Marcella Neri

2.2k citations

37 papers · 785 · h-index 18

Impact in

Cellular and Molecular Neuroscience top 10%
- Genetic Neurodegenerative Diseases
- Hereditary Neurological Disorders
Genetics top 10%
- Neurogenetic and Muscular Disorders Research

Papers in

Molecular Biology 28
- Muscle Physiology and Disorders 14
- RNA Research and Splicing 8
- Ion channel regulation and function 7
- RNA modifications and cancer 4
- Mitochondrial Function and Pathology 4
Cellular and Molecular Neuroscience 8
- Genetic Neurodegenerative Diseases 5

Co-authors: Alessandra Ferlini (31 shared papers)Francesca Gualandi (26 shared papers)Elisa Calzolari (4 shared papers)Paola Rimessi (8 shared papers)Marco Fichera (3 shared papers)Pietro Spitali (6 shared papers)Mariangela Lo Giudice (2 shared papers)Luciano Merlini (5 shared papers)
Journals: Neuromuscular Disorders (9 papers)Human Mutation (2 papers)Neurological Sciences (2 papers)The Journal of Headache and Pain (2 papers)Clinical Neurology and Neurosurgery (1 paper)
Partner nations: Italy United Kingdom United States

In The Last Decade

Marcella Neri

34 papers receiving 770 citations

Peers

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-authors

The 25 scholars most cited alongside Marcella Neri, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Marcella Neri Line = papers co-authored together Marcella Neri links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

Showing the 20 most-cited of 37 papers — load more, or switch the sort, to bring in the rest.

