Giovanni Vazza

1.3k total citations
33 papers, 752 citations indexed

About

Giovanni Vazza is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Giovanni Vazza has authored 33 papers receiving a total of 752 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 13 papers in Cellular and Molecular Neuroscience and 7 papers in Neurology. Recurrent topics in Giovanni Vazza's work include Hereditary Neurological Disorders (10 papers), Neurological diseases and metabolism (7 papers) and Genetic Neurodegenerative Diseases (6 papers). Giovanni Vazza is often cited by papers focused on Hereditary Neurological Disorders (10 papers), Neurological diseases and metabolism (7 papers) and Genetic Neurodegenerative Diseases (6 papers). Giovanni Vazza collaborates with scholars based in Italy, United States and Peru. Giovanni Vazza's co-authors include Maria Luisa Mostacciuolo, Andrea Vettori, Francesca Boaretto, C. Angelini, M.L. Mostacciuolo, Ebe Pastorello, Marta Miorin, Giuliana Galluzzi, Giuliano Tomelleri and Gianluca Occhi and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, Neurology and International Journal of Molecular Sciences.

In The Last Decade

Giovanni Vazza

31 papers receiving 740 citations

Peers

Countries citing papers authored by Giovanni Vazza

Since Specialization

Citations

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

Fields of papers citing papers by Giovanni Vazza

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giovanni Vazza

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Exploring the tumor suppressor role of RIN1 in familial thyroid carcinoma 2025 ·Endocrine Related Cancer ·(unknown), (unknown), (unknown), (unknown), Gianmaria Pennelli, Germano Gaudenzi, (unknown), (unknown), Davide Gentilini, Laura Fugazzola, Antongiulio Faggiano, Giovanni Vitale, Gianluca Occhi, Giovanni Vazza	0
2	GIPR in GH-PitNETs: molecular and functional insights 2025 ·Endocrine Related Cancer ·(unknown), (unknown), (unknown), (unknown), Giorgia Pallafacchina, (unknown), (unknown), (unknown), Gabriele Sales, Giovanni Vazza, Daniela Regazzo, Gianluca Occhi	0
3	The Methylation Analysis of the Glucose-Dependent Insulinotropic Polypeptide Receptor (GIPR) Locus in GH-Secreting Pituitary Adenomas 2023 ·International Journal of Molecular Sciences ·(unknown), (unknown), Giovanni Vazza, Daniela Regazzo, (unknown), Luca Denaro, Giacomo Voltan, Carla Scaroni, Filippo Ceccato, Gianluca Occhi	3
4	Internal validation and improvement of mitochondrial genome sequencing using the Precision ID mtDNA Whole Genome Panel 2021 ·International Journal of Legal Medicine ·(unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Sara De Fanti, Stefania Sarno, (unknown), Donata Luiselli, Alberto Marinò, Giovanni Vazza	9
5	Clinical and genetic characterization of an Italian family with slow-channel syndrome 2018 ·Neurological Sciences ·C. Angelini, (unknown), (unknown), Maria Luisa Mostacciuolo, Giovanni Vazza	9
6	Diagnosis of Primary Ciliary Dyskinesia by a Targeted Next-Generation Sequencing Panel 2016 ·Journal of Molecular Diagnostics ·Francesca Boaretto, Deborah Snijders, (unknown), (unknown), Maria Luisa Mostacciuolo, Mirella Collura, Salvatore Cazzato, (unknown), Michela Silvestri, Giovanni A. Rossi, Angelo Barbato, Giovanni Vazza	32
7	Loss-of-function mutations in theSIGMAR1gene cause distal hereditary motor neuropathy by impairing ER-mitochondria tethering and Ca²⁺signalling 2016 ·Human Molecular Genetics ·(unknown), Giorgia Pallafacchina, Sofia Zanin, V. Crippa, P. Rusmini, Angelo Poletti, Mingyan Fang, (unknown), (unknown), Antonio Petrucci, (unknown), Tiziana Cavallaro, Gian Maria Fabrizi, M. Muglia, Francesca Boaretto, Andrea Vettori, Rosario Rizzuto, Maria Luisa Mostacciuolo, Giovanni Vazza	78
8	Homozygous Desmocollin-2 Mutations and Arrhythmogenic Cardiomyopathy 2015 ·The American Journal of Cardiology ·Alessandra Lorenzon, Kalliopi Pilichou, Ilaria Rigato, Giovanni Vazza, Marzia De Bortoli, Martina Calore, Gianluca Occhi, Elisa Carturan, Elisabetta Lazzarini, (unknown), Elisa Mazzotti, Giulia Poloni, Maria Luisa Mostacciuolo, Luciano Daliento, Gaetano Thiene, Domenico Corrado, Cristina Basso, Barbara Bauce, Alessandra Rampazzo	32
