D Luciano

853 total citations
7 papers, 91 citations indexed

About

D Luciano is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, D Luciano has authored 7 papers receiving a total of 91 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Genetics, 4 papers in Molecular Biology and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in D Luciano's work include Genetics and Neurodevelopmental Disorders (4 papers), Congenital heart defects research (2 papers) and RNA modifications and cancer (1 paper). D Luciano is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Congenital heart defects research (2 papers) and RNA modifications and cancer (1 paper). D Luciano collaborates with scholars based in Italy. D Luciano's co-authors include Lucia Grillo, Marco Fichera, Daniela Benedetto, Maria Bottitta, Antonietta Coppola, Salvatore Striano, Claudia Torniero, Giuseppe Calabrese, Luigi Del Gaudio and Maurizio Elia and has published in prestigious journals such as Gene, Developmental Medicine & Child Neurology and Seizure.

In The Last Decade

D Luciano

7 papers receiving 79 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
D Luciano Italy	5	67	47	21	9	8	7	91
Elsa Delaby France	2	58 0.9×	31 0.7×	30 1.4×	6 0.7×	6 0.8×	3	73
Candace Muss United States	3	114 1.7×	58 1.2×	29 1.4×	13 1.4×	5 0.6×	3	149
Alessandro Calcia Italy	5	60 0.9×	41 0.9×	19 0.9×	10 1.1×	3 0.4×	8	100
Claudia Ismania Samogy Costa Brazil	5	78 1.2×	59 1.3×	30 1.4×	13 1.4×	5 0.6×	8	110
Bärbel Felder Germany	3	74 1.1×	87 1.9×	24 1.1×	15 1.7×	8 1.0×	3	127
Huidan Wu China	8	68 1.0×	65 1.4×	28 1.3×	4 0.4×	3 0.4×	13	126
Natalie Bir United States	4	38 0.6×	47 1.0×	21 1.0×	4 0.4×	4 0.5×	4	79
Isabela Mayá Wayhs Silva Brazil	6	46 0.7×	52 1.1×	23 1.1×	8 0.9×	6 0.8×	8	87
Meron Azage United States	4	91 1.4×	81 1.7×	11 0.5×	10 1.1×	8 1.0×	6	129
Heidi Thiese United States	4	92 1.4×	66 1.4×	11 0.5×	9 1.0×	6 0.8×	4	113

Countries citing papers authored by D Luciano

Since Specialization

Citations

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

Fields of papers citing papers by D Luciano

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of D Luciano

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

All Works

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

1.

Pappalardo, Xena Giada, Angela Ostuni, D Luciano, et al.. (2023). Human VDAC pseudogenes: an emerging role for VDAC1P8 pseudogene in acute myeloid leukemia. Biological Research. 56(1). 33–33. 3 indexed citations

2.

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

3.

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

4.

Barone, Chiara, Sebastiano Bianca, D Luciano, et al.. (2013). Intragenic ILRAPL1 deletion in a male patient with intellectual disability, mild dysmorphic signs, deafness, and behavioral problems. American Journal of Medical Genetics Part A. 161(6). 1381–1385. 11 indexed citations

5.

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

6.

Piccione, Maria, Simona Cavani, Michela Malacarne, et al.. (2011). Molecular and clinical characterization of a small duplication Xp in a human female with psychiatric disorders. Journal of Genetics. 90(3). 473–477. 4 indexed citations

7.

Grosso, Salvatore, Marco Fichera, Ornella Galesi, et al.. (2008). Bilateral periventricular nodular heterotopia and lissencephaly in an infant with unbalanced t(12;17)(q24.31; p13.3) translocation. Developmental Medicine & Child Neurology. 50(6). 473–476. 6 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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