Bernadette Modell

Bernadette Modell's AcademicInfluence.com Rankings

Bernadette Modell

Biology

#8912

World Rank

#12053

Historical Rank

Genetics

#1226

World Rank

#1327

Historical Rank

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Biology

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According to Wikipedia, Professor Bernadette Modell is a British geneticist, specialising in the study of thalassaemia. Modell attended a convent school, and then graduated in zoology, with genetics and embryology from the University of Oxford, in 1955. She then undertook a doctorate in developmental biology at Cambridge University, qualifying in 1959. She next studied medicine at Cambridge and at University College Hospital, qualifying in 1964.

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Bernadette Modell's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

Global epidemiology of haemoglobin disorders and derived service indicators. (2008) (1455)
March of Dimes: global report on birth defects, the hidden toll of dying and disabled children. (2005) (678)
Survival in β-thalassaemia major in the UK: data from the UK Thalassaemia Register (2000) (587)
Improved survival of thalassaemia major in the UK and relation to T2* cardiovascular magnetic resonance (2008) (515)
Folic acid to reduce neonatal mortality from neural tube disorders (2010) (414)
Epidemiology of oral clefts 2012: an international perspective. (2012) (391)
Global Epidemiology of Hemoglobin Disorders (1998) (330)
Iranian national thalassaemia screening programme (2004) (270)
Genetic counselling and customary consanguineous marriage (2002) (247)
The Clinical Approach to Thalassaemia (1984) (220)
What proportion of congenital abnormalities can be prevented? (1993) (201)
Screening extended families for genetic hemoglobin disorders in Pakistan. (2002) (198)
Community control of genetic and congenital disorders (1997) (194)
Method of sampling chorionic villi in first trimester of pregnancy under guidance of real time ultrasound. (1983) (172)
DIRECT GENE ANALYSIS OF CHORIONIC VILLI: A POSSIBLE TECHNIQUE FOR FIRST-TRIMESTER ANTENATAL DIAGNOSIS OF HAEMOGLOBINOPATHIES (1981) (172)
Global regional and national causes of child mortality (2012) (169)
Estimates of global and regional prevalence of neural tube defects for 2015: a systematic analysis (2018) (161)
The frequency of consanguineous marriage among British Pakistanis. (1988) (160)
Medical Research Council European Trial of chorion villus sampling (1991) (159)
Epidemiology of haemoglobin disorders in Europe: an overview (2007) (155)
Medical genetics in developing countries. (2004) (151)
Association of thalassaemia intermedia with a beta‐globin gene haplotype (1987) (135)
Effect of introducing antenatal diagnosis on reproductive behaviour of families at risk for thalassaemia major. (1980) (133)
Science and society: genetic counselling and customary consanguineous marriage. (2002) (127)
Prevention and control of haemoglobinopathies. (1995) (126)
Quality of Life in Thalassemia (2005) (118)
Mapping the prevalence of sickle cell and beta thalassaemia in England: estimating and validating ethnic‐specific rates (1999) (117)
Informed choice in genetic screening for thalassaemia during pregnancy: audit from a national confidential inquiry (2000) (114)
Model for antenatal diagnosis of β-thalassaemia and other monogenic disorders by molecular analysis of linked DNA polymorphisms (1980) (110)
Recommendations for introducing genetics services in developing countries (2003) (106)
Prevention of Thalassaemias and Other Haemoglobin Disorders (2013) (97)
Prenatal diagnosis of beta‐thalassaemia in Pakistan: experience in a Muslim country (2000) (90)
Collecting genetic information in primary care: evaluating a new family history tool. (2005) (83)
CHORIONIC VILLUS SAMPLING Evaluating Safety and Efficacy (1985) (82)
Standards for the Clinical Care of Children and Adults with Thalassaemia in the UK (2005) (80)
Limb abnormalities and chorionic villus sampling (1991) (77)
