B. Modell
Impact in
- Genetics top 0.1%
- Hemoglobinopathies and Related Disorders
- Cleft Lip and Palate Research
- Genomics and Rare Diseases
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- Prenatal Screening and Diagnostics
Papers in
- Genetics 101
- Hemoglobinopathies and Related Disorders 101
- Genomics and Rare Diseases 15
- Genetic Associations and Epidemiology 7
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- Prenatal Screening and Diagnostics 43
- Co-authors
- Matthew W. Darlison (21 shared papers)Maren Khan (4 shared papers)Peter Anthony Mossey (3 shared papers)Mary Petrou (39 shared papers)Michael Angastiniotis (9 shared papers)Hannah K. Blencowe (10 shared papers)Aamra Darr (3 shared papers)Ashraf Samavat (2 shared papers)
- Journals
- The Lancet (15 papers)Annals of the New York Academy of Sciences (8 papers)British Journal of Haematology (7 papers)Prenatal Diagnosis (7 papers)Journal of Medical Genetics (6 papers)
- Partner nations
- United KingdomSouth AfricaUnited States
In The Last Decade
B. Modell
170 papers receiving 8.7k citations
B. Modell's Hit Papers
Peers
Comparison fields: 5 of 150
- Genetics 4.9k
- Pediatrics, Perinatology and Child Health 1.4k
- Hematology 645
- Genetics 1.3k
- Public Health, Environmental and Occupational Health 878
Countries citing papers authored by B. Modell
This map shows the geographic impact of B. Modell'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 B. Modell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites B. Modell more than expected).
Fields of papers citing papers by B. Modell
This network shows the impact of papers produced by B. Modell. 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 B. Modell. The network helps show where B. Modell may publish in the future.
Co-authors
The 25 scholars most cited alongside B. Modell, 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 176 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Global epidemiology of haemoglobin disorders and derived service indicators Hit paper breakdown → | 2008 | 1430 |
| 2 | 2000 | 491 | |
| 3 | 2008 | 477 | |
| 4 | 2012 | 387 | |
| 5 | 2010 | 375 | |
| 6 | 1998 | 261 | |
| 7 | Estimates of global and regional prevalence of neural tube defects for 2015: a systematic analysis Hit paper breakdown → | 2018 | 248 |
| 8 | 2004 | 239 | |
| 9 | 2002 | 221 | |
| 10 | The Clinical Approach to Thalassaemia | 1984 | 203 |
| 11 | 1982 | 176 | |
| 12 | 1993 | 163 | |
| 13 | 1981 | 152 | |
| 14 | 2002 | 146 | |
| 15 | 1983 | 139 | |
| 16 | 2007 | 129 | |
| 17 | 1988 | 120 | |
| 18 | Prevention and control of haemoglobinopathies. | 1995 | 119 |
| 19 | Community control of genetic and congenital disorders | 1997 | 119 |
| 20 | 1980 | 109 |
About B. Modell
B. Modell is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Genetics, Public Health, Environmental and Occupational Health and Clinical Biochemistry, having authored 176 papers that have together received 9.6k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (101 papers), Prenatal Screening and Diagnostics (43 papers), Genomics and Rare Diseases (15 papers), Congenital Anomalies and Fetal Surgery (11 papers), Medical and Health Sciences Research (8 papers), Genetic Associations and Epidemiology (7 papers), Marriage and Family Dynamics (6 papers) and Ethics and bioethics in healthcare (5 papers). The work is most often cited by research in Genetics (4.9k citations), Pediatrics, Perinatology and Child Health (1.4k citations), Hematology (645 citations), Genetics (1.3k citations) and Public Health, Environmental and Occupational Health (878 citations). B. Modell has collaborated with scholars based in United Kingdom, South Africa and United States. Frequent co-authors include Matthew W. Darlison, Maren Khan, Peter Anthony Mossey, Mary Petrou, Michael Angastiniotis, Hannah K. Blencowe, Aamra Darr, Ashraf Samavat, R. H. T. Ward and Joy Elizabeth Lawn. Their work appears in journals such as The Lancet, Annals of the New York Academy of Sciences, British Journal of Haematology, Prenatal Diagnosis 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.