Emanuela Pappalardo

1.7k total citations
29 papers, 1.1k citations indexed

About

Emanuela Pappalardo is a scholar working on Hematology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Emanuela Pappalardo has authored 29 papers receiving a total of 1.1k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Hematology, 12 papers in Genetics and 7 papers in Pathology and Forensic Medicine. Recurrent topics in Emanuela Pappalardo's work include Coagulation, Bradykinin, Polyphosphates, and Angioedema (11 papers), Blood Coagulation and Thrombosis Mechanisms (11 papers) and Hemophilia Treatment and Research (8 papers). Emanuela Pappalardo is often cited by papers focused on Coagulation, Bradykinin, Polyphosphates, and Angioedema (11 papers), Blood Coagulation and Thrombosis Mechanisms (11 papers) and Hemophilia Treatment and Research (8 papers). Emanuela Pappalardo collaborates with scholars based in Italy, Netherlands and United States. Emanuela Pappalardo's co-authors include Marco Cicardi, Lorenza C. Zingale, A Agostoni, Andrea Zanichelli, Ida Martinelli, Paolo Bucciarelli, Christiane Duponchel, Mario Tosi, A. Carugati and L. Maggioni and has published in prestigious journals such as Blood, PLoS ONE and Hepatology.

In The Last Decade

Emanuela Pappalardo

27 papers receiving 1.1k 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 Pappalardo Italy 15 673 333 301 290 193 29 1.1k
Sladjana Andrejević Serbia 15 147 0.2× 257 0.8× 83 0.3× 56 0.2× 45 0.2× 40 618
Paula G. Heller Argentina 23 528 0.8× 176 0.5× 61 0.2× 819 2.8× 8 0.0× 53 1.2k
Ginette Schiby Israel 18 116 0.2× 63 0.2× 220 0.7× 224 0.8× 17 0.1× 53 883
Sophia Jacob United States 7 341 0.5× 95 0.3× 46 0.2× 484 1.7× 14 0.1× 9 1.2k
Carola Metzig Germany 10 124 0.2× 117 0.4× 324 1.1× 110 0.4× 49 0.3× 16 723
Øyvind Hjertner Norway 14 118 0.2× 106 0.3× 76 0.3× 650 2.2× 33 0.2× 27 1.5k
Katsuhiko Matsuo Japan 17 66 0.1× 64 0.2× 104 0.3× 100 0.3× 12 0.1× 23 1.2k
Ken�ichi Sekita Japan 15 129 0.2× 178 0.5× 122 0.4× 289 1.0× 13 0.1× 36 1.1k
Rivka Dresner Pollak Israel 13 153 0.2× 85 0.3× 86 0.3× 128 0.4× 29 0.2× 15 685
Claire Perret France 16 108 0.2× 127 0.4× 33 0.1× 74 0.3× 9 0.0× 30 1.2k

Countries citing papers authored by Emanuela Pappalardo

Since Specialization
Citations

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

Fields of papers citing papers by Emanuela Pappalardo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emanuela Pappalardo