A multidisciplinary approach for improving services in primary care: randomised controlled trial of screening for haemoglobin disorders (1998) (69)
A national register for surveillance of inherited disorders: beta thalassaemia in the United Kingdom. (2001) (67)
Audit of prenatal diagnosis for haemoglobin disorders in the United Kingdom: the first 20 years (1997) (67)
Fourteen-Year Experience of Prenatal Diagnosis of Thalassemia in Iran (2006) (66)
Feasibility of antenatal diagnosis of β thalassaemia by DNA polymorphisms in Asian Indian and Cypriot populations (1984) (62)
The History of Community Genetics: The Contribution of the Haemoglobin Disorders (1998) (57)
Raising the profile of genetics in primary care (2004) (56)
Factors affecting the uptake of prenatal diagnosis for sickle cell disease. (1992) (52)
Systematic Review and Meta-Analysis of the Birth Prevalence of Orofacial Clefts in Low- and Middle-Income Countries (2017) (51)
Presence of gene for β globin in homozygous β0 thalassaemia (1976) (51)
National Confidential Enquiry into counselling for genetic disorders by non‐geneticists: general recommendations and specific standards for improving care (1999) (49)
Prenatal screening for haemoglobin disorders (1995) (47)
EFFECT OF FETAL DIAGNOSTIC TESTING ON BIRTH-RATE OF THALASSAEMIA MAJOR IN BRITAIN (1984) (46)
Risk evaluation of CVS (1993) (45)
Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide (2018) (44)
Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide (2018) (44)
FIRST-TRIMESTER FETAL DIAGNOSIS FOR HAEMOGLOBINOPATHIES: REPORT ON 200 CASES (1986) (42)
Population and genetic studies suggest a single origin for the Indian deletion β° thalassaemia (1984) (42)
Social and genetic implications of customary consanguineous marriage among British Pakistanis. Report of a meeting held at the Ciba Foundation on 15 January 1991 (1991) (42)
Distribution and control of some genetic disorders. (1988) (41)
Cystic fibrosis screening and community genetics. (1990) (38)
Socio-economic inequalities as a predictor of health in South Africa--the Yenza cross-sectional study. (2006) (38)
Thalassemia in Bombay: the role of medical genetics in developing countries. (1990) (38)
GPs' opinions of their role in prenatal genetic services: a cross-sectional survey. (2006) (35)
Study of hemoglobinopathies in Oman through a national register. (2000) (35)
Haematological Aspects of Antenatal Diagnosis for Thalassaemia in Britain (1980) (32)
Alpha thalassaemia hydrops fetalis in the UK: the importance of screening pregnant women of Chinese, other South East Asian and Mediterranean extraction for alpha thalassaemia trait (1992) (32)
OBSTETRIC ASPECTS OF MIDTRIMESTER FETAL BLOOD SAMPLING BY NEEDLING OR FETOSCOPY (1980) (32)
Management of thalassaemia major. (1971) (31)
Accuracy of prenatal diagnosis for haemoglobin disorders in the UK: 25 years' experience (2000) (31)
A scientific basis for cost-benefit analysis of genetics services. (1993) (31)
Addressing key issues in the consanguinity-related risk of autosomal recessive disorders in consanguineous communities: lessons from a qualitative study of British Pakistanis (2015) (29)
Chromosomal disorders: estimating baseline birth prevalence and pregnancy outcomes worldwide (2017) (28)
Chromosomal disorders: estimating baseline birth prevalence and pregnancy outcomes worldwide (2017) (28)
PREVENTION AND CONTROL OF HEMOGLOBINOPATHIES (1995) (27)
Meiotic recombination between two polymorphic restriction sites within the beta globin gene cluster. (1986) (27)
Examining the family-centred approach to genetic testing and counselling among UK Pakistanis: a community perspective (2012) (26)
A Different Molecular Pattern of β‐Thalassemia Mutations in Northeast Brazil (2003) (26)
Community genetics services in Europe (1991) (24)
Rare single gene disorders: estimating baseline prevalence and outcomes worldwide (2018) (24)
Audit of process of antenatal screening for sickle cell disorders at a north London hospital (1997) (24)
