Lista de obras - Lidewij Henneman - Dominio Público Uruguay

A decade of molecular genetic testing for MODY: a retrospective study of utilization in The Netherlands

artículo científico publicado en 2014

Attitudes of cystic fibrosis patients and parents toward carrier screening and related reproductive issues

artículo científico publicado en 2015

Attitudes of general practitioners and midwives towards ethnicity-based haemoglobinopathy-carrier screening

artículo científico publicado en 2012

Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening

artículo científico publicado en 2014

Autosomal recessive disease in children of consanguineous parents: inferences from the proportion of compound heterozygotes

artículo científico publicado en 2010

Causal beliefs and perceptions of risk for diabetes and cardiovascular disease, The Netherlands, 2007.

artículo científico publicado en 2011

Challenges in the care for consanguineous couples: an exploratory interview study among general practitioners and midwives

artículo científico publicado en 2012

Changing to NIPT as a first-tier screening test and future perspectives: opinions of health professionals

artículo científico publicado en 2015

Comment on Gialluisi et al.

artículo científico publicado en 2013

Consanguineous marriage and reproductive risk: attitudes and understanding of ethnic groups practising consanguinity in Western society

artículo científico publicado en 2013

Consanguinity and endogamy in the Netherlands: demographic and medical genetic aspects

artículo científico publicado en 2014

Design of the BRISC study: a multicentre controlled clinical trial to optimize the communication of breast cancer risks in genetic counselling

artículo científico publicado en 2008

Developing a framework for implementation of genetic services: learning from examples of testing for monogenic forms of common diseases

artículo científico publicado en 2014

Direct-to-consumer carrier screening for cystic fibrosis via a hospital website: a 6-year evaluation

artículo científico publicado en 2018

Do Health Professionals Need Additional Competencies for Stratified Cancer Prevention Based on Genetic Risk Profiling?

artículo científico publicado en 2015

Do consanguineous parents of a child affected by an autosomal recessive disease have more DNA identical-by-descent than similarly-related parents with healthy offspring? Design of a case-control study

artículo científico publicado en 2010

Do people from the Jewish community prefer ancestry-based or pan-ethnic expanded carrier screening?

artículo científico publicado en 2015

Effect of comprehensive oncogenetics training interventions for general practitioners, evaluated at multiple performance levels

artículo científico publicado en 2015

Effectiveness of oncogenetics training on general practitioners' consultation skills: a randomized controlled trial

artículo científico publicado en 2013

Ethnic differences and parental beliefs are important for overweight prevention and management in children: a cross-sectional study in the Netherlands

artículo científico publicado en 2012

Ethnicity, educational level and attitudes contribute to parental intentions about genetic testing for child obesity

artículo científico publicado en 2013

Evaluation of cystic fibrosis carrier screening programs according to genetic screening criteria

artículo científico publicado en 2002

Factors for successful implementation of population-based expanded carrier screening: learning from existing initiatives

artículo científico publicado en 2016

Family history of diabetes: exploring perceptions of people at risk in the Netherlands

artículo científico publicado en 2009

Fatalistic responses to different types of genetic risk information: exploring the role of self-malleability

artículo científico publicado en 2010

Genetic educational needs and the role of genetics in primary care: a focus group study with multiple perspectives

artículo científico publicado en 2011

How does a simple enquiry compare to a detailed family history questionnaire to identify coronary heart disease or diabetic familial risk?

artículo científico publicado en 2011

How will new genetic technologies, such as gene editing, change reproductive decision-making? Views of high-risk couples

artículo científico publicado en 2020

Impact of communicating familial risk of diabetes on illness perceptions and self-reported behavioral outcomes: a randomized controlled trial

artículo científico publicado en 2009

Implementing non-invasive prenatal testing for aneuploidy in a national healthcare system: global challenges and national solutions

artículo científico publicado en 2017

International perspectives on the implementation of reproductive carrier screening

scientific article published on 29 November 2019

Lay perceptions of predictive testing for diabetes based on DNA test results versus family history assessment: a focus group study

artículo científico publicado en 2011

Maternal Plasma DNA and RNA Sequencing for Prenatal Testing

artículo científico publicado en 2016

Mothers' