Laura Bernardini

5.1k total citations
126 papers, 2.1k citations indexed

About

Laura Bernardini is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Laura Bernardini has authored 126 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 68 papers in Genetics, 59 papers in Molecular Biology and 23 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Laura Bernardini's work include Genomic variations and chromosomal abnormalities (50 papers), Congenital heart defects research (25 papers) and Genetics and Neurodevelopmental Disorders (21 papers). Laura Bernardini is often cited by papers focused on Genomic variations and chromosomal abnormalities (50 papers), Congenital heart defects research (25 papers) and Genetics and Neurodevelopmental Disorders (21 papers). Laura Bernardini collaborates with scholars based in Italy, United States and France. Laura Bernardini's co-authors include Antonio Novelli, Bruno Dallapiccola, Anna Capalbo, Lorenzo M. Donini, Agatino Battaglia, Sara Loddo, Maria Rosaria De Felice, C. Cannella, Rita Mingarelli and M. Cristina Digilio and has published in prestigious journals such as SHILAP Revista de lepidopterología, Scientific Reports and International Journal of Molecular Sciences.

In The Last Decade

Laura Bernardini

121 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Laura Bernardini Italy	27	1.0k	797	317	234	216	126	2.1k
Amber Burt United States	23	474 0.5×	540 0.7×	223 0.7×	138 0.6×	147 0.7×	57	1.6k
U. Heinrich Germany	26	1.2k 1.1×	1.2k 1.6×	461 1.5×	196 0.8×	231 1.1×	70	2.8k
Joan M. Stoler United States	24	860 0.8×	514 0.6×	538 1.7×	106 0.5×	243 1.1×	63	1.9k
Markus Bettendorf Germany	27	657 0.6×	944 1.2×	328 1.0×	135 0.6×	298 1.4×	117	2.4k
Sabrina Giglio Italy	29	1.3k 1.2×	1.5k 1.8×	422 1.3×	115 0.5×	182 0.8×	116	2.6k
Penelope Feuillan United States	30	1.0k 1.0×	1.0k 1.3×	159 0.5×	206 0.9×	180 0.8×	58	2.6k
M. Jansen Netherlands	29	1.1k 1.1×	1.6k 2.0×	749 2.4×	206 0.9×	269 1.2×	55	3.3k
Jean‐Louis Blouin Switzerland	27	1.1k 1.0×	1.0k 1.3×	280 0.9×	156 0.7×	221 1.0×	75	2.4k
Ingeborg Barišić Croatia	25	525 0.5×	488 0.6×	851 2.7×	88 0.4×	710 3.3×	90	2.2k
Jeffrey M. Sequeira United States	25	398 0.4×	586 0.7×	225 0.7×	141 0.6×	131 0.6×	45	1.7k

Countries citing papers authored by Laura Bernardini

Since Specialization

Citations

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

Fields of papers citing papers by Laura Bernardini

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laura Bernardini

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

Grati, Francesca Romana, Antonio Capalbo, Maria Carla Pittalis, et al.. (2025). Prenatal diagnosis following preimplantation genetic testing (PGT): recommendations of the Italian Society of Human Genetics (SIGU). Journal of Assisted Reproduction and Genetics. 42(3). 1015–1024. 1 indexed citations

Rallis, Dimitrios, et al.. (2024). Single center experience with first-intention high-frequency jet vs. volume-targeted ventilation in extremely preterm neonates. Frontiers in Pediatrics. 11. 1326668–1326668. 2 indexed citations

Bernardini, Laura, Marzia Pollazzon, Maria Grazia Giuffrida, et al.. (2023). Split Hand-Foot and Deafness in a Patient with 7q21.13-q21.3 Deletion Not Including the DLX5/6 Genes. Genes. 14(8). 1526–1526. 2 indexed citations

Fontana, Marco, et al.. (2023). Unaccompanied foreign minors and mental health: Implementation and evaluation of the RHS-15 screening procedure for unaccompanied foreign minors. Journal of Migration and Health. 7. 100177–100177. 2 indexed citations

Giuffrida, Maria Grazia, Marina Goldoni, Giovanna Carpentieri, et al.. (2022). 3′UTR Deletion of NONO Leads to Corpus Callosum Anomaly, Left Ventricular Non-Compaction and Ebstein’s Anomaly in a Male Fetus. Diagnostics. 12(10). 2354–2354. 3 indexed citations

