Lidia Pezzani

1.2k total citations
33 papers, 426 citations indexed

About

Lidia Pezzani is a scholar working on Molecular Biology, Genetics and Cell Biology. According to data from OpenAlex, Lidia Pezzani has authored 33 papers receiving a total of 426 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 19 papers in Genetics and 4 papers in Cell Biology. Recurrent topics in Lidia Pezzani's work include Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (4 papers) and Genetic Syndromes and Imprinting (4 papers). Lidia Pezzani is often cited by papers focused on Genomic variations and chromosomal abnormalities (5 papers), Genomics and Rare Diseases (4 papers) and Genetic Syndromes and Imprinting (4 papers). Lidia Pezzani collaborates with scholars based in Italy, Argentina and United States. Lidia Pezzani's co-authors include Donatella Milani, Susanna Esposito, Gianluca Tadini, Francesca Menni, Francesca Manzoni, Cristina Gervasini, Paola Francesca Ajmone, Caterina Sabatini, Maria Iascone and Paolo Rebulla and has published in prestigious journals such as Human Genetics, Glycobiology and Orphanet Journal of Rare Diseases.

In The Last Decade

Lidia Pezzani

30 papers receiving 416 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Lidia Pezzani Italy 12 174 161 88 62 58 33 426
R Hennekam Netherlands 10 164 0.9× 94 0.6× 107 1.2× 50 0.8× 70 1.2× 14 318
A. David France 13 230 1.3× 326 2.0× 115 1.3× 42 0.7× 19 0.3× 42 579
Diana Carli Italy 14 272 1.6× 279 1.7× 124 1.4× 25 0.4× 97 1.7× 51 599
E Tarantino Italy 13 198 1.1× 217 1.3× 101 1.1× 41 0.7× 31 0.5× 28 460
E K Pivnick United States 11 192 1.1× 166 1.0× 88 1.0× 33 0.5× 118 2.0× 14 422
J. M. Cobben Netherlands 12 388 2.2× 589 3.7× 198 2.3× 59 1.0× 75 1.3× 16 936
Sylvie Manouvrier‐Hanu France 18 395 2.3× 504 3.1× 117 1.3× 36 0.6× 12 0.2× 57 846
J. B. Bijlsma Netherlands 17 335 1.9× 223 1.4× 32 0.4× 56 0.9× 88 1.5× 32 553
Mark J. Stephan United States 15 263 1.5× 279 1.7× 230 2.6× 40 0.6× 26 0.4× 23 762
Ok-Hwa Kim South Korea 11 270 1.6× 153 1.0× 76 0.9× 119 1.9× 13 0.2× 15 458

