Valentino Romano

5.3k total citations
71 papers, 2.1k citations indexed

About

Valentino Romano is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Valentino Romano has authored 71 papers receiving a total of 2.1k indexed citations (citations by other indexed papers that have themselves been cited), including 40 papers in Molecular Biology, 34 papers in Genetics and 17 papers in Clinical Biochemistry. Recurrent topics in Valentino Romano's work include Metabolism and Genetic Disorders (17 papers), Forensic and Genetic Research (14 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Valentino Romano is often cited by papers focused on Metabolism and Genetic Disorders (17 papers), Forensic and Genetic Research (14 papers) and Genetics and Neurodevelopmental Disorders (10 papers). Valentino Romano collaborates with scholars based in Italy, Germany and United States. Valentino Romano's co-authors include Francesco Calı̀, R. Cortese, Vittorio Colantuoni, G. Bensi, Giovanni Raugei, Claudio Santoro, Francesco Costanzo, Rudolf E. Leube, Werner W. Franke and Paolo Bosco and has published in prestigious journals such as The Lancet, Nucleic Acids Research and The EMBO Journal.

In The Last Decade

Valentino Romano

71 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Valentino Romano Italy 23 1.1k 686 595 310 242 71 2.1k
Jürgen Horst Germany 27 1.7k 1.6× 1.1k 1.6× 194 0.3× 112 0.4× 89 0.4× 74 2.9k
Margretta R. Seashore United States 24 943 0.9× 819 1.2× 511 0.9× 159 0.5× 284 1.2× 50 2.5k
Douglas C. Wallace United States 21 2.7k 2.5× 681 1.0× 1.2k 2.1× 66 0.2× 44 0.2× 23 3.4k
Mario C. Rattazzi United States 25 833 0.8× 408 0.6× 167 0.3× 299 1.0× 69 0.3× 54 1.8k
Perttì Aula Finland 30 1.5k 1.4× 939 1.4× 257 0.4× 437 1.4× 243 1.0× 134 3.4k
Corinne D. Boehm United States 22 1.4k 1.3× 812 1.2× 196 0.3× 69 0.2× 156 0.6× 38 3.3k
Pio D’Adamo Italy 24 1.6k 1.5× 349 0.5× 597 1.0× 92 0.3× 107 0.4× 84 2.8k
Marlène Rio France 33 2.2k 2.0× 1.7k 2.4× 525 0.9× 207 0.7× 83 0.3× 112 3.5k
H H Kazazian United States 32 1.7k 1.5× 857 1.2× 81 0.1× 92 0.3× 99 0.4× 64 3.2k
Ian Carr United Kingdom 32 1.7k 1.6× 908 1.3× 38 0.1× 331 1.1× 423 1.7× 111 3.5k

