Bernadette Modell
Impact in
- Genetics top 0.2%
- Hemoglobinopathies and Related Disorders
- Genomics and Rare Diseases
- BRCA gene mutations in cancer
- Hematology top 0.2%
- Iron Metabolism and Disorders
- Blood groups and transfusion
Papers in
-
- Prenatal Screening and Diagnostics 17
- Global Maternal and Child Health 5
- Birth, Development, and Health 4
- Genetics 24
- Hemoglobinopathies and Related Disorders 24
- BRCA gene mutations in cancer 7
- Genomics and Rare Diseases 7
- Co-authors
- Matthew Darlison (12 shared papers)M. Angastiniotis (1 shared paper)Ashraf Samavat (2 shared papers)Aamra Darr (2 shared papers)Mary Petrou (10 shared papers)Dudley J. Pennell (1 shared paper)Mark A. Westwood (1 shared paper)Vasili Berdoukas (1 shared paper)
- Journals
- Prenatal Diagnosis (4 papers)Public Health Genomics (4 papers)Annals of the New York Academy of Sciences (4 papers)Bulletin of the World Health Organization (3 papers)Nature Reviews Genetics (3 papers)
- Partner nations
- United KingdomSouth AfricaPakistan
In The Last Decade
Bernadette Modell
48 papers receiving 3.8k citations
Bernadette Modell's Hit Papers
Peers
Comparison fields: 5 of 135
- Genetics 2.6k
- Hematology 2.1k
- Pediatrics, Perinatology and Child Health 1.3k
- Genetics 573
- Nutrition and Dietetics 249
Countries citing papers authored by Bernadette Modell
This map shows the geographic impact of Bernadette 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 Bernadette Modell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Bernadette Modell more than expected).
Fields of papers citing papers by Bernadette Modell
This network shows the impact of papers produced by Bernadette 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 Bernadette Modell. The network helps show where Bernadette Modell may publish in the future.
Co-authors
The 25 scholars most cited alongside Bernadette 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 50 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 | 1290 |
| 2 | 2008 | 432 | |
| 3 | 1998 | 249 | |
| 4 | 2004 | 231 | |
| 5 | 2018 | 203 | |
| 6 | 2002 | 193 | |
| 7 | The Clinical Approach to Thalassaemia | 1984 | 184 |
| 8 | 2002 | 136 | |
| 9 | 2004 | 92 | |
| 10 | 2002 | 85 | |
| 11 | 2016 | 73 | |
| 12 | 2005 | 62 | |
| 13 | 2006 | 58 | |
| 14 | 2000 | 58 | |
| 15 | 1976 | 56 | |
| 16 | 1985 | 56 | |
| 17 | Prevention of Thalassaemias and Other Haemoglobin Disorders | 2013 | 46 |
| 18 | 1999 | 39 | |
| 19 | 1998 | 38 | |
| 20 | 2004 | 35 |
About Bernadette Modell
Bernadette Modell is a scholar working on Pediatrics, Perinatology and Child Health, Genetics, Genetics, Hematology and General Health Professions, having authored 50 papers that have together received 4.0k indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (24 papers), Prenatal Screening and Diagnostics (17 papers), Iron Metabolism and Disorders (11 papers), BRCA gene mutations in cancer (7 papers), Genomics and Rare Diseases (7 papers), Global Maternal and Child Health (5 papers), Birth, Development, and Health (4 papers) and Folate and B Vitamins Research (4 papers). The work is most often cited by research in Genetics (2.6k citations), Hematology (2.1k citations), Pediatrics, Perinatology and Child Health (1.3k citations), Genetics (573 citations) and Nutrition and Dietetics (249 citations). Bernadette Modell has collaborated with scholars based in United Kingdom, South Africa and Pakistan. Frequent co-authors include Matthew Darlison, M. Angastiniotis, Ashraf Samavat, Aamra Darr, Mary Petrou, Dudley J. Pennell, Mark A. Westwood, Vasili Berdoukas, B Modell and Hannah Blencowe. Their work appears in journals such as Prenatal Diagnosis, Public Health Genomics, Annals of the New York Academy of Sciences, Bulletin of the World Health Organization and Nature Reviews 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.