#	Work
1	Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the human Neuromuscular Disorders ·Marcella Neri, Silvia Torelli, S. Brown, I. Ugo, Patrizia Sabatelli, Luciano Merlini, Pietro Spitali, Paola Rimessi, Francesca Gualandi, Caroline A. Sewry, Alessandra Ferlini, Francesco Muntoni	2007	124
2	Evidence of kinesin heavy chain ( KIF5A ) involvement in pure hereditary spastic paraplegia Neurology ·Marco Fichera, Mariangela Lo Giudice, M. Falco, Maurizio Sturnio, Silvestra Amata, Olga Calabrese, Stefania Bigoni, Elisa Calzolari, Marcella Neri	2004	85
3	The medical genetics of dystrophinopathies: Molecular genetic diagnosis and its impact on clinical practice Neuromuscular Disorders ·Alessandra Ferlini, Marcella Neri, Francesca Gualandi	2012	56
4	A Missense Mutation in the Coiled-Coil Domain of the KIF5A Gene and Late-Onset Hereditary Spastic Paraplegia Archives of Neurology ·Mariangela Lo Giudice, Marcella Neri, Michele Falco, Maurizio Sturnio, Elisa Calzolari, Daniela Benedetto, Marco Fichera	2006	46
5	The DMD Locus Harbours Multiple Long Non-Coding RNAs Which Orchestrate and Control Transcription of Muscle Dystrophin mRNA Isoforms PLoS ONE ·Matteo Bovolenta, Daniela Erriquez, Emanuele Valli, Simona Brioschi, C. Scotton, Marcella Neri, Maria Sofia Falzarano, Samuele Gherardi, M. Fabris, Paola Rimessi, Francesca Gualandi, Giovanni Perini, Alessandra Ferlini	2012	43
6	Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domains Neuromuscular Disorders ·Elizabeth Harris, U. Burki, Chiara Marini‐Bettolo, Marcella Neri, C. Scotton, Judith A. Hudson, Marta Bertoli, Teresinha Evangelista, Bas Vroling, Tuomo Polvikoski, Mark Roberts, Ana Töpf, Kate Bushby, Daniel McArthur, Hanns Lochmüller, Alessandra Ferlini, Volker Straub, Rita Barresi	2017	36
7	Identification and characterization of novel collagen VI non-canonical splicing mutations causing ullrich congenital muscular dystrophy Human Mutation ·E. Martoni, Anna Urciuolo, Patrizia Sabatelli, M. Fabris, Matteo Bovolenta, Marcella Neri, Paolo Grumati, Adele D’Amico, Marika Pane, Eugenio Mercuri, Enrico Bertini, Luciano Merlini, Paolo Bonaldo, Alessandra Ferlini, Francesca Gualandi	2009	34
8	Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5′ mutation hot spot of the dystrophin gene Gene ·Francesca Gualandi, Paola Rimessi, Cecilia Trabanelli, Pietro Spitali, Marcella Neri, Tomaso Patarnello, C. Angelini, Shu C. Yau, Stephen Abbs, Francesco Muntoni, Elisa Calzolari, Alessandra Ferlini	2006	34
9	LAMM syndrome with middle ear dysplasia associated with compound heterozygosity for FGF3 mutations American Journal of Medical Genetics Part A ·Alberto Sensi, Stefano Ceruti, Patrizia Trevisi, Francesca Gualandi, Micol Busi, Ilaria Donati, Marcella Neri, Alessandra Ferlini, Alessandro Martini	2011	27
10	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 ·Matteo Bovolenta, Marcella Neri, E. Martoni, Anna Urciuolo, Patrizia Sabatelli, M. Fabris, Paolo Grumati, Eugenio Mercuri, Enrico Bertini, Luciano Merlini, Paolo Bonaldo, Alessandra Ferlini, Francesca Gualandi	2010	26
11	SERCA1 protein expression in muscle of patients with Brody disease and Brody syndrome and in cultured human muscle fibers Molecular Genetics and Metabolism ·Valeria Guglielmi, Gaetano Vattemi, Francesca Gualandi, Nicol C. Voermans, Matteo Marini, C. Scotton, Elena Pegoraro, Arie Oosterhof, Magdolna Kósa, Ernő Zádor, Enza Maria Valente, D. De Grandis, Marcella Neri, Valentina Codemo, Antonio Novelli, Toin H. Van Kuppevelt, Bruno Dallapiccola, Baziel G.M. van Engelen, Alessandra Ferlini, Giuliano Tomelleri	2013	26
12	A novel KCNA1 mutation in a patient with paroxysmal ataxia, myokymia, painful contractures and metabolic dysfunctions Molecular and Cellular Neuroscience ·Paola Imbrici, Concetta Altamura, Francesca Gualandi, Giuseppe Felice Mangiatordi, Marcella Neri, Giovanni De Maria, Alessandra Ferlini, Alessandro Padovani, Maria Cristina D’Adamo, Orazio Nicolotti, Mauro Pessia, Diana Conte Camerino, Massimiliano Filosto, Jean‐François Desaphy	2017	24
13	Brody Disease: Insights Into Biochemical Features of SERCA1 and Identification of a Novel Mutation Journal of Neuropathology & Experimental Neurology ·Gaetano Vattemi, Francesca Gualandi, Arie Oosterhof, Matteo Marini, Paola Tonin, Paola Rimessi, Marcella Neri, Valeria Guglielmi, Anna Russignan, Consuelo Poli, Toin H. Van Kuppevelt, Alessandra Ferlini, Giuliano Tomelleri	2010	23
14	Biomarkers in rare neuromuscular diseases Experimental Cell Research ·C. Scotton, Chiara Passarelli, Marcella Neri, Alessandra Ferlini	2014	22
15	Custom CGH array profiling of copy number variations (CNVs) on chromosome 6p21.32 (HLA locus) in patients with venous malformations associated with multiple sclerosis BMC Medical Genetics ·Alessandra Ferlini, Matteo Bovolenta, Marcella Neri, Francesca Gualandi, A Balboni, Anton Yuryev, Fabrizio Salvi, Donato Gemmati, A Liboni, Paolo Zamboni	2010	20
16	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 ·Marcella Neri, Rita Selvatici, C. Scotton, Cecilia Trabanelli, Annarita Armaroli, D. De Grandis, Nicolas Lévy, Francesca Gualandi, Alessandra Ferlini	2013	19
17	Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathy. PubMed ·Gaetano Vattemi, Marcella Neri, Silvio Piffer, Patrick Vicart, Francesca Gualandi, Massimiliano Marini, Valeria Guglielmi, Massimiliano Filosto, Paola Tonin, Alessandra Ferlini, Giuliano Tomelleri	2011	19
18	New CACNA1A deletions are associated to migraine phenotypes The Journal of Headache and Pain ·Giulio Grieco, Stella Gagliardi, Ivana Ricca, Orietta Pansarasa, Marcella Neri, Francesca Gualandi, Giuseppe Nappi, Alessandra Ferlini, Cristina Cereda	2018	17
19	Two novel mutations in the spastin gene (SPG4) found by DHPLC mutation analysis Neuromuscular Disorders ·Michele Falco, Carmela Scuderi, S Musumeci, Maurizio Sturnio, Marcella Neri, Stefania Bigoni, Luisa Caniatti, Marco Fichera	2004	15
20	Transcriptional behavior of DMD gene duplications in DMD/BMD males Human Mutation ·Francesca Gualandi, Marcella Neri, Matteo Bovolenta, E. Martoni, Paola Rimessi, Sergio Fini, Pietro Spitali, M. Fabris, Marika Pane, C. Angelini, Marina Mora, Lucía Morandi, Tiziana Mongini, Enrico Bertini, Enzo Ricci, Gaetano Vattemi, Eugenio Mercuri, Luciano Merlini, Alessandra Ferlini	2008	14

About Marcella Neri

Marcella Neri is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience, Cardiology and Cardiovascular Medicine, Cell Biology and Genetics, having authored 37 papers that have together received 785 indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (14 papers), RNA Research and Splicing (8 papers), Cardiomyopathy and Myosin Studies (7 papers), Ion channel regulation and function (7 papers), Genetic Neurodegenerative Diseases (5 papers), RNA modifications and cancer (4 papers), Cellular transport and secretion (4 papers) and Mitochondrial Function and Pathology (4 papers). The work is most often cited by research in Cellular and Molecular Neuroscience (197 citations), Genetics (99 citations), Neurology (69 citations), Sensory Systems (40 citations) and Molecular Biology (546 citations). Marcella Neri has collaborated with scholars based in Italy, United Kingdom and United States. Frequent co-authors include Alessandra Ferlini, Francesca Gualandi, Elisa Calzolari, Paola Rimessi, Marco Fichera, Pietro Spitali, Mariangela Lo Giudice, Luciano Merlini, Patrizia Sabatelli and C. Scotton. Their work appears in journals such as Neuromuscular Disorders, Human Mutation, Neurological Sciences, The Journal of Headache and Pain and Clinical Neurology and Neurosurgery.

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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