Thalassaemia in Britain: a tale of two communities (1998) (24)
THALASSÆMIA AS A MODEL OF RECESSIVE GENETIC DISEASE IN THE COMMUNITY (1980) (24)
Long‐term effect of prospective detection of high genetic risk on couples' reproductive life: data for thalassaemia (2000) (23)
Services for thalassaemia as a model for cost-benefit analysis of genetics services (1991) (22)
Antenatal Diagnosis How to Deliver a Comprehensive Service in the United Kingdom (1990) (22)
Microcytosis, iron deficiency and thalassaemia in a multi‐ethnic community: a pilot study (2007) (22)
Thalassaemia in Azerbaijan. (1994) (21)
Impact of public health on human genetics. (1989) (21)
Genetic screening for ethnic minorities. (1990) (20)
Falling prevalence of beta-thalassaemia and eradication of malaria in the Maldives (2011) (20)
An overview of concepts and approaches used in estimating the burden of congenital disorders globally (2017) (19)
Folic acid: from research to public health practice. (2004) (19)
POPULATION SCREENING FOR CARRIERS OF RECESSIVELY INHERITED DISORDERS (1980) (19)
Epidemiological Methods in Community Genetics and the Modell Global Database of Congenital Disorders (MGDb) (2016) (18)
Delivering genetic screening to the community. (1997) (18)
Prevention of Thalassaemias and Other Haemoglobin Disorders: Volume 1: Principles (2013) (17)
Congenital disorders: epidemiological methods for answering calls for action (2018) (16)
The Changing Epidemiology of β-Thalassemia in the Greek-Cypriot Population (2013) (15)
Problems in the control of genetic disorders. (1990) (15)
OBSTETRIC OUTCOME AND PROBLEMS OF MID‐TRIMESTER FETAL BLOOD SAMPLING FOR ANTENATAL DIAGNOSIS (1981) (15)
The Psychosocial Burden of Cooley's Anemia in Affected Children and Their Parents (1998) (15)
Consanguinity and reproductive behaviour in a tribal population 'the Baiga' in Madhya Pradesh, India. (1995) (14)
Informing Carriers of ß-Thalassemia: Giving the Good News (2004) (13)
Reproductive Reproductive behaviour and natural selection for the sickle gene in the Baiga Tribe of Central India: The role of social parenting (1996) (13)
Sickle-cell disorders: limits of descriptive epidemiology (2013) (12)
Primary care morbidity in Eastern Cape Province. (2010) (12)
Community genetics services in Europe. Report on a survey (1991) (12)
The management of the improved prognosis in thalassemia major. (1982) (12)
Two unusual cases of first trimester prenatal diagnosis of cystic fibrosis using DNA probes (1987) (12)
Kinship and Medical Genetics: A Clinician’s Perspective (1997) (12)
Chorionic villus sampling (CVS): World health organization european regional office (WHO/EURO) meeting statement on the use of CVS in prenatal diagnosis (1992) (11)
Transfusion‐dependent thalassaemia: a new era (2008) (11)
Changes in circulating alphafetoprotein and human chorionic gonadotrophin following chorionic villus sampling. (1988) (11)
A Toolkit to assess health needs for congenital disorders in low- and middle-income countries: an instrument for public health action (2013) (10)
Sickle Cell and Thalassaemia: achieving health gain. Guidance for commisioners and providers (1998) (10)
Ethical aspects of genetic screening. (1992) (9)
Methods to estimate access to care and the effect of interventions on the outcomes of congenital disorders (2018) (9)
The ethics of prenatal diagnosis and genetic counselling. (1990) (9)
Methods to estimate access to care and the effect of interventions on the outcomes of congenital disorders (2018) (9)
The need for a science of community genetics. (1992) (8)
Thalassemia in Britain and Australia. (1976) (8)
Prevention of the haemoglobinopathies. (1983) (8)
Changing paternal age distribution and the human mutation rate in Europe (1990) (8)
A Second Look at the Distribution and Frequency of the Hemoglobinopathies (1985) (7)
Towards an interoperable healthcare information infrastructure — working from the bottom up (2006) (7)
Thalassaemia in the Maldives (1990) (7)
First Trimester Diagnosis of the Hemoglobin Disorders (1985) (6)
The Olivieri case. (2003) (6)
