Roberto Del Bo

8.5k total citations
88 papers, 3.5k citations indexed

About

Roberto Del Bo is a scholar working on Molecular Biology, Genetics and Neurology. According to data from OpenAlex, Roberto Del Bo has authored 88 papers receiving a total of 3.5k indexed citations (citations by other indexed papers that have themselves been cited), including 51 papers in Molecular Biology, 32 papers in Genetics and 29 papers in Neurology. Recurrent topics in Roberto Del Bo's work include Amyotrophic Lateral Sclerosis Research (24 papers), Neurogenetic and Muscular Disorders Research (21 papers) and Muscle Physiology and Disorders (16 papers). Roberto Del Bo is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (24 papers), Neurogenetic and Muscular Disorders Research (21 papers) and Muscle Physiology and Disorders (16 papers). Roberto Del Bo collaborates with scholars based in Italy, United States and Belgium. Roberto Del Bo's co-authors include Giacomo P. Comi, Nereo Bresolin, Stefania Corti, Federica Locatelli, Sandra Strazzer, Sabrina Salani, Chiara Donadoni, Dimitra Papadimitriou, Serena Ghezzi and Andreina Bordoni and has published in prestigious journals such as Nucleic Acids Research, Journal of Clinical Investigation and Journal of Neuroscience.

In The Last Decade

Roberto Del Bo

87 papers receiving 3.4k citations

Peers

Countries citing papers authored by Roberto Del Bo

Since Specialization

Citations

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

Fields of papers citing papers by Roberto Del Bo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Roberto Del Bo. 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 Roberto Del Bo. The network helps show where Roberto Del Bo may publish in the future.

