Manuela Seia

2.9k total citations
70 papers, 1.3k citations indexed

About

Manuela Seia is a scholar working on Pulmonary and Respiratory Medicine, Genetics and Genetics. According to data from OpenAlex, Manuela Seia has authored 70 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Pulmonary and Respiratory Medicine, 16 papers in Genetics and 14 papers in Genetics. Recurrent topics in Manuela Seia's work include Cystic Fibrosis Research Advances (46 papers), Neonatal Respiratory Health Research (26 papers) and Tracheal and airway disorders (18 papers). Manuela Seia is often cited by papers focused on Cystic Fibrosis Research Advances (46 papers), Neonatal Respiratory Health Research (26 papers) and Tracheal and airway disorders (18 papers). Manuela Seia collaborates with scholars based in Italy, Germany and United Kingdom. Manuela Seia's co-authors include Maurizio Ferrari, Annamaria Giunta, Carla Colombo, Carla Colombo, Rita Padoan, Lucy Costantino, Laura Cremonesi, Luigi Porcaro, D. Degiorgio and Lucia Piceni Sereni and has published in prestigious journals such as Journal of Biological Chemistry, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Manuela Seia

68 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Manuela Seia Italy 22 767 235 230 199 198 70 1.3k
M. Claustres France 9 517 0.7× 308 1.3× 108 0.5× 125 0.6× 227 1.1× 18 1.0k
Jörn D. Beck Germany 22 482 0.6× 490 2.1× 188 0.8× 236 1.2× 111 0.6× 71 1.8k
M Super United Kingdom 18 432 0.6× 526 2.2× 184 0.8× 104 0.5× 453 2.3× 47 1.6k
S. Glüer Germany 21 367 0.5× 381 1.6× 645 2.8× 52 0.3× 90 0.5× 68 1.3k
Atsuo Kikuchi Japan 19 229 0.3× 405 1.7× 144 0.6× 105 0.5× 329 1.7× 85 1.5k
Naomi Balamuth United States 14 571 0.7× 351 1.5× 133 0.6× 44 0.2× 54 0.3× 23 1.1k
Josephine Wyatt‐Ashmead United States 19 160 0.2× 174 0.7× 185 0.8× 98 0.5× 70 0.4× 37 836
Marleen Renard Belgium 21 234 0.3× 347 1.5× 138 0.6× 85 0.4× 104 0.5× 50 1.5k
Allison F. O’Neill United States 17 188 0.2× 251 1.1× 234 1.0× 65 0.3× 53 0.3× 65 906
Karen M. Chisholm United States 20 146 0.2× 584 2.5× 110 0.5× 98 0.5× 121 0.6× 68 1.4k

