Marcella Neri

2.2k total citations
37 papers, 785 citations indexed

About

Marcella Neri is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Marcella Neri has authored 37 papers receiving a total of 785 indexed citations (citations by other indexed papers that have themselves been cited), including 28 papers in Molecular Biology, 8 papers in Cellular and Molecular Neuroscience and 8 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Marcella Neri's work include Muscle Physiology and Disorders (14 papers), RNA Research and Splicing (8 papers) and Ion channel regulation and function (7 papers). Marcella Neri is often cited by papers focused on Muscle Physiology and Disorders (14 papers), RNA Research and Splicing (8 papers) and Ion channel regulation and function (7 papers). Marcella Neri collaborates with scholars based in Italy, United Kingdom and United States. Marcella Neri's co-authors include Alessandra Ferlini, Francesca Gualandi, Elisa Calzolari, Paola Rimessi, Marco Fichera, Mariangela Lo Giudice, Luciano Merlini, Pietro Spitali, C. Scotton and Patrizia Sabatelli and has published in prestigious journals such as PLoS ONE, Neurology and Gene.

In The Last Decade

Marcella Neri

34 papers receiving 770 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Marcella Neri Italy	18	546	197	144	121	118	37	785
Malika Chaouch Algeria	10	691 1.3×	275 1.4×	83 0.6×	203 1.7×	85 0.7×	14	910
Andrew Weir United Kingdom	6	886 1.6×	159 0.8×	156 1.1×	131 1.1×	110 0.9×	8	1.1k
Shuhei Kameya Japan	18	968 1.8×	177 0.9×	69 0.5×	135 1.1×	164 1.4×	56	1.1k
Rita C.M. Pavanello Brazil	18	899 1.6×	303 1.5×	254 1.8×	108 0.9×	154 1.3×	50	1.0k
G.W. Padberg Netherlands	16	784 1.4×	218 1.1×	247 1.7×	54 0.4×	90 0.8×	22	1.0k
Carmen Serrano Spain	14	501 0.9×	267 1.4×	98 0.7×	43 0.4×	82 0.7×	31	844
Andrea O’Neill United States	17	629 1.2×	289 1.5×	139 1.0×	285 2.4×	54 0.5×	27	969
Maire Leyne United States	15	689 1.3×	613 3.1×	188 1.3×	241 2.0×	100 0.8×	21	1.3k
Beate Schlotter‐Weigel Germany	15	779 1.4×	338 1.7×	112 0.8×	240 2.0×	59 0.5×	24	1.3k
Hiroki Hagiwara Japan	16	498 0.9×	91 0.5×	85 0.6×	204 1.7×	62 0.5×	29	836

Countries citing papers authored by Marcella Neri

Since Specialization

Citations

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

Fields of papers citing papers by Marcella Neri

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marcella Neri

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

Falzarano, Maria Sofia, Elisa Manzati, Paola Rimessi, et al.. (2025). MECP2 mRNA Profile in Brain Tissues from a Rett Syndrome Patient and Three Human Controls: Mutated Allele Preferential Transcription and In Situ RNA Mapping. Biomolecules. 15(5). 687–687. 1 indexed citations

Scarpa, Maurizio, Marcella Neri, Alessandra Ferlini, et al.. (2024). Miglustat as Disease‐Modifying Therapy in a Patient with SCARB2‐Related Action Myoclonus Renal Failure. Movement Disorders Clinical Practice. 12(2). 231–235.

Bella, Daniela Di, Chiara Pisciotta, Elisa Sarto, et al.. (2022). Beyond canvas: behavioral onset of rfc1-expansion disease in an Italian family—causal or casual?. Neurological Sciences. 43(8). 5095–5098. 4 indexed citations

Gualandi, Francesca, Elisabetta Sette, F. Fortunato, et al.. (2019). Report of a novel ATP7A mutation causing distal motor neuropathy. Neuromuscular Disorders. 29(10). 776–785. 13 indexed citations

