Stavroula Psoni

857 total citations
11 papers, 393 citations indexed

About

Stavroula Psoni is a scholar working on Genetics, Molecular Biology and Cognitive Neuroscience. According to data from OpenAlex, Stavroula Psoni has authored 11 papers receiving a total of 393 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Cognitive Neuroscience. Recurrent topics in Stavroula Psoni's work include Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Stavroula Psoni is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). Stavroula Psoni collaborates with scholars based in Greece, Italy and Germany. Stavroula Psoni's co-authors include Emmanuel Kanavakis, Sophia Kitsiou‐Tzeli, Alessandra Murgia, Stefano Sartori, Marilena Vecchi, Roberta Polli, Meredith Wilson, Simon Williams, Stephanie Fehr and Jenny Downs and has published in prestigious journals such as Pediatric Research, European Journal of Human Genetics and Clinical Genetics.

In The Last Decade

Stavroula Psoni

11 papers receiving 389 citations

Peers

Stavroula Psoni

GENET

PMH

CMN

Adriana Lo‐Castro Italy

Jayon Lihm United States

Sureni V. Mullegama United States

Caroline Nava France

Madeleine Fannemel Norway

Anna Bergo Italy

Moyra Smith United States

Laëtitia Lambert France

Kali Witherspoon United States

Syed K. Rafi United States

Adriana Lo‐Castro Italy

Stavroula Psoni

212 ×0.7

GENET

166 ×0.8

98 ×1.2

77 ×2.1

PMH

12 ×0.6

CMN

Citations per year, relative to Stavroula Psoni Stavroula Psoni (= 1×) peers Adriana Lo‐Castro

Countries citing papers authored by Stavroula Psoni

Since Specialization

Citations

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

Fields of papers citing papers by Stavroula Psoni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stavroula Psoni

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

All Works

Sort: Min cites: Since: Top N: Style:

11 of 11 papers shown

Psoni, Stavroula, et al.. (2017). Cantú Syndrome Associated with Ovarian Agenesis. Molecular Syndromology. 8(4). 206–210. 2 indexed citations

Fryssira, Helen, Stavroula Psoni, Thomas Liehr, et al.. (2016). Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delay. Molecular Cytogenetics. 9(1). 55–55. 7 indexed citations

Kosma, Konstantina, Christalena Sofocleous, Panagiota Pervanidou, et al.. (2016). Recurrent copy number variations as risk factors for autism spectrum disorders: analysis of the clinical implications. Clinical Genetics. 89(6). 708–718. 26 indexed citations

Fehr, Stephanie, Meredith Wilson, Jenny Downs, et al.. (2012). The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy. European Journal of Human Genetics. 21(3). 266–273. 209 indexed citations

Psoni, Stavroula, et al.. (2011). MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disorders. Brain and Development. 34(6). 487–495. 13 indexed citations

Psoni, Stavroula, et al.. (2010). Phenotypic and Genotypic Variability in Four Males With MECP2 Gene Sequence Aberrations Including a Novel Deletion. Pediatric Research. 67(5). 551–556. 22 indexed citations

Leventopoulos, Georgios, Sophia Kitsiou‐Tzeli, K. Kritikos, et al.. (2009). A Clinical Study of Sotos Syndrome Patients With Review of the Literature. Pediatric Neurology. 40(5). 357–364. 51 indexed citations

Psoni, Stavroula, Patrick J. Willems, Emmanuel Kanavakis, et al.. (2009). A novel p.Arg970X mutation in the last exon of the CDKL5 gene resulting in late-onset seizure disorder. European Journal of Paediatric Neurology. 14(2). 188–191. 22 indexed citations

Leventopoulos, Georgios, Sophia Kitsiou‐Tzeli, Stavroula Psoni, et al.. (2008). Three Novel Mutations in Greek Sotos Patients with Rare Clinical Manifestations. Hormone Research in Paediatrics. 71(1). 45–51. 5 indexed citations

10.

Psoni, Stavroula, Kyriaki Kekou, Joanne Traeger‐Synodinos, et al.. (2007). Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome. European Journal of Paediatric Neurology. 11(4). 235–239. 3 indexed citations

11.

Fryssira, Helen, Georgios Leventopoulos, Stavroula Psoni, et al.. (2007). Tumor development in three patients with Noonan syndrome. European Journal of Pediatrics. 167(9). 1025–1031. 33 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.

Explore authors with similar magnitude of impact