Elisabetta Lapi

3.1k total citations
48 papers, 957 citations indexed

About

Elisabetta Lapi is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Elisabetta Lapi has authored 48 papers receiving a total of 957 indexed citations (citations by other indexed papers that have themselves been cited), including 26 papers in Molecular Biology, 24 papers in Genetics and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Elisabetta Lapi's work include Congenital heart defects research (9 papers), Williams Syndrome Research (7 papers) and Genetic Syndromes and Imprinting (6 papers). Elisabetta Lapi is often cited by papers focused on Congenital heart defects research (9 papers), Williams Syndrome Research (7 papers) and Genetic Syndromes and Imprinting (6 papers). Elisabetta Lapi collaborates with scholars based in Italy, Mexico and United Kingdom. Elisabetta Lapi's co-authors include Stefano Stagi, Maurizio de Martino, Francesco Chiarelli, Salvatore Seminara, Roberto Salti, Sabrina Giglio, Maria Luisa Giovannucci Uzielli, G. Bindi, Joseph Upton and Frances R. Goodman and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Kidney International and Human Molecular Genetics.

In The Last Decade

Elisabetta Lapi

48 papers receiving 935 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Elisabetta Lapi Italy 18 534 477 131 96 91 48 957
Alice Goldenberg France 20 678 1.3× 565 1.2× 91 0.7× 36 0.4× 20 0.2× 49 1.1k
Kay Metcalfe United Kingdom 19 502 0.9× 421 0.9× 80 0.6× 20 0.2× 437 4.8× 31 1.2k
H. Enders Germany 18 899 1.7× 933 2.0× 313 2.4× 47 0.5× 15 0.2× 40 1.5k
Beate Albrecht Germany 23 862 1.6× 1.0k 2.2× 264 2.0× 62 0.6× 25 0.3× 45 1.7k
Kwame Anyane‐Yeboa United States 26 1.3k 2.4× 1.2k 2.6× 361 2.8× 45 0.5× 41 0.5× 66 2.3k
N R Dennis United Kingdom 20 628 1.2× 793 1.7× 98 0.7× 42 0.4× 231 2.5× 32 1.3k
Ivan F. M. Lo China 17 740 1.4× 769 1.6× 157 1.2× 9 0.1× 34 0.4× 98 1.3k
Robert F. Stratton United States 19 736 1.4× 916 1.9× 353 2.7× 39 0.4× 44 0.5× 42 1.4k
Chiara Pescucci Italy 19 692 1.3× 745 1.6× 65 0.5× 14 0.1× 33 0.4× 37 1.3k
Uta Grieshammer United States 12 874 1.6× 232 0.5× 141 1.1× 24 0.3× 68 0.7× 14 1.0k

Countries citing papers authored by Elisabetta Lapi

Since Specialization
Citations

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

Fields of papers citing papers by Elisabetta Lapi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Elisabetta Lapi

