Thalia Antoniadi

1.4k total citations
28 papers, 850 citations indexed

About

Thalia Antoniadi is a scholar working on Genetics, Cellular and Molecular Neuroscience and Molecular Biology. According to data from OpenAlex, Thalia Antoniadi has authored 28 papers receiving a total of 850 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 8 papers in Cellular and Molecular Neuroscience and 6 papers in Molecular Biology. Recurrent topics in Thalia Antoniadi's work include Hereditary Neurological Disorders (8 papers), Hearing, Cochlea, Tinnitus, Genetics (5 papers) and Cystic Fibrosis Research Advances (5 papers). Thalia Antoniadi is often cited by papers focused on Hereditary Neurological Disorders (8 papers), Hearing, Cochlea, Tinnitus, Genetics (5 papers) and Cystic Fibrosis Research Advances (5 papers). Thalia Antoniadi collaborates with scholars based in Greece, United Kingdom and Denmark. Thalia Antoniadi's co-authors include Michael B. Petersen, Maria Tzetis, Richard Caswell, Weijia Xie, Konrad Paszkiewicz, Ruth Newbury‐Ecob, Robert Hastings, Lynn Greenhalgh, Michael N. Weedon and Maggie Williams and has published in prestigious journals such as Neurology, The American Journal of Human Genetics and Human Mutation.

In The Last Decade

Thalia Antoniadi

28 papers receiving 829 citations

Peers

Thalia Antoniadi
A. V. Polyakov Russia
Seher Başaran Türkiye
John Wolff United States
Miriam Elbracht Germany
Samuel Clokie United Kingdom
Guy A. Rouleau Canada
V. Volpini Spain
Agnès Guichet France
Jan E. Dumon Belgium
Jr-Gang Cheng United States
A. V. Polyakov Russia
Thalia Antoniadi
Citations per year, relative to Thalia Antoniadi Thalia Antoniadi (= 1×) peers A. V. Polyakov

Countries citing papers authored by Thalia Antoniadi

Since Specialization
Citations

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

Fields of papers citing papers by Thalia Antoniadi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Thalia Antoniadi

This figure shows the co-authorship network connecting the top 25 collaborators of Thalia Antoniadi. A scholar is included among the top collaborators of Thalia Antoniadi 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 Thalia Antoniadi. Thalia Antoniadi 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.
Kulshrestha, R., et al.. (2018). Charcot Marie Tooth disease type 2S with late onset diaphragmatic weakness: An atypical case. Neuromuscular Disorders. 28(12). 1016–1021. 8 indexed citations
2.
Kulshrestha, R., Thalia Antoniadi, Michael J. Rogers, et al.. (2017). Deletion of P2 promoter of GJB1 gene a cause of Charcot-Marie-Tooth disease. Neuromuscular Disorders. 27(8). 766–770. 6 indexed citations
3.
Bánsági, Boglárka, Thalia Antoniadi, Sinéad M. Murphy, et al.. (2015). Genotype/phenotype correlations in AARS-related neuropathy in a cohort of patients from the United Kingdom and Ireland. Journal of Neurology. 262(8). 1899–1908. 32 indexed citations
4.
5.
Evangelista, Teresinha, Boglárka Bánsági, Angela Pyle, et al.. (2015). Phenotypic variability of TRPV4 related neuropathies. Neuromuscular Disorders. 25(6). 516–521. 25 indexed citations
6.
Weedon, Michael N., Robert Hastings, Richard Caswell, et al.. (2011). Exome Sequencing Identifies a DYNC1H1 Mutation in a Large Pedigree with Dominant Axonal Charcot-Marie-Tooth Disease. The American Journal of Human Genetics. 89(2). 308–312. 200 indexed citations
7.
Kokotas, Haris, et al.. (2010). Easy, Rapid, and Cost-Effective Methods for Identifying Carriers of Recurrent GJB2 Mutations Causing Nonsyndromic Hearing Impairment in the Greek Population. Genetic Testing and Molecular Biomarkers. 14(2). 189–192. 1 indexed citations
8.
Karadimas, Charalampos, et al.. (2006). Prenatal diagnosis of achondroplasia presenting with multiple‐suture synostosis: a novel association. Prenatal Diagnosis. 26(3). 258–261. 11 indexed citations
9.
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
10.
Antoniadi, Thalia, Christos Yapijakis, P. Kaminopetros, et al.. (2002). A simple and effective approach for detecting maternal cell contamination in molecular prenatal diagnosis. Prenatal Diagnosis. 22(5). 425–429. 20 indexed citations
11.
Παμπάνος, Ανδρέας, John R. Economides, Vasiliki Iliadou, et al.. (2002). Prevalence of GJB2 mutations in prelingual deafness in the Greek population. International Journal of Pediatric Otorhinolaryngology. 65(2). 101–108. 56 indexed citations
12.
Velissariou, Voula, et al.. (2002). Maternal uniparental isodisomy 20 in a foetus with trisomy 20 mosaicism: clinical, cytogenetic and molecular analysis. European Journal of Human Genetics. 10(11). 694–698. 36 indexed citations
13.
Velissariou, Voula, et al.. (2001). Prenatal diagnosis of two rare de novo structural aberrations of the Y chromosome: cytogenetic and molecular analysis. Prenatal Diagnosis. 21(6). 484–487. 4 indexed citations
14.
Antoniadi, Thalia, Ανδρέας Παμπάνος, & Michael B. Petersen. (2001). Prenatal diagnosis of prelingual deafness: carrier testing and prenatal diagnosis of the common GJB2 35delG mutation. Prenatal Diagnosis. 21(1). 10–13. 12 indexed citations
15.
Antoniadi, Thalia, et al.. (2000). Mutation analysis of the GJB2 (connexin 26) gene by DGGE in Greek patients with sensorineural deafness. Human Mutation. 16(1). 7–12. 43 indexed citations
16.
Antoniadi, Thalia, et al.. (1999). Prevalence of factor V Leiden, prothrombin G20210A, and MTHFR C677T mutations in a Greek population of blood donors. American Journal of Hematology. 61(4). 265–267. 59 indexed citations
17.
Kanavakis, Emmanouel, et al.. (1998). Cystic fibrosis mutation screening in CBAVD patients and men with obstructive azoospermia or severe oligozoospermia. Molecular Human Reproduction. 4(4). 333–337. 46 indexed citations
18.
Kanavakis, Emmanuel, et al.. (1996). Characterization of more than 85% of cystic fibrosis alleles in the Greek population, including five novel mutations. Human Genetics. 99(1). 121–125. 36 indexed citations
19.
20.
Tzetis, Maria, et al.. (1995). Identification of two novel mutations (296 + 1G − C and A46D) in exon 2 of the CFTR gene in Greek cystic fibrosis patients. Molecular and Cellular Probes. 9(4). 283–285. 2 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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