This figure shows the co-authorship network connecting the top 25 collaborators of Emanuela Pappalardo. A scholar is included among the top collaborators of Emanuela Pappalardo 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 Pappalardo. Emanuela Pappalardo 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.
Mesolella, Massimo, et al.. (2023). Subjective Perception and Psychoacoustic Aspects of the Laryngectomee Voice: The Impact on Quality of Life. Journal of Personalized Medicine. 13(3). 570–570. 5 indexed citations
2.
Spena, Silvia, Francesca Gianniello, Emanuela Pappalardo, et al.. (2023). Genetic Variants Identified by Whole Exome Sequencing in a Large Italian Family with High Plasma Levels of Factor VIII and Von Willebrand Factor. International Journal of Molecular Sciences. 24(18). 14167–14167.
3.
Agosti, Pasquale, Ilaria Mancini, Saeed Sadeghian, et al.. (2023). Factor V Leiden but not the factor II 20210G>A mutation is a risk factor for premature coronary artery disease: a case-control study in Iran. Research and Practice in Thrombosis and Haemostasis. 7(1). 100048–100048. 5 indexed citations
4.
Gambino, Caterina Maria, Luisa Agnello, Bruna Lo Sasso, et al.. (2022). The role of serum free light chain as biomarker of Myasthenia Gravis. Clinica Chimica Acta. 528. 29–33. 6 indexed citations
5.
Pagliari, M, Ilaria Mancini, Emanuela Pappalardo, et al.. (2021). Role of ADAMTS13, VWF and F8 genes in deep vein thrombosis. PLoS ONE. 16(10). e0258675–e0258675. 6 indexed citations
6.
Gorski, Marcin M., Anna Lecchi, Eti Alessandra Femia, et al.. (2019). Complications of whole-exome sequencing for causal gene discovery in primary platelet secretion defects. Haematologica. 104(10). 2084–2090. 10 indexed citations
7.
Gorski, Marcin M., Hugoline G. de Haan, Ilaria Mancini, et al.. (2018). Next-generation DNA sequencing to identify novel genetic risk factors for cerebral vein thrombosis. Thrombosis Research. 169. 76–81. 4 indexed citations
8.
Gorski, Marcin M., Kevin Blighe, Luca A. Lotta, et al.. (2016). Whole-exome sequencing to identify genetic risk variants underlying inhibitor development in severe hemophilia A patients. Blood. 127(23). 2924–2933. 24 indexed citations
9.
Gorski, Marcin M., Luca A. Lotta, Emanuela Pappalardo, et al.. (2016). Single Nucleotide Variant rs2232710 in the Protein Z-Dependent Protease Inhibitor (ZPI, SERPINA10) Gene Is Not Associated with Deep Vein Thrombosis. PLoS ONE. 11(3). e0151347–e0151347. 9 indexed citations
10.
Passamonti, Serena M., Federica Di Berardino, Paolo Bucciarelli, et al.. (2015). Risk factors for idiopathic sudden sensorineural hearing loss and their association with clinical outcome. Thrombosis Research. 135(3). 508–512. 55 indexed citations
11.
Lotta, Luca A., Giacomo Tuana, Jin Yu, et al.. (2013). Next‐generation sequencing study finds an excess of rare, coding single‐nucleotide variants of ADAMTS13 in patients with deep vein thrombosis. Journal of Thrombosis and Haemostasis. 11(7). 1228–1239. 42 indexed citations
12.
Lotta, Luca A., Mark L. Wang, Jin Yu, et al.. (2012). Identification of genetic risk variants for deep vein thrombosis by multiplexed next-generation sequencing of 186 hemostatic/pro-inflammatory genes. BMC Medical Genomics. 5(1). 7–7. 29 indexed citations
13.
Pappalardo, Emanuela, Sonia Caccia, Chiara Suffritti, et al.. (2008). Mutation screening of C1 inhibitor gene in 108 unrelated families with hereditary angioedema: Functional and structural correlates. Molecular Immunology. 45(13). 3536–3544. 96 indexed citations
14.
Zingale, Lorenza C., L. Beltrami, Andrea Zanichelli, et al.. (2006). Angioedema without urticaria: a large clinical survey. Canadian Medical Association Journal. 175(9). 1065–1070. 147 indexed citations
15.
Cicardi, Marco, et al.. (2005). C1 inhibitor: molecular and clinical aspects. Springer Seminars in Immunopathology. 27(3). 286–298. 73 indexed citations
16.
Primignani, Massimo, Ida Martinelli, Paolo Bucciarelli, et al.. (2005). Risk factors for thrombophilia in extrahepatic portal vein obstruction†. Hepatology. 41(3). 603–608. 146 indexed citations
17.
Pappalardo, Emanuela, Lorenza C. Zingale, & Marco Cicardi. (2003). Increased expression of C1-inhibitor mRNA in patients with hereditary angioedema treated with Danazol. Immunology Letters. 86(3). 271–276. 58 indexed citations
18.
Cicardi, Marco, et al.. (2003). Autoantibodies and Lymphoproliferative Diseases in Acquired C1-Inhibitor Deficiencies. Medicine. 82(4). 274–281. 100 indexed citations
19.
Pappalardo, Emanuela, Marco Cicardi, Christiane Duponchel, et al.. (2000). Frequent de novo mutations and exon deletions in the C1inhibitor gene of patients with angioedema. Journal of Allergy and Clinical Immunology. 106(6). 1147–1154. 174 indexed citations
20.
Brancolini, Valeria, Elena Belloni, Emanuela Pappalardo, et al.. (1995). Search for mutations in pancreatic sufficient cystic fibrosis Italian patients: detection of 90% of molecular defects and identification of three novel mutations. Human Genetics. 96(3). 312–8. 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Sladjana Andrejević Breakdown of academic impact, for papers by Paula G. Heller Breakdown of academic impact, for papers by Ginette Schiby Breakdown of academic impact, for papers by Sophia Jacob Breakdown of academic impact, for papers by Carola Metzig Breakdown of academic impact, for papers by Øyvind Hjertner Breakdown of academic impact, for papers by Katsuhiko Matsuo Breakdown of academic impact, for papers by Ken�ichi Sekita Breakdown of academic impact, for papers by Rivka Dresner Pollak Breakdown of academic impact, for papers by Claire Perret
Rankless by CCL
2026