Amre Shahwan

1.5k total citations
37 papers, 1.0k citations indexed

About

Amre Shahwan is a scholar working on Psychiatry and Mental health, Pediatrics, Perinatology and Child Health and Genetics. According to data from OpenAlex, Amre Shahwan has authored 37 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Psychiatry and Mental health, 17 papers in Pediatrics, Perinatology and Child Health and 14 papers in Genetics. Recurrent topics in Amre Shahwan's work include Epilepsy research and treatment (18 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Genomics and Rare Diseases (7 papers). Amre Shahwan is often cited by papers focused on Epilepsy research and treatment (18 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Genomics and Rare Diseases (7 papers). Amre Shahwan collaborates with scholars based in Ireland, United States and United Kingdom. Amre Shahwan's co-authors include Norman Delanty, A. Simon Harvey, Michael A. Farrell, Veronica Lambert, Pamela Gallagher, Joan K. Austin, Ailbhe Benson, Mary D. King, Nicholas M. Allen and Sally Ann Lynch and has published in prestigious journals such as Neurology, The Lancet Neurology and Epilepsia.

In The Last Decade

Amre Shahwan

37 papers receiving 1.0k citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Amre Shahwan Ireland 16 515 387 265 210 170 37 1.0k
Gabriella Di Rosa Italy 21 348 0.7× 212 0.5× 288 1.1× 269 1.3× 169 1.0× 82 1.1k
Anne Tournay United States 13 560 1.1× 333 0.9× 187 0.7× 141 0.7× 179 1.1× 20 1.1k
Iris E. Martínez‐Juárez Mexico 19 607 1.2× 323 0.8× 204 0.8× 139 0.7× 163 1.0× 60 1000
Sharon Whiting Canada 19 624 1.2× 460 1.2× 166 0.6× 231 1.1× 265 1.6× 46 1.5k
Edda Haberlandt Austria 25 641 1.2× 477 1.2× 288 1.1× 371 1.8× 180 1.1× 89 1.7k
Nerses Bebek Türkiye 22 964 1.9× 515 1.3× 266 1.0× 187 0.9× 316 1.9× 126 1.5k
Barbara Mostacci Italy 18 359 0.7× 191 0.5× 128 0.5× 164 0.8× 175 1.0× 69 971
Francesca Darra Italy 24 819 1.6× 440 1.1× 522 2.0× 365 1.7× 285 1.7× 86 1.6k
Sophia Varadkar United Kingdom 13 438 0.9× 183 0.5× 135 0.5× 213 1.0× 121 0.7× 30 1.1k
Antonino Romeo Italy 21 853 1.7× 498 1.3× 249 0.9× 179 0.9× 120 0.7× 43 1.2k

Countries citing papers authored by Amre Shahwan

Since Specialization
Citations

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

Fields of papers citing papers by Amre Shahwan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Amre Shahwan