The Prevention of Thalassemia Revisited: A Historical and Ethical Perspective by the Thalassemia International Federation (2021) (6)
Fetoplacental Products as a Prognostic Guide Following Chorionic Villi Sampling (1985) (6)
Haemoglobin disorders—a point of entry for community genetics services in India? (2019) (6)
THE BAIGAS OF MADHYA PRADESH: A DEMOGRAPHIC STUDY (1997) (6)
Social consequences of introducing antenatal diagnosis for thalassemia. (1982) (6)
Confidential inquiries should be funded in clinical genetics (2001) (6)
Why do some practices respond to an educational intervention? (2000) (6)
OBSTETRIC OUTCOME IN FIRST TRIMESTER FETAL DIAGNOSIS FOR THE HAEMOGLOBINOPATHIES (1983) (5)
Informing carriers of beta-thalassemia: giving the good news. (2004) (5)
Role of Genetic Diagnosis Registers in Ongoing Consultation with the Community (2000) (5)
SECOND TRIMESTER CHORIONIC VILLUS (PLACENTAL) BIOPSY (1986) (5)
Prenatal diagnosis of haemoglobin disorders by cordocentesis at 12 weeks' gestation (1991) (4)
DTPA in the management of iron overload in thalassaemia (1983) (4)
Thalassaemia, abnormal haemoglobins and iron deficiency in a British Asian population (2008) (4)
Audit of Prenatal Diagnosis for Hemoglobin Disorders in the United Kingdom: The First Twenty Years (1998) (4)
Thalassemia and its problems in Indonesia by the year 2000. (1988) (3)
Chorionic Villi Sampling in a High-Risk Population Using the Portex Cannula (1985) (3)
Historical overview of development in methods to estimate burden of disease due to congenital disorders (2018) (3)
Modelled epidemiological data for selected congenital disorders in South Africa (2021) (3)
New Developments in Genetics for the New Millennium: The Concept of Clinical Bioinformatics (2000) (3)
ANTENATAL SEARCH FOR β‐THALASSAEMIA IN A TWIN PREGNANCY. (1979) (3)
Giving the good news (2004) (3)
Ethical Issues in the Control of Genetic Diseases (1991) (3)
Code of Practice on Human Genetic Testing Services Supplied Direct to the Public (1998) (3)
Thalassaemia screening: ethics and practice (1989) (3)
Genetic screening for ethnic minorities: Author's reply (1990) (3)
THALASSEMIA IN AZERBAIJAN (1994) (3)
Diagnostic fetal blood sampling for the haemoglobinopathies--10-year experience. (1985) (2)
Social Aspects of First Trimester Diagnosis (1985) (2)
Review of control programs and future trends in the United Kingdom. (1988) (2)
TRANSABDOMINAL CHORIONIC VILLUS SAMPLING (1986) (2)
Alpha thalassemia hydrops fetalis in the UK: The importance of screening pregnant women of Chinese, other South East Asian and Mediterranean extraction for alpha thalassemia trait (1993) (1)
Impact and future of screening for haemoglobin disorders (1998) (1)
Antenatal search for fetal beta-thalassaemia in a twin pregnancy. (1979) (1)
Genetic screening for ethnic minorities (I: Reply) (1990) (1)
Biochemical neonatal screening. (1990) (1)
Methods to estimate access to care and the effect of interventions on the outcomes of congenital disorders (2018) (1)
Rate of change of sickle allele frequency may be influenced by total fertility rate: a sesquicentenary reflection on human micro‐evolution (2009) (1)
Methods to estimate access to care and the effect of interventions on the outcomes of congenital disorders (2018) (1)
Screening for carriers of recessive disease. (1983) (1)
Audit for prenatal diagnosis for haemoglobin disorders in the United Kingdom (1998) (1)
Carrier Screening for Inherited Hemoglobin Disorders in Cyprus and the United Kingdom (2006) (1)
Sickle Cell Disease (1988) (0)
The comparative value of prospective and retrospective fetal diagnosis in preventing inherited disease. (1985) (0)
An overview of concepts and approaches used in estimating the burden of congenital disorders globally (2017) (0)
An overview of concepts and approaches used in estimating the burden of congenital disorders globally (2017) (0)
ALPHA THALASSAEMIA MUTATION DATA TABLES (2013) (0)
[The deontology of prenatal diagnosis and genetic counseling]. (1991) (0)
Transcervical chorionic villus sampling. (1987) (0)
