Nadia Zanetti

1.6k total citations · 1 hit paper
10 papers, 1.2k citations indexed

About

Nadia Zanetti is a scholar working on Molecular Biology, Clinical Biochemistry and Cellular and Molecular Neuroscience. According to data from OpenAlex, Nadia Zanetti has authored 10 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 7 papers in Clinical Biochemistry and 2 papers in Cellular and Molecular Neuroscience. Recurrent topics in Nadia Zanetti's work include Mitochondrial Function and Pathology (7 papers), Metabolism and Genetic Disorders (7 papers) and ATP Synthase and ATPases Research (2 papers). Nadia Zanetti is often cited by papers focused on Mitochondrial Function and Pathology (7 papers), Metabolism and Genetic Disorders (7 papers) and ATP Synthase and ATPases Research (2 papers). Nadia Zanetti collaborates with scholars based in Italy, Australia and United States. Nadia Zanetti's co-authors include Giuseppe Lamorte, Brent A. Reynolds, Elena Binda, Francesco DiMeco, Angelo L. Vescovi, Sara Piccirillo, Giovanni Broggi, Henry Brem, Alessandro Olivi and Daniele Ghezzi and has published in prestigious journals such as Nature, Cancer Cell and Cells.

In The Last Decade

Nadia Zanetti

9 papers receiving 1.2k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Bone morphogenetic proteins inhibit the tumorigenic potential of human brain tumour-initiating cells

2006 914 citations Sara Piccirillo, Brent A. Reynolds et al. Nature profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Nadia Zanetti Italy	7	750	567	364	281	130	10	1.2k
Thant S. Zhu United States	9	614 0.8×	534 0.9×	360 1.0×	365 1.3×	54 0.4×	10	1.1k
Karisa C. Schreck United States	16	946 1.3×	418 0.7×	505 1.4×	290 1.0×	44 0.3×	55	1.4k
Juyoun Jin South Korea	19	758 1.0×	646 1.1×	478 1.3×	395 1.4×	48 0.4×	30	1.5k
Sascha Seidel Germany	8	752 1.0×	308 0.5×	252 0.7×	447 1.6×	237 1.8×	10	1.2k
Koos E. Hovinga Netherlands	11	762 1.0×	659 1.2×	606 1.7×	539 1.9×	61 0.5×	25	1.5k
Michael Masterman‐Smith United States	10	922 1.2×	954 1.7×	711 2.0×	484 1.7×	77 0.6×	12	1.8k
Anne-Marie Bleau United States	8	798 1.1×	785 1.4×	487 1.3×	447 1.6×	33 0.3×	9	1.5k
Lung-Kuo Tai Taiwan	8	499 0.7×	416 0.7×	153 0.4×	205 0.7×	47 0.4×	9	918
Marie‐Thérése Stockhausen Denmark	18	557 0.7×	281 0.5×	412 1.1×	272 1.0×	132 1.0×	24	1.1k
Elena Rampazzo Italy	21	932 1.2×	490 0.9×	541 1.5×	592 2.1×	47 0.4×	35	1.6k

Countries citing papers authored by Nadia Zanetti

Since Specialization

Citations

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

Fields of papers citing papers by Nadia Zanetti

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nadia Zanetti

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

All Works

Sort: Min cites: Since: Top N: Style:

10 of 10 papers shown

1.

Invernizzi, Federica, Andrea Legati, Nadia Zanetti, et al.. (2023). NGS-Based Genetic Analysis in a Cohort of Italian Patients with Suspected Inherited Myopathies and/or HyperCKemia. Genes. 14(7). 1393–1393. 3 indexed citations

2.

Frascarelli, Chiara, Nadia Zanetti, Alessia Nasca, et al.. (2023). Nanopore long-read next-generation sequencing for detection of mitochondrial DNA large-scale deletions. Frontiers in Genetics. 14. 1089956–1089956. 22 indexed citations

3.

Zanetti, Nadia, Marco Bobbo, Egidio Barbi, et al.. (2023). A new family with a case of severe early-onset muscle fatigue and a peculiar maternally inherited painful swelling in chewing muscles associated with homoplasmic m.15992A>T mutation in mitochondrial tRNAPro. Neuromuscular Disorders. 33(12). 972–977.

4.

Nasca, Alessia, Andrea Legati, Megi Meneri, et al.. (2022). Biallelic Variants in ENDOG Associated with Mitochondrial Myopathy and Multiple mtDNA Deletions. Cells. 11(6). 974–974. 6 indexed citations

5.

Legati, Andrea, Nadia Zanetti, Alessia Nasca, et al.. (2021). Current and New Next-Generation Sequencing Approaches to Study Mitochondrial DNA. Journal of Molecular Diagnostics. 23(6). 732–741. 26 indexed citations

6.

Marchet, Silvia, Andrea Legati, Alessia Nasca, et al.. (2020). Homozygous mutations in C1QBP as cause of progressive external ophthalmoplegia (PEO) and mitochondrial myopathy with multiple mtDNA deletions. Human Mutation. 41(10). 1745–1750. 11 indexed citations

7.

Catania, Alessia, Andrea Legati, Lorenzo Peverelli, et al.. (2019). Homozygous variant in OTX2 and possible genetic modifiers identified in a patient with combined pituitary hormone deficiency, ocular involvement, myopathy, ataxia, and mitochondrial impairment. American Journal of Medical Genetics Part A. 179(5). 827–831. 4 indexed citations

8.

Torraco, Alessandra, Anna Ardissone, Federica Invernizzi, et al.. (2016). Novel mutations in IBA57 are associated with leukodystrophy and variable clinical phenotypes. Journal of Neurology. 264(1). 102–111. 34 indexed citations

9.

Binda, Elena, Alberto Visioli, Fabrizio Giani, et al.. (2012). The EphA2 Receptor Drives Self-Renewal and Tumorigenicity in Stem-like Tumor-Propagating Cells from Human Glioblastomas. Cancer Cell. 22(6). 765–780. 169 indexed citations

10.

Piccirillo, Sara, Brent A. Reynolds, Nadia Zanetti, et al.. (2006). Bone morphogenetic proteins inhibit the tumorigenic potential of human brain tumour-initiating cells. Nature. 444(7120). 761–765. 914 indexed citations breakdown →

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