L.F. Bernini
Impact in
- Genetics top 10%
- Forensic and Genetic Research
- Hemoglobinopathies and Related Disorders
- Genetic diversity and population structure
- Race, Genetics, and Society
- Hematology top 10%
- Blood groups and transfusion
- Iron Metabolism and Disorders
Papers in
- Genetics 7
- Hemoglobinopathies and Related Disorders 7
- Genetic diversity and population structure 2
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- Blood groups and transfusion 5
- Iron Metabolism and Disorders 2
- Co-authors
- Giuseppe Passarino (2 shared papers)Ornella Semino (2 shared papers)A. Silvana Santachiara‐Benerecetti (1 shared paper)G. Modiano (4 shared papers)Monique Losekoot (2 shared papers)Erna van Loghem (3 shared papers)Paola Giordano (1 shared paper)Cornelis L. Harteveld (1 shared paper)
- Journals
- Human Heredity (4 papers)British Journal of Haematology (2 papers)Nature (2 papers)Journal of Medical Genetics (1 paper)Blood (1 paper)
- Partner nations
- ItalyNetherlandsUnited Kingdom
In The Last Decade
L.F. Bernini
17 papers receiving 355 citations
Peers
Comparison fields: 5 of 82
- Genetics 94
- Hematology 87
- Genetics 166
- Clinical Biochemistry 16
- Archeology 26
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 | 78 |
| 2 | Pre-Caucasoid and Caucasoid genetic features of the Indian population, revealed by mtDNA polymorphisms. | 1996 | 65 |
| 3 | 1994 | 57 | |
| 4 | 1974 | 53 | |
| 5 | 1978 | 27 | |
| 6 | Survey of several red cell and serum genetic markers in a Peruvian population. | 1972 | 25 |
| 7 | 1974 | 15 | |
| 8 | 1970 | 15 | |
| 9 | 1996 | 14 | |
| 10 | 1979 | 12 | |
| 11 | 1991 | 11 | |
| 12 | 1981 | 7 | |
| 13 | Genetic heterogeneity in Sardinia: 15 polymorphisms examined in 11 isolates. | 1991 | 7 |
| 14 | Hemoglobin Sabine [beta 91 (F7) Leu-->Pro]: occurrence in a Sardinian individual with hemolytic anemia and inclusion bodies. | 1993 | 5 |
| 15 | 1974 | 3 | |
| 16 | 1963 | 2 | |
| 17 | [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, Hematology, Genetics, Molecular Biology and Physiology, having authored 17 papers that have together received 397 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (7 papers), Blood groups and transfusion (5 papers), Erythrocyte Function and Pathophysiology (3 papers), Neonatal Health and Biochemistry (2 papers), Iron Metabolism and Disorders (2 papers), Genetic diversity and population structure (2 papers), Folate and B Vitamins Research (1 paper) and Forensic Anthropology and Bioarchaeology Studies (1 paper). The work is most often cited by research in Genetics (94 citations), Hematology (87 citations), Genetics (166 citations), Clinical Biochemistry (16 citations) and Archeology (26 citations). L.F. Bernini has collaborated with scholars based in Italy, Netherlands and United Kingdom. Frequent co-authors include Giuseppe Passarino, Ornella Semino, A. Silvana Santachiara‐Benerecetti, G. Modiano, Monique Losekoot, Erna van Loghem, Paola Giordano, Cornelis L. Harteveld, G. R. Fraser and W.S. Volkers. Their work appears in journals such as Human Heredity, British Journal of Haematology, Nature, Journal of Medical Genetics and Blood.
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.