9	High prevalence of chitotriosidase deficiency in Peruvian Amerindians exposed to chitin-bearing food and enteroparasites 2014 ·Carbohydrate Polymers ·Nicola Manno, (unknown), Francesca Boaretto, (unknown), (unknown), (unknown), Salvatore Musumeci, Andrea Battisti, Rupert J. Quinnell, (unknown), Giovanni Vazza, M.L. Mostacciuolo, Maurizio G. Paoletti, Franco H. Falcone	10
10	Mutation Analysis of MFN2, GJB1, MPZ and PMP22 in Italian Patients with Axonal Charcot–Marie–Tooth Disease 2014 ·NeuroMolecular Medicine ·(unknown), Francesca Boaretto, Chiara Briani, Elena Pegoraro, Mario Cacciavillani, Andrea Martinuzzi, M. Muglia, Andrea Vettori, Giovanni Vazza, Maria Luisa Mostacciuolo	23
11	Improving the knowledge of amyotrophic lateral sclerosis genetics: novel SOD1 and FUS variants 2013 ·Neurobiology of Aging ·Cinzia Bertolin, Carla D’Ascenzo, Giorgia Querin, Alessandra Gaiani, Francesca Boaretto, (unknown), Giovanni Vazza, C. Angelini, Annachiara Cagnin, Elena Pegoraro, Gianni Sorarú, Maria Luisa Mostacciuolo	8
12	Analysis of complete mitochondrial genomes of patients with schizophrenia and bipolar disorder 2011 ·Journal of Human Genetics ·Cinzia Bertolin, Chiara Magri, Sergio Barlati, Andrea Vettori, Giulia Perini, (unknown), Maria Luisa Mostacciuolo, Giovanni Vazza	16
13	Novel mutations in the L1CAM gene support the complexity of L1 syndrome 2010 ·Journal of the Neurological Sciences ·Cinzia Bertolin, Francesca Boaretto, Giovanni Barbon, Leonardo Salviati, Elisabetta Lapi, Maria Teresa Divizia, Livia Garavelli, Gianluca Occhi, Giovanni Vazza, Maria Luisa Mostacciuolo	6
14	Developmental defects and neuromuscular alterations due to mitofusin 2 gene (MFN2) silencing in zebrafish: a new model for Charcot-Marie-Tooth type 2A neuropathy 2010 ·Neuromuscular Disorders ·Andrea Vettori, (unknown), Enrico Moro, Giovanni Vazza, Giulia Polo, Natascia Tiso, Francesco Argenton, Maria Luisa Mostacciuolo	35
15	Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north‐east Italian population sample 2009 ·Clinical Genetics ·(unknown), Ebe Pastorello, Giovanni Vazza, Marta Miorin, C. Angelini, Giuliano Tomelleri, Giuliana Galluzzi, (unknown)	106
16	Familial epilepsy and developmental dysphasia: Description of an Italian pedigree with autosomal dominant inheritance and screening of candidate loci 2008 ·Epilepsy Research ·Roberto Michelucci, (unknown), S. Testoni, D. Passarelli, P. Riguzzi, Erica Diani, Giovanni Vazza, (unknown), Aldo Scabar, Maria Luisa Mostacciuolo, L. Volpi, Guido Rubboli, (unknown), Maria Margherita Mancardi, C. A. Tassinari, Carlo Nobile	6
17	Genome-wide scan supports the existence of a susceptibility locus for schizophrenia and bipolar disorder on chromosome 15q26 2006 ·Molecular Psychiatry ·Giovanni Vazza, Cinzia Bertolin, (unknown), Andrea Vettori, Francesca Boaretto, (unknown), (unknown), Giulia Perini, (unknown), Maria Luisa Mostacciuolo	38
18	A Locus for Migraine without Aura Maps on Chromosome 14q21.2-q22.3 2003 ·The American Journal of Human Genetics ·D. Soragna, Andrea Vettori, Gianni Carraro, Enrico Marchioni, Giovanni Vazza, Silvia Bellini, Rossella Tupler, F Savoldi, M.L. Mostacciuolo	70
19	A New Locus for Autosomal Recessive Spastic Paraplegia Associated with Mental Retardation and Distal Motor Neuropathy, SPG14, Maps to Chromosome 3q27-q28 2000 ·The American Journal of Human Genetics ·Giovanni Vazza, (unknown), Francesca Boaretto, (unknown), (unknown), Maria Luisa Mostacciuolo	48
20	Hereditary spastic paraplegia associated with peripheral neuropathy: a distinct clinical and genetic entity 2000 ·Neuromuscular Disorders ·Maria Luisa Mostacciuolo, Luca Rampoldi, (unknown), Giovanni Vazza, (unknown), C. Angelini	5

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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