Alessandra Govoni

3.0k total citations
32 papers, 1.0k citations indexed

About

Alessandra Govoni is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Alessandra Govoni has authored 32 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 13 papers in Genetics and 8 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Alessandra Govoni's work include Neurogenetic and Muscular Disorders Research (13 papers), Muscle Physiology and Disorders (9 papers) and RNA modifications and cancer (7 papers). Alessandra Govoni is often cited by papers focused on Neurogenetic and Muscular Disorders Research (13 papers), Muscle Physiology and Disorders (9 papers) and RNA modifications and cancer (7 papers). Alessandra Govoni collaborates with scholars based in Italy, United States and Germany. Alessandra Govoni's co-authors include Giacomo P. Comi, Stefania Corti, Nereo Bresolin, Lyndsey Braun, Brian K. Kaspar, Francesca Magri, Delia Gagliardi, Vicki L. McGovern, Laura Ferraiuolo and Shibi Likhite and has published in prestigious journals such as Neurology, Clinical Infectious Diseases and The Journal of Infectious Diseases.

In The Last Decade

Alessandra Govoni

30 papers receiving 977 citations

Peers

Countries citing papers authored by Alessandra Govoni

Since Specialization

Citations

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

Fields of papers citing papers by Alessandra Govoni

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alessandra Govoni

This figure shows the co-authorship network connecting the top 25 collaborators of Alessandra Govoni. A scholar is included among the top collaborators of Alessandra Govoni 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 Alessandra Govoni. Alessandra Govoni 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	Characterization of Phenotypic Variability in Becker Muscular Dystrophy for Clinical Practice and Towards Trial Readiness: A Two-Years Follow up Study 2024 ·Journal of Neuromuscular Diseases ·Giulia Ricci, Alessandra Govoni, (unknown), Guja Astrea, (unknown), (unknown), Roberta Battini, Maria Laura Manca, Vincenzo Castiglione, Alberto Giannoni, Michele Emdin, Gabriele Siciliano	2
2	Multi-omics profiling of CSF from spinal muscular atrophy type 3 patients after nusinersen treatment: a 2-year follow-up multicenter retrospective study 2023 ·Cellular and Molecular Life Sciences ·Irene Faravelli, Delia Gagliardi, Elena Abati, Megi Meneri, (unknown), Francesca Magri, Valeria Parente, Lucia Petrozzi, Giulia Ricci, (unknown), (unknown), (unknown), Donatella Caruso, Gabriele Siciliano, Giacomo P. Comi, Alessandra Govoni, Stefania Corti, Linda Ottoboni	14
3	Ischemic optic neuropathy as first presentation in patient with m.3243 A > G MELAS classic mutation 2023 ·BMC Neurology ·Simone Scarcella, Laura Dell’Arti, Delia Gagliardi, Francesca Magri, Alessandra Govoni, Daniele Velardo, (unknown), (unknown), Dario Ronchi, Daniela Piga, Giacomo P. Comi, Stefania Corti, Megi Meneri	0
4	Bridging the Gap: Gene Therapy in a Patient With Spinal Muscular Atrophy Type 1 2022 ·Neurology ·Gianluca Costamagna, Alessandra Govoni, (unknown), Stefania Corti	2
5	Diagnostic and prognostic value of CSF neurofilaments in a cohort of patients with motor neuron disease: A cross‐sectional study 2021 ·Journal of Cellular and Molecular Medicine ·Delia Gagliardi, Irene Faravelli, Megi Meneri, (unknown), Alessandra Govoni, Francesca Magri, Giulia Ricci, Gabriele Siciliano, Giacomo P. Comi, Stefania Corti	13
6	Current understanding of and emerging treatment options for spinal muscular atrophy with respiratory distress type 1 (SMARD1) 2020 ·Cellular and Molecular Life Sciences ·M. Perego, (unknown), Monica Nizzardo, Alessandra Govoni, Michela Taiana, Nereo Bresolin, Giacomo P. Comi, Stefania Corti	18
7	Spinal muscular atrophy with respiratory distress type 1: Clinical phenotypes, molecular pathogenesis and therapeutic insights 2019 ·Journal of Cellular and Molecular Medicine ·(unknown), Monica Nizzardo, Alessandra Govoni, Michela Taiana, Nereo Bresolin, Giacomo P. Comi, Stefania Corti	25
8	Can Intestinal Pseudo-Obstruction Drive Recurrent Stroke-Like Episodes in Late-Onset MELAS Syndrome? A Case Report and Review of the Literature 2019 ·Frontiers in Neurology ·Delia Gagliardi, Eleonora Mauri, Francesca Magri, Daniele Velardo, Megi Meneri, Elena Abati, (unknown), Irene Faravelli, Daniela Piga, Dario Ronchi, Fabio Triulzi, Lorenzo Peverelli, Monica Sciacco, Nereo Bresolin, Giacomo P. Comi, Stefania Corti, Alessandra Govoni	13
