Manuela Ergoli

515 total citations
12 papers, 205 citations indexed

About

Manuela Ergoli is a scholar working on Molecular Biology, Cardiology and Cardiovascular Medicine and Cellular and Molecular Neuroscience. According to data from OpenAlex, Manuela Ergoli has authored 12 papers receiving a total of 205 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 6 papers in Cardiology and Cardiovascular Medicine and 4 papers in Cellular and Molecular Neuroscience. Recurrent topics in Manuela Ergoli's work include Muscle Physiology and Disorders (7 papers), Nuclear Structure and Function (5 papers) and Genetic Neurodegenerative Diseases (4 papers). Manuela Ergoli is often cited by papers focused on Muscle Physiology and Disorders (7 papers), Nuclear Structure and Function (5 papers) and Genetic Neurodegenerative Diseases (4 papers). Manuela Ergoli collaborates with scholars based in Italy, Poland and France. Manuela Ergoli's co-authors include Luisa Politano, Esther Picillo, Emanuela Viggiano, Paola D′Ambrosio, Roberta Petillo, Gerardo Nigro, Alberto Palladino, Antonella Taglia, Annalaura Torella and Massimo Venditti and has published in prestigious journals such as Human Genetics, Journal of Cellular and Molecular Medicine and Frontiers in Neurology.

In The Last Decade

Manuela Ergoli

12 papers receiving 203 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Manuela Ergoli Italy	8	179	66	39	33	32	12	205
Xavière Lornage France	10	186 1.0×	105 1.6×	43 1.1×	54 1.6×	40 1.3×	19	243
Carola Hedberg Sweden	7	158 0.9×	97 1.5×	29 0.7×	30 0.9×	45 1.4×	9	216
Benjamin M. Nash Australia	7	152 0.8×	39 0.6×	38 1.0×	26 0.8×	20 0.6×	17	200
S. Makri France	5	140 0.8×	27 0.4×	23 0.6×	43 1.3×	12 0.4×	8	156
S. Llense France	8	288 1.6×	83 1.3×	33 0.8×	50 1.5×	49 1.5×	11	304
Kyriaki Kekou Greece	8	148 0.8×	29 0.4×	77 2.0×	28 0.8×	27 0.8×	24	195
Vasantha Gowda United Kingdom	6	157 0.9×	57 0.9×	23 0.6×	22 0.7×	75 2.3×	15	204
Carrie Stephan United States	6	119 0.7×	49 0.7×	11 0.3×	52 1.6×	35 1.1×	13	136
Yo Okizuka Japan	10	307 1.7×	69 1.0×	66 1.7×	37 1.1×	75 2.3×	18	363
Irene Colombo Italy	7	155 0.9×	63 1.0×	14 0.4×	30 0.9×	53 1.7×	14	198

Countries citing papers authored by Manuela Ergoli

Since Specialization

Citations

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

Fields of papers citing papers by Manuela Ergoli

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuela Ergoli

This figure shows the co-authorship network connecting the top 25 collaborators of Manuela Ergoli. A scholar is included among the top collaborators of Manuela Ergoli 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 Manuela Ergoli. Manuela Ergoli is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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12 of 12 papers shown

Petillo, Roberta, Paola D′Ambrosio, Manuela Ergoli, et al.. (2020). CLCN1 Molecular Characterization in 19 South-Italian Patients With Dominant and Recessive Type of Myotonia Congenita. Frontiers in Neurology. 11. 63–63. 5 indexed citations

Palladino, Alberto, Andrea Antonio Papa, Vincenzo Russo, et al.. (2019). Are there real benefits to implanting cardiac devices in patients with end-stage dilated dystrophinopathic cardiomyopathy? Review of literature and personal results.. PubMed. 38(1). 1–7. 10 indexed citations

D′Ambrosio, Paola, Roberta Petillo, Annalaura Torella, et al.. (2019). Cardiac diseases as a predictor warning of hereditary muscle diseases. The case of laminopathies.. PubMed. 38(2). 33–36. 3 indexed citations

Viggiano, Emanuela, Agnieszka Madej‐Pilarczyk, Nicola Carboni, et al.. (2019). X-Linked Emery–Dreifuss Muscular Dystrophy: Study Of X-Chromosome Inactivation and Its Relation with Clinical Phenotypes in Female Carriers. Genes. 10(11). 919–919. 6 indexed citations

Ergoli, Manuela, Massimo Venditti, Esther Picillo, Sergio Minucci, & Luisa Politano. (2019). Study of expression of genes potentially responsible for reduced fitness in patients with myotonic dystrophy type 1 and identification of new biomarkers of testicular function. Molecular Reproduction and Development. 87(1). 45–52. 18 indexed citations

Spitali, Pietro, Kristina Hettne, Roula Tsonaka, et al.. (2018). Cross‐sectional serum metabolomic study of multiple forms of muscular dystrophy. Journal of Cellular and Molecular Medicine. 22(4). 2442–2448. 27 indexed citations

Viggiano, Emanuela, et al.. (2017). Skewed X‐chromosome inactivation plays a crucial role in the onset of symptoms in carriers of Becker muscular dystrophy. The Journal of Gene Medicine. 19(4). 18 indexed citations

Ergoli, Manuela, et al.. (2017). Study of anti-Müllerian hormone levels in patients with Myotonic Dystrophy Type 1. Preliminary results.. PubMed. 36(4). 199–202. 3 indexed citations

Viggiano, Emanuela, Manuela Ergoli, Esther Picillo, & Luisa Politano. (2016). Determining the role of skewed X-chromosome inactivation in developing muscle symptoms in carriers of Duchenne muscular dystrophy. Human Genetics. 135(7). 685–698. 48 indexed citations

10.

Astrea, Guja, Ilaria Pezzini, Rosa Pasquariello, et al.. (2016). TMEM5-associated dystroglycanopathy presenting with CMD and mild limb-girdle muscle involvement. Neuromuscular Disorders. 26(7). 459–461. 12 indexed citations

11.

Petillo, Roberta, Paola D′Ambrosio, Annalaura Torella, et al.. (2015). Novel mutations in LMNA A/C gene and associated phenotypes.. PubMed Central. 34(2-3). 116–9. 18 indexed citations

12.

Taglia, Antonella, Roberta Petillo, Paola D′Ambrosio, et al.. (2015). Clinical features of patients with dystrophinopathy sharing the 45-55 exon deletion of DMD gene.. PubMed. 34(1). 9–13. 37 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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