Elisabetta Lapi

3.1k citations
48 papers · 966 · h-index 18

Impact in

Papers in

    • Congenital heart defects research 6
    • Epigenetics and DNA Methylation 4
    • Genetics and Neurodevelopmental Disorders 4
    • Genomic variations and chromosomal abnormalities 4
    • Connective tissue disorders research 4
    • Genetic Syndromes and Imprinting 4

Elisabetta Lapi

48 papers receiving 944 citations

Peers

Elisabetta Lapi
Comparison fields: 5 of 70
  • Developmental Biology 91
  • Developmental Neuroscience 88
  • Genetics 440
  • Molecular Biology 434
  • Pediatrics, Perinatology and Child Health 104
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Citations per field
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Citations per year

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-authors

The 25 scholars most cited alongside Elisabetta Lapi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Elisabetta Lapi Line = papers co-authored together Elisabetta Lapi links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 48 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1997170
2 201198
3 200267
4 199965
5 200944
6 201540
7 200537
8 200732
9 201529
10 201627
11 200925
12 201523
13 200821
14 201420
15 201019
16 201419
17 200118
18 200717
19 201516
20 201616

About Elisabetta Lapi

Elisabetta Lapi is a scholar working on Molecular Biology, Genetics, Developmental Neuroscience, Pediatrics, Perinatology and Child Health and Surgery, having authored 48 papers that have together received 966 indexed citations. Recurring topics across this work include Congenital heart defects research (6 papers), Williams Syndrome Research (6 papers), Genetics and Neurodevelopmental Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Connective tissue disorders research (4 papers), Epigenetics and DNA Methylation (4 papers), Genetic Syndromes and Imprinting (4 papers) and Congenital limb and hand anomalies (4 papers). The work is most often cited by research in Developmental Biology (91 citations), Developmental Neuroscience (88 citations), Genetics (440 citations), Molecular Biology (434 citations) and Pediatrics, Perinatology and Child Health (104 citations). Elisabetta Lapi has collaborated with scholars based in Italy, Ireland and Poland. Frequent co-authors include Stefano Stagi, Maurizio de Martino, Francesco Chiarelli, Salvatore Seminara, Roberto Salti, Sabrina Giglio, Maria Luisa Giovannucci Uzielli, G. Bindi, Stefan Mundlos and William Reardon. Their work appears in journals such as HORMONES, Clinical Endocrinology, BMC Endocrine Disorders, Fertility and Sterility and Neuromuscular Disorders.

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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