Marika Pane

13.1k total citations
127 papers, 3.9k citations indexed

About

Marika Pane is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Marika Pane has authored 127 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 72 papers in Molecular Biology, 57 papers in Genetics and 32 papers in Surgery. Recurrent topics in Marika Pane's work include Neurogenetic and Muscular Disorders Research (57 papers), Muscle Physiology and Disorders (47 papers) and Congenital Anomalies and Fetal Surgery (22 papers). Marika Pane is often cited by papers focused on Neurogenetic and Muscular Disorders Research (57 papers), Muscle Physiology and Disorders (47 papers) and Congenital Anomalies and Fetal Surgery (22 papers). Marika Pane collaborates with scholars based in Italy, United Kingdom and United States. Marika Pane's co-authors include Eugenio Mercuri, Sonia Messina, Francesco Muntoni, Enrico Bertini, Joanna Allsop, Anna Pichiecchio, Adele D’Amico, Valeria Ricotti, Elena Mazzone and Francesco Muntoni and has published in prestigious journals such as PLoS ONE, Neurology and Annals of Neurology.

In The Last Decade

Marika Pane

121 papers receiving 3.8k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Marika Pane Italy	36	2.5k	1.6k	894	587	541	127	3.9k
Brenda Wong United States	36	2.9k 1.2×	1.1k 0.7×	714 0.8×	914 1.6×	346 0.6×	142	4.2k
Sonia Messina Italy	37	3.0k 1.2×	1.5k 1.0×	866 1.0×	628 1.1×	505 0.9×	114	4.3k
Wendy King United States	27	2.5k 1.0×	828 0.5×	602 0.7×	529 0.9×	602 1.1×	45	3.8k
Emma Ciafaloni United States	35	2.8k 1.1×	766 0.5×	435 0.5×	599 1.0×	678 1.3×	113	4.3k
Julaine Florence United States	36	2.9k 1.2×	1.4k 0.9×	528 0.6×	562 1.0×	631 1.2×	66	5.0k
Jean Tomezsko United States	10	2.4k 1.0×	697 0.4×	379 0.4×	612 1.0×	288 0.5×	11	3.4k
Shree Pandya United States	27	4.2k 1.7×	1.2k 0.8×	472 0.5×	1.0k 1.8×	860 1.6×	59	5.4k
Linda Lowes United States	27	1.7k 0.7×	932 0.6×	492 0.6×	351 0.6×	152 0.3×	128	2.9k
K. Bushby United Kingdom	19	3.6k 1.5×	1.1k 0.7×	317 0.4×	955 1.6×	733 1.4×	38	4.7k
Nicolas Deconinck Belgium	25	2.2k 0.9×	626 0.4×	387 0.4×	336 0.6×	403 0.7×	91	3.0k

Countries citing papers authored by Marika Pane

Since Specialization

Citations

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

Fields of papers citing papers by Marika Pane

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marika Pane

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

D’Alatri, Lucia, Claudia Manfredi, Roberta Onesimo, et al.. (2025). Do Rare Genetic Conditions Exhibit a Specific Phonotype? A Comprehensive Description of the Vocal Traits Associated with Crisponi/Cold-Induced Sweating Syndrome Type 1. Genes. 16(8). 881–881. 1 indexed citations

Cutrona, Costanza, Roberta Onesimo, Giorgia Coratti, et al.. (2025). Application of the neonatal ‘floppy module’ to older infants: can it be used for differential diagnosis?. European Journal of Pediatrics. 184(11). 661–661.

Mercuri, Eugenio, Giorgia Coratti, Costanza Cutrona, et al.. (2025). Development of the “SMA NNE,” a short neonatal neurological examination for newborns with spinal muscular atrophy. European Journal of Pediatrics. 184(9). 562–562.

