Bertil Hall
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Neurology top 5%
- Neurofibromatosis and Schwannoma Cases
Papers in
- Genetics 12
- Genomic variations and chromosomal abnormalities 4
- Dermatoglyphics and Human Traits 4
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 2
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- Chromosomal and Genetic Variations 5
- Co-authors
- Bëngt Källén (2 shared papers)Mitchell S. Golbus (1 shared paper)M. J. Simpkiss (1 shared paper)Jaime O. Claudio (1 shared paper)Dilys M. Parry (1 shared paper)Nathalie Chrétien (1 shared paper)Virginia V. Michels (1 shared paper)Priscilla Short (1 shared paper)
- Journals
- The Lancet (8 papers)Hereditas (6 papers)Acta Paediatrica (5 papers)Clinical Genetics (3 papers)Acta Obstetricia Et Gynecologica Scandinavica (2 papers)
- Partner nations
- SwedenCanadaUnited States
In The Last Decade
Bertil Hall
35 papers receiving 727 citations
Peers
Comparison fields: 5 of 87
- Developmental Biology 75
- Neurology 176
- Genetics 300
- Pediatrics, Perinatology and Child Health 172
- Rheumatology 66
Countries citing papers authored by Bertil Hall
This map shows the geographic impact of Bertil Hall'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 Bertil Hall with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bertil Hall more than expected).
Fields of papers citing papers by Bertil Hall
This network shows the impact of papers produced by Bertil Hall. 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 Bertil Hall. The network helps show where Bertil Hall may publish in the future.
Co-authors
The 25 scholars most cited alongside Bertil Hall, 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 38 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Type of mutation in the neurofibromatosis type 2 gene (NF2) frequently determines severity of disease. | 1996 | 216 |
| 2 | 1966 | 70 | |
| 3 | 1964 | 63 | |
| 4 | 1976 | 57 | |
| 5 | 1977 | 51 | |
| 6 | 1964 | 42 | |
| 7 | 1962 | 30 | |
| 8 | 1985 | 29 | |
| 9 | 1968 | 25 | |
| 10 | 1961 | 25 | |
| 11 | 1963 | 23 | |
| 12 | 1968 | 22 | |
| 13 | Ocular manifestations of branchio-oculo-facial syndrome: report of a novel mutation and review of the literature. | 2010 | 19 |
| 14 | Cooccurrence of collagenous colitis with seronegative spondyloarthropathy: report of a case and literature review. | 1993 | 19 |
| 15 | 2009 | 18 | |
| 16 | 1972 | 14 | |
| 17 | 1972 | 12 | |
| 18 | Presentation of multicentric Castleman's disease with sicca syndrome, cardiomyopathy, palmar and plantar rash. | 1993 | 12 |
| 19 | 1965 | 10 | |
| 20 | 1970 | 9 |
About Bertil Hall
Bertil Hall is a scholar working on Genetics, Plant Science, Molecular Biology, Pediatrics, Perinatology and Child Health and Surgery, having authored 38 papers that have together received 836 indexed citations. Recurring topics across this work include Congenital limb and hand anomalies (5 papers), Chromosomal and Genetic Variations (5 papers), Prenatal Screening and Diagnostics (4 papers), Metabolism and Genetic Disorders (4 papers), Genomic variations and chromosomal abnormalities (4 papers), Dermatoglyphics and Human Traits (4 papers), Botanical Research and Chemistry (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (2 papers). The work is most often cited by research in Developmental Biology (75 citations), Neurology (176 citations), Genetics (300 citations), Pediatrics, Perinatology and Child Health (172 citations) and Rheumatology (66 citations). Bertil Hall has collaborated with scholars based in Sweden, Canada and United States. Frequent co-authors include Bëngt Källén, Mitchell S. Golbus, M. J. Simpkiss, Jaime O. Claudio, Dilys M. Parry, Nathalie Chrétien, Virginia V. Michels, Priscilla Short, Katsumasa Kitamura and Peter Propping. Their work appears in journals such as The Lancet, Hereditas, Acta Paediatrica, Clinical Genetics and Acta Obstetricia Et Gynecologica Scandinavica.
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.