Daniela Giardino

2.5k total citations
61 papers, 1.0k citations indexed

About

Daniela Giardino is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Daniela Giardino has authored 61 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 46 papers in Genetics, 22 papers in Molecular Biology and 14 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Daniela Giardino's work include Genomic variations and chromosomal abnormalities (39 papers), Prenatal Screening and Diagnostics (14 papers) and Chromosomal and Genetic Variations (13 papers). Daniela Giardino is often cited by papers focused on Genomic variations and chromosomal abnormalities (39 papers), Prenatal Screening and Diagnostics (14 papers) and Chromosomal and Genetic Variations (13 papers). Daniela Giardino collaborates with scholars based in Italy, Argentina and United Kingdom. Daniela Giardino's co-authors include Lidia Larizza, Palma Finelli, Nicoletta Rizzi, Daniela Bettio, Lucia Ballarati, Marco Losa, Maria Paola Recalcati, Silvia Russo, Ornella Rodeschini and Graziano Grugni and has published in prestigious journals such as Neuroscience, International Journal of Cancer and Neuropsychologia.

In The Last Decade

Daniela Giardino

60 papers receiving 976 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Daniela Giardino Italy 19 608 432 205 149 103 61 1.0k
Géraldine Viot France 21 647 1.1× 674 1.6× 280 1.4× 82 0.6× 144 1.4× 56 1.4k
György Kosztolányi Hungary 16 394 0.6× 392 0.9× 221 1.1× 94 0.6× 68 0.7× 84 921
Stefania Gimelli Switzerland 21 900 1.5× 787 1.8× 228 1.1× 225 1.5× 174 1.7× 64 1.6k
Katrin Õunap Estonia 25 857 1.4× 1.0k 2.4× 264 1.3× 103 0.7× 75 0.7× 106 1.8k
Emmanuelle Lemyre Canada 22 879 1.4× 550 1.3× 276 1.3× 95 0.6× 129 1.3× 52 1.3k
Helen Kingston United Kingdom 24 645 1.1× 839 1.9× 161 0.8× 76 0.5× 122 1.2× 63 1.9k
Elisabetta Lapi Italy 18 477 0.8× 534 1.2× 131 0.6× 31 0.2× 70 0.7× 48 957
Giovanni Sorge Italy 22 553 0.9× 486 1.1× 153 0.7× 85 0.6× 150 1.5× 75 1.3k
Brigitte Benzacken France 20 737 1.2× 462 1.1× 426 2.1× 156 1.0× 57 0.6× 61 1.3k
Patricia G. Wheeler United States 22 400 0.7× 529 1.2× 194 0.9× 45 0.3× 151 1.5× 41 1.1k

