Anthi Drousiotou

1.6k total citations
47 papers, 1.1k citations indexed

About

Anthi Drousiotou is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Anthi Drousiotou has authored 47 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 29 papers in Molecular Biology, 14 papers in Clinical Biochemistry and 14 papers in Physiology. Recurrent topics in Anthi Drousiotou's work include Metabolism and Genetic Disorders (14 papers), Mitochondrial Function and Pathology (13 papers) and Lysosomal Storage Disorders Research (13 papers). Anthi Drousiotou is often cited by papers focused on Metabolism and Genetic Disorders (14 papers), Mitochondrial Function and Pathology (13 papers) and Lysosomal Storage Disorders Research (13 papers). Anthi Drousiotou collaborates with scholars based in Cyprus, United States and United Kingdom. Anthi Drousiotou's co-authors include Sarah A. Tishkoff, Jacques Loiselet, Giovanni Destro‐Bisol, Marie‐Paule Lefranc, George Argyropoulos, Salem Abbès, Andrew G. Clark, Anna Piro, Mark Stoneking and Scott M. Williams and has published in prestigious journals such as Science, SHILAP Revista de lepidopterología and Journal of Cell Science.

In The Last Decade

Anthi Drousiotou

44 papers receiving 1.1k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Anthi Drousiotou Cyprus 14 465 368 188 159 150 47 1.1k
Laurie D. Smith United States 19 467 1.0× 482 1.3× 186 1.0× 28 0.2× 136 0.9× 40 1.1k
Nobuaki Wakamatsu Japan 19 562 1.2× 240 0.7× 138 0.7× 39 0.2× 78 0.5× 59 1.2k
Ronald G. Davidson Canada 20 639 1.4× 446 1.2× 324 1.7× 75 0.5× 150 1.0× 59 1.4k
Feige Kaplan Canada 24 588 1.3× 266 0.7× 367 2.0× 37 0.2× 78 0.5× 57 1.3k
Maria Luisa Tenchini Italy 24 555 1.2× 198 0.5× 209 1.1× 138 0.9× 55 0.4× 74 1.6k
Sebastian Eck Germany 12 366 0.8× 448 1.2× 59 0.3× 70 0.4× 40 0.3× 23 1.0k
Mutsumi Inaba Japan 18 381 0.8× 123 0.3× 431 2.3× 73 0.5× 96 0.6× 71 968
Yulan Lu China 19 527 1.1× 314 0.9× 37 0.2× 55 0.3× 120 0.8× 83 1.2k
Eija H. Seppälä Finland 17 436 0.9× 417 1.1× 94 0.5× 25 0.2× 47 0.3× 34 1.1k
Kyriacos Markianos United States 17 546 1.2× 219 0.6× 74 0.4× 445 2.8× 37 0.2× 35 1.6k

Countries citing papers authored by Anthi Drousiotou

Since Specialization
Citations

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

Fields of papers citing papers by Anthi Drousiotou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anthi Drousiotou

