Giuseppe Marangi

3.9k total citations
54 papers, 1.5k citations indexed

About

Giuseppe Marangi is a scholar working on Molecular Biology, Neurology and Genetics. According to data from OpenAlex, Giuseppe Marangi has authored 54 papers receiving a total of 1.5k indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 25 papers in Neurology and 24 papers in Genetics. Recurrent topics in Giuseppe Marangi's work include Amyotrophic Lateral Sclerosis Research (25 papers), Neurogenetic and Muscular Disorders Research (20 papers) and Genomic variations and chromosomal abnormalities (19 papers). Giuseppe Marangi is often cited by papers focused on Amyotrophic Lateral Sclerosis Research (25 papers), Neurogenetic and Muscular Disorders Research (20 papers) and Genomic variations and chromosomal abnormalities (19 papers). Giuseppe Marangi collaborates with scholars based in Italy, United States and Japan. Giuseppe Marangi's co-authors include Marcella Zollino, Serena Lattante, Amelia Conte, Mario Sabatelli, Bryan J. Traynor, Daniela Orteschi, Giovanni Neri, Marco Luigetti, Alessandra Del Grande and Marina Murdolo and has published in prestigious journals such as Nature Genetics, Neurology and Brain Research.

In The Last Decade

Giuseppe Marangi

52 papers receiving 1.4k citations

Peers

Giuseppe Marangi

NEURO

GENET

NEURO

Marie Mangelsdorf Australia

Serena Lattante Italy

Pavel Seeman Czechia

Sascha Vermeer Netherlands

José Manuel Morante‐Redolat Spain

Chantal Sellier France

James R. Lupski United States

Véronique Belzil Canada

A. Nazlı Başak Türkiye

Ma Salomé Sirerol-Piquer Spain

Marie Mangelsdorf Australia

Giuseppe Marangi

1.1k ×1.5

167 ×0.3

NEURO

950 ×1.6

GENET

148 ×0.3

GENET

49 ×0.2

NEURO

Citations per year, relative to Giuseppe Marangi Giuseppe Marangi (= 1×) peers Marie Mangelsdorf

Countries citing papers authored by Giuseppe Marangi

Since Specialization

Citations

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

Fields of papers citing papers by Giuseppe Marangi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Giuseppe Marangi

This figure shows the co-authorship network connecting the top 25 collaborators of Giuseppe Marangi. A scholar is included among the top collaborators of Giuseppe Marangi 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 Giuseppe Marangi. Giuseppe Marangi 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

Lattante, Serena, Daniela Bernardo, Agata Katia Patanella, et al.. (2025). Burden of pathogenetic and likely pathogenetic variants in SPG7, SPG11 and AP4 genes in Amyotrophic Lateral Sclerosis. A case-control study. Journal of Neurology. 272(7). 455–455.

Lattante, Serena, Mario Sabatelli, Giulia Bisogni, et al.. (2023). Evaluating the contribution of the gene TARDBP in Italian patients with amyotrophic lateral sclerosis. European Journal of Neurology. 30(5). 1246–1255. 5 indexed citations

Marangi, Giuseppe, Daniela Orteschi, Domenica Battaglia, et al.. (2023). Linear Diagnostic Procedure Elicited by Clinical Genetics and Validated by mRNA Analysis in Neuronal Ceroid Lipofuscinosis 7 Associated with a Novel Non-Canonical Splice Site Variant in MFSD8. Genes. 14(2). 245–245. 3 indexed citations

Bigoni, Stefania, et al.. (2020). Clinical Genetics Can Solve the Pitfalls of Genome-Wide Investigations: Lesson from Mismapping a Loss-of-Function Variant in KANSL1. Genes. 11(10). 1177–1177. 13 indexed citations

Currò, Aurora, Gabriella Doddato, Mirella Bruttini, et al.. (2020). CDKL5 mutations may mimic Pitt-Hopkins syndrome phenotype. European Journal of Medical Genetics. 64(1). 104102–104102. 1 indexed citations

