L.F. Bernini
Impact in
- Genetics top 10%
- Forensic and Genetic Research
- Hemoglobinopathies and Related Disorders
- Genetic diversity and population structure
- Genetic Associations and Epidemiology
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- Protease and Inhibitor Mechanisms
Papers in
- Genetics 10
- Forensic and Genetic Research 6
- Genetic diversity and population structure 5
- Hemoglobinopathies and Related Disorders 5
- Genetic Associations and Epidemiology 5
- High Altitude and Hypoxia 1
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- Blood groups and transfusion 1
- Co-authors
- Ornella Semino (2 shared papers)Giuseppe Passarino (2 shared papers)Erna van Loghem (5 shared papers)Lourens E. Nijenhuis (4 shared papers)A. Silvana Santachiara‐Benerecetti (1 shared paper)Guido Modiano (4 shared papers)Monique Losekoot (1 shared paper)Paola Giordano (1 shared paper)
- Journals
- Human Heredity (4 papers)Nature (2 papers)British Journal of Haematology (2 papers)Annals of Human Biology (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- NetherlandsItalyUnited Kingdom
In The Last Decade
L.F. Bernini
16 papers receiving 338 citations
Peers
Comparison fields: 5 of 49
- Genetics 67
- Genetics 218
- Cancer Research 17
- Hematology 13
- Cell Biology 10
Countries citing papers authored by L.F. Bernini
This map shows the geographic impact of L.F. Bernini'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.F. Bernini with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites L.F. Bernini more than expected).
Fields of papers citing papers by L.F. Bernini
This network shows the impact of papers produced by L.F. Bernini. 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.F. Bernini. The network helps show where L.F. Bernini may publish in the future.
Co-authors
The 25 scholars most cited alongside L.F. Bernini, 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 | Studies on African Pygmies. I. A pilot investigation of Babinga Pygmies in the Central African Republic (with an analysis of genetic distances). | 1969 | 75 |
| 2 | Pre-Caucasoid and Caucasoid genetic features of the Indian population, revealed by mtDNA polymorphisms. | 1996 | 64 |
| 3 | 1994 | 58 | |
| 4 | 1974 | 53 | |
| 5 | 1978 | 28 | |
| 6 | Survey of several red cell and serum genetic markers in a Peruvian population. | 1972 | 26 |
| 7 | 1974 | 15 | |
| 8 | 1970 | 14 | |
| 9 | 1996 | 14 | |
| 10 | 1979 | 12 | |
| 11 | 1981 | 8 | |
| 12 | Genetic heterogeneity in Sardinia: 15 polymorphisms examined in 11 isolates. | 1991 | 7 |
| 13 | Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodies. | 1993 | 7 |
| 14 | 1963 | 3 | |
| 15 | 1974 | 2 | |
| 16 | [Hemolytic disease of the newborn and chronic hypochromic microcytic anemia in one family: gamma-delta-beta thalassemia]. | 1981 | 1 |
About L.F. Bernini
L.F. Bernini is a scholar working on Genetics, Genetics, Hematology, Cancer Research and Cell Biology, having authored 16 papers that have together received 387 indexed citations. Recurring topics across this work include Forensic and Genetic Research (6 papers), Genetic diversity and population structure (5 papers), Hemoglobinopathies and Related Disorders (5 papers), Genetic Associations and Epidemiology (5 papers), Protease and Inhibitor Mechanisms (1 paper), Blood groups and transfusion (1 paper), Hemoglobin structure and function (1 paper) and High Altitude and Hypoxia (1 paper). The work is most often cited by research in Genetics (67 citations), Genetics (218 citations), Cancer Research (17 citations), Hematology (13 citations) and Cell Biology (10 citations). L.F. Bernini has collaborated with scholars based in Netherlands, Italy and United Kingdom. Frequent co-authors include Ornella Semino, Giuseppe Passarino, Erna van Loghem, Lourens E. Nijenhuis, A. Silvana Santachiara‐Benerecetti, Guido Modiano, Monique Losekoot, Paola Giordano, J. G. A. M. Heister and H. L. Haak. Their work appears in journals such as Human Heredity, Nature, British Journal of Haematology, Annals of Human Biology and Journal of Medical Genetics.
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.