Countries citing papers authored by Daniela Giardino

Since Specialization
Citations

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

Fields of papers citing papers by Daniela Giardino

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Daniela Giardino

This figure shows the co-authorship network connecting the top 25 collaborators of Daniela Giardino. A scholar is included among the top collaborators of Daniela Giardino 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 Daniela Giardino. Daniela Giardino 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.
2.
Recalcati, Maria Paola, Ornella Rodeschini, Chiara Barone, et al.. (2019). Ten new cases of Balanced Reciprocal Translocation Mosaicism (BRTM): Reproductive implications, frequency and mechanism. European Journal of Medical Genetics. 63(2). 103639–103639. 5 indexed citations
3.
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Cirello, Valentina, Chiara Castronovo, Susan Marelli, et al.. (2018). Segmental Maternal UPD of Chromosome 7q in a Patient With Pendred and Silver Russell Syndromes-Like Features. Frontiers in Genetics. 9. 600–600. 3 indexed citations
5.
Recalcati, Maria Paola, Maria Teresa Bonati, Isabella Mammi, et al.. (2017). Molecular cytogenetics characterization of seven small supernumerary marker chromosomes derived from chromosome 19: Genotype-phenotype correlation and review of the literature. European Journal of Medical Genetics. 61(3). 173–180. 2 indexed citations
6.
Castronovo, Chiara, M. Crippa, Daniela Giardino, et al.. (2013). A novel mosaic NSD1 intragenic deletion in a patient with an atypical phenotype. American Journal of Medical Genetics Part A. 161(3). 611–618. 5 indexed citations
7.
Castronovo, Chiara, Emanuele Valtorta, M. Crippa, et al.. (2013). Design and validation of a pericentromeric BAC clone set aimed at improving diagnosis and phenotype prediction of supernumerary marker chromosomes. Molecular Cytogenetics. 6(1). 45–45. 8 indexed citations
8.
Finelli, Palma, Silvia Maria Sirchia, Maura Masciadri, et al.. (2012). Juxtaposition of heterochromatic and euchromatic regions by chromosomal translocation mediates a heterochromatic long-range position effect associated with a severe neurological phenotype. Molecular Cytogenetics. 5(1). 16–16. 21 indexed citations
9.
Ballarati, Lucia, Anna Cereda, Rossella Caselli, et al.. (2011). Deletion of the AP1S2 gene in a child with psychomotor delay and hypotonia. European Journal of Medical Genetics. 55(2). 124–127. 8 indexed citations
10.
Ballarati, Lucia, Anna Cereda, Rossella Caselli, et al.. (2010). Genotype–phenotype correlations in a new case of 8p23.1 deletion and review of the literature. European Journal of Medical Genetics. 54(1). 55–59. 38 indexed citations
11.
Giardino, Daniela, Aglaia Vignoli, Lucia Ballarati, et al.. (2010). Genetic investigations on 8 patients affected by ring 20 chromosome syndrome. BMC Medical Genetics. 11(1). 146–146. 17 indexed citations
12.
Lenzini, Elisabetta, Lucia Ballarati, Paola Drigo, et al.. (2009). 1q44-qter Trisomy:Clinical Report and Review of the Literature. Genetic Testing and Molecular Biomarkers. 13(1). 79–86. 3 indexed citations
13.
Giardino, Daniela, et al.. (2007). Prenatal diagnosis of a small chromosome 2‐derived supernumerary marker, and review of the reported cases. American Journal of Medical Genetics Part A. 143A(18). 2200–2203. 1 indexed citations
14.
Giardino, Daniela, Lucia Ballarati, Palma Finelli, et al.. (2006). Prenatal diagnosis of a de novo complex chromosome rearrangement (CCR) mediated by six breakpoints, and a review of 20 prenatally ascertained CCRs. Prenatal Diagnosis. 26(6). 565–570. 31 indexed citations
15.
Bonati, Maria Teresa, et al.. (2005). Trisomy 15q25.2‐qter in an autistic child: Genotype–phenotype correlations. American Journal of Medical Genetics Part A. 133A(2). 184–188. 17 indexed citations
16.
Giardino, Daniela, et al.. (2004). Unbalanced segregation of a complex four-break 5q23–31 insertion in the 5p13 band in a malformed child. European Journal of Human Genetics. 12(6). 455–459. 3 indexed citations
17.
Giardino, Daniela, Palma Finelli, Silvia Russo, et al.. (2002). Small familial supernumerary ring chromosome 2: FISH characterization and genotype‐phenotype correlation. American Journal of Medical Genetics. 111(3). 319–323. 23 indexed citations
18.
Finelli, Palma, Daniela Giardino, Silvia Russo, et al.. (2001). Refined FISH characterization of a de novo 1p22-p36.2 paracentric inversion and associated 1p21-22 deletion in a patient with signs of 1p36 microdeletion syndrome. American Journal of Medical Genetics. 99(4). 308–313. 7 indexed citations
19.
Bettio, Daniela, Nicoletta Rizzi, & Daniela Giardino. (1994). Familial translocation (X;3) (p22.3;p23): chromosomal in situ suppression (CISS) hybridization and inactivation pattern study. Clinical Genetics. 46(5). 360–363. 10 indexed citations
20.
Giardino, Daniela, et al.. (1990). Angelman's Syndrome in the First Year of Life. Developmental Medicine & Child Neurology. 32(11). 1011–1016. 33 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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