Putotto, Carolina, Federica Pulvirenti, Flaminia Pugnaloni, et al.. (2022). Clinical Risk Factors for Aortic Root Dilation in Patients with 22q11.2 Deletion Syndrome: A Longitudinal Single-Center Study. Genes. 13(12). 2334–2334. 3 indexed citations

Bernardini, Laura, et al.. (2021). Koolen‐de Vries syndrome in a 63‐year‐old woman: Report of the oldest patient and a review of the adult phenotype. American Journal of Medical Genetics Part A. 188(2). 692–707. 3 indexed citations

Fontana, Paolo, Laura Bernardini, Cinzia Lombardi, et al.. (2020). De Novo Inverted Duplication Deletion of 4p in a 14-Week-Old Male Fetus Aborted Due to Multiple Anomalies. Journal of Pediatric Genetics. 10(3). 245–249.

Ferrari, Daniela, Laura Bernardini, Giuseppe Lamorte, et al.. (2019). Production and characterization of human induced pluripotent stem cells (iPSC) CSSi007-A (4383) from Joubert Syndrome. Stem Cell Research. 38. 101480–101480. 3 indexed citations

10.

Ferrari, Daniela, Bárbara Torres, Marina Goldoni, et al.. (2018). Copy number variations in healthy subjects. Case study: iPSC line CSSi005-A (3544) production from an individual with variation in 15q13.3 chromosome duplicating gene CHRNA7. Stem Cell Research. 32. 73–77. 2 indexed citations

11.

Torres, Bárbara, Daniela Ferrari, Antonella De Jaco, et al.. (2018). Production and characterization of CSSI003 (2961) human induced pluripotent stem cells (iPSCs) carrying a novel puntiform mutation in RAI1 gene, Causative of Smith–Magenis syndrome. Stem Cell Research. 28. 153–156. 1 indexed citations

12.

Ferrari, Daniela, Laura Bernardini, Federica Consoli, et al.. (2018). Generation of the induced pluripotent stem cell line CSSi006-A (3681) from a patient affected by advanced-stage Juvenile Onset Huntington's Disease. Stem Cell Research. 29. 174–178. 1 indexed citations

13.

Ferrari, Daniela, Laura Bernardini, Federica Consoli, et al.. (2018). Generation of induced pluripotent stem cell line, CSSi004-A (2962), from a patient diagnosed with Huntington's disease at the presymptomatic stage. Stem Cell Research. 28. 145–148. 6 indexed citations

14.

Rosati, Jessica, Daniela Ferrari, Bárbara Torres, et al.. (2018). Generation of induced pluripotent stem cell line, CSSi002-A (2851), from a patient with juvenile Huntington Disease. Stem Cell Research. 27. 86–89. 3 indexed citations

15.

Rosati, Jessica, Marina Goldoni, Daniela Ferrari, et al.. (2018). Production and characterization of human induced pluripotent stem cells (iPSCs) from Joubert Syndrome: CSSi001-A (2850). Stem Cell Research. 27. 74–77. 1 indexed citations

16.

Prontera, Paolo, Valerio Napolioni, Daniela Rogaia, et al.. (2014). DPP6 gene disruption in a family with Gilles de la Tourette syndrome. Neurogenetics. 15(4). 237–242. 22 indexed citations

17.

Torrente, Isabella, Federica Consoli, Rosangela Ferese, et al.. (2012). Novel and recurrent EVC and EVC2 mutations in Ellis-van Creveld syndrome and Weyers acrofacial dyostosis. European Journal of Medical Genetics. 56(2). 80–87. 49 indexed citations

18.

Gervasini, Cristina, Francesca Romana Grati, Faustina Lalatta, et al.. (2010). SHOX duplications found in some cases with type I Mayer-Rokitansky-Kuster-Hauser syndrome. Genetics in Medicine. 12(10). 634–640. 55 indexed citations

19.

Spitalieri, Paola, Giancarlo Cortese, Adalgisa Pietropolli, et al.. (2009). Identification of Multipotent Cytotrophoblast Cells from Human First Trimester Chorionic Villi. Cloning and Stem Cells. 11(4). 535–556. 22 indexed citations

20.

Donini, Lorenzo M., Maria Rosaria De Felice, Laura Tassi, et al.. (2002). A "proportional and objective score" for the mini nutritional assessment in long-term geriatric care.. PubMed. 6(2). 141–6. 30 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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