Elisa Pisaneschi

1.1k total citations
41 papers, 579 citations indexed

About

Elisa Pisaneschi is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Elisa Pisaneschi has authored 41 papers receiving a total of 579 indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Molecular Biology, 16 papers in Cell Biology and 12 papers in Genetics. Recurrent topics in Elisa Pisaneschi's work include Skin and Cellular Biology Research (14 papers), RNA regulation and disease (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Elisa Pisaneschi is often cited by papers focused on Skin and Cellular Biology Research (14 papers), RNA regulation and disease (6 papers) and Genomic variations and chromosomal abnormalities (4 papers). Elisa Pisaneschi collaborates with scholars based in Italy, United States and Egypt. Elisa Pisaneschi's co-authors include Adriano Angioni, Bruno Dallapiccola, Antonio Novelli, M. Cristina Digilio, May El Hachem, Francesca Romana Lepri, Andrea Diociaiuti, Maria Lisa Dentici, Giovanna Zambruno and Maria Gnazzo and has published in prestigious journals such as International Journal of Molecular Sciences, The American Journal of Human Genetics and Annals of the Rheumatic Diseases.

In The Last Decade

Elisa Pisaneschi

37 papers receiving 547 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elisa Pisaneschi Italy 12 346 258 96 55 46 41 579
Nisha Patel Saudi Arabia 17 428 1.2× 267 1.0× 69 0.7× 52 0.9× 24 0.5× 39 727
Davor Lessel Germany 17 523 1.5× 181 0.7× 72 0.8× 48 0.9× 39 0.8× 44 733
Shehla Mohammed United Kingdom 12 497 1.4× 248 1.0× 57 0.6× 61 1.1× 26 0.6× 25 680
Patricio Barros‐Núñez Mexico 15 359 1.0× 302 1.2× 99 1.0× 26 0.5× 42 0.9× 71 688
Wouter Steyaert Belgium 14 392 1.1× 318 1.2× 59 0.6× 28 0.5× 16 0.3× 27 639
Muneera Alshammari Saudi Arabia 14 473 1.4× 406 1.6× 85 0.9× 25 0.5× 24 0.5× 18 749
Avni Santani United States 16 405 1.2× 439 1.7× 34 0.4× 93 1.7× 65 1.4× 39 781
Christopher R. Futtner United States 12 695 2.0× 232 0.9× 36 0.4× 60 1.1× 23 0.5× 16 983
Pelin Özlem Şimşek‐Kiper Türkiye 14 377 1.1× 326 1.3× 70 0.7× 48 0.9× 16 0.3× 99 662
Ghislaine Plessis France 18 431 1.2× 341 1.3× 46 0.5× 29 0.5× 32 0.7× 31 810

Countries citing papers authored by Elisa Pisaneschi

Since Specialization
Citations

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

Fields of papers citing papers by Elisa Pisaneschi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisa Pisaneschi

