Ignazio Calì

2.6k total citations
40 papers, 1.2k citations indexed

About

Ignazio Calì is a scholar working on Molecular Biology, Neurology and Nutrition and Dietetics. According to data from OpenAlex, Ignazio Calì has authored 40 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 39 papers in Molecular Biology, 22 papers in Neurology and 12 papers in Nutrition and Dietetics. Recurrent topics in Ignazio Calì's work include Prion Diseases and Protein Misfolding (39 papers), Neurological diseases and metabolism (22 papers) and Trace Elements in Health (12 papers). Ignazio Calì is often cited by papers focused on Prion Diseases and Protein Misfolding (39 papers), Neurological diseases and metabolism (22 papers) and Trace Elements in Health (12 papers). Ignazio Calì collaborates with scholars based in United States, Italy and United Kingdom. Ignazio Calì's co-authors include Pierluigi Gambetti, Qingzhong Kong, Wen‐Quan Zou, Witold K. Surewicz, Jue Yuan, Krystyna Surewicz, Silvio Notari, Liuting Qing, Lawrence B. Schonberger and Piero Parchi and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Ignazio Calì

39 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Ignazio Calì United States 19 1.1k 549 371 142 131 40 1.2k
Jackie Linehan United Kingdom 10 769 0.7× 332 0.6× 257 0.7× 112 0.8× 46 0.4× 11 829
A Fletcher Australia 7 900 0.8× 370 0.7× 116 0.3× 65 0.5× 198 1.5× 11 974
Patrick J. Bosque United States 11 1.1k 0.9× 530 1.0× 397 1.1× 76 0.5× 48 0.4× 14 1.1k
C.M. Goodsir United Kingdom 17 821 0.7× 502 0.9× 384 1.0× 128 0.9× 53 0.4× 22 853
James F. Striebel United States 17 832 0.7× 537 1.0× 230 0.6× 224 1.6× 46 0.4× 30 927
Don C. Guiroy United States 14 459 0.4× 256 0.5× 114 0.3× 153 1.1× 91 0.7× 21 581
Gary Hsich United States 7 472 0.4× 159 0.3× 66 0.2× 59 0.4× 96 0.7× 10 603
Etienne Levavasseur France 12 426 0.4× 318 0.6× 99 0.3× 45 0.3× 34 0.3× 18 652
Rita Moos Switzerland 14 614 0.6× 338 0.6× 192 0.5× 261 1.8× 33 0.3× 22 830
J.P. Deslys France 12 485 0.4× 260 0.5× 105 0.3× 48 0.3× 78 0.6× 17 548

