Maria Tzetis

5.7k total citations
115 papers, 2.3k citations indexed

About

Maria Tzetis is a scholar working on Genetics, Molecular Biology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, Maria Tzetis has authored 115 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Genetics, 38 papers in Molecular Biology and 30 papers in Pulmonary and Respiratory Medicine. Recurrent topics in Maria Tzetis's work include Genomic variations and chromosomal abnormalities (25 papers), Cystic Fibrosis Research Advances (22 papers) and Prenatal Screening and Diagnostics (14 papers). Maria Tzetis is often cited by papers focused on Genomic variations and chromosomal abnormalities (25 papers), Cystic Fibrosis Research Advances (22 papers) and Prenatal Screening and Diagnostics (14 papers). Maria Tzetis collaborates with scholars based in Greece, United States and Switzerland. Maria Tzetis's co-authors include Emmanuel Kanavakis, Joanne Traeger‐Synodinos, Sofia Kitsiou‐Tzeli, Christina Vrettou, Stavros Doudounakis, Aspasia Tsezou, Alexandra Efthymiadou, C. Kattamis, Emmanouel Kanavakis and Myrto Poulou and has published in prestigious journals such as SHILAP Revista de lepidopterología, Human Molecular Genetics and Clinical Chemistry.

In The Last Decade

Maria Tzetis

111 papers receiving 2.3k citations

Peers

Maria Tzetis

PRM

GENET

PPCH

GENET

Dongli Song China

Shuan‐Pei Lin Taiwan

Véronique David France

Tetsuya Hirata Japan

Ramazan Demir Türkiye

M. Castellucci Italy

Elizabeth M. Rohlfs United States

Akihiro Yasoda Japan

Allan M. Lund Denmark

M Garabédian France

Dongli Song China

Maria Tzetis

773 ×1.1

414 ×0.7

PRM

117 ×0.3

GENET

417 ×1.0

PPCH

112 ×0.3

GENET

Citations per year, relative to Maria Tzetis Maria Tzetis (= 1×) peers Dongli Song

Countries citing papers authored by Maria Tzetis

Since Specialization

Citations

This map shows the geographic impact of Maria Tzetis'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 Maria Tzetis with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maria Tzetis more than expected).

Fields of papers citing papers by Maria Tzetis

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maria Tzetis. 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 Maria Tzetis. The network helps show where Maria Tzetis may publish in the future.

Co-authorship network of co-authors of Maria Tzetis

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Tzetis. A scholar is included among the top collaborators of Maria Tzetis 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 Maria Tzetis. Maria Tzetis 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

Kosma, Konstantina, Andromachi Mitsioni, Christina Kanaka‐Gantenbein, et al.. (2024). Alport Syndrome: Clinical Utility of Early Genetic Diagnosis in Children. Genes. 15(8). 1016–1016. 2 indexed citations

Tzetis, Maria, Talia Kakourou, Christina Kanaka‐Gantenbein, et al.. (2023). Characteristics of Café-au-lait Macules and their Association with the Neurofibromatosis type I Genotype in a Cohort of Greek Children. Acta Dermato Venereologica. 103. adv5758–adv5758. 5 indexed citations

Kokkali, Georgia, David Iles, John Huntriss, et al.. (2021). The effects of aging on molecular modulators of human embryo implantation. iScience. 24(7). 102751–102751. 8 indexed citations

Ράμπιας, Θεόδωρος, Dimitris Karagiannis, Margaritis Avgeris, et al.. (2019). The lysine‐specific methyltransferase KMT 2C/ MLL 3 regulates DNA repair components in cancer. EMBO Reports. 20(3). 96 indexed citations

Tzetis, Maria, et al.. (2019). Therapeutic Effects of Mesenchymal Stem Cells Derived From Bone Marrow, Umbilical Cord Blood, and Pluripotent Stem Cells in a Mouse Model of Chemically Induced Inflammatory Bowel Disease. Inflammation. 42(5). 1730–1740. 30 indexed citations

