Vito Guzzetta

1.6k citations
7 papers · 1.2k · 1 hit paper · h-index 6

Impact in

    • Hereditary Neurological Disorders
    • Genetic Neurodegenerative Diseases
  • Neurology top 5%
    • Neurological diseases and metabolism
    • Botulinum Toxin and Related Neurological Disorders
    • Peripheral Neuropathies and Disorders

Papers in

    • RNA and protein synthesis mechanisms 1
    • RNA modifications and cancer 1
    • Neurogenetic and Muscular Disorders Research 2
    • Genomic variations and chromosomal abnormalities 2
    • Connective tissue disorders research 1

Vito Guzzetta

7 papers receiving 1.2k citations

Hit Papers

DNA duplication associated with Charcot-Marie-Tooth disease type 1A 1991 · 1.0k citations
1.0k0+11+23Years since publication2505007501000

Peers

Vito Guzzetta
Comparison fields: 5 of 55
  • Cellular and Molecular Neuroscience 810
  • Neurology 263
  • Neurology 324
  • Genetics 105
  • Genetics 273
Replace Carlos A. Garcia with:
Carlos A. Garcia United States
Friedmar R. Kreuz Germany
JoAnn Bergoffen United States
Sascha Vermeer Netherlands
Laura E. Warner United States
Félix Prieto Spain
Nacer Abbas France
Nazha Birouk France
A. V. Polyakov Russia
Collette K. Hand Canada
Vito Guzzetta relative to Carlos A. Garcia United States Carlos A. Garcia's profile →
Citations per field
00.5×1.5×
Carlos A. Garcia · 1×
Citations per year

Countries citing papers authored by Vito Guzzetta

Since Specialization
Citations

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

Fields of papers citing papers by Vito Guzzetta

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Vito Guzzetta, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Vito Guzzetta Line = papers co-authored together Vito Guzzetta links everyone, so they are left out of the graph.

All Works

7 of 7 papers shown
#Work
1
DNA duplication associated with Charcot-Marie-Tooth disease type 1A
Hit paper breakdown →
19911013
2 199689
3 199237
4 199126
5 199611
6 20026
7 19962

About Vito Guzzetta

Vito Guzzetta is a scholar working on Molecular Biology, Genetics, Genetics, Cellular and Molecular Neuroscience and Surgery, having authored 7 papers that have together received 1.2k indexed citations. Recurring topics across this work include Hereditary Neurological Disorders (2 papers), Neurogenetic and Muscular Disorders Research (2 papers), Genomic variations and chromosomal abnormalities (2 papers), Connective tissue disorders research (1 paper), Cholesterol and Lipid Metabolism (1 paper), RNA and protein synthesis mechanisms (1 paper), T-cell and Retrovirus Studies (1 paper) and RNA modifications and cancer (1 paper). The work is most often cited by research in Cellular and Molecular Neuroscience (810 citations), Neurology (263 citations), Neurology (324 citations), Genetics (105 citations) and Genetics (273 citations). Vito Guzzetta has collaborated with scholars based in Italy and United States. Frequent co-authors include Pragna I. Patel, Roberto Montes‐de‐Oca‐Luna, James R. Lupski, Odila Saucedo‐Cárdenas, Carlos A. Garcia, Barbara J. Trask, James M. Killian, Susan Slaugenhaupt, David F. Barker and Pentao Liu. Their work appears in journals such as Genomics, Epilepsia, Cell and American Journal of Medical Genetics.

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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