Elisa Savin

495 total citations
6 papers, 57 citations indexed

About

Elisa Savin is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Elisa Savin has authored 6 papers receiving a total of 57 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Molecular Biology, 4 papers in Genetics and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Elisa Savin's work include Genomic variations and chromosomal abnormalities (3 papers), Prenatal Screening and Diagnostics (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). Elisa Savin is often cited by papers focused on Genomic variations and chromosomal abnormalities (3 papers), Prenatal Screening and Diagnostics (2 papers) and Hedgehog Signaling Pathway Studies (2 papers). Elisa Savin collaborates with scholars based in Italy, Germany and Singapore. Elisa Savin's co-authors include Cristiana Marchese, Francesca Carozzi, G Pagliano, Mario Marchi, M Campogrande, A. O. Carbonara, E. Viora, Simona Cavalieri, Enrico Grosso and Barbara Pasini and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of Medical Genetics and Cytogenetic and Genome Research.

In The Last Decade

Elisa Savin

6 papers receiving 54 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Elisa Savin Italy	4	30	29	15	12	10	6	57
S. Pritchard United States	4	31 1.0×	10 0.3×	7 0.5×	15 1.3×	2 0.2×	7	53
Nicolas Pangaud France	4	8 0.3×	11 0.4×	6 0.4×	8 0.7×	7 0.7×	7	52
Madelena Martin United States	3	19 0.6×	53 1.8×	18 1.2×	14 1.2×	1 0.1×	4	90
Audrey Lacalm France	8	110 3.7×	17 0.6×	18 1.2×	17 1.4×	6 0.6×	11	142
G Girschick Germany	4	13 0.4×	26 0.9×	6 0.4×	9 0.8×	5 0.5×	9	78
John Williams United States	4	64 2.1×	24 0.8×	49 3.3×	18 1.5×	2 0.2×	6	115
Brigitte Leroy France	5	66 2.2×	39 1.3×	20 1.3×	34 2.8×	3 0.3×	8	122
Elisabeth Alanio France	4	52 1.7×	35 1.2×	15 1.0×	33 2.8×	18 1.8×	6	92
Kelly Cohen United Kingdom	5	44 1.5×	23 0.8×	15 1.0×	5 0.4×	1 0.1×	8	65
Ljubica Odak Croatia	5	14 0.5×	7 0.2×	28 1.9×	15 1.3×	4 0.4×	13	60

Countries citing papers authored by Elisa Savin

Since Specialization

Citations

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

Fields of papers citing papers by Elisa Savin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisa Savin

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

All Works

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6 of 6 papers shown

1.

Sirchia, Fabio, Eleonora Di Gregorio, Gabriella Restagno, et al.. (2017). A case of Feingold type 2 syndrome associated with keratoconus refines keratoconus type 7 locus on chromosome 13q. European Journal of Medical Genetics. 60(4). 224–227. 8 indexed citations

2.

Gregorio, Eleonora Di, Giovanni Botta, Alessandro Calcia, et al.. (2015). Array-Comparative Genomic Hybridization Analysis in Fetuses with Major Congenital Malformations Reveals that 24% of Cases Have Pathogenic Deletions/Duplications. Cytogenetic and Genome Research. 147(1). 10–16. 2 indexed citations

3.

Mandrile, Giorgia, Eleonora Di Gregorio, Alessandro Calcia, et al.. (2014). A New Case of 13q12.2q13.1 Microdeletion Syndrome Contributes to Phenotype Delineation. SHILAP Revista de lepidopterología. 2014. 1–5. 1 indexed citations

4.

Temperani, Paola, et al.. (1989). Ring chromosome in a patient with MEN IIA S. Cancer Genetics and Cytogenetics. 37(1). 23–27. 4 indexed citations

5.

Savin, Elisa, et al.. (1987). Translocation X;13 in a patient with retinoblastoma.. Journal of Medical Genetics. 24(7). 431–434. 6 indexed citations

6.

Marchese, Cristiana, Elisa Savin, Francesca Carozzi, et al.. (1985). Cystic hygroma: Prenatal diagnosis and genetic counselling. Prenatal Diagnosis. 5(3). 221–227. 36 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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