Luigina Spaccini

1.6k total citations
47 papers, 455 citations indexed

About

Luigina Spaccini is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Luigina Spaccini has authored 47 papers receiving a total of 455 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 19 papers in Genetics and 12 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Luigina Spaccini's work include Genetics and Neurodevelopmental Disorders (8 papers), Fetal and Pediatric Neurological Disorders (7 papers) and Prenatal Screening and Diagnostics (6 papers). Luigina Spaccini is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Fetal and Pediatric Neurological Disorders (7 papers) and Prenatal Screening and Diagnostics (6 papers). Luigina Spaccini collaborates with scholars based in Italy, United States and Finland. Luigina Spaccini's co-authors include Massimo Mastrangelo, Cecilia Parazzini, Barbara Scelsa, Andrea Righini, Lidia Larizza, Angela Peron, Mariangela Rustico, Angelo Selicorni, Pierangelo Veggiotti and Cristina Gervasini and has published in prestigious journals such as SHILAP Revista de lepidopterología, International Journal of Molecular Sciences and International Journal of Environmental Research and Public Health.

In The Last Decade

Luigina Spaccini

41 papers receiving 441 citations

Peers

Luigina Spaccini

GENET

PPCH

SURGE

Maria Descartes United States

Mathilde Nizon France

Ho‐Ming Luk China

Carlos E. Speck‐Martins Brazil

Alice S. Brooks Netherlands

Mary K. Bofinger United States

Göran Brandberg Sweden

Maya Chopra United States

Ohsuke Migita Japan

Daniel R. Carvalho Brazil

Maria Descartes United States

Luigina Spaccini

399 ×1.9

431 ×2.7

GENET

94 ×0.9

PPCH

72 ×1.3

SURGE

20 ×0.5

Citations per year, relative to Luigina Spaccini Luigina Spaccini (= 1×) peers Maria Descartes

Countries citing papers authored by Luigina Spaccini

Since Specialization

Citations

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

Fields of papers citing papers by Luigina Spaccini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Luigina Spaccini

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

Spaccini, Luigina, S. Faiola, Arianna Laoreti, et al.. (2025). Monochorionic Diamniotic Twins with Sex Discordance: Case Series. Diagnostics. 15(3). 372–372.

Faiola, S., Chiara Doneda, Arianna Laoreti, et al.. (2025). Neurodevelopmental Outcome in Isolated Vermian Hypoplasia: A Single-Center Retrospective Cohort Study and Literature Review. The Cerebellum. 24(3). 64–64.

Spagnoli, Carlotta, Stefano Giuseppe Caraffi, A Cavalli, et al.. (2024). Genetic Epilepsies and Developmental Epileptic Encephalopathies with Early Onset: A Multicenter Study. International Journal of Molecular Sciences. 25(2). 1248–1248. 9 indexed citations

Cattaneo, Elisa, Luigina Spaccini, Maria Iascone, et al.. (2024). Novel Genetic Variant in HUWE1. Neurology Genetics. 10(4). e200169–e200169. 1 indexed citations

Cattaneo, Elisa, et al.. (2024). Giant congenital fibroblastic connective tissue nevus associated with vascular anomalies. Journal of Cutaneous Pathology. 51(7). 485–489.

Laoreti, Arianna, et al.. (2024). Amnioreduction for Polyhydramnios in a Consecutive Series at a Single Center: Indications, Risks and Perinatal Outcomes. Children. 11(4). 502–502. 2 indexed citations

Spaccini, Luigina, et al.. (2023). Case report: Early-onset parkinsonism among the neurological features in children with PHACTR1 variants. Frontiers in Neurology. 14. 1181015–1181015.

Masnada, Silvia, Paola Anna Erba, Anna Camporesi, et al.. (2023). FDXR-associated disease: a challenging differential diagnosis with inflammatory peripheral neuropathy. Neurological Sciences. 44(9). 3037–3043. 4 indexed citations

Jokela, Manu, Meriel McEntagart, Tessa Homfray, et al.. (2023). The crucial role of titin in fetal development: recurrent miscarriages and bone, heart and muscle anomalies characterise the severe end of titinopathies spectrum. Journal of Medical Genetics. 60(9). 866–873. 8 indexed citations

10.

Lanna, Mariano, Dario Consonni, S. Faiola, et al.. (2023). Fetal Hydrothorax Treated with Pleuro-Amniotic Shunting: Fetal and Maternal Complications and Long-Term Outcomes. Fetal Diagnosis and Therapy. 50(2). 115–120. 1 indexed citations

11.

Pezzani, Lidia, Laura Pezzoli, Daniela Marchetti, et al.. (2023). Comparison of first‐tier whole‐exome sequencing with a multi‐step traditional approach for diagnosing paediatric outpatients: An Italian prospective study. Molecular Genetics & Genomic Medicine. 12(1). e2316–e2316. 4 indexed citations

12.

Pezzani, Lidia, Enrico Alfei, Laura Pezzoli, et al.. (2023). Rock around DYRK1A: Ethnic diversity, clinical challenges. American Journal of Medical Genetics Part A. 191(5). 1459–1464.

13.

Iascone, Maria, Luigina Spaccini, Davide Tonduti, et al.. (2022). Mucopolysaccharidosis-Plus Syndrome, a Rapidly Progressive Disease: Favorable Impact of a Very Prolonged Steroid Treatment on the Clinical Course in a Child. Genes. 13(3). 442–442. 14 indexed citations

14.

Olivotto, Sara, Eleonora Basso, Barbara Castellotti, et al.. (2022). Successful use of perampanel in GABRA1-related myoclonic epilepsy with photosensitivity. Epilepsy & Behavior Reports. 19. 100544–100544. 4 indexed citations

15.

Moneghini, Laura, Delfina Tosi, Daniela Graziani, et al.. (2020). CD10 and CD34 as markers in vascular malformations with PIK3CA and TEK mutations. Human Pathology. 99. 98–106. 4 indexed citations

16.

Redaelli, Serena, Silvia Maitz, Francesca Crosti, et al.. (2019). Refining the Phenotype of Recurrent Rearrangements of Chromosome 16. International Journal of Molecular Sciences. 20(5). 1095–1095. 28 indexed citations

17.

Paccagnini, S., Elena Pozzi, Luigina Spaccini, et al.. (2018). Currarino syndrome and microcephaly due to a rare 7q36.2 microdeletion: a case report. The Italian Journal of Pediatrics/Italian journal of pediatrics. 44(1). 59–59. 1 indexed citations

18.

Scelsa, Barbara, Mariangela Rustico, Andrea Righini, et al.. (2018). Mild ventriculomegaly from fetal consultation to neurodevelopmental assessment: A single center experience and review of the literature. European Journal of Paediatric Neurology. 22(6). 919–928. 26 indexed citations

19.

Costanzo, Sara, Luigina Spaccini, Luca Pio, et al.. (2017). Currarino syndrome: does the presence of a genetic anomaly correlate with a more severe phenotype? A multicentre study. Journal of Pediatric Surgery. 52(10). 1591–1596. 12 indexed citations

20.

Giorda, Roberto, Silvana Beri, María Clara Bonaglia, et al.. (2011). Common structural features characterize interstitial intrachromosomal Xp and 18q triplications. American Journal of Medical Genetics Part A. 155(11). 2681–2687. 6 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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