium on Diabetes, Hypertention, Metabolic Syndrome and Pregnancy, DIPAP2017, Barchelona, Spain, 8 March 2017.
● “A New Generation Non-invasive Prenatal Test for Genetics Disorders”. The First International Personalized Medicine Congress. Tehran, Iran. February 24-27, 2017.
● “Circulating Tumour DNA as a Non-invasive Biomarker in Cancer”. Genetics in Oncology, University of Kaunas, Kaunas, Lithuania. February 1-3, 2017.
● “Non Invasive Prenatal Testing of Genetic Disorders”. The 1st Asia-Pacific Symposium on Diabetes, Hypertention, Metabolic Syndrome and Pregnancy, DIPAP2016, Colombo, Sri Lanka, 8-10 September 2016.
● “Genetics Meets Fetal and Perinatal Medicine”. The 1st Asia-Pacific Symposium on Diabetes, Hypertention, Metabolic Syndrome and Pregnancy, DIPAP2016, Colombo, Sri Lanka, 8-10 September 2016.
● “Non Invasive Prenatal Diagnosis of Chromosomal Disorders”. 2nd International Conference of the Hellenic Society of Human Genetics, Athens, Greece. 4-6 November 2016, Invited Lecturer.
● “Non Invasive Prenatal Diagnosis of Genomic Disorders”. 5th International Conference of the Cyprus Society of Human Genetics, Nicosia, Cyprus. 14-15 October 2016.
● “When IVF meets NIPT: Another challenge to look at…”. Annual Meeting of the National Society of Obstetric and Gynegology, Tel Aviv, Israel. 8 March 2016.
● “Multiplex Parallel Analysis of Targeted Genomic Regions for NIPT”. Molecular Diagnostic Europe, Lisbon, Portugal. 4-7 April 2016.
● “New Generation Non-Invasive Prenatal Diagnosis with competitive advandages”, Eurogenetics Center, Thessaloniki, Greece, 25 April, 2016.
● “NIPT: Present and Future”, Two Forum – EXPO Athens, Athens, Greece.
● “Non-Invasive Prenatal Diagnosis using cffDNA”, Biomedical Center, Thessaloniki, Greece, 26 April, 2016.
● “Non-Invasive Prenatal Diagnosis using cffDNA”, University of Ioannina, Greece, 29 June, 2016.
● “Non-Invasive Prenatal Diagnosis of aneuploidies”, Biomedical Center, Athens, Greece,15 June, 2016.
● “The Veracity Test. Advances in Fetal Medicine Course. London, UK, 5-7 December 2015.
● “Development and Validation of the Veracity Non Invasive Prenatal Test., Advances in Prenatal Diagnosis. 16-19 November 2015. Boston, USA.
● “Development and Validation of the Veracity: a non-invasive prenatal test”, Vilnious University, Lithuania, 7 November, 2015.
●“Barriers and Drivers for the Implementation of Clinical Sequencing: An International Discussion Symposium”, American Society of Human Genetics Meeting, 6-10 October, 2015, Baltimore, USA. Invited Lecturer, Plenary Lecture.
● “Development and Validation of the Veracity: a newly highly accurate and cost effective non-invasive prenatal test”, Advance course in Ultrasound and Fetal Medicine, 2-4 October 2015, Belfast, UK.
● “Development and Validation of the Veracity: a non-invasive prenatal test”, Pan-Hellenic Perinatal Conference, 15-18 October 2015, Athens, Greece.
● “DNA-based Non Invasive Prenatal Diagnosis for Down Syndrome”, World Medical Summit, 7-9 July 2015, Macau, China.
● “Non Invasive Prenatal Diagnosis”, Lithuenian Academy of Science, Vilnious, Lithuenia, 16 December 2014.
● “Non Invasive Prenatal Diagnosis of Genetic Diseases”. Femmes d’ Europe, Brussels, Belgium, 16 October 2013.
● “Non Invasive Prenatal Diagnosis of Genetic Disorders”. BrainTrain EU Conference, Riken Institute, Yokahama, Japan, 19 September 2013.
● “Development of a New Non-Invasive Prenatal Diagnostic Method using Peripheral Maternal Blood Sample”. 1st Conference of the Society of Medical Geneticists, 30 May to 1 June 2013, Greece, Athens.
● “Non-Invasive Prenatal Diagnosis: From inception of the idea to the development of the product”. University of Ioannina School of Medicine, Ioannina, Greece.
● “Non Invasive prenatal diagnosis”. 11th World Congress in Fetal Medicine, 24-28 June 2012, Kos, Greece.
● “Further development and larger validation of non-invasive prenatal diagnosis for trisomy 21 using MeDIP real time qPCR”. European Society of Human Genetics 2012, 23-26 June 2012, Nurnberg, Germany.
● “Non-Invasive Prenatal Diagnosis for Trisomy 21 using MeDIP real time qPCR”. 4th Slovene Medical Genetics Symposium – New technologies and approaches in medical genetic diagnostics, 6 April 2012, Ljubljana, Slovenia.
● “Prenatal Diagnosis of Genetic Disorders: From Invasive to Non Invasive Prenatal Diagnosis”. International Down Syndrome Day, Hadassah Hospital, 22 March 2012, Jerusalem, Israel.
●“Development and Commercial Exploitation of Non-Invasive Prenatal Diagnosis”. Advanced Technologies in Medicine, Conference in Innovation, University of Crete, 25 – 26 February 2012, Greece, Cyprus.
● “Non-Invasive Prenatal Diagnosis of Down Syndrome”. 14th Conference of the Italian Society of Human Genetics (XIV SIGU), 13-16 Nov 2011, Milan, Italy.
● “Non-Invasive Prenatal Diagnosis of Down Syndrome”. 7th International Conference on Circulating Nucleic Acids in Plasma and Serum (CNAPS VII), 24-25 Oct 2011, Madrid, Spain.
● “Fetal-specific DNA methylation ratio permits non-invasive prenatal diagnosis of trisomy 21”. Cold Spring Harbor Laboratory: Personal Genomes, 30 Sept – 2 Oct 2011, New York, USA.
● “From invasive to non-invasive prenatal diagnosis”. The 5th International Conference on Birth Defects and Disabilities in the Developing World, 24-27 September 2011, Lodz, Poland.
● “Non-Invasive Prenatal Diagnosis of Down Syndrome”, Isida Clinic, 16 Sept 2011, Kiev, Ukraine.
● “Development and Validation of Non-Invasive Prenatal Diagnosis for Trisomy 21”. 8th European Cytogenetics Conference, European Cytogenetic Association, 2-5 July, 2011, Porto, Portugal.
● “Diagnosis of Aneuploides: Epigenetic Approach – Fetal-Specific DNA Methylation Ration Permits Non-Invasive Prenatal Diagnosis of Trisomy 21”. 10th Fetal Medicine World Congress, 26-30 June 2011, Malta.
● “Development and Validation of Non-Invasive Prenatal Diagnosis of Trisomy 21”. European Genetics Conference, European Society of Human Genetics, 28-31 May, 2011, Amsterdam, Netherlands.
● “Non-Invasive Prenatal Diagnosis of Down Syndrome”. University of Ioannina Medical School, 23 May, 2011, Ioannina, Greece.
● “Non-Invasive Prenatal Diagnosis of Down Syndrome”. Annual Conference of UK Clinical Molecular Genetics Society and UK Association of Clinical Cytogenetics, 4-8 April, 2011, Durham, UK.
● “Non-Invasive Prenatal Diagnosis of Down Syndrome”. MHTERA Hospital, 2-4 December 2010, Athens, Greece.