Emanuele Panza

1.4k total citations
32 papers, 507 citations indexed

About

Emanuele Panza is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Emanuele Panza has authored 32 papers receiving a total of 507 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Genetics, 8 papers in Molecular Biology and 7 papers in Surgery. Recurrent topics in Emanuele Panza's work include Hereditary Neurological Disorders (6 papers), Neurological diseases and metabolism (5 papers) and Platelet Disorders and Treatments (5 papers). Emanuele Panza is often cited by papers focused on Hereditary Neurological Disorders (6 papers), Neurological diseases and metabolism (5 papers) and Platelet Disorders and Treatments (5 papers). Emanuele Panza collaborates with scholars based in Italy, United States and Spain. Emanuele Panza's co-authors include Marco Seri, Roberto De Giorgio, Charles H. Knowles, Greger Lindberg, Antonio Orlacchio, Arun Meyyazhagan, Alessandro Pecci, Valeria Bozzi, Pamela Magini and Carlo Balduini and has published in prestigious journals such as Journal of Clinical Investigation, Blood and International Journal of Molecular Sciences.

In The Last Decade

Emanuele Panza

31 papers receiving 501 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Emanuele Panza Italy 15 133 125 101 79 78 32 507
Igor Kovačević Netherlands 15 284 2.1× 71 0.6× 15 0.1× 30 0.4× 41 0.5× 21 643
Paolo Fontana Italy 16 224 1.7× 160 1.3× 18 0.2× 36 0.5× 120 1.5× 47 884
Rania Shamekh United States 12 100 0.8× 78 0.6× 16 0.2× 39 0.5× 33 0.4× 21 329
Karen Verity Australia 12 233 1.8× 81 0.6× 55 0.5× 119 1.5× 39 0.5× 12 568
Rumiko Izumi Japan 16 327 2.5× 37 0.3× 26 0.3× 138 1.7× 68 0.9× 50 609
Yutaka Harita Japan 19 427 3.2× 124 1.0× 60 0.6× 55 0.7× 21 0.3× 66 934
Guanghong Wu United States 11 277 2.1× 33 0.3× 39 0.4× 102 1.3× 40 0.5× 17 558
Alina Kurolap Israel 12 150 1.1× 36 0.3× 15 0.1× 28 0.4× 36 0.5× 42 399
H Jani United Kingdom 6 107 0.8× 141 1.1× 69 0.7× 47 0.6× 52 0.7× 11 372
J E Barker United States 9 236 1.8× 53 0.4× 81 0.8× 74 0.9× 34 0.4× 15 501