Countries citing papers authored by Valentino Romano

Since Specialization
Citations

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

Fields of papers citing papers by Valentino Romano

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Valentino Romano

This figure shows the co-authorship network connecting the top 25 collaborators of Valentino Romano. A scholar is included among the top collaborators of Valentino Romano 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 Valentino Romano. Valentino Romano 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.
Romano, Valentino, et al.. (2021). Neuronal Cytoskeleton in Intellectual Disability: From Systems Biology and Modeling to Therapeutic Opportunities. International Journal of Molecular Sciences. 22(11). 6167–6167. 18 indexed citations
2.
Vetri, Luigi, Francesco Calı̀, Mirella Vinci, et al.. (2020). A de novo heterozygous mutation in KCNC2 gene implicated in severe developmental and epileptic encephalopathy. European Journal of Medical Genetics. 63(4). 103848–103848. 18 indexed citations
3.
Calı̀, Francesco, Carmela Scuderi, Sebastiano Bianca, et al.. (2014). Carrier screening for spinal muscular atrophy in Italian population. Journal of Genetics. 93(1). 179–181. 6 indexed citations
4.
Marrale, Maurizio, Nadia Ninfa Albanese, Francesco Calı̀, & Valentino Romano. (2014). Assessing the Impact of Copy Number Variants on miRNA Genes in Autism by Monte Carlo Simulation. PLoS ONE. 9(3). e90947–e90947. 23 indexed citations
5.
Romano, Valentino, et al.. (2013). Percolation model of axon guidance. Nova Science Publishers (Nova Science Publishers, Inc.). 65–70. 1 indexed citations
6.
Calı̀, Francesco, et al.. (2013). Multiplex ligation-dependent probe amplification detection of an unknown large deletion of the CREB-binding protein gene in a patient with Rubinstein-Taybi Syndrome. Genetics and Molecular Research. 12(AOP). 2809–15. 4 indexed citations
7.
Romano, Valentino, Mirella Vinci, Salvatore Miccichè, et al.. (2010). Exon deletions of the PAH gene in Italian hyperphenylalaninemics. Experimental & Molecular Medicine. 42. 1 indexed citations
8.
Calı̀, Francesco, Giuseppe Calabrese, Marco Fichera, et al.. (2010). Novel deletion of the E3A ubiquitin protein ligase gene detected by multiplex ligation-dependent probe amplification in a patient with Angelman syndrome. Experimental & Molecular Medicine. 42(12). 842–842. 4 indexed citations
9.
Acquadro, Francesco, et al.. (2010). Functional Annotation of Genes Overlapping Copy Number Variants in Autistic Patients: Focus on Axon Pathfinding. Current Genomics. 11(2). 136–145. 23 indexed citations
10.
Laumonnier, Frédéric, Sébastien Roger, Pascaline Guérin, et al.. (2006). Association of a Functional Deficit of the BK Ca Channel, a Synaptic Regulator of Neuronal Excitability, With Autism and Mental Retardation. American Journal of Psychiatry. 163(9). 1622–1629. 135 indexed citations
11.
Romano, Valentino, Gregorio Seidita, Mario G. Mirisola, et al.. (2005). Suggestive evidence for association of D2S2188 marker (2q31.1) with autism in 143 Sicilian (Italian) TRIO families. Psychiatric Genetics. 15(2). 149–150. 6 indexed citations
12.
Szibor, R., Jeanett Edelmann, Sandra Hering, et al.. (2003). Cell line DNA typing in forensic genetics—the necessity of reliable standards. Forensic Science International. 138(1-3). 37–43. 91 indexed citations
13.
Romano, Valentino, Francesco Calı̀, A. Flugý, et al.. (2003). Autosomal Microsatellite and mtDNA Genetic Analysis in Sicily (Italy). Annals of Human Genetics. 67(1). 42–53. 17 indexed citations
14.
Puglisi‐Allegra, Stefano, Simona Cabib, Tiziana Pascucci, et al.. (2000). Dramatic brain aminergic deficit in a genetic mouse model of phenylketonuria. Neuroreport. 11(6). 1361–1364. 79 indexed citations
15.
Yılmaz, Engin, Francesco Calı̀, Valentino Romano, et al.. (2000). Molecular basis of mild hyperphenylalaninaemia in Turkey. Journal of Inherited Metabolic Disease. 23(5). 523–525. 9 indexed citations
16.
Bosco, Paolo, Raffaele Ferri, Francesco Calı̀, et al.. (1995). Analysis of the FMR-1 gene and correlation with phenotype in Sicilian families with the fragile X syndrome. 20. 149–151. 1 indexed citations
17.
Romano, Valentino, Friedemann Call, Per Guldberg, et al.. (1994). Association between haplotypes, Hind III‐VNTR alleles and mutations at the PAH locus in Sicily. Acta Paediatrica. 83(s407). 39–40. 5 indexed citations
18.
Goonewardena, P., Anne C. Gross, Carl Dobkin, et al.. (1991). Linkage analysis of the fragile X syndrome using a new DNA marker U6.2 defining locus DXS304. American Journal of Medical Genetics. 38(2-3). 322–327. 3 indexed citations
19.
Cross, Nicholas C.P., Timothy M. Cox, R. de Franchis, et al.. (1990). Molecular analysis of aldolase B genes in hereditary fructose intolerance. The Lancet. 335(8685). 306–309. 82 indexed citations
20.
Fürst, Dieter O., Rüdiger Nave, Mary Osborn, et al.. (1987). Nebulin and titin expression in Duchenne muscular dystrophy appears normal. FEBS Letters. 224(1). 49–53. 16 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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