This figure shows the co-authorship network connecting the top 25 collaborators of Amre Shahwan. A scholar is included among the top collaborators of Amre Shahwan 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 Amre Shahwan. Amre Shahwan 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.
Gorman, Kathleen M., et al.. (2024). Epileptic dyskinetic encephalopathy in KBG syndrome: Expansion of the phenotype. Epilepsy & Behavior Reports. 25. 100647–100647. 2 indexed citations
2.
Harvey, Susan, et al.. (2023). Relationship Between Electroencephalography and Seizure Outcome in Typical Absence Seizures in Children. Pediatric Neurology. 148. 56–64. 1 indexed citations
3.
Benson, Ailbhe & Amre Shahwan. (2021). Monitoring the frequency and duration of epileptic seizures: “A journey through time”. European Journal of Paediatric Neurology. 33. 168–178. 4 indexed citations
4.
Raftery, Tara, Robert Cunney, Richard J. Drew, et al.. (2021). Neurological involvement in children with hemolytic uremic syndrome. European Journal of Pediatrics. 181(2). 501–512. 18 indexed citations
5.
Benson, Ailbhe, et al.. (2018). Development and psychometric evaluation of the youth and parent versions of the Epilepsy Disclosure Scale (EDS). Epilepsy & Behavior. 82. 111–118. 3 indexed citations
6.
Byrne, Susan, et al.. (2017). The Temple Star Transitional Model of Care for epilepsy; the outcome of a quality improvement project. Epilepsy & Behavior. 79. 4–8. 11 indexed citations
7.
Conroy, Judith, Nicholas M. Allen, Kathleen M. Gorman, et al.. (2016). Novel European SLC1A4 variant: infantile spasms and population ancestry analysis. Journal of Human Genetics. 61(8). 761–764. 15 indexed citations
8.
Gorman, Kathleen M. & Amre Shahwan. (2016). Sultiame revisited: treatment of refractory absence seizures. Epileptic Disorders. 18(3). 329–333. 10 indexed citations
9.
Allen, Nicholas M., Judith Conroy, Thierry Deonna, et al.. (2016). Atypical benign partial epilepsy of childhood with acquired neurocognitive, lexical semantic, and autistic spectrum disorder. Epilepsy & Behavior Case Reports. 6. 42–48. 8 indexed citations
10.
Benson, Ailbhe, et al.. (2016). The stigma experiences and perceptions of families living with epilepsy: Implications for epilepsy-related communication within and external to the family unit. Patient Education and Counseling. 99(9). 1473–1481. 43 indexed citations
11.
Benson, Ailbhe, et al.. (2015). To tell or not to tell: A systematic review of the disclosure practices of children living with epilepsy and their parents. Epilepsy & Behavior. 51. 73–95. 49 indexed citations
12.
Benson, Ailbhe, et al.. (2015). Family communication in the context of pediatric epilepsy: A systematic review. Epilepsy & Behavior. 51. 225–239. 40 indexed citations
13.
Benson, Ailbhe, Veronica Lambert, Pamela Gallagher, Amre Shahwan, & Joan K. Austin. (2015). “I don't want them to look at me and think of my illness, I just want them to look at me and see me”: Child perspectives on the challenges associated with disclosing an epilepsy diagnosis to others. Epilepsy & Behavior. 53. 83–91. 29 indexed citations
14.
Allen, Nicholas M., Judith Conroy, Amre Shahwan, et al.. (2014). Excellent outcome with de novo 15q13.3 microdeletion causing infantile spasms—A further patient. American Journal of Medical Genetics Part A. 164(7). 1863–1866. 3 indexed citations
15.
Shahwan, Amre, Catherine Bailey, Lara Shekerdemian, & A. Simon Harvey. (2010). The prevalence of seizures in comatose children in the pediatric intensive care unit: A prospective video‐EEG study. Epilepsia. 51(7). 1198–1204. 86 indexed citations
16.
Kinirons, Peter, Gianpiero L. Cavalleri, Amre Shahwan, et al.. (2006). Examining the role of common genetic variation in the γ2 subunit of the GABAA receptor in epilepsy using tagging SNPs. Epilepsy Research. 70(2-3). 229–238. 15 indexed citations
17.
Shahwan, Amre, Kevin Murphy, Colin P. Doherty, et al.. (2006). The controversial association of ABCB1 polymorphisms in refractory epilepsy: An analysis of multiple SNPs in an Irish population. Epilepsy Research. 73(2). 192–198. 60 indexed citations
18.
Shahwan, Amre, et al.. (2006). Atypical presentation of ataxia–oculomotor apraxia type 1. Developmental Medicine & Child Neurology. 48(6). 529–529. 8 indexed citations
19.
Shahwan, Amre, Michael A. Farrell, & Norman Delanty. (2005). Progressive myoclonic epilepsies: a review of genetic and therapeutic aspects. The Lancet Neurology. 4(4). 239–248. 154 indexed citations
20.
Shahwan, Amre, et al.. (2004). Malignant Refractory Epilepsy in Identical Twins Mosaic for a Supernumerary Ring Chromosome 19. Epilepsia. 45(8). 997–1000. 18 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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