Countries citing papers authored by Emanuele Panza

Since Specialization
Citations

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

Fields of papers citing papers by Emanuele Panza

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Emanuele Panza

This figure shows the co-authorship network connecting the top 25 collaborators of Emanuele Panza. A scholar is included among the top collaborators of Emanuele Panza 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 Emanuele Panza. Emanuele Panza 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.
Coccia, Emanuele, Stefania Calabrese, Flavia Palombo, et al.. (2024). Effectiveness and Impact of Transcript Analysis in Clinical Genetics Daily Practice. Clinical Genetics. 107(5). 570–575. 1 indexed citations
2.
Meyyazhagan, Arun, et al.. (2024). Effects of APOE isoforms in diabetic nephropathy patients of South India. Acta Diabetologica. 62(4). 487–497.
3.
4.
Rossi, Cesare, Cecilia Evangelisti, Simona Ferrari, et al.. (2023). Case report: Functional characterization of a novel CHD7 intronic variant in patients with CHARGE syndrome. Frontiers in Genetics. 14. 1082100–1082100. 3 indexed citations
5.
Panza, Emanuele, Arun Meyyazhagan, & Antonio Orlacchio. (2022). Hereditary spastic paraplegia: Genetic heterogeneity and common pathways. Experimental Neurology. 357. 114203–114203. 30 indexed citations
6.
Toydemir, Reha M., et al.. (2020). Seizures and Cardiomyopathy in a Patient with Pallister-Killian Syndrome due to Hexasomy 12p Mosaicism. Molecular Syndromology. 11(3). 125–129. 1 indexed citations
7.
Avnet, Sofia, Silvia Lemma, Costantino Errani, et al.. (2020). Benign albeit glycolytic: MCT4 expression and lactate release in giant cell tumour of bone. Bone. 134. 115302–115302. 3 indexed citations
8.
Dugan, Sarah, et al.. (2018). Delineation of the 9q31 deletion syndrome: Genomic microarray characterization of two patients with overlapping deletions. American Journal of Medical Genetics Part A. 176(12). 2901–2906. 4 indexed citations
9.
Knowles, Charles H., Greger Lindberg, Emanuele Panza, & Roberto De Giorgio. (2013). New perspectives in the diagnosis and management of enteric neuropathies. Nature Reviews Gastroenterology & Hepatology. 10(4). 206–218. 81 indexed citations
10.
Panza, Emanuele, Charles H. Knowles, Claudio Graziano, et al.. (2012). Genetics of human enteric neuropathies. Progress in Neurobiology. 96(2). 176–189. 30 indexed citations
11.
Bozzi, Valeria, Emanuele Panza, Serena Barozzi, et al.. (2011). Mutations responsible for MYH9-related thrombocytopenia impair SDF-1-driven migration of megakaryoblastic cells. Thrombosis and Haemostasis. 106(10). 693–704. 23 indexed citations
12.
Rocco, Daniela De, Emanuele Panza, Valeria Bozzi, et al.. (2010). Heavy chain myosin 9-related disease (MYH9-RD): Neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder. Thrombosis and Haemostasis. 103(4). 826–832. 66 indexed citations
13.
Brussino, Alessandro, Giovanna Vaula, Cinzia Cagnoli, et al.. (2009). A family with autosomal dominant leukodystrophy linked to 5q23.2–q23.3 without lamin B1 mutations. European Journal of Neurology. 17(4). 541–549. 31 indexed citations
14.
Panza, Emanuele, Monica Marini, Alessandro Pecci, et al.. (2008). Transfection of the mutant MYH9 cDNA reproduces the most typical cellular phenotype of MYH9-related disease in different cell lines. PubMed. 1(1). 5–5. 5 indexed citations
15.
Pippucci, Tommaso, Emanuele Panza, Eva Pompilii, et al.. (2008). Autosomal recessive hereditary spastic paraplegia with thin corpus callosum: a novel mutation in the SPG11 gene and further evidence for genetic heterogeneity. European Journal of Neurology. 16(1). 121–126. 12 indexed citations
16.
Panza, Emanuele, Tommaso Pippucci, Roberto Cusano, et al.. (2008). Refinement of the SPG9 locus on chromosome 10q23.3‐24.2 and exclusion of candidate genes. European Journal of Neurology. 15(5). 520–524. 3 indexed citations
17.
Deglincerti, Alessia, Roberto De Giorgio, Kıvanç Çefle, et al.. (2007). A novel locus for syndromic chronic idiopathic intestinal pseudo-obstruction maps to chromosome 8q23–q24. European Journal of Human Genetics. 15(8). 889–897. 21 indexed citations
18.
Longo, Luca, Emanuele Panza, Francesca Schena, et al.. (2007). Genetic Predisposition to Familial Neuroblastoma: Identification of Two Novel Genomic Regions at 2p and 12p. Human Heredity. 63(3-4). 205–211. 20 indexed citations
19.
Panza, Emanuele, Giorgio Gimelli, Mario Passalacqua, et al.. (2007). The breakpoint identified in a balanced de novo translocation t(7;9)(p14.1;q31.3) disrupts the A-kinase (PRKA) anchor protein 2 gene (AKAP2) on chromosome 9 in a patient with Kallmann syndrome and bone anomalies. International Journal of Molecular Medicine. 19(3). 429–35. 13 indexed citations
20.
Leggett, Barbara, Roberto Corinaldesi, G Dobrilla, et al.. (1986). A double-blind controlled trial of ranitidine 300 mg nocte and ranitidine 150 mg b.i.d. in the short-term treatment of gastric ulcer.. PubMed. 24(2). 104–7. 2 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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