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Pierpaolo Mastroiacovo

Biographic Data

ID6058171
NAMEPierpaolo Mastroiacovo
GIVEN NAMESPierpaolo
FAMILY NAMEMastroiacovo
SIGNATUREMASTROIACOVO P
AFFILIATIONSQueen Mary University of London
ORCID0000-0002-8318-8664
VERIFIEDYes
TOTAL WORKS7
TOTAL CITATIONS7
AUTHOR COUNT7
EDITOR COUNT0
FIRST PUBLICATION YEAR1996
LATEST PUBLICATION YEAR2018
H-INDEX1
  • Value of sharing and networking among birth defects surveillance programs

    Open Access•Eva Bermejo, Lorenzo D Botto et al.•ARTICLE•Journal of Community Genetics•2018

  • Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide

    Open Access•Sowmiya Moorthie, Hannah Blencowe et al.•ARTICLE•Journal of Community Genetics•2018

    Congenital anomaly registries have two main surveillance aims: firstly to define baseline epidemiology of important congenital anomalies to facilitate programme, policy and resource planning, and secondly to identify clusters of cases and any other epidemiological changes that could give early warning of environmental or infectious hazards. However, setting up a sustainable registry and surveillance system is resource-intensive requiring national…

  • An overview of concepts and approaches used in estimating the burden of congenital disorders globally

    Open Access•Sowmiya Moorthie, Hannah Blencowe et al.•ARTICLE•Journal of Community Genetics•2017

    Congenital disorders are an important cause of pregnancy loss, premature death and life-long disability. A range of interventions can greatly reduce their burden, but the absence of local epidemiological data on their prevalence and the impact of interventions impede policy and service development in many countries. In an attempt to overcome these deficiencies, we have developed a tool-The Modell Global Database of Congenital Disorders (MGDb) tha…

  • Chromosomal disorders

    Open Access•Sowmiya Moorthie, Hannah Blencowe et al.•ARTICLE•Journal of Community Genetics•2017

    Chromosomal disorders, of which Down syndrome is the most common, can cause multi-domain disability. In addition, compared to the general population, there is a higher frequency of death before the age of five. In many settings, large gaps in data availability have hampered policy-making, programme priorities and resource allocation for these important conditions. We have developed methods, which overcome this lack of data and allow estimation of…

  • Fostering International Collaboration in Birth Defects Research and Prevention

    Lorenzo D Botto, Elisabeth Robert-Gnansia et al.•ARTICLE•American Journal of Public Health•2006•References: 14

    The International Clearing-house for Birth Defects Surveillance and Research, formerly known as International Clearinghouse of Birth Defects Monitoring Systems, consists of 40 registries worldwide that collaborate in monitoring 40 types of birth defects. Clearinghouse activities include the sharing and joint monitoring of birth defect data, epidemiologic and public health research, and capacity building, with the goal of reducing disease and prom…

  • Infant mortality and congenital anomalies from 1950 to 1994

    Aldo Rosano, Lorenzo D Botto et al.•ARTICLE•Journal of Epidemiology and…•2000•Cited by: 7•References: 6

    STUDY OBJECTIVE: To provide an international perspective on the impact of congenital anomalies on infant mortality from 1950 to 1994. DESIGN: Population-based study based on data obtained from vital statistics reported to the World Health Organisation. SETTINGS: 36 countries from Europe, the Middle East, the Americas, Asia, and the South Pacific. RESULTS: On average, infant mortality declined 68.8 per cent from 1950 to 1994. In the countries stud…

  • What proportion of multiple births are due to ovulation induction? A register-based study in Italy

    Carlo Corchia, Pierpaolo Mastroiacovo et al.•ARTICLE•American Journal of Public Health•1996•References: 14

    OBJECTIVES: This study evaluated the increase in risk of multiple births associated with ovulation induction and calculated the proportion of multiple births attributable to this treatment. METHODS: Cases were 350 multiple births and controls were 737 single births enrolled from April 1993 to March 1994 in the Mercurio Project, an investigation of reproductive outcomes in Italy. RESULTS: Ovulation induction was used in 45 case births (12.9%) and …

  • Infant mortality and congenital anomalies from 1950 to 1994

    Aldo Rosano, Lorenzo D Botto et al.•ARTICLE•Journal of Epidemiology and…•2000•Cited by: 7•References: 6

