Giuseppe Bonapace

784 total citations
24 papers, 439 citations indexed

About

Giuseppe Bonapace is a scholar working on Molecular Biology, Clinical Biochemistry and Cell Biology. According to data from OpenAlex, Giuseppe Bonapace has authored 24 papers receiving a total of 439 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 6 papers in Clinical Biochemistry and 6 papers in Cell Biology. Recurrent topics in Giuseppe Bonapace's work include Metabolism and Genetic Disorders (6 papers), Cellular transport and secretion (5 papers) and Neurological diseases and metabolism (3 papers). Giuseppe Bonapace is often cited by papers focused on Metabolism and Genetic Disorders (6 papers), Cellular transport and secretion (5 papers) and Neurological diseases and metabolism (3 papers). Giuseppe Bonapace collaborates with scholars based in Italy, United States and United Kingdom. Giuseppe Bonapace's co-authors include William S. Sly, Gul N. Shah, Abdül Waheed, Pietro Strisciuglio, Peiyi Hu, Daniela Concolino, Rupak Datta, Lisa Roberts, Jacquie Greenberg and Soraya Bardien and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Neurobiology of Aging and Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease.

In The Last Decade

Giuseppe Bonapace

24 papers receiving 431 citations

Peers

Giuseppe Bonapace
Zhenlian Wang China
R. Kraetzner Germany
Erin Conboy United States
Gonzalo L. Vilas Canada
Kateřina Hodaňová Czechia
T A Diggle United Kingdom
Neelanjan Vishnu Sweden
Patricia Yuste‐Checa Spain
Timothy C. Kenny United States
S. Sekine Japan
Zhenlian Wang China
Giuseppe Bonapace
Citations per year, relative to Giuseppe Bonapace Giuseppe Bonapace (= 1×) peers Zhenlian Wang

Countries citing papers authored by Giuseppe Bonapace

Since Specialization
Citations

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

Fields of papers citing papers by Giuseppe Bonapace

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giuseppe Bonapace

This figure shows the co-authorship network connecting the top 25 collaborators of Giuseppe Bonapace. A scholar is included among the top collaborators of Giuseppe Bonapace 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 Giuseppe Bonapace. Giuseppe Bonapace 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.
Gagliardi, Monica, Andrea Quattrone, Gennarina Arabia, et al.. (2023). ANXA1 mutation analysis in Italian patients with early onset PD. Neurobiology of Aging. 125. 123–124. 1 indexed citations
2.
3.
Salatino, Alessandro, Maria Mirabelli, Eusebio Chiefari, et al.. (2022). The anticancer effects of Metformin in the male germ tumor SEM-1 cell line are mediated by HMGA1. Frontiers in Endocrinology. 13. 1051988–1051988. 9 indexed citations
4.
Bonapace, Giuseppe, Francesco Gentile, Nicola Coppedé, et al.. (2021). Methylglyoxal Adducts Levels in Blood Measured on Dried Spot by Portable Near-Infrared Spectroscopy. Nanomaterials. 11(9). 2432–2432. 3 indexed citations
5.
Bonapace, Giuseppe, Monica Gagliardi, Maurizio Morelli, et al.. (2021). Multiple system atrophy and C9orf72 hexanucleotide repeat expansions in a cohort of Italian patients. Neurobiology of Aging. 112. 12–15. 4 indexed citations
6.
Gagliardi, Monica, Marco D’Amelio, Laura Brighina, et al.. (2020). DCTN1 mutation analysis in Italian patients with PSP, MSA, and DLB. Neurobiology of Aging. 93. 143.e5–143.e7. 3 indexed citations
7.
Bonapace, Giuseppe, Daniela Concolino, Monica Gagliardi, et al.. (2019). Intracellular FMRpolyG-Hsp70 complex in fibroblast cells from a patient affected by fragile X tremor ataxia syndrome. Heliyon. 5(6). e01954–e01954. 6 indexed citations
8.
Gagliardi, Monica, Grazia Annesi, Maurizio Morelli, et al.. (2018). DNAJC13 mutation screening in patients with Parkinson's disease from South Italy. Parkinsonism & Related Disorders. 55. 134–137. 13 indexed citations
9.
Sestito, Simona, et al.. (2018). Genetics and Gene Therapy in Hunter Disease. Current Gene Therapy. 18(2). 90–95. 8 indexed citations
10.
Concolino, Daniela, et al.. (2016). Long-term treatment of phenylketonuria with a new medical food containing large neutral amino acids. European Journal of Clinical Nutrition. 71(1). 51–55. 24 indexed citations
11.
Sestito, Simona, Vincenzo Salpietro, Agata Polizzi, et al.. (2016). Pathobiological Insights into Neurological Involvement in Cobalamin C Deficiency. CINECA IRIS Institutial Research Information System (University of Genoa). 6(1). 25–29. 1 indexed citations
12.
Scala, Iris, Daniela Concolino, Roberto Della Casa, et al.. (2015). Long-term follow-up of patients with phenylketonuria treated with tetrahydrobiopterin: a seven years experience. Orphanet Journal of Rare Diseases. 10(1). 14–14. 26 indexed citations
13.
Bonapace, Giuseppe, et al.. (2014). Identification of two novel mutations on CLCN7 gene in a patient with malignant ostopetrosis. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 40(1). 90–90. 7 indexed citations
14.
Bonapace, Giuseppe, et al.. (2010). Germline mosaicism for the c.2021G > A (p.Arg674Gln) mutation in siblings with trismus pseudocamptodactyly. American Journal of Medical Genetics Part A. 152A(11). 2898–2900. 4 indexed citations
15.
Concolino, Daniela, Maria Anna Rapsomaniki, Eliana Disabella, et al.. (2010). Co-existence of Phenylketonuria and Fabry disease on a 3 year-old boy: case report. BMC Pediatrics. 10(1). 32–32. 7 indexed citations
16.
Concolino, Daniela, et al.. (2009). Long-term treatment with recombinant insulin-like growth factor 1 (IGF-1) in a child with IGF-1 gene mutation. European Journal of Pediatrics. 169(2). 245–247. 6 indexed citations
17.
Datta, Rupak, Abdül Waheed, Giuseppe Bonapace, Gul N. Shah, & William S. Sly. (2009). Pathogenesis of retinitis pigmentosa associated with apoptosis-inducing mutations in carbonic anhydrase IV. Proceedings of the National Academy of Sciences. 106(9). 3437–3442. 50 indexed citations
18.
Bonapace, Giuseppe, Francesco Iuliano, Stefano Molica, Antonio Peta, & Pietro Strisciuglio. (2004). Cytosolic carbonic anhydrase activity in chronic myeloid disorders with different clinical phenotype. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1689(3). 179–181. 6 indexed citations
19.
20.
Rebello, George, Raj Ramesar, Lisa Roberts, et al.. (2004). Apoptosis-inducing signal sequence mutation in carbonic anhydrase IV identified in patients with the RP17 form of retinitis pigmentosa. Proceedings of the National Academy of Sciences. 101(17). 6617–6622. 87 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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