Xenia Iona

2.4k total citations
13 papers, 795 citations indexed

About

Xenia Iona is a scholar working on Psychiatry and Mental health, Genetics and Molecular Biology. According to data from OpenAlex, Xenia Iona has authored 13 papers receiving a total of 795 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Psychiatry and Mental health, 7 papers in Genetics and 4 papers in Molecular Biology. Recurrent topics in Xenia Iona's work include Epilepsy research and treatment (12 papers), Genomics and Rare Diseases (5 papers) and Ion channel regulation and function (3 papers). Xenia Iona is often cited by papers focused on Epilepsy research and treatment (12 papers), Genomics and Rare Diseases (5 papers) and Ion channel regulation and function (3 papers). Xenia Iona collaborates with scholars based in Australia, United Kingdom and Italy. Xenia Iona's co-authors include Samuel F. Berkovic, Ingrid E. Scheffer, Jacinta M. McMahon, Leanne M. Dibbens, John C. Mulley, Louise A. Harkin, Sameer M. Zuberi, Deepak Gill, Sarah E. Heron and Elaine Wirrell and has published in prestigious journals such as New England Journal of Medicine, SHILAP Revista de lepidopterología and Neurology.

In The Last Decade

Xenia Iona

13 papers receiving 756 citations

Peers

Countries citing papers authored by Xenia Iona

Since Specialization

Citations

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

Fields of papers citing papers by Xenia Iona

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Xenia Iona

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

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	A variant of KCC 2 from patients with febrile seizures impairs neuronal Cl ⁻ extrusion and dendritic spine formation 2014 ·EMBO Reports ·Martin Puskarjov, Patricia Seja, Sarah E. Heron, (unknown), Faraz Ahmad, Xenia Iona, Karen Oliver, Bronwyn E. Grinton, László Vutskits, Ingrid E. Scheffer, Steven Petrou, Peter Blaesse, Leanne M. Dibbens, Samuel F. Berkovic, Kai Kaila	131
2	Atypical multifocal Dravet syndrome lacks generalized seizures and may show later cognitive decline 2013 ·Developmental Medicine & Child Neurology ·Young Ok Kim, Susannah T. Bellows, Jacinta M. McMahon, Xenia Iona, John A. Damiano, Leanne M. Dibbens, Kent R. Kelley, Deepak Gill, J. Helen Cross, Samuel F. Berkovic, Ingrid E. Scheffer	13
3	Autosomal dominant vasovagal syncope 2013 ·Neurology ·Karl Martin Klein, Catherine Bromhead, Katherine R. Smith, Christopher J. O’Callaghan, (unknown), Sarah E. Heron, Xenia Iona, Bree Hodgson, Jacinta M. McMahon, Kate Lawrence, Ingrid E. Scheffer, Leanne M. Dibbens, Melanie Bahlo, Samuel F. Berkovic	17
4	Role of the sodium channel SCN9A in genetic epilepsy with febrile seizures plus and Dravet syndrome 2013 ·Epilepsia ·John C. Mulley, Bree Hodgson, Jacinta M. McMahon, Xenia Iona, Susannah T. Bellows, Saul A. Mullen, K Farrell, Mark T. Mackay, Lynette G. Sadleir, Andrew Bleasel, Deepak Gill, Richard Webster, Elaine Wirrell, Michael Harbord, (unknown), Eva Andermann, Sara Kivity, Samuel F. Berkovic, Ingrid E. Scheffer, Leanne M. Dibbens	56
5	Do mutations in SCN1B cause Dravet syndrome? 2012 ·Epilepsy Research ·Young Ok Kim, Leanne M. Dibbens, Carla Marini, Arvid Suls, Nicole Chémaly, Davide Mei, Jacinta M. McMahon, Xenia Iona, Samuel F. Berkovic, Peter De Jonghe, Renzo Guerrini, Rima Nabbout, Ingrid E. Scheffer	12
6	Febrile infection-related epilepsy syndrome is not caused by SCN1A mutations 2012 ·Epilepsy Research ·(unknown), A. Simon Harvey, Xenia Iona, Leanne M. Dibbens, John A. Damiano, Todor Arsov, Deepak Gill, Jeremy L. Freeman, Richard J. Leventer, Angela Vincent, Samuel F. Berkovic, Jacinta M. McMahon, Ingrid E. Scheffer	10
7	PRRT2 phenotypic spectrum includes sporadic and fever-related infantile seizures 2012 ·Neurology ·Ingrid E. Scheffer, Bronwyn E. Grinton, Sarah E. Heron, Sara Kivity, Zaid Afawi, Xenia Iona, Hadassa Goldberg‐Stern, Maria Kinali, Ian Andrews, Renzo Guerrini, Carla Marini, Lynette G. Sadleir, Samuel F. Berkovic, Leanne M. Dibbens	63
8	The Role of Seizure-RelatedSEZ6as a Susceptibility Gene in Febrile Seizures 2011 ·SHILAP Revista de lepidopterología ·John C. Mulley, Xenia Iona, Bree Hodgson, Sarah E. Heron, Samuel F. Berkovic, Ingrid E. Scheffer, Leanne M. Dibbens	19
9	Effects of vaccination on onset and outcome of Dravet syndrome: a retrospective study 2010 ·The Lancet Neurology ·Anne M. McIntosh, Jacinta M. McMahon, Leanne M. Dibbens, Xenia Iona, John C. Mulley, Ingrid E. Scheffer, Samuel F. Berkovic	101
10	Timing of De Novo Mutagenesis — A Twin Study of Sodium-Channel Mutations 2010 ·New England Journal of Medicine ·Lata Vadlamudi, Leanne M. Dibbens, Kate Lawrence, Xenia Iona, Jacinta M. McMahon, Wayne Murrell, Alan Mackay‐Sim, Ingrid E. Scheffer, Samuel F. Berkovic	74
11	De novo SCN1A mutations in Dravet syndrome and related epileptic encephalopathies are largely of paternal origin: Table 1 2009 ·Journal of Medical Genetics ·Sarah E. Heron, Ingrid E. Scheffer, Xenia Iona, Sameer M. Zuberi, Rachael Birch, Jacinta M. McMahon, (unknown), Samuel F. Berkovic, John C. Mulley	43
12	De-novo mutations of the sodium channel gene SCN1A in alleged vaccine encephalopathy: a retrospective study 2006 ·The Lancet Neurology ·Samuel F. Berkovic, Louise A. Harkin, Jacinta M. McMahon, James T. Pelekanos, Sameer M. Zuberi, Elaine Wirrell, Deepak Gill, Xenia Iona, John C. Mulley, Ingrid E. Scheffer	173
13	A new molecular mechanism for severe myoclonic epilepsy of infancy: Exonic deletions in SCN1A 2006 ·Neurology ·John C. Mulley, Paul V. Nelson, (unknown), Leanne M. Dibbens, Xenia Iona, Jacinta M. McMahon, Louise A. Harkin, Jan Schouten, Shuancang Yu, Samuel F. Berkovic, Ingrid E. Scheffer	83

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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