9	Time Is Motor Neuron: Therapeutic Window and Its Correlation with Pathogenetic Mechanisms in Spinal Muscular Atrophy 2018 ·Molecular Neurobiology ·Alessandra Govoni, Delia Gagliardi, Giacomo P. Comi, Stefania Corti	54
10	Central Nervous System Involvement in Common Variable Immunodeficiency: A Case of Acute Unilateral Optic Neuritis in a 26-Year-Old Italian Patient 2018 ·Frontiers in Neurology ·Elena Abati, Irene Faravelli, Francesca Magri, Alessandra Govoni, Daniele Velardo, Delia Gagliardi, Eleonora Mauri, (unknown), Nereo Bresolin, Giovanna Fabio, Giacomo P. Comi, Maria Carrabba, Stefania Corti	5
11	A Phase 1/2a Follistatin Gene Therapy Trial for Becker Muscular Dystrophy 2014 ·Molecular Therapy ·Jerry R. Mendell, Zarife Sahenk, Vinod Malik, Ana M. Gómez, Kevin M. Flanigan, Linda Lowes, Lindsay N. Alfano, Katherine Berry, Eric S. Meadows, Sarah Lewis, Lyndsey Braun, Kim Shontz, (unknown), K. Reed Clark, Xiomara Q. Rosales, Samiah Al-Zaidy, Alessandra Govoni, Louise R. Rodino‐Klapac, Mark Hogan, Brian K. Kaspar	189
12	Growing Evidence about the Relationship between Vessel Dissection and Scuba Diving 2013 ·Case Reports in Neurology ·Simona Brajkovic, Giulietta Riboldi, Alessandra Govoni, Stefania Corti, Nereo Bresolin, Giacomo P. Comi	3
13	Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophy 2013 ·Cellular and Molecular Life Sciences ·Alessandra Govoni, Francesca Magri, Simona Brajkovic, Chiara Zanetta, Irene Faravelli, Stefania Corti, Nereo Bresolin, Giacomo P. Comi	50
14	Frequency and characterisation of anoctamin 5 mutations in a cohort of Italian limb-girdle muscular dystrophy patients 2012 ·Neuromuscular Disorders ·Francesca Magri, Roberto Del Bo, Maria Grazia D’Angelo, Monica Sciacco, S. Gandossini, Alessandra Govoni, Laura Napoli, Patrizia Ciscato, Francesco Fortunato, Erika Brighina, Sara Bonato, Andreina Bordoni, Valeria Lucchini, Stefania Corti, Maurizio Moggio, Nereo Bresolin, Giacomo P. Comi	47
15	Clinical and molecular characterization of a cohort of patients with novel nucleotide alterations of the Dystrophin gene detected by direct sequencing 2011 ·BMC Medical Genetics ·Francesca Magri, Roberto Del Bo, Maria Grazia D’Angelo, Alessandra Govoni, Serena Ghezzi, S. Gandossini, Monica Sciacco, Patrizia Ciscato, Andreina Bordoni, Silvana Tedeschi, Francesco Fortunato, Valeria Lucchini, Matteo Cereda, Stefania Corti, Maurizio Moggio, Nereo Bresolin, Giacomo P. Comi	28
16	Systemic transplantation of c-kit+ cells exerts a therapeutic effect in a model of amyotrophic lateral sclerosis 2010 ·Human Molecular Genetics ·Stefania Corti, Monica Nizzardo, Martina Nardini, Chiara Donadoni, Sabrina Salani, Chiara Simone, Marianna Falcone, Giulietta Riboldi, Alessandra Govoni, Nereo Bresolin, Giacomo P. Comi	50
17	The m.12316G>A mutation in the mitochondrial tRNALeu(CUN) gene is associated with mitochondrial myopathy and respiratory impairment 2010 ·Journal of the Neurological Sciences ·Dario Ronchi, (unknown), Andreina Bordoni, Elisa Fassone, Monica Sciacco, Patrizia Ciscato, Maurizio Moggio, Alessandra Govoni, Stefania Corti, Nereo Bresolin, Giacomo P. Comi	1
18	New molecular findings in congenital myopathies due to selenoprotein N gene mutations 2010 ·Journal of the Neurological Sciences ·Rachele Cagliani, (unknown), Angela Berardinelli, Maria Grazia D’Angelo, A. Prelle, Stefania Riva, Laura Napoli, Ksenija Gorni, Simona Orcesi, Costanza Lamperti, Anna Pichiecchio, (unknown), Rossella Tupler, Francesca Magri, Alessandra Govoni, Stefania Corti, Nereo Bresolin, Maurizio Moggio, Giacomo P. Comi	14
19	Cidofovir added to HAART improves virological and clinical outcome in AIDS-associated progressive multifocal leukoencephalopathy 2000 ·AIDS ·Andrea De Luca, Maria Letizia Giancola, Adriana Ammassari, Susanna Grisetti, Antonella Cingolani, Maria Grazia Paglia, Alessandra Govoni, Rita Murri, Letizia Testa, Antonella d’Arminio Monforte, Andrea Antinori	63
20	Discontinuation of Primary Prophylaxis forPneumocystis cariniiPneumonia and Toxoplasmic Encephalitis in Human Immunodeficiency Virus Type I–Infected Patients: The Changes in Opportunistic Prophylaxis Study 2000 ·The Journal of Infectious Diseases ·Cristina Mussini, Patrizio Pezzotti, Alessandra Govoni, (unknown), Andrea Antinori, Antonella d'Arminio Monforte, Andrea De Luca, Nicola Mongiardo, (unknown), Francesco Chiodo, Ercole Concia, L Bonazzi, Mauro Moroni, L Ortona, Roberto Esposito, Andrea Cossarizza, Bruno De Rienzo	66

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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