Gemma D’Elia

518 total citations
10 papers, 333 citations indexed

About

Gemma D’Elia is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Gemma D’Elia has authored 10 papers receiving a total of 333 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Molecular Biology and 3 papers in Surgery. Recurrent topics in Gemma D’Elia's work include Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Chromosomal and Genetic Variations (2 papers). Gemma D’Elia is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genetics and Neurodevelopmental Disorders (2 papers) and Chromosomal and Genetic Variations (2 papers). Gemma D’Elia collaborates with scholars based in Italy and United States. Gemma D’Elia's co-authors include Adriano Angioni, Massimo Negrini, Luigi Bolondi, Giovanni Lanza, Laura Lupini, Angelo Veronese, Jessica Consiglio, Nicola Zanesi, Francesca Fornari and Hansjüerg Alder and has published in prestigious journals such as Cancer Research, The Journal of Pediatrics and BMC Cancer.

In The Last Decade

Gemma D’Elia

10 papers receiving 308 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Gemma D’Elia Italy	8	210	134	97	33	24	10	333
Essam Al Ageeli Saudi Arabia	11	237 1.1×	169 1.3×	110 1.1×	16 0.5×	14 0.6×	29	388
Annemieke H. van der Hout Netherlands	8	227 1.1×	88 0.7×	223 2.3×	21 0.6×	19 0.8×	13	451
Eddy N. de Boer Netherlands	8	213 1.0×	90 0.7×	202 2.1×	26 0.8×	7 0.3×	17	425
Alessandra Franzoni Italy	11	166 0.8×	63 0.5×	53 0.5×	21 0.6×	10 0.4×	33	307
Stanisław Zajączek Poland	10	198 0.9×	26 0.2×	129 1.3×	30 0.9×	37 1.5×	36	354
A G McGuckin United Kingdom	9	198 0.9×	97 0.7×	91 0.9×	14 0.4×	10 0.4×	11	365
Chau‐To Kwok Australia	12	362 1.7×	226 1.7×	114 1.2×	42 1.3×	5 0.2×	15	599
Alice Goldenberg France	9	382 1.8×	155 1.2×	87 0.9×	68 2.1×	3 0.1×	12	527
Samaneh Farashi Iran	9	149 0.7×	39 0.3×	87 0.9×	7 0.2×	22 0.9×	31	452
Hessa S. Alsaif Saudi Arabia	10	254 1.2×	31 0.2×	130 1.3×	71 2.2×	38 1.6×	18	417

Countries citing papers authored by Gemma D’Elia

Since Specialization

Citations

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

Fields of papers citing papers by Gemma D’Elia

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Gemma D’Elia. 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 Gemma D’Elia. The network helps show where Gemma D’Elia may publish in the future.

Co-authorship network of co-authors of Gemma D’Elia

This figure shows the co-authorship network connecting the top 25 collaborators of Gemma D’Elia. A scholar is included among the top collaborators of Gemma D’Elia 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 Gemma D’Elia. Gemma D’Elia 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

Piglionica, Marilidia, et al.. (2024). Molecular Basis and Diagnostic Approach to Isolated and Syndromic Lateralized Overgrowth in Childhood. The Journal of Pediatrics. 274. 114177–114177. 1 indexed citations

Pignata, Laura, Giuseppina Vitiello, Viola Alesi, et al.. (2022). Different Mechanisms Cause Hypomethylation of Both H19 and KCNQ1OT1 Imprinted Differentially Methylated Regions in Two Cases of Silver–Russell Syndrome Spectrum. Genes. 13(10). 1875–1875. 2 indexed citations

Pascolini, Giulia, Emanuele Agolini, Nicole Fleischer, et al.. (2020). A novel patient with White–Sutton syndrome refines the mutational and clinical repertoire of the POGZ‐related phenotype and suggests further observations. American Journal of Medical Genetics Part A. 182(7). 1791–1795. 10 indexed citations

D’Elia, Gemma, Silvia Genovese, Cecilia Surace, et al.. (2015). Advantages of a next generation sequencing targeted approach for the molecular diagnosis of retinoblastoma. BMC Cancer. 15(1). 841–841. 21 indexed citations

Ciocca, Leonardo, M. Cristina Digilio, Gemma D’Elia, et al.. (2015). Hypoplastic left heart syndrome and 21q22.3 deletion. American Journal of Medical Genetics Part A. 167(3). 579–586. 19 indexed citations

Surace, Cecilia, Francesco Berardinelli, Andrea Masotti, et al.. (2014). Telomere shortening and telomere position effect in mild ring 17 syndrome. Epigenetics & Chromatin. 7(1). 1–1. 59 indexed citations

D’Elia, Gemma, Francesca Del Bufalo, Maria Antonietta De Ioris, et al.. (2013). Two novel cases of trilateral retinoblastoma: genetics and review of the literature. Cancer Genetics. 206(11). 398–401. 9 indexed citations

Roberti, María P., Cecilia Surace, M. Cristina Digilio, et al.. (2011). Complex chromosome rearrangements related 15q14 microdeletion plays a relevant role in phenotype expression and delineates a novel recurrent syndrome. Orphanet Journal of Rare Diseases. 6(1). 17–17. 9 indexed citations

Veronese, Angelo, Laura Lupini, Jessica Consiglio, et al.. (2010). Oncogenic Role of miR-483-3p at the IGF2/483 Locus. Cancer Research. 70(8). 3140–3149. 182 indexed citations

10.

Surace, Cecilia, Pietro Sirleto, Gemma D’Elia, et al.. (2009). Mild ring 17 syndrome shares common phenotypic features irrespective of the chromosomal breakpoints location. Clinical Genetics. 76(3). 256–262. 21 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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