Fortunato Lonardo

1.7k total citations
52 papers, 645 citations indexed

About

Fortunato Lonardo is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Fortunato Lonardo has authored 52 papers receiving a total of 645 indexed citations (citations by other indexed papers that have themselves been cited), including 33 papers in Genetics, 24 papers in Molecular Biology and 10 papers in Surgery. Recurrent topics in Fortunato Lonardo's work include Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (9 papers) and Congenital limb and hand anomalies (6 papers). Fortunato Lonardo is often cited by papers focused on Genomic variations and chromosomal abnormalities (19 papers), Prenatal Screening and Diagnostics (9 papers) and Congenital limb and hand anomalies (6 papers). Fortunato Lonardo collaborates with scholars based in Italy, United States and Portugal. Fortunato Lonardo's co-authors include Gioacchino Scarano, Matteo Della Monica, Di Fiore, S A Aaronson, Paul Arnstein, Fabio Acquaviva, Paolo Fontana, Lucia Perone, Mariateresa Falco and M Stabile and has published in prestigious journals such as International Journal of Molecular Sciences, Human Mutation and Ultrasound in Obstetrics and Gynecology.

In The Last Decade

Fortunato Lonardo

48 papers receiving 590 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fortunato Lonardo Italy 16 350 258 110 99 73 52 645
Gülen Eda Ütine Türkiye 14 373 1.1× 367 1.4× 64 0.6× 77 0.8× 66 0.9× 114 715
Giuseppe Calabrese Italy 14 173 0.5× 257 1.0× 77 0.7× 154 1.6× 31 0.4× 45 711
Pelin Özlem Şimşek‐Kiper Türkiye 14 326 0.9× 377 1.5× 87 0.8× 35 0.4× 57 0.8× 99 662
Pamela Brock United States 15 286 0.8× 277 1.1× 68 0.6× 45 0.5× 63 0.9× 39 712
Greg B. Peters Australia 14 385 1.1× 382 1.5× 262 2.4× 101 1.0× 49 0.7× 22 785
Shlomit Rienstein Israel 14 161 0.5× 277 1.1× 60 0.5× 107 1.1× 46 0.6× 28 559
Shehla Mohammed United Kingdom 17 456 1.3× 577 2.2× 250 2.3× 80 0.8× 58 0.8× 24 949
Patricio Barros‐Núñez Mexico 15 302 0.9× 359 1.4× 83 0.8× 74 0.7× 28 0.4× 71 688
Olaf Rittinger Austria 17 384 1.1× 433 1.7× 13 0.1× 81 0.8× 66 0.9× 40 785
A Munnich France 14 347 1.0× 685 2.7× 166 1.5× 55 0.6× 254 3.5× 37 1.1k

Countries citing papers authored by Fortunato Lonardo

Since Specialization
Citations

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

Fields of papers citing papers by Fortunato Lonardo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fortunato Lonardo

This figure shows the co-authorship network connecting the top 25 collaborators of Fortunato Lonardo. A scholar is included among the top collaborators of Fortunato Lonardo 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 Fortunato Lonardo. Fortunato Lonardo 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.
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
2.
Fontana, Paolo, et al.. (2025). MODY5 and 17q12 Microdeletion Syndrome: Phenotype Variability, Prenatal and Postnatal Counseling. Genes. 16(9). 1002–1002. 1 indexed citations
3.
Marzano, Flaviana, Matteo Chiara, Arianna Consiglio, et al.. (2023). Whole-Exome and Transcriptome Sequencing Expands the Genotype of Majewski Osteodysplastic Primordial Dwarfism Type II. International Journal of Molecular Sciences. 24(15). 12291–12291.
4.
5.
Lonardo, Fortunato, M. Cristina Digilio, Daniela Rogaia, et al.. (2021). Clinical and molecular characterizations of 11 new patients with type 1 Feingold syndrome: Proposal for selecting diagnostic criteria and further genetic testing in patients with severe phenotype. American Journal of Medical Genetics Part A. 185(4). 1204–1210. 5 indexed citations
6.
Fontana, Paolo, Monia Ginevrino, Giuseppina Cantalupo, et al.. (2021). A ZFHX4 mutation associated with a recognizable neuropsychological and facial phenotype. European Journal of Medical Genetics. 64(11). 104321–104321. 9 indexed citations
7.
8.
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.
9.
Fontana, Paolo, Marina Grasso, Fabio Acquaviva, et al.. (2017). SNORD116 deletions cause Prader‐Willi syndrome with a mild phenotype and macrocephaly. Clinical Genetics. 92(4). 440–443. 34 indexed citations
10.
Vetro, Annalisa, Didier Goidin, Ivan Limongelli, et al.. (2017). Diagnostic application of a capture based NGS test for the concurrent detection of variants in sequence and copy number as well as LOH. Clinical Genetics. 93(3). 545–556. 10 indexed citations
11.
Lonardo, Fortunato, Paola Di Natale, Susanna Lualdi, et al.. (2014). Mucopolysaccharidosis type II in a female patient with a reciprocal X;9 translocation and skewed X chromosome inactivation. American Journal of Medical Genetics Part A. 164(10). 2627–2632. 27 indexed citations
12.
Filippo, Gianpaolo De, Domenico Rendina, A. Nazzaro, et al.. (2013). Baseline Inhibin B Levels for Diagnosis of Central Precocious Puberty in Girls. Hormone Research in Paediatrics. 80(3). 207–212. 10 indexed citations
13.
Monica, Matteo Della, Domenico Galzerano, Fabio Acquaviva, et al.. (2013). Science, art, and mistery in the statues and in the anatomical machines of the prince of sansevero: The masterpieces of the “Sansevero Chapel”. American Journal of Medical Genetics Part A. 161(11). 2920–2929. 3 indexed citations
14.
Monica, Matteo Della, et al.. (2013). The Salernitan school of medicine: Women, men, and children. A syndromological review of the oldest medical school in the western world. American Journal of Medical Genetics Part A. 161(4). 809–816. 1 indexed citations
15.
Piane, Maria, Matteo Della Monica, Gianluca Piatelli, et al.. (2009). Majewski osteodysplastic primordial dwarfism type II (MOPD II) syndrome previously diagnosed as Seckel syndrome: Report of a novel mutation of the PCNT gene. American Journal of Medical Genetics Part A. 149A(11). 2452–2456. 29 indexed citations
16.
Lonardo, Fortunato, et al.. (2007). Al‐Awadi/Raas‐Rothschild syndrome: Two new cases and review. American Journal of Medical Genetics Part A. 143A(24). 3169–3174. 4 indexed citations
17.
Guanciali‐Franchi, Paolo, Giuseppe Calabrese, Elisena Morizio, et al.. (2004). Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. American Journal of Medical Genetics Part A. 127A(2). 144–148. 17 indexed citations
18.
Scarano, Gioacchino, Matteo Della Monica, Fortunato Lonardo, & Giovanni Neri. (1996). Novel findings in a patient with Weaver or a Weaver-like syndrome. American Journal of Medical Genetics. 63(2). 378–381. 5 indexed citations
19.
Scarano, Gioacchino, et al.. (1996). A case of short-rib syndrome without polydactyly in a stillborn: a new type?. PubMed. 30(1). 95–101. 1 indexed citations
20.
Arnstein, Paul, et al.. (1991). Oncogenic potential of erbB-2 in human mammary epithelial cells.. PubMed. 6(7). 1189–94. 117 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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