L Perroni
Impact in
- Immunology top 2%
- T-cell and B-cell Immunology
- Immune Cell Function and Interaction
- Immunotherapy and Immune Responses
- Immunodeficiency and Autoimmune Disorders
- Genetics top 5%
- Diabetes and associated disorders
- Genetics and Neurodevelopmental Disorders
Papers in
- Genetics 24
- Genomic variations and chromosomal abnormalities 11
- Genetics and Neurodevelopmental Disorders 9
- Diabetes and associated disorders 4
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- Neonatal Health and Biochemistry 7
- Prenatal Screening and Diagnostics 5
- Co-authors
- F. Dagna Bricarelli (12 shared papers)Francesca Faravelli (5 shared papers)Olivier Goulet (1 shared paper)Mary E. Brunkow (1 shared paper)Massimo Mazzella (1 shared paper)Geoffrey C Byrne (1 shared paper)Mark W. Appleby (1 shared paper)Ephrat Levy‐Lahad (1 shared paper)
- Journals
- British Journal of Haematology (4 papers)Human Genetics (3 papers)The Journal of Pediatrics (1 paper)Journal of Alzheimer s Disease (1 paper)Nucleic Acids Research (1 paper)
- Partner nations
- ItalyUnited StatesCanada
In The Last Decade
L Perroni
37 papers receiving 2.1k citations
L Perroni's Hit Papers
Peers
Comparison fields: 5 of 82
- Immunology 1.3k
- Genetics 539
- Gastroenterology 56
- Hematology 113
- Transplantation 18
Countries citing papers authored by L Perroni
This map shows the geographic impact of L Perroni'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 L Perroni with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites L Perroni more than expected).
Fields of papers citing papers by L Perroni
This network shows the impact of papers produced by L Perroni. 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 L Perroni. The network helps show where L Perroni may publish in the future.
Co-authors
The 25 scholars most cited alongside L Perroni, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 39 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | X-linked neonatal diabetes mellitus, enteropathy and endocrinopathy syndrome is the human equivalent of mouse scurfy Hit paper breakdown → | 2001 | 1431 |
| 2 | 2005 | 83 | |
| 3 | 1980 | 73 | |
| 4 | 2011 | 62 | |
| 5 | 2006 | 48 | |
| 6 | 2009 | 41 | |
| 7 | 1996 | 36 | |
| 8 | 2008 | 35 | |
| 9 | 1989 | 32 | |
| 10 | An extensive search for RFLP in the human glucose-6-phosphate dehydrogenase locus has revealed a silent mutation in the coding sequence. | 1988 | 31 |
| 11 | 1980 | 25 | |
| 12 | 1999 | 25 | |
| 13 | 1998 | 18 | |
| 14 | 2008 | 18 | |
| 15 | 1988 | 17 | |
| 16 | 1988 | 17 | |
| 17 | 2010 | 16 | |
| 18 | 2010 | 16 | |
| 19 | 1988 | 15 | |
| 20 | 1975 | 14 |
About L Perroni
L Perroni is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Immunology and Surgery, having authored 39 papers that have together received 2.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (11 papers), Genetics and Neurodevelopmental Disorders (9 papers), Neonatal Health and Biochemistry (7 papers), Immune Cell Function and Interaction (5 papers), Prenatal Screening and Diagnostics (5 papers), Diabetes and associated disorders (4 papers), T-cell and B-cell Immunology (4 papers) and Chromosomal and Genetic Variations (4 papers). The work is most often cited by research in Immunology (1.3k citations), Genetics (539 citations), Gastroenterology (56 citations), Hematology (113 citations) and Transplantation (18 citations). L Perroni has collaborated with scholars based in Italy, United States and Canada. Frequent co-authors include F. Dagna Bricarelli, Francesca Faravelli, Olivier Goulet, Mary E. Brunkow, Massimo Mazzella, Geoffrey C Byrne, Mark W. Appleby, Ephrat Levy‐Lahad, Fred Ramsdell and Jean‐Laurent Casanova. Their work appears in journals such as British Journal of Haematology, Human Genetics, The Journal of Pediatrics, Journal of Alzheimer s Disease 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.