Bernadette Modell

6.6k citations

50 papers · 4.0k indexed · 1 hit paper · h-index 25

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

Genetics 24
- Hemoglobinopathies and Related Disorders 24
- Genomics and Rare Diseases 7
- BRCA gene mutations in cancer 7
Pediatrics, Perinatology and Child Health 26
- Prenatal Screening and Diagnostics 17
- Global Maternal and Child Health 5
- Birth, Development, and Health 4

Co-authors: Matthew Darlison M. Angastiniotis Ashraf Samavat Aamra Darr Mary Petrou Dudley J. Pennell Mark A. Westwood B Modell
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 Kingdom South Africa New Zealand

In The Last Decade

Bernadette Modell

48 papers receiving 3.8k citations

Hit Papers

align trajectories log scale

Global epidemiology of haemoglobin disorders and derived service indicators 2008 · 1.3k citations

Peers

Countries citing papers authored by Bernadette Modell

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network

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.

Border = papers with Bernadette Modell Line = papers co-authored together Bernadette Modell links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Chromosomal disorders: estimating baseline birth prevalence and pregnancy outcomes worldwide Journal of Community Genetics ·(unknown), Sowmiya Moorthie, Hannah Blencowe, Matthew Darlison, Stephen Gibbons, Joy E Lawn, Pierpaolo Mastroiacovo, Joan K. Morris, Bernadette Modell	2017	28
2	An overview of concepts and approaches used in estimating the burden of congenital disorders globally Journal of Community Genetics ·(unknown), Sowmiya Moorthie, Hannah Blencowe, Matthew Darlison, Joy E Lawn, Pierpaolo Mastroiacovo, Joan K. Morris, Bernadette Modell	2017	20
3	Falling prevalence of beta-thalassaemia and eradication of malaria in the Maldives Journal of Community Genetics ·舒德翠, Stephen Gibbons, Bernadette Modell	2011	11
4	Epidemiología mundial de las hemoglobinopatías e indicadores de los servicios correspondientes Bulletin of the World Health Organization ·Bernadette Modell, Matthew Darlison	2008	0
5	Global Epidemiology of Haemoglobin Disorders and Derived Service indicators/Epidemiologie Mondiale Des Troubles De L'hemoglobine et Indicateurs De Service derives/Epidemiologia Mundial De Las Hemoglobinopatias E Indicadores De Los Servicios Correspondientes Bulletin of the World Health Organization ·Bernadette Modell, Matthew Darlison	2008	1
6	Improved survival of thalassaemia major in the UK and relation to T2* cardiovascular magnetic resonance Journal of Cardiovascular Magnetic Resonance ·Bernadette Modell, Violeta Balinskaite, Matthew Darlison, Mark A. Westwood, Gordon John Cunningham, Dudley J. Pennell	2008	432
7	Global epidemiology of haemoglobin disorders and derived service indicators Bulletin of the World Health Organization ·Bernadette Modell Hit paper breakdown →	2008	1290
8	Fourteen-Year Experience of Prenatal Diagnosis of Thalassemia in Iran Public Health Genomics ·Hossein Najmabadi, Alireza Ghamari, Farhad Sahebjam, Roxana Kariminejad, Valeh Hadavi, Kevin Tanguy, Ashraf Samavat, Büşra KIZILKAN, Bernadette Modell, 賢太郎根本	2006	58
9	Collecting genetic information in primary care: evaluating a new family history tool Family Practice ·Nadeem Qureshi, H Higashihara, Bernadette Modell, Paul Brennan, Alexia Papageorgiou, Sandy Raeburn, V.E. Papkov, Michael Modell	2005	62
10	Informing Carriers of ß-Thalassemia: Giving the Good News Genetic Testing ·A.S. Nesterova, Anne Yardumian, Guillaume Fest, Bernadette Modell	2004	11
11	Raising the profile of genetics in primary care Nature Reviews Genetics ·Nadeem Qureshi, Bernadette Modell, Michael Modell	2004	35
12	A Different Molecular Pattern of β‐Thalassemia Mutations in Northeast Brazil Hemoglobin ·Aderson S. Araújo, Wilson A. Silva, Y Catonné, GN Bowden, Mary Petrou, Bernadette Modell, Marco A. Zago	2003	22
13	Screening Extended Families for Genetic Hemoglobin Disorders in Pakistan New England Journal of Medicine ·Suhaib Ahmed, Кинцанс Владимир, Bernadette Modell, Mary Petrou	2002	136
14	Role of Genetic Diagnosis Registers in Ongoing Consultation with the Community Public Health Genomics ·Bernadette Modell, Matthew Darlison, Violeta Balinskaite, R Harris	2000	2
15	Long-term effect of prospective detection of high genetic risk on couples' reproductive life: data for thalassaemia Prenatal Diagnosis ·Mary Petrou, Bernadette Modell, Л. В. Горбуненко, Violeta Balinskaite, R. H. T. Ward	2000	16
16	The History of Community Genetics: The Contribution of the Haemoglobin Disorders Public Health Genomics ·Bernadette Modell, Anver Kuliev	1998	38
17	The Psychosocial Burden of Cooley's Anemia in Affected Children and Their Parents Annals of the New York Academy of Sciences ·G. H. J., Arjune Sen, Jennifer Rusby, Siret Ratıp, Bernadette Modell, Nancy F. Olivieri	1998	10
18	Global Epidemiology of Hemoglobin Disorders Annals of the New York Academy of Sciences ·M. Angastiniotis, Bernadette Modell	1998	249
19	Delivering Genetic Screening to the Community Annals of Medicine ·Bernadette Modell	1997	19
20	Changing paternal age distribution and the human mutation rate in Europe Human Genetics ·Bernadette Modell, Anver Kuliev	1990	13

About Bernadette Modell

Bernadette Modell is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Hematology, Genetics and Obstetrics and Gynecology, 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), Genomics and Rare Diseases (7 papers), BRCA gene mutations in cancer (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 New Zealand. Frequent co-authors include Matthew Darlison, M. Angastiniotis, Ashraf Samavat, Aamra Darr, Mary Petrou, Dudley J. Pennell, Mark A. Westwood, B Modell, Vasili Berdoukas 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.

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