A review of key terminology and definitions used for birth defects globally. (2023) (0)
Obstetric outcome and problems of mid-trimester fetal blood sampling for antenatal diagnosis (1982) (0)
COST-BENEFIT ANALYSIS AND PRENATAL DIAGNOSIS (1989) (0)
Rare single gene disorders: estimating baseline prevalence and outcomes worldwide (2018) (0)
The method of chorion villus sampling under real-time ultrasound guidance using the 'Portex' cannula (1987) (0)
Rare single gene disorders: estimating baseline prevalence and outcomes worldwide (2018) (0)
AToolkit to assess health needs for congenital disorders in low- and middle-income countries: an instrument for public health action (2020) (0)
Presence of gene for beta globin in homozygous beta0 thalassaemia. (1976) (0)
The Accessible Publishing of Genetic Information (APoGI) web resource and international network. (2001) (0)
Historical overview of development in methods to estimate burden of disease due to congenital disorders (2018) (0)
Screening for Genetic Disease in the Community (1999) (0)
Antenatal diagnosis of beta-thalassaemia. (1983) (0)
Congenital disorders: epidemiological methods for answering calls for action (2018) (0)
Population Screening for Carriers of Recessively Inherited Disorders (1980) (0)
Addressing key issues in the consanguinity-related risk of autosomal recessive disorders in consanguineous communities: lessons from a qualitative study of British Pakistanis (2015) (0)
DEDICATED TO PROFESSOR RENZO GALANELLO (2013) (0)
DELTA BETA THALASSAEMIA AND HPFH MUTATION DATA TABLE (2013) (0)
A heartfelt "thank you" to all the reviewers of the Journal of Community Genetics in 2010 (2011) (0)
Examining the family-centred approach to genetic testing and counselling among UK Pakistanis: a community perspective (2012) (0)
DELTA THALASSAEMIA MUTATION TABLE (2013) (0)
Preventing congenital abnormalities: Authors' reply (1993) (0)
GLOBAL EPIDEMIOLOGY TABLES (2013) (0)
thalassaemia during pregnancy : audit from a Informed choice in genetic screening for (2000) (0)
Contents Vol. 3, 2000 (2001) (0)
THE PUBLISHERS-THALASSAEMIA INTERNATIONAL FEDERATION (TIF) (2013) (0)
NON-DELETIONAL HPFH MUTATION DATA TABLE (2013) (0)
Biochemical neonatal screening. Preconceptional and antenatal screening may be preferable in some cases (1990) (0)
BETA THALASSAEMIA MUTATION DATA TABLES (2013) (0)
Information delivery in primary care: deployment of information about rare genetic disorders (2001) (0)
Costs and benefits of antenatal screening for couples at risk of thalassaemia (1998) (0)
Chromosomal disorders: estimating baseline birth prevalence and pregnancy outcomes worldwide (2017) (0)
Chromosomal disorders: estimating baseline birth prevalence and pregnancy outcomes worldwide (2017) (0)
The Science behind Jeans for Genes Day: Teaching Packs for Primary (Key Stage 2) and Secondary (Key Stage 4) Schools (1998) (0)
Thefrequency ofconsanguineous marriage among (1988) (0)
Screening in practice : genetic scrrening for ethnic mimorities (1990) (0)
Subject Index Vol. 3, 2000 (2001) (0)
Chorionic Villi Sampling (1987) (0)
Reviews /Analyses Prevention andcontrol ofhaemoglobinopathies* (1995) (0)
TRANS-CERVICAL CHORIONIC VILLUS SAMPLING (1987) (0)
ANTENATAL DIAGNOSIS OF β‐THALASSAEMIA (1983) (0)
PREVENTING CONGENITAL-ABNORMALITIES - REPLY (1993) (0)
and Secondary (Key Stage 4) Schools Teaching Packs for Primary (Key Stage 2) The Science behind Jeans for Genes Day (2017) (0)
Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide (2018) (0)
ALPHA THALASSAEMIA MUTATIONS: FREQUENCY AND DISTRIBUTION TABLES (2013) (0)
Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide (2018) (0)
Haemoglobin disorders—a point of entry for community genetics services in India? (2019) (0)
From DNA to the Community: International Conference on Community Genetics, Jonquire, Qubec, June 2000 (2001) (0)
Proposal for a joint WHO/ICF-(M)A programme for neonatal screening for cystic fibrosis (1991) (0)

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