Diego Vozzi

4.9k total citations
36 papers, 516 citations indexed

About

Diego Vozzi is a scholar working on Molecular Biology, Sensory Systems and Genetics. According to data from OpenAlex, Diego Vozzi has authored 36 papers receiving a total of 516 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 12 papers in Sensory Systems and 8 papers in Genetics. Recurrent topics in Diego Vozzi's work include Hearing, Cochlea, Tinnitus, Genetics (12 papers), Genomics and Rare Diseases (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Diego Vozzi is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (12 papers), Genomics and Rare Diseases (6 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Diego Vozzi collaborates with scholars based in Italy, Qatar and United Kingdom. Diego Vozzi's co-authors include Paolo Gasparini, Giorgia Girotto, Anna Morgan, Ramin Badii, Dragana Vuckovic, Pio D’Adamo, Angela D’Eustacchio, Danilo Licastro, Flavio Faletra and Massimo Mezzavilla and has published in prestigious journals such as Nature Communications, Neuron and PLoS ONE.

In The Last Decade

Diego Vozzi

33 papers receiving 506 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Diego Vozzi Italy 16 250 204 130 72 54 36 516
Atteeq U. Rehman United States 12 373 1.5× 315 1.5× 93 0.7× 118 1.6× 65 1.2× 19 588
Amal Abu Rayyan Palestinian Territory 12 356 1.4× 223 1.1× 228 1.8× 81 1.1× 45 0.8× 18 632
Valérie Faugère France 14 438 1.8× 277 1.4× 85 0.7× 83 1.2× 25 0.5× 21 550
Marta Lucía Tamayo Colombia 11 469 1.9× 338 1.7× 75 0.6× 89 1.2× 41 0.8× 35 647
Sigrid Wayne United States 11 344 1.4× 364 1.8× 55 0.4× 115 1.6× 74 1.4× 19 543
Arnaud P. J. Giese United States 11 248 1.0× 224 1.1× 42 0.3× 61 0.8× 42 0.8× 13 438
Kazunori Namba Japan 15 331 1.3× 187 0.9× 38 0.3× 116 1.6× 44 0.8× 28 586
Marie Teixeira France 13 374 1.5× 120 0.6× 142 1.1× 114 1.6× 15 0.3× 26 596
Asadollah Aghaie France 13 641 2.6× 403 2.0× 76 0.6× 153 2.1× 97 1.8× 16 904
Pranav Dinesh Mathur United States 12 359 1.4× 318 1.6× 43 0.3× 123 1.7× 42 0.8× 16 550

Countries citing papers authored by Diego Vozzi

Since Specialization
Citations

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

Fields of papers citing papers by Diego Vozzi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Diego Vozzi

