Erika Salvi

12.0k total citations
53 papers, 1.3k citations indexed

About

Erika Salvi is a scholar working on Molecular Biology, Physiology and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Erika Salvi has authored 53 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 13 papers in Physiology and 11 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Erika Salvi's work include Ion channel regulation and function (8 papers), Hereditary Neurological Disorders (7 papers) and Hormonal Regulation and Hypertension (5 papers). Erika Salvi is often cited by papers focused on Ion channel regulation and function (8 papers), Hereditary Neurological Disorders (7 papers) and Hormonal Regulation and Hypertension (5 papers). Erika Salvi collaborates with scholars based in Italy, Netherlands and United States. Erika Salvi's co-authors include Fabìo Macciardi, Daniele Cusi, Sara Lupoli, Alessandro Orro, Guia Guffanti, Anita Lakatos, Steven G. Potkin, Frithjof Kruggel, Margherita Marchi and Giuseppe Lauria and has published in prestigious journals such as PLoS ONE, Brain and Cancer.

In The Last Decade

Erika Salvi

51 papers receiving 1.3k citations

Peers

Countries citing papers authored by Erika Salvi

Since Specialization

Citations

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

Fields of papers citing papers by Erika Salvi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Erika Salvi

This figure shows the co-authorship network connecting the top 25 collaborators of Erika Salvi. A scholar is included among the top collaborators of Erika Salvi 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 Erika Salvi. Erika Salvi 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	Painful diabetic neuropathy is associated with accelerated epigenetic aging 2025 ·GeroScience ·(unknown), Paolo Garagnani, Massimiliano Bonafè, Maria Giulia Bacalini, Luciano Calzari, Davide Gentilini, Dan Ziegler, Monique M. Gerrits, Catharina G. Faber, Rayaz A. Malik, Margherita Marchi, Erika Salvi, Giuseppe Lauria, Chiara Pirazzini	2
2	Broadening the Genetic Spectrum of Painful Small-Fiber Neuropathy through Whole-Exome Study in Early-Onset Cases 2024 ·International Journal of Molecular Sciences ·(unknown), (unknown), Silvia Santoro, Monique M. Gerrits, Elisabetta Mascia, Margherita Marchi, Erika Salvi, Hubert J.M. Smeets, Janneke G. J. Hoeijmakers, Filippo Martinelli Boneschi, Massimo Filippi, Giuseppe Lauria, Catharina G. Faber, Federica Esposito	2
3	Autophagy Markers Are Altered in Alzheimer’s Disease, Dementia with Lewy Bodies and Frontotemporal Dementia 2024 ·International Journal of Molecular Sciences ·(unknown), Marcella Catania, (unknown), Erika Salvi, (unknown), (unknown), Claudia Saraceno, (unknown), Rosanna Squitti, Giuliano Binetti, Giuseppe Di Fede, Roberta Ghidoni	7
4	Integrative miRNA–mRNA profiling of human epidermis: unique signature of SCN9A painful neuropathy 2023 ·Brain ·(unknown), Erika Salvi, Stefania Marcuzzo, Margherita Marchi, Raffaella Lombardi, Daniele Cartelli, Daniele Cazzato, (unknown), Andrea Gelemanović, (unknown), (unknown), Ilaria D’Amato, Janneke G. J. Hoeijmakers, Sulayman D. Dib‐Hajj, Stephen G. Waxman, Catharina G. Faber, Giuseppe Lauria	5
5	Archival skin biopsy specimens as a tool for miRNA-based diagnosis: Technical and post-analytical considerations 2023 ·Molecular Therapy — Methods & Clinical Development ·(unknown), Margherita Marchi, Stefania Marcuzzo, Raffaella Lombardi, Catharina G. Faber, Giuseppe Lauria, Erika Salvi	1
6	Peripheral Ion Channel Gene Screening in Painful- and Painless-Diabetic Neuropathy 2022 ·International Journal of Molecular Sciences ·(unknown), Rowida Almomani, Margherita Marchi, Bianca T. A. de Greef, (unknown), Janneke G. J. Hoeijmakers, Patrick Lindsey, Erika Salvi, Gidon J. Bönhof, Dan Ziegler, Rayaz A. Malik, Stephen G. Waxman, Giuseppe Lauria, Catharina G. Faber, Hubert J.M. Smeets, Monique M. Gerrits	14
7	Peripheral Ion Channel Genes Screening in Painful Small Fiber Neuropathy 2022 ·International Journal of Molecular Sciences ·(unknown), Rowida Almomani, Margherita Marchi, Erika Salvi, Bianca T. A. de Greef, (unknown), Janneke G. J. Hoeijmakers, Patrick Lindsey, Stephen G. Waxman, Giuseppe Lauria, Catharina G. Faber, Hubert J.M. Smeets, Monique M. Gerrits	15
8	The PINK1 p.Asn521Thr Variant Is Associated with Earlier Disease Onset in GRN/C9orf72 Frontotemporal Lobar Degeneration 2022 ·International Journal of Molecular Sciences ·Giacomina Rossi, Erika Salvi, Luisa Benussi, (unknown), (unknown), (unknown), (unknown), (unknown), Matteo Carrara, Cristian Bonvicini, (unknown), Claudia Saraceno, (unknown), Giorgio Giaccone, Giuliano Binetti, Roberta Ghidoni	2