Countries citing papers authored by Ignazio Calì

Since Specialization
Citations

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

Fields of papers citing papers by Ignazio Calì

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ignazio Calì

This figure shows the co-authorship network connecting the top 25 collaborators of Ignazio Calì. A scholar is included among the top collaborators of Ignazio Calì 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 Ignazio Calì. Ignazio Calì 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.
Cohen, Mark L., Ignazio Calì, J. Ludwig, et al.. (2025). Case report: Atypical young case of MV1 Creutzfeldt-Jakob disease with unusually long survival. Frontiers in Cellular Neuroscience. 18. 1518542–1518542. 1 indexed citations
2.
Orrú, Christina D., Yvonne Cohen, Rossana Occhipinti, et al.. (2023). A novel subtype of sporadic Creutzfeldt–Jakob disease with PRNP codon 129MM genotype and PrP plaques. Acta Neuropathologica. 146(1). 121–143. 5 indexed citations
3.
Cracco, Laura, Ignazio Calì, Mark L. Cohen, et al.. (2023). Efficient transmission of human prion diseases to a glycan-free prion protein-expressing host. Brain. 147(4). 1539–1552.
4.
Cracco, Laura, Gianfranco Puoti, Zerui Wang, et al.. (2023). Novel histotypes of sporadic Creutzfeldt–Jakob disease linked to 129MV genotype. Acta Neuropathologica Communications. 11(1). 141–141. 2 indexed citations
5.
Calì, Ignazio, Tze How Mok, Helen E. Speedy, et al.. (2021). Characterization of Prion Disease Associated with a Two-Octapeptide Repeat Insertion. Viruses. 13(9). 1794–1794. 5 indexed citations
6.
Calì, Ignazio, Juan Carlos Espinosa, Satish Kumar Nemani, et al.. (2021). Two distinct conformers of PrPD type 1 of sporadic Creutzfeldt–Jakob disease with codon 129VV genotype faithfully propagate in vivo. Acta Neuropathologica Communications. 9(1). 55–55. 5 indexed citations
7.
Wang, Zerui, Kefeng Qin, Manuel V. Camacho, et al.. (2021). Generation of human chronic wasting disease in transgenic mice. Acta Neuropathologica Communications. 9(1). 158–158. 26 indexed citations
8.
Baiardi, Simone, Marcello Rossi, Angela Mammana, et al.. (2021). Phenotypic diversity of genetic Creutzfeldt–Jakob disease: a histo-molecular-based classification. Acta Neuropathologica. 142(4). 707–728. 30 indexed citations
9.
Nemani, Satish Kumar, Xiangzhu Xiao, Ignazio Calì, et al.. (2020). A novel mechanism of phenotypic heterogeneity in Creutzfeldt-Jakob disease. Acta Neuropathologica Communications. 8(1). 85–85. 11 indexed citations
10.
Calì, Ignazio, Laura Cracco, Dario Saracino, et al.. (2020). Case Report: Histopathology and Prion Protein Molecular Properties in Inherited Prion Disease With a De Novo Seven-Octapeptide Repeat Insertion. Frontiers in Cellular Neuroscience. 14. 150–150. 3 indexed citations
11.
Cracco, Laura, Silvio Notari, Ignazio Calì, et al.. (2017). Novel strain properties distinguishing sporadic prion diseases sharing prion protein genotype and prion type. Scientific Reports. 7(1). 38280–38280. 16 indexed citations
12.
Calì, Ignazio, et al.. (2015). Distinct pathological phenotypes of Creutzfeldt-Jakob disease in recipients of prion-contaminated growth hormone. Acta Neuropathologica Communications. 3(1). 37–37. 18 indexed citations
13.
Xiao, Xiangzhu, Jue Yuan, Stéphane Haı̈k, et al.. (2013). Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease. PLoS ONE. 8(3). e58786–e58786. 31 indexed citations
14.
Xiao, Xiangzhu, Jue Yuan, Ignazio Calì, et al.. (2013). Correction: Glycoform-Selective Prion Formation in Sporadic and Familial Forms of Prion Disease. PLoS ONE. 8(10). 17 indexed citations
15.
Calì, Ignazio, Abby Oehler, Jamie Fong, et al.. (2013). Genetic CJD with a novel E200G mutation in the prion protein gene and comparison with E200K mutation cases. Acta Neuropathologica Communications. 1(1). 80–80. 22 indexed citations
16.
Kong, Qingzhong, Jeffrey Mills, Bishwajit Kundu, et al.. (2013). Thermodynamic Stabilization of the Folded Domain of Prion Protein Inhibits Prion Infection in Vivo. Cell Reports. 4(2). 248–254. 26 indexed citations
17.
Moody, Karen, Lawrence B. Schonberger, Ryan A. Maddox, et al.. (2011). Sporadic fatal insomnia in a young woman: A diagnostic challenge: Case Report. BMC Neurology. 11(1). 136–136. 9 indexed citations
18.
Gambetti, Pierluigi, Ignazio Calì, Silvio Notari, et al.. (2010). Molecular biology and pathology of prion strains in sporadic human prion diseases. Acta Neuropathologica. 121(1). 79–90. 75 indexed citations
19.
Tartaglia, Maria Carmela, Julie Thai, Tricia See, et al.. (2010). Pathologic Evidence That the T188R Mutation inPRNPIs Associated With Prion Disease. Journal of Neuropathology & Experimental Neurology. 69(12). 1220–1227. 9 indexed citations
20.
Calì, Ignazio. (2006). Classification of sporadic Creutzfeldt-Jakob disease revisited. Brain. 129(9). 2266–2277. 100 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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