Kokkali, Georgia, David Iles, John Huntriss, et al.. (2019). Can trophectoderm RNA analysis predict human blastocyst competency?. Systems Biology in Reproductive Medicine. 65(4). 312–325. 15 indexed citations

Poulou, Myrto, et al.. (2018). Phenotypic expression of a spectrum of Neurofibromatosis Type 1 (NF1) mutations identified through NGS and MLPA. Journal of the Neurological Sciences. 395. 95–105. 29 indexed citations

Destouni, Aspasia, Myrto Poulou, Georgia Kakourou, et al.. (2015). Single-cell high resolution melting analysis: A novel, generic, pre-implantation genetic diagnosis (PGD) method applied to cystic fibrosis (HRMA CF-PGD). Journal of Cystic Fibrosis. 15(2). 163–170. 1 indexed citations

Tzetis, Maria, Marianna Tzanoudaki, George Vassilopoulos, et al.. (2014). Generation of Human β-Thalassemia Induced Pluripotent Cell Lines by Reprogramming of Bone Marrow–Derived Mesenchymal Stromal Cells Using Modified mRNA. Cellular Reprogramming. 16(6). 447–455. 13 indexed citations

10.

Poulou, Myrto, et al.. (2014). Are ALOX5AP gene SNPs a risk or protective factor for stroke?. Gene. 548(1). 56–60. 3 indexed citations

11.

Γιαννίκου, Κρινιώ, Maria Tzetis, George Paterakis, et al.. (2013). Mesenchymal Derivatives of Genetically Unstable Human Embryonic Stem Cells Are Maintained Unstable but Undergo Senescence in Culture As Do Bone Marrow–Derived Mesenchymal Stem Cells. Cellular Reprogramming. 16(1). 1–8. 6 indexed citations

12.

Karamanou, Marianna, et al.. (2011). Anton van Leeuwenhoek (1632-1723): father of micromorphology and discoverer of spermatozoa.. PubMed. 42(4). 311–4. 13 indexed citations

13.

Tsezou, Aspasia, et al.. (2009). Gilbert Syndrome as a Predisposing Factor for Cholelithiasis Risk in the Greek Adult Population. Genetic Testing. 0(0). 3971321277–3971321277. 9 indexed citations

14.

Tsezou, Aspasia, et al.. (2009). Gilbert Syndrome as a Predisposing Factor for Cholelithiasis Risk in the Greek Adult Population. Genetic Testing and Molecular Biomarkers. 13(1). 143–146. 26 indexed citations

15.

Poulou, Myrto, Marios Kaliakatsos, Aspasia Tsezou, et al.. (2008). Association of the CALM1 Core Promoter Polymorphism with Knee Osteoarthritis in Patients of Greek Origin. Genetic Testing. 12(2). 263–265. 19 indexed citations

16.

Tsezou, Aspasia, et al.. (2007). Genetic Polymorphisms in the UGT1A1 Gene and Breast Cancer Risk in Greek Women. Genetic Testing. 11(3). 303–306. 10 indexed citations

17.

Nicolaidou, Polyxeni, et al.. (2006). Steroid hormones polymorphisms and cholelithiasis in Greek population. Liver International. 27(1). 61–68. 5 indexed citations

18.

Kaliakatsos, Marios, Maria Tzetis, Emmanuel Kanavakis, et al.. (2005). Asporin and knee osteoarthritis in patients of Greek origin. Osteoarthritis and Cartilage. 14(6). 609–611. 60 indexed citations

19.

Radivojevic, Danijela, Tanja Lalic, Marija Guć‐Šćekić, et al.. (2004). Spectrum of Cystic Fibrosis Mutations in Serbia and Montenegro and Strategy for Prenatal Diagnosis. Genetic Testing. 8(3). 276–280. 20 indexed citations

20.

Loudianos, Georgios, Mario Lovicu, Paola Solinas, et al.. (2000). Delineation of the Spectrum of Wilson Disease Mutations in the Greek Population and the Identification of Six Novel Mutations. Genetic Testing. 4(4). 399–402. 25 indexed citations

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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