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

All Works

20 of 20 papers shown
1.
Alesi, Viola, Silvia Genovese, Silvia Di Tommaso, et al.. (2024). Structural rearrangements as a recurrent pathogenic mechanism for SETBP1 haploinsufficiency. Human Genomics. 18(1). 29–29. 1 indexed citations
2.
3.
Colona, Vito Luigi, Enrico Bertini, M. Cristina Digilio, et al.. (2023). A New Case of Autosomal-Dominant POLR3B-Related Disorder: Widening Genotypic and Phenotypic Spectrum. Brain Sciences. 13(11). 1567–1567. 1 indexed citations
4.
Campi, Francesca, Domenico Umberto De Rose, Flaminia Pugnaloni, et al.. (2023). Neurodevelopmental and genetic findings in neonates with intracranial arteriovenous shunts: A case series. Frontiers in Pediatrics. 11. 1111527–1111527. 3 indexed citations
5.
Rotunno, Roberta, et al.. (2022). PIK3CA-related overgrowth with an uncommon phenotype: case report. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 48(1). 71–71. 3 indexed citations
6.
Radenkovic, Silvia, Diego Martinelli, Yuebo Zhang, et al.. (2022). TRAPPC9-CDG: A novel congenital disorder of glycosylation with dysmorphic features and intellectual disability. Genetics in Medicine. 24(4). 894–904. 13 indexed citations
7.
Diociaiuti, Andrea, Diego Martinelli, Francesco Nicita, et al.. (2021). Two Italian Patients with ELOVL4-Related Neuro-Ichthyosis:  Expanding the Genotypic and Phenotypic Spectrum and Ultrastructural Characterization. Genes. 12(3). 343–343. 9 indexed citations
8.
Rossi, Sabrina, Daniele Castiglia, Elisa Pisaneschi, et al.. (2020). Immunofluorescence mapping, electron microscopy and genetics in the diagnosis and sub‐classification of inherited epidermolysis bullosa: a single‐centre retrospective comparative study of 87 cases with long‐term follow‐up. Journal of the European Academy of Dermatology and Venereology. 35(4). 1007–1016. 8 indexed citations
9.
Diociaiuti, Andrea, Simona Giancristoforo, Elisa Pisaneschi, et al.. (2020). Hoarse cry in a newborn with epidermolysis bullosa simplex, generalized severe. Pediatric Dermatology. 37(2). 393–395. 1 indexed citations
10.
Diociaiuti, Andrea, Mario Cutrone, Roberta Rotunno, et al.. (2019). Angioma serpiginosum: a case report and review of the literature. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 45(1). 53–53. 3 indexed citations
11.
Guzzetti, Chiara, Carla Bizzarri, Elisa Pisaneschi, et al.. (2018). Next-Generation Sequencing Identifies Different Genetic Defects in 2 Patients with Primary Adrenal Insufficiency and Gonadotropin-Independent Precocious Puberty. Hormone Research in Paediatrics. 90(3). 203–211. 8 indexed citations
12.
Bizzarri, Carla, Elisa Pisaneschi, Mafalda Mucciolo, et al.. (2017). Lipoid congenital adrenal hyperplasia by steroidogenic acute regulatory protein (STAR) gene mutation in an Italian infant: an uncommon cause of adrenal insufficiency. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 43(1). 57–57. 4 indexed citations
13.
Alesi, Viola, Silvia Genovese, Sara Loddo, et al.. (2017). Interstitial 10q21.1q23.31 Duplication due to Meiotic Recombination of a Paternal Balanced Complex Rearrangement: Cytogenetic and Molecular Characterization. Cytogenetic and Genome Research. 151(4). 179–185. 2 indexed citations
14.
Masotti, Andrea, Paolo Uva, Laura Davis‐Keppen, et al.. (2015). Keppen-Lubinsky Syndrome Is Caused by Mutations in the Inwardly Rectifying K+ Channel Encoded by KCNJ6. The American Journal of Human Genetics. 96(2). 295–300. 86 indexed citations
15.
Pisaneschi, Elisa, Pietro Sirleto, Francesca Romana Lepri, et al.. (2015). CHARGE syndrome due to deletion of region upstream of CHD7 gene START codon. BMC Medical Genetics. 16(1). 78–78. 3 indexed citations
16.
Lepri, Francesca Romana, M. Cristina Digilio, Maria Gnazzo, et al.. (2014). Diagnosis of Noonan syndrome and related disorders using target next generation sequencing. BMC Medical Genetics. 15(1). 14–14. 48 indexed citations
17.
Dentici, Maria Lisa, Francesca Romana Lepri, Maria Gnazzo, et al.. (2014). Kabuki syndrome: clinical and molecular diagnosis in the first year of life. Archives of Disease in Childhood. 100(2). 158–164. 62 indexed citations
18.
Modoni, Anna, Adele D’Amico, Bruno Dallapiccola, et al.. (2011). Low-Rate Repetitive Nerve Stimulation Protocol in an Italian Cohort of Patients Affected by Recessive Myotonia Congenita. Journal of Clinical Neurophysiology. 28(1). 39–44. 16 indexed citations
19.
Pisaneschi, Elisa, Giovanna Zambruno, Pernille Axél Gregersen, et al.. (2011). A founder synonymous COL7A1 mutation in three Danish families with dominant dystrophic epidermolysis bullosa pruriginosa identifies exonic regulatory sequences required for exon 87 splicing. British Journal of Dermatology. 165(3). 678–682. 16 indexed citations
20.
Castiglia, Daniele, Marco Castori, Elisa Pisaneschi, et al.. (2009). Trisomic rescue causing reduction to homozygosity for a novel ABCA12 mutation in harlequin ichthyosis. Clinical Genetics. 76(4). 392–397. 27 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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