Ivana Spiga

725 total citations
10 papers, 163 citations indexed

About

Ivana Spiga is a scholar working on Molecular Biology, Genetics and Ophthalmology. According to data from OpenAlex, Ivana Spiga has authored 10 papers receiving a total of 163 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 3 papers in Genetics and 2 papers in Ophthalmology. Recurrent topics in Ivana Spiga's work include Retinal Development and Disorders (3 papers), Genomics and Rare Diseases (2 papers) and Metabolism and Genetic Disorders (2 papers). Ivana Spiga is often cited by papers focused on Retinal Development and Disorders (3 papers), Genomics and Rare Diseases (2 papers) and Metabolism and Genetic Disorders (2 papers). Ivana Spiga collaborates with scholars based in Italy and United States. Ivana Spiga's co-authors include Francesca Fumagalli, Mirella Filocamo, Laura Lorioli, Martina Cesani, Serena Grossi, Alessandra Biffi, Paola Carrera, Maurizio Ferrari, Pier Giorgio Righetti and Cecilia Gelfi and has published in prestigious journals such as Human Mutation, Clinical Chemistry and Laboratory Medicine (CCLM) and Haemophilia.

In The Last Decade

Ivana Spiga

10 papers receiving 162 citations

Peers

Ivana Spiga

MB

PHYSI

EPIDE

GENET

HEMAT

Kim D. Falkenberg Netherlands

A. Kohlschuetter Germany

Mohammad A. Al–Muhaizea Saudi Arabia

Andrea Curtabbi Spain

Brandon R. Desousa United States

Jacob M. Winter United States

Laura Lorioli Italy

Ahsen Chaudhry Canada

João Paulo Gabriel Portugal

S. Romano France

Kim D. Falkenberg Netherlands

Ivana Spiga

188 ×2.0

MB

40 ×0.6

PHYSI

23 ×0.8

EPIDE

23 ×1.1

GENET

4 ×0.3

HEMAT

Citations per year, relative to Ivana Spiga Ivana Spiga (= 1×) peers Kim D. Falkenberg

Countries citing papers authored by Ivana Spiga

Since Specialization

Citations

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

Fields of papers citing papers by Ivana Spiga

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ivana Spiga

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

All Works

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10 of 10 papers shown

1.

Zambon, Alberto A., Daniele Ghezzi, Cristina Baldoli, et al.. (2023). Expanding the spectrum of neonatal‐onset AIFM1‐associated disorders. Annals of Clinical and Translational Neurology. 10(10). 1844–1853. 1 indexed citations

2.

Bianco, Lorenzo, Alessandro Arrigo, Alessio Antropoli, et al.. (2022). PRPH2-Associated Retinopathy. Ophthalmology Retina. 7(5). 450–461. 12 indexed citations

3.

Bianco, Lorenzo, Alessandro Arrigo, Alessio Antropoli, et al.. (2022). Multimodal imaging evaluation of occult macular dystrophy associated with a novel RP1L1 variant. American Journal of Ophthalmology Case Reports. 26. 101550–101550. 3 indexed citations

4.

Baroni, Marcello, Patrizia Della Valle, Ivana Spiga, et al.. (2019). Missense changes in the catalytic domain of coagulation factor X account for minimal function preventing a perinatal lethal condition. Haemophilia. 25(4). 685–692. 9 indexed citations

5.

Resta, Chiara Di, Ivana Spiga, Stefania Merella, et al.. (2018). Integration of multigene panels for the diagnosis of hereditary retinal disorders using Next Generation Sequencing and bioinformatics approaches.. PubMed. 29(1). 15–25. 6 indexed citations

6.

Cesani, Martina, Laura Lorioli, Serena Grossi, et al.. (2015). Mutation Update ofARSAandPSAPGenes Causing Metachromatic Leukodystrophy. Human Mutation. 37(1). 16–27. 83 indexed citations

7.

Soriani, Nadia, Domenico Girelli, Clara Camaschella, et al.. (2010). High resolution melting for the identification of mutations in the iron responsive element of the ferritin light chain gene. Clinical Chemistry and Laboratory Medicine (CCLM). 48(10). 1415–1418. 6 indexed citations

8.

Gelfi, Cecilia, et al.. (1995). Amplification of 18 dystrophin gene exons in DMD/BMD patients: simultaneous resolution by capillary electrophoresis in sieving liquid polymers.. PubMed. 19(2). 254–8, 260. 25 indexed citations

9.

Carrera, Paola, Maurizio Ferrari, Ivana Spiga, et al.. (1993). Molecular Characterization of 21-Hydroxylase Deficiency in 70 Italian Families. Human Heredity. 43(3). 190–196. 13 indexed citations

10.

Privitera, Enrica, et al.. (1990). Double minute chromosomes and a homogeneously staining chromosome region in C3H10T1/2 murine cells transformed “in vitro” by proton radiation. Cancer Genetics and Cytogenetics. 49(1). 75–86. 5 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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