Co-authorship network of co-authors of Roberto Del Bo

This figure shows the co-authorship network connecting the top 25 collaborators of Roberto Del Bo. A scholar is included among the top collaborators of Roberto Del Bo 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 Roberto Del Bo. Roberto Del Bo 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	Investigating the prevalence of MFN2 mutations in amyotrophic lateral sclerosis: insights from an Italian cohort 2024 ·Brain Communications ·Elena Abati, Delia Gagliardi, Arianna Manini, Roberto Del Bo, Dario Ronchi, Megi Meneri, Francesca Beretta, (unknown), Federica Rizzo, Edoardo Monfrini, Alessio Di Fonzo, Maria Teresa Pellecchia, (unknown), Vincenzo Silani, Giacomo P. Comi, Antonia Ratti, Federico Verde, Nicola Ticozzi, Stefania Corti	1
2	Exploiting the role of CSF NfL, CHIT1, and miR-181b as potential diagnostic and prognostic biomarkers for ALS 2024 ·Journal of Neurology ·Delia Gagliardi, Mafalda Rizzuti, Pegah Masrori, (unknown), Roberto Del Bo, (unknown), Megi Meneri, Simone Scarcella, (unknown), Nicole Hersmus, (unknown), (unknown), Vincenzo Silani, Koen Poesen, Philip Van Damme, Giacomo P. Comi, Stefania Corti, Federico Verde	3
3	NOTCH2NLC GGC repeats are not expanded in Italian amyotrophic lateral sclerosis patients 2023 ·Scientific Reports ·Arianna Manini, Delia Gagliardi, Megi Meneri, (unknown), Roberto Del Bo, Giacomo P. Comi, Stefania Corti, Dario Ronchi	2
4	Analysis of HTT CAG repeat expansion in Italian patients with amyotrophic lateral sclerosis 2022 ·Annals of Clinical and Translational Neurology ·Arianna Manini, Delia Gagliardi, Megi Meneri, (unknown), Roberto Del Bo, Cesa Scaglione, Giacomo P. Comi, Stefania Corti, Dario Ronchi	4
5	Homozygous SOD1 Variation L144S Produces a Severe Form of Amyotrophic Lateral Sclerosis in an Iranian Family 2021 ·Neurology Genetics ·Delia Gagliardi, (unknown), Roberto Del Bo, Megi Meneri, Giacomo P. Comi, Stefania Corti, Dario Ronchi	11
6	MFN2-related neuropathies: Clinical features, molecular pathogenesis and therapeutic perspectives 2015 ·Journal of the Neurological Sciences ·(unknown), Federica Rizzo, Giulietta Riboldi, Roberto Del Bo, Monica Nizzardo, Chiara Simone, Giacomo P. Comi, Nereo Bresolin, Stefania Corti	100
7	Novel optineurin mutations in patients with familial and sporadic amyotrophic lateral sclerosis 2011 ·Journal of Neurology Neurosurgery & Psychiatry ·Roberto Del Bo, Cinzia Tiloca, Viviana Pensato, Lucia Corrado, Antonia Ratti, Nicola Ticozzi, Stefania Corti, Barbara Castellotti, Letizia Mazzini, Gianni Sorarú, Cristina Cereda, Sandra D’Alfonso, Cinzia Gellera, Giacomo P. Comi, Vincenzo Silani	77
8	Motoneuron Transplantation Rescues the Phenotype of SMARD1 (Spinal Muscular Atrophy with Respiratory Distress Type 1) 2009 ·Journal of Neuroscience ·Stefania Corti, Monica Nizzardo, Martina Nardini, Chiara Donadoni, Sabrina Salani, Roberto Del Bo, Dimitra Papadimitriou, Federica Locatelli, Nicoletta Mezzina, Francesca Gianni, Nereo Bresolin, Giacomo P. Comi	28
9	TARDBP (TDP‐43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations 2009 ·European Journal of Neurology ·Roberto Del Bo, Serena Ghezzi, Stefania Corti, Massimo Pandolfo, Michela Ranieri, Domenico Santoro, (unknown), A. Prelle, (unknown), Michelangelo Mancuso, Gianni Sorarú, Chiara Briani, C. Angelini, Gabriele Siciliano, Nereo Bresolin, Giacomo P. Comi	81
10	DMD Trp3X nonsense mutation associated with a founder effect in North American families with mild Becker muscular dystrophy 2009 ·Neuromuscular Disorders ·Kevin M. Flanigan, Diane M. Dunn, Andrew von Niederhausern, Michael Howard, Jerry R. Mendell, Anne M. Connolly, Carol Saunders, Ann Modrcin, Majed Dasouki, Giacomo P. Comi, Roberto Del Bo, (unknown), Richard D. Jacobson, Richard S. Finkel, Līvija Medne, Robert B. Weiss	34
11	Neural stem cell transplantation can ameliorate the phenotype of a mouse model of spinal muscular atrophy 2008 ·Journal of Clinical Investigation ·Stefania Corti, Monica Nizzardo, Martina Nardini, Chiara Donadoni, Sabrina Salani, Dario Ronchi, Francesca Saladino, Andreina Bordoni, Francesco Fortunato, Roberto Del Bo, Dimitra Papadimitriou, Federica Locatelli, Giorgia Menozzi, Sandra Strazzer, Nereo Bresolin, Giacomo P. Comi	113
12	Neural stem cells LewisX + CXCR4 + modify disease progression in an amyotrophic lateral sclerosis model 2007 ·Brain ·Stefania Corti, Federica Locatelli, Dimitra Papadimitriou, Roberto Del Bo, Monica Nizzardo, Martina Nardini, Chiara Donadoni, Sabrina Salani, Francesco Fortunato, Sandra Strazzer, Nereo Bresolin, Giacomo P. Comi	110
13	SPG11: a consistent clinical phenotype in a family with homozygous Spatacsin truncating mutation 2007 ·Neurogenetics ·Roberto Del Bo, Alessio Di Fonzo, Serena Ghezzi, Federica Locatelli, Giovanni Stévanin, Antonella Costa, Stefania Corti, Nereo Bresolin, Giacomo P. Comi	30
14	Transplanted ALDHhiSSClo neural stem cells generate motor neurons and delay disease progression of nmd mice, an animal model of SMARD1 2005 ·Human Molecular Genetics ·Stefania Corti, Federica Locatelli, Dimitra Papadimitriou, Chiara Donadoni, Roberto Del Bo, Marco Crimi, Andreina Bordoni, Francesco Fortunato, Sandra Strazzer, Giorgia Menozzi, Sabrina Salani, Nereo Bresolin, Giacomo P. Comi	80
15	Neuronal Differentiation of Murine Bone Marrow Thy-1- and Sca-1-Positive Cells 2003 ·Journal of Hematotherapy & Stem Cell Research ·Federica Locatelli, Stefania Corti, Chiara Donadoni, Michela Guglieri, (unknown), Sandra Strazzer, Sabrina Salani, Roberto Del Bo, Franco Fortunato, Andreina Bordoni, Giacomo P. Comi	37
16	Mitochondrial A12308G polymorphism affects clinical features in patients with single mtDNA macrodeletion 2003 ·European Journal of Human Genetics ·Marco Crimi, Roberto Del Bo, Sara Galbiati, Monica Sciacco, Andreina Bordoni, Nereo Bresolin, Giacomo P. Comi	17
17	High mutational burden in the mtDNA control region from aged muscles: a single-fiber study 2003 ·Neurobiology of Aging ·Roberto Del Bo	38
18	Neuroectodermal and microglial differentiation of bone marrow cells in the mouse spinal cord and sensory ganglia 2002 ·Journal of Neuroscience Research ·Stefania Corti, Federica Locatelli, Chiara Donadoni, Sandra Strazzer, Sabrina Salani, Roberto Del Bo, M. Caccialanza, Nereo Bresolin, G. Scarlato, Giacomo P. Comi	78
19	Evidence and age-related distribution of mtDNA D-loop point mutations in skeletal muscle from healthy subjects and mitochondrial patients 2002 ·Journal of the Neurological Sciences ·Roberto Del Bo, Andreina Bordoni, Filippo Martinelli Boneschi, Marco Crimi, Monica Sciacco, Nereo Bresolin, G. Scarlato, Giacomo P. Comi	35
20	Modulated Generation of Neuronal Cells from Bone Marrow by Expansion and Mobilization of Circulating Stem Cells with in Vivo Cytokine Treatment 2002 ·Experimental Neurology ·Stefania Corti, Federica Locatelli, Sandra Strazzer, Sabrina Salani, Roberto Del Bo, Davide Soligo, Patrizia Bossolasco, Nereo Bresolin, G. Scarlato, Giacomo P. Comi	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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