Berti, Beatrice, Daniela Verrigni, Alessia Nasca, et al.. (2024). De Novo DNM1L Mutation in a Patient with Encephalopathy, Cardiomyopathy and Fatal Non-Epileptic Paroxysmal Refractory Vomiting. International Journal of Molecular Sciences. 25(14). 7782–7782. 2 indexed citations

Panicucci, Chiara, Martina Bartolucci, Noemi Brolatti, et al.. (2024). Proteomics profiling and machine learning in nusinersen-treated patients with spinal muscular atrophy. Cellular and Molecular Life Sciences. 81(1). 393–393. 3 indexed citations

Mennini, Francesco Saverio, et al.. (2024). Cost-Effectiveness Analysis of Newborn Screening for Spinal Muscular Atrophy in Italy. Clinical Drug Investigation. 44(9). 687–701. 4 indexed citations

Trucco, Federica, Emilio Albamonte, Marika Pane, et al.. (2024). Parental diagnostic delay and developmental outcomes in congenital and childhood‐onset myotonic dystrophy type 1. Developmental Medicine & Child Neurology. 67(3). 365–373. 2 indexed citations

Benemei, Silvia, Francesca Gatto, Luca Boni, & Marika Pane. (2024). “If you cannot measure it, you cannot improve it”. Outcome measures in Duchenne Muscular Dystrophy: current and future perspectives. Acta Neurologica Belgica. 125(1). 1–12. 2 indexed citations

Onesimo, Roberta, Elizabeth Katherine Anna Triumbari, Chiara Leoni, et al.. (2023). Validation and cross‐cultural adaptation of the Italian version of the paediatric eating assessment tool (I‐PEDI‐EAT‐10) in genetic syndromes. International Journal of Language & Communication Disorders. 59(3). 1152–1162. 2 indexed citations

10.

Brogna, Claudia, Marika Pane, Giorgia Coratti, et al.. (2023). Upper Limb Changes in DMD Patients Amenable to Skipping Exons 44, 45, 51 and 53: A 24-Month Study. Children. 10(4). 746–746. 2 indexed citations

11.

Chieffo, Daniela Pia Rosaria, Marika Pane, Simona Lucibello, et al.. (2023). A Longitudinal Follow-Up Study of Intellectual Function in Duchenne Muscular Dystrophy over Age: Is It Really Stable?. Journal of Clinical Medicine. 12(2). 403–403. 7 indexed citations

12.

Pera, Maria Carmela, Giorgia Coratti, Chiara Bravetti, et al.. (2023). Caregivers’ Expectations on Possible Functional Changes following Disease-Modifying Treatment in Type II and III Spinal Muscular Atrophy: A Comparative Study. Journal of Clinical Medicine. 12(13). 4183–4183. 3 indexed citations

13.

Ricci, Martina, Anna Capasso, Giorgia Coratti, et al.. (2023). Profile of cognitive abilities in spinal muscular atrophy type II and III: what is the role of motor impairment?. Neuromuscular Disorders. 33(10). 711–717. 9 indexed citations

14.

Canonico, Francesco, Maila Chirivì, Fabio Maiullari, et al.. (2021). Focus on the road to modelling cardiomyopathy in muscular dystrophy. Cardiovascular Research. 118(8). 1872–1884. 6 indexed citations

15.

Mercuri, Eugenio, Giuseppe Zampino, Alisha Morsella, et al.. (2021). Contactless: a new personalised telehealth model in chronic pediatric diseases and disability during the COVID-19 era. The Italian Journal of Pediatrics/Italian journal of pediatrics. 47(1). 29–29. 13 indexed citations

16.

Sansone, Valeria, Giorgia Coratti, Maria Carmela Pera, et al.. (2020). Sometimes they come back: New and old spinal muscular atrophy adults in the era of nusinersen. European Journal of Neurology. 28(2). 602–608. 8 indexed citations

17.

Jokela, Manu, Giorgio Tasca, Anna Vihola, et al.. (2019). An unusual ryanodine receptor 1 (RYR1) phenotype. Neurology. 92(14). e1600–e1609. 12 indexed citations

18.

Sanctis, Roberto De, Giorgia Coratti, Amy Pasternak, et al.. (2016). Developmental milestones in type I spinal muscular atrophy. Neuromuscular Disorders. 26(11). 754–759. 90 indexed citations

19.

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

20.

Mercuri, Eugenio, Daniela Ricci, Marika Pane, & Giovanni Baranello. (2005). The neurological examination of the newborn baby. Early Human Development. 81(12). 947–956. 25 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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