Grieco, Giulio, Stella Gagliardi, Ivana Ricca, et al.. (2018). New CACNA1A deletions are associated to migraine phenotypes. The Journal of Headache and Pain. 19(1). 75–75. 17 indexed citations

Gherardi, Samuele, Matteo Bovolenta, Chiara Passarelli, et al.. (2017). Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expression. Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1860(11). 1138–1147. 8 indexed citations

Gagliardi, Stella, Gaetano S. Grieco, Francesca Gualandi, et al.. (2017). De novo exonic duplication of ATP1A2 in Italian patient with hemiplegic migraine: a case report. The Journal of Headache and Pain. 18(1). 63–63. 6 indexed citations

Imbrici, Paola, Concetta Altamura, Francesca Gualandi, et al.. (2017). A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions. Molecular and Cellular Neuroscience. 83. 6–12. 24 indexed citations

Neri, Marcella, Rita Selvatici, C. Scotton, et al.. (2013). A patient with limb girdle muscular dystrophy carries a TRIM32 deletion, detected by a novel CGH array, in compound heterozygosis with a nonsense mutation. Neuromuscular Disorders. 23(6). 478–482. 19 indexed citations

10.

Neri, Marcella, Emanuele Valli, Giovanna Alfano, et al.. (2012). The absence of dystrophin brain isoform expression in healthy human heart ventricles explains the pathogenesis of 5' X-linked dilated cardiomyopathy. BMC Medical Genetics. 13(1). 20–20. 12 indexed citations

11.

Ferlini, Alessandra, Marcella Neri, & Francesca Gualandi. (2012). The medical genetics of dystrophinopathies: Molecular genetic diagnosis and its impact on clinical practice. Neuromuscular Disorders. 23(1). 4–14. 56 indexed citations

12.

Bovolenta, Matteo, Emanuele Valli, Simona Brioschi, et al.. (2012). The DMD Locus Harbours Multiple Long Non-Coding RNAs Which Orchestrate and Control Transcription of Muscle Dystrophin mRNA Isoforms. PLoS ONE. 7(9). e45328–e45328. 43 indexed citations

13.

Sensi, Alberto, Stefano Ceruti, Patrizia Trevisi, et al.. (2011). LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutations. American Journal of Medical Genetics Part A. 155(5). 1096–1101. 27 indexed citations

14.

Bovolenta, Matteo, Marcella Neri, E. Martoni, et al.. (2010). Identification of a deep intronic mutation in the COL6A2 gene by a novel custom oligonucleotide CGH array designed to explore allelic and genetic heterogeneity in collagen VI-related myopathies. BMC Medical Genetics. 11(1). 44–44. 26 indexed citations

15.

Vattemi, Gaetano, Francesca Gualandi, Arie Oosterhof, et al.. (2010). Brody Disease: Insights Into Biochemical Features of SERCA1 and Identification of a Novel Mutation. Journal of Neuropathology & Experimental Neurology. 69(3). 246–252. 23 indexed citations

16.

Martoni, E., Anna Urciuolo, Patrizia Sabatelli, et al.. (2009). Identification and characterization of novel collagen VI non-canonical splicing mutations causing ullrich congenital muscular dystrophy. Human Mutation. 30(5). E662–E672. 34 indexed citations

17.

Gualandi, Francesca, Marcella Neri, Matteo Bovolenta, et al.. (2008). Transcriptional behavior of DMD gene duplications in DMD/BMD males. Human Mutation. 30(2). E310–E319. 14 indexed citations

18.

Gualandi, Francesca, Paola Rimessi, Cecilia Trabanelli, et al.. (2006). Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5′ mutation hot spot of the dystrophin gene. Gene. 370. 26–33. 34 indexed citations

19.

Rimessi, Paola, Francesca Gualandi, Laurence Duprez, et al.. (2005). Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutation. American Journal of Medical Genetics Part A. 132A(4). 391–394. 7 indexed citations

20.

Scuderi, Carmela, S Musumeci, Marcella Neri, et al.. (2004). Two novel mutations in the spastin gene (SPG4) found by DHPLC mutation analysis. Neuromuscular Disorders. 14(11). 750–753. 15 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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