Lucia Grillo

819 total citations
11 papers, 185 citations indexed

About

Lucia Grillo is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Lucia Grillo has authored 11 papers receiving a total of 185 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 8 papers in Genetics and 2 papers in Genetics. Recurrent topics in Lucia Grillo's work include Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Glycosylation and Glycoproteins Research (2 papers). Lucia Grillo is often cited by papers focused on Genetics and Neurodevelopmental Disorders (6 papers), Genomic variations and chromosomal abnormalities (5 papers) and Glycosylation and Glycoproteins Research (2 papers). Lucia Grillo collaborates with scholars based in Italy. Lucia Grillo's co-authors include Maria Bottitta, Maurizio Elia, Giuseppe Calabrese, Marco Fichera, Corrado Romano, D Luciano, S Reitano, Maria Esposito, Marco Carotenuto and Daniela Benedetto and has published in prestigious journals such as Gene, Human Genetics and Seizure.

In The Last Decade

Lucia Grillo

11 papers receiving 159 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lucia Grillo Italy 8 118 103 31 20 13 11 185
Naila Cristina Vilaça Lourenço Brazil 9 129 1.1× 125 1.2× 46 1.5× 28 1.4× 8 0.6× 16 214
Katrin Männik Estonia 7 163 1.4× 124 1.2× 41 1.3× 25 1.3× 14 1.1× 9 222
Yoko Hiraki Japan 10 131 1.1× 97 0.9× 14 0.5× 22 1.1× 7 0.5× 17 219
Diane Hu‐Lince United States 7 144 1.2× 143 1.4× 24 0.8× 22 1.1× 9 0.7× 7 253
Emilie Landais France 10 177 1.5× 117 1.1× 40 1.3× 26 1.3× 24 1.8× 15 253
Carmen Esmer Mexico 5 157 1.3× 116 1.1× 46 1.5× 33 1.6× 7 0.5× 16 225
Bénédicte Duban‐Bedu France 10 154 1.3× 93 0.9× 21 0.7× 39 1.9× 10 0.8× 12 214
Alfonso Caro‐Llopis Spain 7 132 1.1× 102 1.0× 16 0.5× 16 0.8× 8 0.6× 14 190
Ping Yee Billie Au Canada 9 121 1.0× 119 1.2× 14 0.5× 16 0.8× 18 1.4× 21 216
Angelo Selicorni Italy 8 204 1.7× 139 1.3× 31 1.0× 12 0.6× 9 0.7× 9 348

Countries citing papers authored by Lucia Grillo

Since Specialization
Citations

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

Fields of papers citing papers by Lucia Grillo

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucia Grillo

This figure shows the co-authorship network connecting the top 25 collaborators of Lucia Grillo. A scholar is included among the top collaborators of Lucia Grillo 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 Lucia Grillo. Lucia Grillo is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

11 of 11 papers shown
1.
2.
Vinci, Mirella, Lucia Castiglia, Lucia Grillo, et al.. (2016). Identification of novel mutations in L1CAM gene by a DHPLC-based assay. Genes & Genomics. 38(12). 1159–1164. 1 indexed citations
3.
Salemi, Michele, Concetta Barone, Corrado Romano, et al.. (2015). A peculiar VNTR in the cystathionine β-synthase gene is a risk factor for Down Syndrome.. Cellular and Molecular Biology. 61(5). 49–51. 3 indexed citations
4.
Benedetto, Daniela, S Musumeci, Emanuela Avola, et al.. (2014). Definition of minimal duplicated region encompassing the XIAP and STAG2 genes in the Xq25 microduplication syndrome. American Journal of Medical Genetics Part A. 164(8). 1923–1930. 9 indexed citations
5.
Coppola, Antonietta, Maria Bottitta, Giuseppe Calabrese, et al.. (2014). Seizures and EEG pattern in the 22q13.3 deletion syndrome: Clinical report of six Italian cases. Seizure. 23(9). 774–779. 43 indexed citations
6.
Fichera, Marco, Rita Barone, Lucia Grillo, et al.. (2014). Familial 1q22 microduplication associated with psychiatric disorders, intellectual disability and late-onset autoimmune inflammatory response. Molecular Cytogenetics. 7(1). 90–90. 3 indexed citations
7.
Benedetto, Daniela, Corrado Romano, Mariangela Lo Giudice, et al.. (2013). 6p22.3 deletion: report of a patient with autism, severe intellectual disability and electroencephalographic anomalies. Molecular Cytogenetics. 6(1). 4–4. 19 indexed citations
8.
Grillo, Lucia, Donatella Greco, Rosa Pettinato, et al.. (2013). Increased FGF3 and FGF4 gene dosage is a risk factor for craniosynostosis. Gene. 534(2). 435–439. 15 indexed citations
9.
Elia, Maurizio, Maria Bottitta, Lucia Grillo, et al.. (2012). An atypical patient with Cowden syndrome and PTEN gene mutation presenting with cortical malformation and focal epilepsy. Brain and Development. 34(10). 873–876. 38 indexed citations
10.
Grillo, Lucia, S Reitano, Maria Bottitta, et al.. (2010). Familial 1.1 Mb deletion in chromosome Xq22.1 associated with mental retardation and behavioural disorders in female patients. European Journal of Medical Genetics. 53(2). 113–116. 33 indexed citations
11.
Failla, Pinella, Corrado Romano, S Reitano, et al.. (2008). 12q12 deletion: A new patient contributing to genotype–phenotype correlation. American Journal of Medical Genetics Part A. 146A(10). 1354–1357. 10 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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2026