Countries citing papers authored by Lidia Pezzani

Since Specialization
Citations

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

Fields of papers citing papers by Lidia Pezzani

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Lidia Pezzani

This figure shows the co-authorship network connecting the top 25 collaborators of Lidia Pezzani. A scholar is included among the top collaborators of Lidia Pezzani 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 Lidia Pezzani. Lidia Pezzani 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.
Pezzani, Lidia, Angelo Selicorni, Maria Francesca Bedeschi, et al.. (2025). Portrait of a Spectrum: Clinical and Genetic Characterization of a Large Cohort of Chromatinopathies—30 Years' Experience From a Third Level Center. Clinical Genetics. 109(4). 707–716.
2.
Lettieri, Antonella, Chiara Parodi, Elisa Adele Colombo, et al.. (2024). Characterization of a novel HDAC2 pathogenetic variant: a missing puzzle piece for chromatinopathies. Human Genetics. 143(6). 747–759. 1 indexed citations
3.
Pezzoli, Laura, Lidia Pezzani, Antonella Lettieri, et al.. (2024). Expanding the clinical spectrum of PPP3CA variants - alternative isoforms matter. Orphanet Journal of Rare Diseases. 19(1). 481–481. 1 indexed citations
4.
Pezzani, Lidia, Rosamaria Silipigni, Silvia Russo, et al.. (2024). A long way to syndromic short stature. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 50(1). 192–192.
5.
Pezzani, Lidia, Enrico Alfei, Laura Pezzoli, et al.. (2023). Rock around DYRK1A: Ethnic diversity, clinical challenges. American Journal of Medical Genetics Part A. 191(5). 1459–1464.
6.
Pezzani, Lidia, Laura Pezzoli, Anna Cereda, et al.. (2023). Double somatic mosaicism in Cornelia de Lange syndrome. American Journal of Medical Genetics Part A. 194(5). e63512–e63512. 3 indexed citations
7.
Pezzani, Lidia, Laura Pezzoli, Daniela Marchetti, et al.. (2023). Comparison of first‐tier whole‐exome sequencing with a multi‐step traditional approach for diagnosing paediatric outpatients: An Italian prospective study. Molecular Genetics & Genomic Medicine. 12(1). e2316–e2316. 4 indexed citations
8.
Milani, Donatella, Federica Alberti, Claudia Cesaretti, et al.. (2023). CATSHL syndrome, a new family and phenotypic expansion. Clinical Genetics. 105(3). 313–316. 1 indexed citations
9.
Pezzani, Lidia, Laura Pezzoli, Daniela Marchetti, et al.. (2022). Atypical, Composite, or Blended Phenotypes: How Different Molecular Mechanisms Could Associate in Double-Diagnosed Patients. Genes. 13(7). 1275–1275. 17 indexed citations
10.
Pezzani, Lidia, et al.. (2022). SBIDDS Syndrome: A New Spoke of the Epigenetic Machinery Wheel. Molecular Syndromology. 13(6). 543–550. 1 indexed citations
11.
Pezzani, Lidia, Laura Pezzoli, Daniela Marchetti, et al.. (2020). Double homozygosity in CEP57 and DYNC2H1 genes detected by WES: Composite or expanded phenotype?. Molecular Genetics & Genomic Medicine. 8(3). e1064–e1064. 8 indexed citations
12.
Pezzani, Lidia, Lucia Mauri, Angelo Selicorni, et al.. (2020). Aortic dilation in Sotos syndrome: An underestimated feature?. American Journal of Medical Genetics Part A. 182(7). 1819–1823. 6 indexed citations
13.
Paganini, Leda, Loubna Abdel Hadi, Massimiliano Chetta, et al.. (2018). A HS6ST2 gene variant associated with X‐linked intellectual disability and severe myopia in two male twins. Clinical Genetics. 95(3). 368–374. 17 indexed citations
14.
Pezzani, Lidia, Daniela Marchetti, Anna Cereda, et al.. (2018). Atypical presentation of pediatric BRAF RASopathy with acute encephalopathy. American Journal of Medical Genetics Part A. 176(12). 2867–2871. 24 indexed citations
15.
Pezzani, Lidia, Donatella Milani, Francesca Manzoni, et al.. (2015). HOXA genes cluster: clinical implications of the smallest deletion. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 41(1). 31–31. 8 indexed citations
16.
Milani, Donatella, Francesca Manzoni, Lidia Pezzani, et al.. (2015). Rubinstein-Taybi syndrome: clinical features, genetic basis, diagnosis, and management. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 41(1). 4–4. 86 indexed citations
17.
Ronzoni, Luisa, Lidia Pezzani, Donatella Milani, et al.. (2015). A Novel Intragenic Deletion in Ophn1 in A Boy with Developmental Delay, Strabismus and Cerebellar Hypoplasia. 1(1). 2 indexed citations
18.
Milani, Donatella, Marta Cerutti, Lidia Pezzani, et al.. (2014). Syndromic obesity: clinical implications of a correct diagnosis. ˜The œItalian Journal of Pediatrics/Italian journal of pediatrics. 40(1). 33–33. 16 indexed citations
19.
Tadini, Gianluca, et al.. (2013). Anemic Nevus in Neurofibromatosis Type 1. Dermatology. 226(2). 115–118. 10 indexed citations
20.
Dordoni, Chiara, Marco Ritelli, Marina Venturini, et al.. (2013). Recurring and Generalized Visceroptosis in Ehlers–Danlos Syndrome Hypermobility Type. American Journal of Medical Genetics Part A. 161(5). 1143–1147. 21 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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