Zollino, Marcella, Serena Lattante, Daniela Orteschi, et al.. (2017). Syndromic Craniosynostosis Can Define New Candidate Genes for Suture Development or Result from the Non-specifc Effects of Pleiotropic Genes: Rasopathies and Chromatinopathies as Examples. Frontiers in Neuroscience. 11. 587–587. 19 indexed citations

Marangi, Giuseppe, Serena Lattante, Amelia Conte, et al.. (2016). Matrin 3 variants are frequent in Italian ALS patients. Neurobiology of Aging. 49. 218.e1–218.e7. 34 indexed citations

Chiò, Adriano, Andrea Calvo, Cristina Moglia, et al.. (2015). ATXN2 PolyQ Intermediate Repeat Modifies ALS Phenotype and Survival (I8-3B). Neurology. 84(14_supplement). 1 indexed citations

Marangi, Giuseppe & Bryan J. Traynor. (2014). Genetic causes of amyotrophic lateral sclerosis: New genetic analysis methodologies entailing new opportunities and challenges. Brain Research. 1607. 75–93. 110 indexed citations

10.

Marangi, Giuseppe, et al.. (2013). Interstitial deletion of 3p22.3p22.2 encompassing ARPP21 and CLASP2 is a potential pathogenic factor for a syndromic form of intellectual disability: A co‐morbidity model with additional copy number variations in a large family. American Journal of Medical Genetics Part A. 161(11). 2890–2893. 20 indexed citations

11.

Sabatelli, Mario, Alice Moncada, Amelia Conte, et al.. (2013). Mutations in the 3′ untranslated region of FUS causing FUS overexpression are associated with amyotrophic lateral sclerosis. Human Molecular Genetics. 22(23). 4748–4755. 86 indexed citations

12.

Marangi, Giuseppe, Vincenzo Leuzzi, Filippo Manti, et al.. (2012). TRAPPC9-related autosomal recessive intellectual disability: report of a new mutation and clinical phenotype. European Journal of Human Genetics. 21(2). 229–232. 54 indexed citations

13.

Marangi, Giuseppe, Daniela Orteschi, Federico Vigevano, et al.. (2012). Expanding the spectrum of rearrangements involving chromosome 19: A mild phenotype associated with a 19p13.12–p13.13 deletion. American Journal of Medical Genetics Part A. 158A(4). 888–893. 6 indexed citations

14.

Sabatelli, Mario, Marcella Zollino, Marco Luigetti, et al.. (2011). Uncovering amyotrophic lateral sclerosis phenotypes: Clinical features and long-term follow-up of upper motor neuron-dominant ALS. Amyotrophic Lateral Sclerosis. 12(4). 278–282. 31 indexed citations

15.

Grande, Alessandra Del, Amelia Conte, Serena Lattante, et al.. (2011). D11Y SOD1 mutation and benign ALS: A consistent genotype-phenotype correlation. Journal of the Neurological Sciences. 309(1-2). 31–33. 7 indexed citations

16.

Grande, Alessandra Del, Marco Luigetti, Amelia Conte, et al.. (2011). A novel L67P SOD1 mutation in an Italian ALS patient. Amyotrophic Lateral Sclerosis. 12(2). 150–152. 11 indexed citations

17.

Luigetti, Marco, Serena Lattante, Marcella Zollino, et al.. (2011). SOD1 G93D sporadic amyotrophic lateral sclerosis (SALS) patient with rapid progression and concomitant novel ANG variant. Neurobiology of Aging. 32(10). 1924.e15–1924.e18. 30 indexed citations

18.

Zollino, Marcella, Daniela Orteschi, Giuseppe Marangi, et al.. (2009). A case of Beckwith–Wiedemann syndrome caused by a cryptic 11p15 deletion encompassing the centromeric imprinted domain of the BWS locus. Journal of Medical Genetics. 47(6). 429–432. 39 indexed citations

19.

Luigetti, Marco, Francesca Madia, Amelia Conte, et al.. (2009). SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis. 10(5-6). 479–482. 10 indexed citations

20.

Faravelli, Francesca, Marina Murdolo, Giuseppe Marangi, et al.. (2007). Mother to son amplification of a small subtelomeric deletion: A new mechanism of familial recurrence in microdeletion syndromes. American Journal of Medical Genetics Part A. 143A(11). 1169–1173. 42 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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