Lucia Pucci

493 total citations
21 papers, 286 citations indexed

About

Lucia Pucci is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Lucia Pucci has authored 21 papers receiving a total of 286 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 8 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Lucia Pucci's work include Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genetic Syndromes and Imprinting (5 papers). Lucia Pucci is often cited by papers focused on Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (10 papers) and Genetic Syndromes and Imprinting (5 papers). Lucia Pucci collaborates with scholars based in Italy and United States. Lucia Pucci's co-authors include Salvatore Grosso, Sabrina Buoni, G Morgese, A. Fois, Rosario Berardi, Cecilia Anichini, Paolo Balestri, Daniela Galimberti, G. Bartalini and Raffaella Zannolli and has published in prestigious journals such as Obstetrics and Gynecology, Developmental Medicine & Child Neurology and Epilepsy Research.

In The Last Decade

Lucia Pucci

21 papers receiving 280 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 Pucci Italy 11 210 143 54 51 25 21 286
Eve Õiglane‐Shlik Estonia 10 185 0.9× 177 1.2× 76 1.4× 39 0.8× 16 0.6× 17 320
Dima El‐Khechen United States 8 208 1.0× 125 0.9× 26 0.5× 25 0.5× 11 0.4× 10 294
Midori Sugawara Japan 11 234 1.1× 157 1.1× 26 0.5× 44 0.9× 45 1.8× 12 323
Ivana Ricca Italy 10 123 0.6× 156 1.1× 16 0.3× 74 1.5× 10 0.4× 20 303
Emma McCann United Kingdom 6 177 0.8× 153 1.1× 80 1.5× 18 0.4× 34 1.4× 10 315
Ulrike Thies Germany 10 126 0.6× 258 1.8× 30 0.6× 141 2.8× 16 0.6× 19 357
Daniel Amsallem France 10 222 1.1× 173 1.2× 29 0.5× 25 0.5× 19 0.8× 21 335
Wout H. Deelen Netherlands 11 256 1.2× 232 1.6× 69 1.3× 41 0.8× 12 0.5× 16 413
M. A. Mori Spain 10 216 1.0× 156 1.1× 82 1.5× 63 1.2× 33 1.3× 15 378
Carolyn Dunn United Kingdom 3 240 1.1× 134 0.9× 40 0.7× 15 0.3× 70 2.8× 3 304

Countries citing papers authored by Lucia Pucci

Since Specialization
Citations

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

Fields of papers citing papers by Lucia Pucci

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lucia Pucci

This figure shows the co-authorship network connecting the top 25 collaborators of Lucia Pucci. A scholar is included among the top collaborators of Lucia Pucci 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 Pucci. Lucia Pucci 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.
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
2.
Grosso, Salvatore, Lucia Pucci, Paolo Curatolo, et al.. (2008). Epilepsy and electroencephalographic anomalies in chromosome 2 aberrations. Epilepsy Research. 79(1). 63–70. 12 indexed citations
3.
Grosso, Salvatore, Lucia Pucci, G. Bartalini, et al.. (2006). Photoparoxysmal responses in children with chromosomal aberrations. Epilepsy Research. 72(2-3). 164–170. 5 indexed citations
4.
Buoni, Sabrina, Raffaella Zannolli, Lucia Pucci, et al.. (2006). Familial Robertsonian 13;14 Translocation With Mental Retardation and Epilepsy. Journal of Child Neurology. 21(6). 531–533. 3 indexed citations
5.
Grosso, Salvatore, Lucia Pucci, Rosanna Maria Di Bartolo, et al.. (2005). Chromosome 18 aberrations and epilepsy: A review. American Journal of Medical Genetics Part A. 134A(1). 88–94. 20 indexed citations
6.
Grosso, Salvatore, Lucia Pucci, Rosanna Maria Di Bartolo, et al.. (2004). Epilepsy and Electroencephalographic Findings in Pericentric Inversion of Chromosome 12. Journal of Child Neurology. 19(8). 604–608. 7 indexed citations
7.
Grosso, Salvatore, Rosanna Maria Di Bartolo, Rosario Berardi, et al.. (2004). Electroencephalographic and Epileptic Patterns in X Chromosome Anomalies. Journal of Clinical Neurophysiology. 21(4). 249–253. 28 indexed citations
8.
Battisti, Carla, María Clara Bonaglia, Sabrina Giglio, et al.. (2003). De novo double translocation 3;13 and 4;8;18 in a patient with mental retardation and skeletal abnormalities. American Journal of Medical Genetics Part A. 117A(3). 207–211. 8 indexed citations
9.
Grosso, Salvatore, M. Cioni, Lucia Pucci, et al.. (2002). De novo complete trisomy 5p: Clinical and neuroradiological findings. American Journal of Medical Genetics. 112(1). 56–60. 16 indexed citations
10.
Zannolli, Raffaella, Sid Gilman, Símone Rossi, et al.. (2002). Hereditary Neuronal Intranuclear Inclusion Disease With Autonomic Failure and Cerebellar Degeneration. Archives of Neurology. 59(8). 1319–1319. 47 indexed citations
11.
Zannolli, Raffaella, Rosa Mostardini, Lucia Pucci, et al.. (2001). Corpus callosum agenesis, multiple cysts, skin defects, and subtle ocular abnormalities with a de novo mutation [45,XX,der(5), t(5;14) (pter;q11.2)]. American Journal of Medical Genetics. 102(1). 29–35. 6 indexed citations
12.
Grosso, Salvatore, Cecilia Anichini, Rosario Berardi, et al.. (2000). Central Precocious Puberty and Abnormal Chromosomal Patterns. Endocrine Pathology. 11(1). 69–76. 14 indexed citations
13.
Zannolli, Raffaella, et al.. (2000). Char syndrome: An additional family with polythelia, a new finding. American Journal of Medical Genetics. 95(3). 201–203. 7 indexed citations
14.
Buoni, Sabrina, et al.. (2000). The Syndrome of Inv Dup (15): Clinical, Electroencephalographic, and Imaging Findings. Journal of Child Neurology. 15(6). 380–385. 17 indexed citations
15.
Zannolli, Raffaella, Antonio Acquaviva, Alfonso D’Ambrosio, et al.. (2000). Vagal and Hypoglossal Bell's Palsy. Journal of Child Neurology. 15(2). 130–132. 2 indexed citations
16.
Grosso, Salvatore, Rosario Berardi, Lucia Pucci, & Paolo Balestri. (1999). PRECOCIOUS PUBERTY WITH TRISOMY X SYNDROME. Obstetrics and Gynecology. 94(Supplement). 861–861. 2 indexed citations
17.
Buoni, Sabrina, Salvatore Grosso, Lucia Pucci, & A. Fois. (1999). Diagnosis of Angelman syndrome: clinical and EEG criteria. Brain and Development. 21(5). 296–302. 48 indexed citations
18.
Grosso, Salvatore, M. Cioni, Sabrina Buoni, et al.. (1998). Growth hormone secretion in Prader-Willi syndrome. Journal of Endocrinological Investigation. 21(7). 418–422. 15 indexed citations
19.
Anichini, Cecilia, et al.. (1992). [Correlations between karyotype and phenotype in structural and numerical abnormalities of chromosome 18].. PubMed. 68(4). 263–9. 2 indexed citations
20.
Anichini, Cecilia, et al.. (1992). [Correlation of the clinical phenotype with a pericentric inversion of chromosome 9].. PubMed. 68(3). 175–81. 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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