9	Association of colorectal cancer with genetic and epigenetic variation in PEAR1—A population-based cohort study 2022 ·PLoS ONE ·Wen‐Yi Yang, Benedetta Izzi, Adam P. Bress, Lutgarde Thijs, Lorena Citterio, Fang‐Fei Wei, Erika Salvi, Simona Delli Carpini, Paolo Manunta, Daniele Cusi, Marc Hoylaerts, Aernout Luttun, Peter Verhamme, Sheetal Hardikar, Tim S. Nawrot, Jan A. Staessen, Zhen‐Yu Zhang	3
10	Identification of a cytokine profile in serum and cerebrospinal fluid of pediatric and adult spinal muscular atrophy patients and its modulation upon nusinersen treatment 2022 ·Frontiers in Cellular Neuroscience ·Silvia Bonanno, Paola Cavalcante, Erika Salvi, (unknown), (unknown), (unknown), Francesca Andreetta, Anna Venerando, Viviana Pensato, (unknown), Riccardo Zanin, Maria Teresa Arnoldi, Claudia Dosi, Renato Mantegazza, Riccardo Masson, Lorenzo Maggi, Stefania Marcuzzo	21
11	Congenital insensitivity to pain: a novel mutation affecting a U12-type intron causes multiple aberrant splicing of SCN9A 2021 ·Pain ·Margherita Marchi, Ilaria D’Amato, (unknown), Daniele Cartelli, Erika Salvi, Raffaella Lombardi, (unknown), Giuseppe Lauria	4
12	Evaluation of molecular inversion probe versus TruSeq® custom methods for targeted next-generation sequencing 2020 ·PLoS ONE ·Rowida Almomani, Margherita Marchi, (unknown), Patrick Lindsey, Erika Salvi, Bart de Koning, Silvia Santoro, Stefania Magri, H.J.M. Smeets, Filippo Martinelli Boneschi, (unknown), Dan Ziegler, Janneke G. J. Hoeijmakers, Gidon J. Bönhof, Sulayman D. Dib‐Hajj, Stephen G. Waxman, Ingemar S.J. Merkies, Giuseppe Lauria, Catharina G. Faber, Monique M. Gerrits, (unknown)	13
13	Diagnostic criteria for small fibre neuropathy in clinical practice and research 2019 ·Brain ·Grazia Devigili, Sara Rinaldo, Raffaella Lombardi, Daniele Cazzato, Margherita Marchi, Erika Salvi, Roberto Eleopra, Giuseppe Lauria	141
14	A red orange and lemon by‐products extract rich in anthocyanins inhibits the progression of diabetic nephropathy 2019 ·Journal of Cellular Physiology ·Sara Damiano, (unknown), Erika Salvi, Massimo Papale, Antonio Giordano, Margherita Amenta, Gabriele Ballistreri, Simona Fabroni, Paolo Rapisarda, Giovambattista Capasso, Iris Maria Forte, Daniela Barone, Roberto Ciarcia	22
15	A novel SCN9A splicing mutation in a compound heterozygous girl with congenital insensitivity to pain, hyposmia and hypogeusia 2018 ·Journal of the Peripheral Nervous System ·Margherita Marchi, Vincenzo Provitera, Maria Nolano, Marcello Romano, Simona Maccora, Ilaria D’Amato, Erika Salvi, Monique M. Gerrits, Lucio Santoro, Giuseppe Lauria	22
16	Next‐generation sequencing of a family with a high penetrance of monoclonal gammopathies for the identification of candidate risk alleles 2017 ·Cancer ·Niccolò Bolli, Matteo Barcella, Erika Salvi, Francesca D’Avila, Antonio Vendramin, Chiara De Philippis, Nikhil C. Munshi, Hervé Avet‐Loiseau, Peter J. Campbell, Alberto Mussetti, Cristiana Carniti, Francesco Maura, Cristina Barlassina, Paolo Corradini, Vittorio Montefusco	15
17	PEAR1 is not a major susceptibility gene for cardiovascular disease in a Flemish population 2017 ·BMC Medical Genetics ·Wen‐Yi Yang, Thibault Petit, Nicholas Cauwenberghs, Zhen‐Yu Zhang, Chang‐Sheng Sheng, Lutgarde Thijs, Erika Salvi, Benedetta Izzi, Christophe Vandenbriele, Fang‐Fei Wei, Yumei Gu, Lotte Jacobs, Lorena Citterio, Simona Delli Carpini, Cristina Barlassina, Daniele Cusi, Marc Hoylaerts, Peter Verhamme, Tatiana Kuznetsova, Jan A. Staessen	11
18	Interaction between polyphenols intake and PON1 gene variants on markers of cardiovascular disease: a nutrigenetic observational study 2016 ·Journal of Translational Medicine ·Federica Rizzi, Costanza Conti, Elena Dogliotti, Annalisa Terranegra, Erika Salvi, Daniele Braga, (unknown), Sara Lupoli, Alessandra Mingione, Francesca Pivari, Caterina Brasacchio, Matteo Barcella, Martina Chittani, Francesca D’Avila, Maurizio Turiel, (unknown), Laura Soldati, Daniele Cusi, Cristina Barlassina	36
19	Genes Involved in Vasoconstriction and Vasodilation System Affect Salt-Sensitive Hypertension 2011 ·PLoS ONE ·Lorena Citterio, Marco Simonini, Laura Zagato, Erika Salvi, Simona Delli Carpini, Chiara Lanzani, Elisabetta Messaggio, Nunzia Casamassima, Francesca Frau, Francesca D’Avila, Daniele Cusi, Cristina Barlassina, Paolo Manunta	63
20	SNPLims: a data management system for genome wide association studies 2008 ·BMC Bioinformatics ·Alessandro Orro, Guia Guffanti, Erika Salvi, Fabìo Macciardi, Luciano Milanesi	20

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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