This figure shows the co-authorship network connecting the top 25 collaborators of Anthi Drousiotou. A scholar is included among the top collaborators of Anthi Drousiotou 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 Anthi Drousiotou. Anthi Drousiotou is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Grafakou, Olga, Theodoros Georgiou, Jana Křížová, et al.. (2025). YME1L1 Dysfunction Associated With 3‐Methylglutaconic Aciduria. Journal of Inherited Metabolic Disease. 48(3). e70029–e70029.
2.
Tomazou, Marios, Theodoros Georgiou, Carolina Sismani, et al.. (2024). A novel large intragenic DPYD deletion causing dihydropyrimidine dehydrogenase deficiency: a case report. BMC Medical Genomics. 17(1). 78–78. 2 indexed citations
3.
Georgiou, Theodoros, Petros Petrou, Nicos Skordis, et al.. (2024). Inherited metabolic disorders in Cyprus. Molecular Genetics and Metabolism Reports. 39. 101083–101083.
4.
Theodosiou, Athina, Carolina Sismani, Edwin H. Jacobs, et al.. (2023). GAA variants associated with reduced enzymatic activity but lack of Pompe-related symptoms, incidentally identified by exome sequencing. Molecular Genetics and Metabolism Reports. 36. 100997–100997. 2 indexed citations
5.
Schumacher, Fabian, Margarita Zachariou, Burkhard Kleuser, et al.. (2022). Stbd1-deficient mice display insulin resistance associated with enhanced hepatic ER-mitochondria contact. Biochimie. 200. 172–183. 6 indexed citations
6.
Nicolaou, Paschalis, Petros Petrou, Anthi Drousiotou, et al.. (2020). A novel SLC30A10 missense variant associated with parkinsonism and dystonia without hypermanganesemia. Journal of the Neurological Sciences. 418. 117101–117101. 7 indexed citations
7.
Georgiou, Theodoros, George Christopoulos, Violetta Anastasiadou, et al.. (2014). The first family with Tay-Sachs disease in Cyprus: Genetic analysis reveals a nonsense (c.78G>A) and a silent (c.1305C>T) mutation and allows preimplantation genetic diagnosis. Meta Gene. 2. 200–205. 6 indexed citations
8.
Georgiou, Theodoros, et al.. (2012). The spectrum of mutations identified in Cypriot patients with phenylalanine hydroxylase deficiency detected through neonatal screening. Clinical Biochemistry. 45(7-8). 588–592. 6 indexed citations
9.
Georgiou, Theodoros, Jacinta L. Chuang, Richard Wynn, et al.. (2009). Maple Syrup Urine Disease in Cypriot Families: Identification of Three Novel Mutations and Biochemical Characterization of the p.Thr211Met Mutation in the E1α Subunit. Genetic Testing and Molecular Biomarkers. 13(5). 657–664. 9 indexed citations
10.
Kleopa, Kleopas A., et al.. (2006). Naturally occurring utrophin correlates with disease severity in Duchenne muscular dystrophy. Human Molecular Genetics. 15(10). 1623–1628. 70 indexed citations
11.
Georgiou, Theodoros, Violetta Anastasiadou, Anna Caciotti, et al.. (2005). The Arg482His Mutation in the β-Galactosidase Gene Is Responsible for a High Frequency of GM1 Gangliosidosis Carriers in a Cypriot Village. PubMed. 9(2). 126–132. 17 indexed citations
12.
Drousiotou, Anthi, et al.. (2004). Molecular characterization of G6PD deficiency in Cyprus. Blood Cells Molecules and Diseases. 33(1). 25–30. 22 indexed citations
13.
Georgiou, Theodoros, Anthi Drousiotou, Yvan Campos, et al.. (2004). Four novel mutations in patients from the Middle East with the infantile form of GM1-gangliosidosis. Human Mutation. 24(4). 352–352. 13 indexed citations
14.
Kyriakides, Tassos C., et al.. (2003). A comparative morphological study in 33 cases of respiratory chain encephalomyopathies.. PubMed. 22(2). 48–51. 2 indexed citations
15.
Verrelli, Brian C., John H. McDonald, George Argyropoulos, et al.. (2002). Evidence for Balancing Selection from Nucleotide Sequence Analyses of Human G6PD. The American Journal of Human Genetics. 71(5). 1112–1128. 119 indexed citations
16.
Kleanthous, Marina, et al.. (2001). Alpha‐thalassaemia prenatal diagnosis by two PCR‐based methods. Prenatal Diagnosis. 21(5). 413–417. 7 indexed citations
17.
Drousiotou, Anthi, Violetta Anastasiadou, George Christopoulos, et al.. (2000). Sandhoff disease in Cyprus: population screening by biochemical and DNA analysis indicates a high frequency of carriers in the Maronite community. Human Genetics. 107(1). 12–17. 13 indexed citations
18.
Drousiotou, Anthi, P.A. Ioannou, Georgios Christopoulos, et al.. (1998). Neonatal Screening for Duchenne Muscular Dystrophy: A Novel Semiquantitative Application of the Bioluminescence Test for Creatine Kinase in a Pilot National Program in Cyprus. Genetic Testing. 2(1). 55–60. 48 indexed citations
19.
Drousiotou, Anthi, et al.. (1994). Dystrophinopathy presenting as congenital muscular dystrophy. Neuromuscular Disorders. 4(4). 387–392. 8 indexed citations
20.
Ioannou, Panos, et al.. (1994). Mutation analysis of a Sandhoff disease patient in the Maronite community in Cyprus. Human Genetics. 94(2). 136–40. 8 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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