Emanuela Abiusi

1.4k total citations
8 papers, 376 citations indexed

About

Emanuela Abiusi is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Emanuela Abiusi has authored 8 papers receiving a total of 376 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 5 papers in Genetics and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Emanuela Abiusi's work include Neurogenetic and Muscular Disorders Research (5 papers), RNA modifications and cancer (2 papers) and Ion channel regulation and function (2 papers). Emanuela Abiusi is often cited by papers focused on Neurogenetic and Muscular Disorders Research (5 papers), RNA modifications and cancer (2 papers) and Ion channel regulation and function (2 papers). Emanuela Abiusi collaborates with scholars based in Italy, United States and United Kingdom. Emanuela Abiusi's co-authors include Melanie Care, Michael H. Gollob, Wojciech Zaręba, Arnon Adler, Eline A. Nannenberg, Arthur A.M. Wilde, John Garcia, Valeria Novelli, James S. Ware and Amy C. Sturm and has published in prestigious journals such as Circulation, European Heart Journal and Human Molecular Genetics.

In The Last Decade

Emanuela Abiusi

8 papers receiving 369 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emanuela Abiusi Italy 7 254 214 61 48 35 8 376
B. Kerem Israel 9 145 0.6× 237 1.1× 56 0.9× 21 0.4× 55 1.6× 12 456
Yo Okizuka Japan 10 69 0.3× 307 1.4× 75 1.2× 21 0.4× 66 1.9× 18 363
Julian Schröter Germany 9 172 0.7× 172 0.8× 21 0.3× 29 0.6× 50 1.4× 20 312
Colleen M. Donlin‐Smith United States 7 70 0.3× 194 0.9× 64 1.0× 19 0.4× 18 0.5× 7 209
Vasantha Gowda United Kingdom 6 57 0.2× 157 0.7× 75 1.2× 20 0.4× 23 0.7× 15 204
A. Ya. Gudkova Russia 10 169 0.7× 184 0.9× 20 0.3× 12 0.3× 16 0.5× 46 299
M. Hinton United Kingdom 4 214 0.8× 220 1.0× 8 0.1× 33 0.7× 15 0.4× 6 321
Liliana Vercelli Italy 9 46 0.2× 167 0.8× 79 1.3× 52 1.1× 16 0.5× 17 276
Philip A. Wahr United States 10 309 1.2× 265 1.2× 18 0.3× 15 0.3× 25 0.7× 13 438
Sherin I. Hashem United States 8 105 0.4× 185 0.9× 11 0.2× 32 0.7× 22 0.6× 11 280

Countries citing papers authored by Emanuela Abiusi

Since Specialization
Citations

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

Fields of papers citing papers by Emanuela Abiusi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emanuela Abiusi

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

All Works

8 of 8 papers shown
1.
Scala, Marcello, Emanuela Abiusi, Ilaria Contaldo, et al.. (2022). Phosphatase and tensin homolog (PTEN) variants and epilepsy: A multicenter case series. Seizure. 100. 82–86. 12 indexed citations
2.
Walsh, Roddy, Arnon Adler, Ahmad S. Amin, et al.. (2021). Evaluation of gene validity for CPVT and short QT syndrome in sudden arrhythmic death. European Heart Journal. 43(15). 1500–1510. 71 indexed citations
3.
Adler, Arnon, Valeria Novelli, Ahmad S. Amin, et al.. (2020). An International, Multicentered, Evidence-Based Reappraisal of Genes Reported to Cause Congenital Long QT Syndrome. Circulation. 141(6). 418–428. 204 indexed citations
4.
Sanctis, Roberto De, Marika Pane, Giorgia Coratti, et al.. (2017). Clinical phenotypes and trajectories of disease progression in type 1 spinal muscular atrophy. Neuromuscular Disorders. 28(1). 24–28. 38 indexed citations
5.
Pane, Marika, Leonardo Lapenta, Emanuela Abiusi, et al.. (2017). Longitudinal assessments in discordant twins with SMA. Neuromuscular Disorders. 27(10). 890–893. 8 indexed citations
6.
Abiusi, Emanuela, Klaus Dieterich, Paulette Mezin, et al.. (2017). Biallelic mutation of UNC50, encoding a protein involved in AChR trafficking, is responsible for arthrogryposis. Human Molecular Genetics. 26(20). 3989–3994. 9 indexed citations
7.
Rubboli, Guido, Pierangelo Veggiotti, Antonella Pini, et al.. (2015). Spinal muscular atrophy associated with progressive myoclonic epilepsy: A rare condition caused by mutations in ASAH1. Epilepsia. 56(5). 692–698. 30 indexed citations
8.
Morandi, Lucía, Emanuela Abiusi, Maria Barbara Pasanisi, et al.. (2013). P.6.4 Salbutamol tolerability and efficacy in adult type III SMA patients: Results of a multicentric, molecular and clinical, double-blind, placebo-controlled study. Neuromuscular Disorders. 23(9-10). 771–771. 4 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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2026