This figure shows the co-authorship network connecting the top 25 collaborators of Diego Vozzi. A scholar is included among the top collaborators of Diego Vozzi 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 Diego Vozzi. Diego Vozzi 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.
Rastogi, Mohit, Martina Bartolucci, Marina Nanni, et al.. (2024). Integrative multi-omic analysis reveals conserved cell-projection deficits in human Down syndrome brains. Neuron. 112(15). 2503–2523.e10. 6 indexed citations
2.
Divizia, Maria Teresa, Livia Pisciotta, Maria Margherita Mancardi, et al.. (2023). Novel SYNGAP1 Variant in an Adult Individual Affected by Intellectual Disability and Epilepsy: A Cold Case Solved through Whole-Exome Sequencing. Molecular Syndromology. 14(5). 433–438.
3.
Scala, Marcello, Patrizia De Marco, Marzia Ognibene, et al.. (2023). Somatic Double Inactivation of NF1 Associated with NF1-Related Pectus Excavatum Deformity. Human Mutation. 2023. 1–7. 3 indexed citations
4.
Scala, Marcello, Francesca Madia, Diego Vozzi, et al.. (2023). MYT1L variant inherited by a mosaic father in a case of severe developmental and epileptic encephalopathy. Epileptic Disorders. 25(6). 874–879.
5.
Mangoni, Damiano, Alessandro Simi, Pierre Lau, et al.. (2023). LINE-1 regulates cortical development by acting as long non-coding RNAs. Nature Communications. 14(1). 4974–4974. 22 indexed citations
6.
Pisciotta, Livia, Margherita Squillario, Maria Teresa Divizia, et al.. (2021). Case Report: Whole Exome Sequencing Revealed Disease-Causing Variants in Two Genes in a Patient With Autism Spectrum Disorder, Intellectual Disability, Hyperactivity, Sleep and Gastrointestinal Disturbances. Frontiers in Genetics. 12. 625564–625564. 9 indexed citations
7.
Stazio, Mariateresa Di, Chiara Collesi, Diego Vozzi, et al.. (2018). TBL1Y: a new gene involved in syndromic hearing loss. European Journal of Human Genetics. 27(3). 466–474. 15 indexed citations
8.
Morgan, Anna, Dragana Vuckovic, Navaneethakrishnan Krishnamoorthy, et al.. (2018). Next-generation sequencing identified SPATC1L as a possible candidate gene for both early-onset and age-related hearing loss. European Journal of Human Genetics. 27(1). 70–79. 18 indexed citations
9.
10.
Mezzavilla, Massimo, et al.. (2015). Increased Rate of Deleterious Variants in Long Runs of Homozygosity of an Inbred Population from Qatar. Human Heredity. 79(1). 14–19. 20 indexed citations
11.
Morgan, Anna, Ilaria Gandin, Pietro Palumbo, et al.. (2015). Target sequencing approach intended to discover new mutations in non-syndromic intellectual disability. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 781. 32–36. 9 indexed citations
12.
Lenarduzzi, Stefania, Diego Vozzi, Anna Morgan, et al.. (2015). Usher syndrome: An effective sequencing approach to establish a genetic and clinical diagnosis. Hearing Research. 320. 18–23. 22 indexed citations
13.
Bianco, Anna Monica, Flavio Faletra, Diego Vozzi, et al.. (2015). Two-gene mutation in a single patient: Biochemical and functional analysis for a correct interpretation of exome results. Molecular Medicine Reports. 12(4). 6128–6132. 2 indexed citations
14.
Girotto, Giorgia, Massimo Mezzavilla, Dragana Vuckovic, et al.. (2014). Consanguinity and Hereditary Hearing Loss in Qatar. Human Heredity. 77(1-4). 175–182. 16 indexed citations
15.
Vozzi, Diego, Anna Morgan, Dragana Vuckovic, et al.. (2014). Hereditary hearing loss: a 96 gene targeted sequencing protocol reveals novel alleles in a series of Italian and Qatari patients. Gene. 542(2). 209–216. 45 indexed citations
16.
Athanasakis, Emmanouil, Danilo Licastro, Flavio Faletra, et al.. (2013). Next generation sequencing in nonsyndromic intellectual disability: From a negative molecular karyotype to a possible causative mutation detection. American Journal of Medical Genetics Part A. 164(1). 170–176. 31 indexed citations
17.
Girotto, Giorgia, Annalisa Buniello, Diego Vozzi, et al.. (2013). Linkage Study and Exome Sequencing Identify a BDP1 Mutation Associated with Hereditary Hearing Loss. PLoS ONE. 8(12). e80323–e80323. 44 indexed citations
18.
Faletra, Flavio, Giorgia Girotto, Pio D’Adamo, et al.. (2013). A novel P2RX2 mutation in an Italian family affected by autosomal dominant nonsyndromic hearing loss. Gene. 534(2). 236–239. 31 indexed citations
19.
Potrich, Cristina, Lorenzo Lunelli, Stefania Forti, et al.. (2009). Effect of materials for micro-electro-mechanical systems on PCR yield. European Biophysics Journal. 39(6). 979–986. 15 indexed citations
20.
Fagoonee, Sharmila, Ferdinando Di Cunto, Diego Vozzi, et al.. (2006). Microarray and Large-Scale In Silico –Based Identification of Genes Functionally Related to Haptoglobin and/or Hemopexin. DNA and Cell Biology. 25(6). 323–330. 9 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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