Stavroula Psoni

857 citations

11 papers · 393 indexed · h-index 8

Co-authors: Emmanuel Kanavakis Sophia Kitsiou‐Tzeli Alessandra Murgia Stefano Sartori Marilena Vecchi Roberta Polli Meredith Wilson Simon Williams
Topics: Genetics and Neurodevelopmental Disorders (6 papers)Autism Spectrum Disorder Research (4 papers)Genomic variations and chromosomal abnormalities (3 papers)
Cited by: Genetics Cognitive Neuroscience Molecular Biology
Journals: Pediatric Research European Journal of Human Genetics Clinical Genetics
Partner nations: Greece Italy Germany

In The Last Decade

Stavroula Psoni

11 papers receiving 389 citations

Peers

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

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11 of 11 papers shown

#	Work	Indexed citations
1	Cantú Syndrome Associated with Ovarian Agenesis 2017 ·Molecular Syndromology ·(unknown),Stavroula Psoni,(unknown),(unknown),Christalena Sofocleous,Emmanouil Manolakos,Maria Gavra,(unknown),(unknown)	2
2	Partial monosomy14q involving FOXG1 and NOVA1 in an infant with microcephaly, seizures and severe developmental delay 2016 ·Molecular Cytogenetics ·Helen Fryssira,(unknown),Stavroula Psoni,(unknown),Thomas Liehr,(unknown),(unknown),(unknown),Ioannis Papoulidis,Emmanouil Manolakos,Nikolaos Chaliasos	7
3	Recurrent copy number variations as risk factors for autism spectrum disorders: analysis of the clinical implications 2016 ·Clinical Genetics ·(unknown),Konstantina Kosma,(unknown),Christalena Sofocleous,Panagiota Pervanidou,(unknown),Ανδρέας Παμπάνος,Stavroula Psoni,(unknown),Emmanouel Kanavakis,(unknown),Maria Tzetis	26
4	The CDKL5 disorder is an independent clinical entity associated with early-onset encephalopathy 2012 ·European Journal of Human Genetics ·Stephanie Fehr,Meredith Wilson,Jenny Downs,Simon Williams,Alessandra Murgia,Stefano Sartori,Marilena Vecchi,Gladys Ho,Roberta Polli,Stavroula Psoni,Xinhua Bao,Nicholas de Klerk,Helen Leonard,John Christodoulou	209
5	MECP2 mutations and clinical correlations in Greek children with Rett syndrome and associated neurodevelopmental disorders 2011 ·Brain and Development ·Stavroula Psoni,Christalena Sofocleous,Joanne Traeger‐Synodinos,Sophia Kitsiou‐Tzeli,Emmanuel Kanavakis,(unknown)	13
6	Phenotypic and Genotypic Variability in Four Males With MECP2 Gene Sequence Aberrations Including a Novel Deletion 2010 ·Pediatric Research ·Stavroula Psoni,Christalena Sofocleous,Joanne Traeger‐Synodinos,Sophia Kitsiou‐Tzeli,Emmanuel Kanavakis,(unknown)	22
7	A Clinical Study of Sotos Syndrome Patients With Review of the Literature 2009 ·Pediatric Neurology ·Georgios Leventopoulos,Sophia Kitsiou‐Tzeli,K. Kritikos,Stavroula Psoni,Ariadni Mavrou,Emmanuel Kanavakis,Helen Fryssira	51
8	A novel p.Arg970X mutation in the last exon of the CDKL5 gene resulting in late-onset seizure disorder 2009 ·European Journal of Paediatric Neurology ·Stavroula Psoni,Patrick J. Willems,Emmanuel Kanavakis,A Mavrou,(unknown),Joanne Traeger‐Synodinos,(unknown),(unknown),Sophia Kitsiou‐Tzeli	22
9	Three Novel Mutations in Greek Sotos Patients with Rare Clinical Manifestations 2008 ·Hormone Research in Paediatrics ·Georgios Leventopoulos,Sophia Kitsiou‐Tzeli,Stavroula Psoni,Ariadni Mavrou,Emmanuel Kanavakis,P J Willems,Helen Fryssira	5
10	Coinheritance of mutated SMN1 and MECP2 genes in a child with phenotypic features of spinal muscular atrophy (SMA) type II and Rett syndrome 2007 ·European Journal of Paediatric Neurology ·(unknown),Stavroula Psoni,(unknown),(unknown),Kyriaki Kekou,Joanne Traeger‐Synodinos,Sofìa Kitsiou,Emmanuel Kanavakis,Helen Fryssira	3
11	Tumor development in three patients with Noonan syndrome 2007 ·European Journal of Pediatrics ·Helen Fryssira,Georgios Leventopoulos,Stavroula Psoni,Sophia Kitsiou‐Tzeli,Nikolaos Stavrianeas,Emmanuel Kanavakis	33

About Stavroula Psoni

Stavroula Psoni is a scholar working on Developmental Biology, Genetics and Cognitive Neuroscience, having authored 11 papers that have together received 393 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (6 papers), Autism Spectrum Disorder Research (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Genetics (313 citations), Cognitive Neuroscience (81 citations) and Molecular Biology (212 citations). Stavroula Psoni has collaborated with scholars based in Greece, Italy and Germany. Frequent 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. Their work appears in journals such as Pediatric Research, European Journal of Human Genetics and Clinical Genetics.

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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