L. Culpi
Impact in
-
- Congenital Ear and Nasal Anomalies
-
- Cystic Fibrosis Research Advances
- Neonatal Respiratory Health Research
- Tracheal and airway disorders
Papers in
- Genetics 9
- Congenital Ear and Nasal Anomalies 7
- Hemoglobinopathies and Related Disorders 2
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- Cystic Fibrosis Research Advances 9
- Tracheal and airway disorders 2
- Co-authors
- Maria Luiza Petzl‐Erler (4 shared papers)Angelica Beate Winter Boldt (2 shared papers)Jürgen F. J. Kun (2 shared papers)Luiza Tamie Tsuneto (2 shared papers)Salmo Raskin (9 shared papers)Noemi F. Pereira (1 shared paper)Karin Braun-Prado (1 shared paper)Tatiana Rozov (4 shared papers)
- Journals
- Human Heredity (2 papers)Genetica (1 paper)Journal of Biosocial Science (1 paper)Clinical Genetics (1 paper)Human Immunology (1 paper)
- Partner nations
- BrazilUnited StatesGermany
In The Last Decade
L. Culpi
17 papers receiving 292 citations
Peers
Comparison fields: 5 of 48
- Genetics 56
- Pulmonary and Respiratory Medicine 131
- Immunology 82
- Virology 11
- Hematology 17
Countries citing papers authored by L. Culpi
This map shows the geographic impact of L. Culpi'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. Culpi with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites L. Culpi more than expected).
Fields of papers citing papers by L. Culpi
This network shows the impact of papers produced by L. Culpi. 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. Culpi. The network helps show where L. Culpi may publish in the future.
Co-authors
The 25 scholars most cited alongside L. Culpi, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2006 | 57 | |
| 2 | 2007 | 53 | |
| 3 | 2000 | 46 | |
| 4 | Geographic heterogeneity of 4 common worldwide cystic fibrosis non-DF508 mutations in Brazil. | 1999 | 22 |
| 5 | 2003 | 19 | |
| 6 | Cystic fibrosis in the Brazilian population: DF508 mutation and KM-19/XV-2C haplotype distribution. | 1997 | 16 |
| 7 | Frequencies of the butyrylcholinesterase K mutation in Brazilian populations of European and African origin. | 1998 | 14 |
| 8 | Regional distribution of cystic fibrosis-linked DNA haplotypes in Brazil: multicenter study. | 1997 | 13 |
| 9 | 2009 | 13 | |
| 10 | 2007 | 12 | |
| 11 | 1999 | 9 | |
| 12 | 2005 | 7 | |
| 13 | 1984 | 5 | |
| 14 | 1991 | 3 | |
| 15 | 1984 | 3 | |
| 16 | 2017 | 1 | |
| 17 | 2007 | 1 | |
| 18 | Valongo, an isolated braziliann black community. I. Structure of the population | 1992 | 0 |
About L. Culpi
L. Culpi is a scholar working on Genetics, Pulmonary and Respiratory Medicine, Hematology, Immunology and Plant Science, having authored 18 papers that have together received 294 indexed citations. Recurring topics across this work include Cystic Fibrosis Research Advances (9 papers), Congenital Ear and Nasal Anomalies (7 papers), Blood groups and transfusion (3 papers), T-cell and B-cell Immunology (3 papers), Pesticide Exposure and Toxicity (3 papers), Cholinesterase and Neurodegenerative Diseases (2 papers), Hemoglobinopathies and Related Disorders (2 papers) and Tracheal and airway disorders (2 papers). The work is most often cited by research in Genetics (56 citations), Pulmonary and Respiratory Medicine (131 citations), Immunology (82 citations), Virology (11 citations) and Hematology (17 citations). L. Culpi has collaborated with scholars based in Brazil, United States and Germany. Frequent co-authors include Maria Luiza Petzl‐Erler, Angelica Beate Winter Boldt, Jürgen F. J. Kun, Luiza Tamie Tsuneto, Salmo Raskin, Noemi F. Pereira, Karin Braun-Prado, Tatiana Rozov, Paulo José Cauduro Maróstica and Fernando Abreu. Their work appears in journals such as Human Heredity, Genetica, Journal of Biosocial Science, Clinical Genetics and Human Immunology.
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.