Irina Stefanova

856 total citations
10 papers, 204 citations indexed

About

Irina Stefanova is a scholar working on Pediatrics, Perinatology and Child Health, Psychiatry and Mental health and Genetics. According to data from OpenAlex, Irina Stefanova has authored 10 papers receiving a total of 204 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Pediatrics, Perinatology and Child Health, 4 papers in Psychiatry and Mental health and 3 papers in Genetics. Recurrent topics in Irina Stefanova's work include Epilepsy research and treatment (3 papers), Genomics and Rare Diseases (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Irina Stefanova is often cited by papers focused on Epilepsy research and treatment (3 papers), Genomics and Rare Diseases (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Irina Stefanova collaborates with scholars based in Germany, Bulgaria and Netherlands. Irina Stefanova's co-authors include Gabriele Gillessen‐Kaesbach, Ulrich Stephani, Hiltrud Muhle, Almuth Caliebe, Reiner Siebert, Holger Tönnies, Sarah von Spiczak, Ingo Helbig, Rainer Boor and Andreas van Baalen and has published in prestigious journals such as SHILAP Revista de lepidopterología, Epilepsia and Epilepsy & Behavior.

In The Last Decade

Irina Stefanova

10 papers receiving 191 citations

Peers

Irina Stefanova

GENET

PMH

PPCH

CMN

Rita Teek Estonia

Theresa Scattergood United States

Auli Sirén Finland

Aurora Arghir Romania

Ornella Galesi Italy

Uzma Abdullah Pakistan

Gérald Bussy France

Lucia Pucci Italy

Charlly Kao United States

Elysa J. Marco United States

Rita Teek Estonia

Irina Stefanova

124 ×1.0

GENET

126 ×1.9

14 ×0.3

PMH

36 ×0.9

PPCH

34 ×1.0

CMN

Citations per year, relative to Irina Stefanova Irina Stefanova (= 1×) peers Rita Teek

Countries citing papers authored by Irina Stefanova

Since Specialization

Citations

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

Fields of papers citing papers by Irina Stefanova

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Irina Stefanova

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

All Works

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10 of 10 papers shown

Stefanova, Irina, et al.. (2021). Familial hyperinsulinaemic hypoglycaemia with epileptic syndrome, cognitive impairment and detected mutation of the ABCC 8 (SUR1) gene: a case report. SHILAP Revista de lepidopterología. 63(5). 805–808. 1 indexed citations

Stefanova, Irina, et al.. (2017). Significance of noncompliance when treating patients with epilepsy. Neurologia i Neurochirurgia Polska. 52(2). 215–221. 4 indexed citations

Stefanova, Irina, et al.. (2015). Translation, Adaptation And Validation Of The Bulgarian Version Of The SIDAED Questionnaire. SHILAP Revista de lepidopterología. 8(1). 19–25. 1 indexed citations

Stefanova, Irina, et al.. (2014). Translation, cross-cultural adaptation, and validation of the Bulgarian version of the Liverpool Adverse Event Profile. Epilepsy & Behavior. 39. 88–91. 11 indexed citations

Jähn, Johanna, Almuth Caliebe, Sarah von Spiczak, et al.. (2012). CDKL5 Mutations as a Cause of Severe Epilepsy in Infancy. Journal of Child Neurology. 28(7). 937–941. 14 indexed citations

Unger, Sheila, Ekkehart Lausch, Franco Stanzial, et al.. (2011). Fetal akinesia in metatropic dysplasia: The combined phenotype of chondrodysplasia and neuropathy?. American Journal of Medical Genetics Part A. 155(11). 2860–2864. 26 indexed citations

Weichert, J., Andreas Schröer, Dániel Beyer, Gabriele Gillessen‐Kaesbach, & Irina Stefanova. (2011). Cornelia de Lange syndrome: antenatal diagnosis in two consecutive pregnancies due to rare gonadal mosaicism ofNIPBLgene mutation. The Journal of Maternal-Fetal & Neonatal Medicine. 24(7). 978–982. 5 indexed citations

Helbig, Ingo, Holger Tönnies, Hiltrud Muhle, et al.. (2010). Deletions in 16p13 including GRIN2A in patients with intellectual disability, various dysmorphic features, and seizure disorders of the rolandic region. Epilepsia. 51(9). 1870–1873. 65 indexed citations

Stefanova, Irina, et al.. (2010). Mosaic and complete tetraploidy in live-born infants: two new patients and review of the literature. Clinical Dysmorphology. 19(3). 123–127. 23 indexed citations

10.

Caliebe, Almuth, Hester Y. Kroes, Jasper J. van der Smagt, et al.. (2010). Four patients with speech delay, seizures and variable corpus callosum thickness sharing a 0.440 Mb deletion in region 1q44 containing the HNRPU gene. European Journal of Medical Genetics. 53(4). 179–185. 54 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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