Countries citing papers authored by Manuela Seia

Since Specialization
Citations

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

Fields of papers citing papers by Manuela Seia

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Manuela Seia

This figure shows the co-authorship network connecting the top 25 collaborators of Manuela Seia. A scholar is included among the top collaborators of Manuela Seia 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 Seia. Manuela Seia 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.
Monfrini, Edoardo, Francesca Spagnolo, Margherita Canesi, et al.. (2021). VPS13C-associated Parkinson's disease: Two novel cases and review of the literature. Parkinsonism & Related Disorders. 94. 37–39. 13 indexed citations
2.
Curcio, Cristina, et al.. (2020). Unexpected Genotype in a Non-Transfusion Dependent Thalassemia Family. Journal of Medical Cases. 11(4). 90–93.
3.
Lucarelli, Marco, Luigi Porcaro, Lucy Costantino, et al.. (2017). A New Targeted CFTR Mutation Panel Based on Next-Generation Sequencing Technology. Journal of Molecular Diagnostics. 19(5). 788–800. 27 indexed citations
4.
Cortini, Francesca, et al.. (2016). Next-generation sequencing and a novel COL3A1 mutation associated with vascular Ehlers–Danlos syndrome with severe intestinal involvement: a case report. Journal of Medical Case Reports. 10(1). 303–303. 9 indexed citations
5.
Straniero, Letizia, Giulia Soldà, Lucy Costantino, et al.. (2016). Whole-gene CFTR sequencing combined with digital RT-PCR improves genetic diagnosis of cystic fibrosis. Journal of Human Genetics. 61(12). 977–984. 12 indexed citations
6.
Costantino, Lucy, Giulia Soldà, Manuela Seia, et al.. (2013). Fine Characterization of the Recurrent c.1584+18672A>G Deep-Intronic Mutation in the Cystic Fibrosis Transmembrane Conductance Regulator Gene. American Journal of Respiratory Cell and Molecular Biology. 48(5). 619–625. 15 indexed citations
7.
Degiorgio, D., Paola Antonia Corsetto, Angela Maria Rizzo, et al.. (2013). Two ABCB4 point mutations of strategic NBD-motifs do not prevent protein targeting to the plasma membrane but promote MDR3 dysfunction. European Journal of Human Genetics. 22(5). 633–639. 24 indexed citations
8.
Sironi, Francesca, Paola Primignani, Sara Tùnesi, et al.. (2013). DJ1 analysis in a large cohort of Italian early onset Parkinson Disease patients. Neuroscience Letters. 557. 165–170. 9 indexed citations
9.
Paffoni, Alessio, Valentina Paracchini, Stefania Ferrari, et al.. (2011). Use of parthenogenetic activation of human oocytes as an experimental model for evaluation of polar body based PGD assay performance. Journal of Assisted Reproduction and Genetics. 28(5). 461–470. 3 indexed citations
10.
Castellani, Carlo, Vera Bianchi, Manuela Seia, et al.. (2011). An interactive computer program can effectively educate potential users of cystic fibrosis carrier tests. American Journal of Medical Genetics Part A. 155(4). 778–785. 16 indexed citations
11.
Costantino, Lucy, Laura Claut, Carla Colombo, et al.. (2011). A wide methodological approach to identify a large duplication in CFTR gene in a CF patient uncharacterised by sequencing analysis. Journal of Cystic Fibrosis. 10(6). 412–417. 5 indexed citations
12.
Costantino, Lucy, Laura Claut, Valentina Paracchini, et al.. (2010). A novel donor splice site characterized by CFTR mRNA analysis induces a new pseudo-exon in CF patients. Journal of Cystic Fibrosis. 9(6). 411–418. 13 indexed citations
13.
Degiorgio, D., Carla Colombo, Manuela Seia, et al.. (2007). Molecular characterization and structural implications of 25 new ABCB4 mutations in progressive familial intrahepatic cholestasis type 3 (PFIC3). European Journal of Human Genetics. 15(12). 1230–1238. 71 indexed citations
14.
Padoan, Rita, et al.. (2000). A novel missense mutation (Y89C) in exon 3 of the CFTR (ABCC7) gene in a young male. Human Mutation. 15(5). 486–486. 1 indexed citations
15.
Seia, Manuela, et al.. (2000). A novel stop mutation in exon 18 (W1145X) of the CFTR (ABCC7) gene in an adult CF patient. Human Mutation. 16(6). 532–533. 1 indexed citations
16.
Magnani, Carmelina, Laura Cremonesi, Elena Belloni, et al.. (1994). Informativity of intragenic microsatellites for carrier detection and prenatal diagnosis of cystic fibrosis in the Italian population. Clinical Genetics. 45(3). 135–139. 5 indexed citations
17.
Belloni, Elena, et al.. (1992). Multiplex PCR for rapid detection of three mutations in the cystic fibrosis gene.. Genome Research. 1(4). 297–298. 9 indexed citations
18.
Ronchetto, Patrizia, Juan José Tellería Orriols, Pascale Fanen, et al.. (1992). A nonsense mutation (R1158X) and a splicing mutation (3849 + 4A → G) in exon 19 of the cystic fibrosis transmembrane conductance regulator gene. Genomics. 12(2). 417–418. 17 indexed citations
19.
Cremonesi, Laura, Manuela Seia, Silvia Russo, et al.. (1990). Frequency of the ΔF508 mutation in a sample of 175 Italian cystic fibrosis patients. Human Genetics. 85(4). 400–402. 7 indexed citations
20.
Camaschella, Clara, Anna Serra, Maria Tiziana Bertero, et al.. (1989). Molecular Characterization of Italian Chromosomes Carrying the Lepore Boston Gene. Acta Haematologica. 81(3). 136–139. 3 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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