This figure shows the co-authorship network connecting the top 25 collaborators of Elisabetta Lapi. A scholar is included among the top collaborators of Elisabetta Lapi 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 Elisabetta Lapi. Elisabetta Lapi 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.
Pignata, Laura, Angela Sparago, Orazio Palumbo, et al.. (2021). Mosaic Segmental and Whole-Chromosome Upd(11)mat in Silver-Russell Syndrome. Genes. 12(4). 581–581. 5 indexed citations
2.
3.
Stagi, Stefano, Mariarosaria Di Tommaso, Elisabetta Lapi, et al.. (2016). Triple X syndrome and puberty: focus on the hypothalamus-hypophysis-gonad axis. Fertility and Sterility. 105(6). 1547–1553. 15 indexed citations
4.
Stagi, Stefano, Francesco Chiarelli, Alberto Verrotti, et al.. (2016). Bone mineral status and metabolism in patients with Williams-Beuren syndrome. HORMONES. 15(3). 404–412. 7 indexed citations
5.
Stagi, Stefano, Anna Virginia Gulino, Elisabetta Lapi, & Donato Rigante. (2015). Epigenetic control of the immune system: a lesson from Kabuki syndrome. Immunologic Research. 64(2). 345–359. 40 indexed citations
6.
Stagi, Stefano, Elisabetta Lapi, Maria A. Pantaleo, et al.. (2015). A new case of de novo 6q24.2-q25.2 deletion on paternal chromosome 6 with growth hormone deficiency: a twelve-year follow-up and literature review. BMC Medical Genetics. 16(1). 69–69. 16 indexed citations
7.
Stagi, Stefano, et al.. (2015). Bone status in genetic syndromes: A review. HORMONES. 14(1). 19–31. 12 indexed citations
8.
Stagi, Stefano, et al.. (2015). Giant multiple bladder diverticula in Williams–Beuren syndrome. Kidney International. 88(2). 416–416. 1 indexed citations
9.
Stagi, Stefano, Giovanna Traficante, Elisabetta Lapi, et al.. (2015). Agenesis of internal carotid artery associated with isolated growth hormone deficiency: a case report and literature review. BMC Endocrine Disorders. 15(1). 58–58. 9 indexed citations
10.
Stagi, Stefano, Elisabetta Lapi, Silvia Romano, et al.. (2014). Coeliac disease and risk for other autoimmune diseases in patients with Williams-Beuren syndrome. BMC Medical Genetics. 15(1). 61–61. 14 indexed citations
11.
Stagi, Stefano, Elisabetta Lapi, Salvatore Seminara, et al.. (2014). Long-term auxological and endocrinological evaluation of patients with 9p trisomy: a focus on the growth hormone-insulin-like growth factor-I axis. BMC Endocrine Disorders. 14(1). 3–3. 13 indexed citations
12.
Chiesa, Nicoletta, Agostina De Crescenzo, Kankadeb Mishra, et al.. (2011). The KCNQ1OT1 imprinting control region and non-coding RNA: new properties derived from the study of Beckwith–Wiedemann syndrome and Silver–Russell syndrome cases. Human Molecular Genetics. 21(1). 10–25. 98 indexed citations
13.
Bertolin, Cinzia, Francesca Boaretto, Giovanni Barbon, et al.. (2010). Novel mutations in the L1CAM gene support the complexity of L1 syndrome. Journal of the Neurological Sciences. 294(1-2). 124–126. 6 indexed citations
14.
Gambineri, Eleonora, Elisabetta Lapi, Tommaso Casini, et al.. (2010). Evans Syndrome and Antibody Deficiency: An Atypical Presentation of Chromosome 22q11.2 Deletion Syndrome. Pediatric Reports. 2(2). e13–e13. 3 indexed citations
15.
Stagi, Stefano, Elisabetta Lapi, Eleonora Gambineri, et al.. (2009). Thyroid function and morphology in subjects with microdeletion of chromosome 22q11 (del(22)(q11)). Clinical Endocrinology. 72(6). 839–844. 24 indexed citations
16.
Stagi, Stefano, et al.. (2008). Congenital Hypothyroidism in Young-Simpson Syndrome. Journal of Pediatric Endocrinology and Metabolism. 21(11). 1089–92. 2 indexed citations
17.
Wieland, Ilse, Carola I. Weidner, Roberto Ciccone, et al.. (2007). Contiguous gene deletions involving EFNB1, OPHN1, PJA1 and EDA in patients with craniofrontonasal syndrome. Clinical Genetics. 72(6). 506–516. 32 indexed citations
18.
Stagi, Stefano, G. Bindi, Anna Silvia Neri, et al.. (2003). Thyroid hypoplasia of the left lobe in two girls affected by Williams syndrome. Clinical Dysmorphology. 12(4). 267–268. 10 indexed citations
19.
Baumer, Alessandra, Maria Luisa Giovannucci Uzielli, Silvia Guarducci, et al.. (2002). Meiotic origin of two ring chromosomes 18 in a girl with developmental delay. American Journal of Medical Genetics. 113(1). 101–104. 12 indexed citations
20.
Giunti, Laura, Silvia Guarducci, Elisabetta Lapi, et al.. (2001). Spectrum and distribution of MECP2 mutations in 64 Italian Rett syndrome girls: tentative genotype/phenotype correlation. Brain and Development. 23. S242–S245. 18 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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