    STUDY OBJECTIVE: To provide an international perspective on the impact of congenital anomalies on infant mortality from 1950 to 1994. DESIGN: Population-based study based on data obtained from vital statistics reported to the World Health Organisation. SETTINGS: 36 countries from Europe, the Middle East, the Americas, Asia, and the South Pacific. RESULTS: On average, infant mortality declined 68.8 per cent from 1950 to 1994. In the countries stud…

  • What proportion of multiple births are due to ovulation induction? A register-based study in Italy

    Carlo Corchia, Pierpaolo Mastroiacovo et al.•ARTICLE•American Journal of Public Health•1996•References: 14

    OBJECTIVES: This study evaluated the increase in risk of multiple births associated with ovulation induction and calculated the proportion of multiple births attributable to this treatment. METHODS: Cases were 350 multiple births and controls were 737 single births enrolled from April 1993 to March 1994 in the Mercurio Project, an investigation of reproductive outcomes in Italy. RESULTS: Ovulation induction was used in 45 case births (12.9%) and …

  • Infant mortality and congenital anomalies from 1950 to 1994

    Aldo Rosano, Lorenzo D Botto et al.•ARTICLE•Journal of Epidemiology and…•2000•Cited by: 7•References: 6

    STUDY OBJECTIVE: To provide an international perspective on the impact of congenital anomalies on infant mortality from 1950 to 1994. DESIGN: Population-based study based on data obtained from vital statistics reported to the World Health Organisation. SETTINGS: 36 countries from Europe, the Middle East, the Americas, Asia, and the South Pacific. RESULTS: On average, infant mortality declined 68.8 per cent from 1950 to 1994. In the countries stud…

  • Fostering International Collaboration in Birth Defects Research and Prevention

    Lorenzo D Botto, Elisabeth Robert-Gnansia et al.•ARTICLE•American Journal of Public Health•2006•References: 14

    The International Clearing-house for Birth Defects Surveillance and Research, formerly known as International Clearinghouse of Birth Defects Monitoring Systems, consists of 40 registries worldwide that collaborate in monitoring 40 types of birth defects. Clearinghouse activities include the sharing and joint monitoring of birth defect data, epidemiologic and public health research, and capacity building, with the goal of reducing disease and prom…

  • An overview of concepts and approaches used in estimating the burden of congenital disorders globally

    Open Access•Sowmiya Moorthie, Hannah Blencowe et al.•ARTICLE•Journal of Community Genetics•2017

    Congenital disorders are an important cause of pregnancy loss, premature death and life-long disability. A range of interventions can greatly reduce their burden, but the absence of local epidemiological data on their prevalence and the impact of interventions impede policy and service development in many countries. In an attempt to overcome these deficiencies, we have developed a tool-The Modell Global Database of Congenital Disorders (MGDb) tha…

  • Chromosomal disorders

    Open Access•Sowmiya Moorthie, Hannah Blencowe et al.•ARTICLE•Journal of Community Genetics•2017

    Chromosomal disorders, of which Down syndrome is the most common, can cause multi-domain disability. In addition, compared to the general population, there is a higher frequency of death before the age of five. In many settings, large gaps in data availability have hampered policy-making, programme priorities and resource allocation for these important conditions. We have developed methods, which overcome this lack of data and allow estimation of…

  • Value of sharing and networking among birth defects surveillance programs

    Open Access•Eva Bermejo, Lorenzo D Botto et al.•ARTICLE•Journal of Community Genetics•2018

  • Estimating the birth prevalence and pregnancy outcomes of congenital malformations worldwide

    Open Access•Sowmiya Moorthie, Hannah Blencowe et al.•ARTICLE•Journal of Community Genetics•2018

    Congenital anomaly registries have two main surveillance aims: firstly to define baseline epidemiology of important congenital anomalies to facilitate programme, policy and resource planning, and secondly to identify clusters of cases and any other epidemiological changes that could give early warning of environmental or infectious hazards. However, setting up a sustainable registry and surveillance system is resource-intensive requiring national…

Environmental health (7 works) · Medicine (7 works) · Pediatrics (5 works) · Public health (5 works) · Folate and B Vitamins Research (4 works) · Demography (3 works) · Epidemiology (3 works) · Pregnancy (3 works) · Assisted Reproductive Technology and Twin Pregnancy (2 works) · Child Nutrition and Water Access (2 works)

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