Michele D’Urso

7.5k citations
100 papers · 4.2k · h-index 35

Impact in

Papers in

    • Genomics and Chromatin Dynamics 15
    • CRISPR and Genetic Engineering 10
    • RNA Research and Splicing 9
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 11
    • Genetics and Neurodevelopmental Disorders 9

Michele D’Urso

100 papers receiving 4.1k citations

Peers

Michele D’Urso
Comparison fields: 5 of 108
  • Genetics 1.3k
  • Pediatrics, Perinatology and Child Health 688
  • Molecular Biology 2.6k
  • Cell Biology 432
  • Clinical Biochemistry 167
Replace Gudrun Nürnberg with:
Gudrun Nürnberg Germany
A. Westerveld Netherlands
Andreas Winterpacht Germany
Anita Rauch Germany
Michael B. Petersen Greece
E. Viégas-Pèquignot France
Célia Bádenas Spain
Rolph Pfundt Netherlands
Alan Buckler United States
Hülya Kayserili Türkiye
Michele D’Urso relative to Gudrun Nürnberg Germany Gudrun Nürnberg's profile →
Citations per field
00.5×2.9×
Gudrun Nürnberg · 1×
Citations per year

Countries citing papers authored by Michele D’Urso

Since Specialization
Citations

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

Fields of papers citing papers by Michele D’Urso

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Michele D’Urso, 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 Michele D’Urso Line = papers co-authored together Michele D’Urso links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 100 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1996393
2 2003327
3 1986216
4 1988202
5 1986188
6 199699
7 199296
8 200195
9 199191
10 200185
11
Human Xq24-Xq28: approaches to mapping with yeast artificial chromosomes.
199083
12 200877
13 199676
14 199575
15 199375
16 198474
17 199869
18
New ABCR mutations and clinical phenotype in Italian patients with Stargardt disease.
200069
19 198562
20 198959

About Michele D’Urso

Michele D’Urso is a scholar working on Molecular Biology, Genetics, Plant Science, Pediatrics, Perinatology and Child Health and Surgery, having authored 100 papers that have together received 4.2k indexed citations. Recurring topics across this work include Genomics and Chromatin Dynamics (15 papers), Neonatal Health and Biochemistry (14 papers), Chromosomal and Genetic Variations (14 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (11 papers), CRISPR and Genetic Engineering (10 papers), RNA Research and Splicing (9 papers), Genetics and Neurodevelopmental Disorders (9 papers) and Metabolism and Genetic Disorders (8 papers). The work is most often cited by research in Genetics (1.3k citations), Pediatrics, Perinatology and Child Health (688 citations), Molecular Biology (2.6k citations), Cell Biology (432 citations) and Clinical Biochemistry (167 citations). Michele D’Urso has collaborated with scholars based in Italy, United States and United Kingdom. Frequent co-authors include Alfredo Ciccodicola, Daniela Toniolo, Lucio Luzzatto, G. Martini, David Schlessinger, M. Graziella Persico, David Schlessinger, G. Battistuzzi, Giuseppe Viglietto and Maurizio D’Esposito. Their work appears in journals such as Genomics, Proceedings of the National Academy of Sciences, Gene, Human Molecular Genetics and Nucleic Acids Research.

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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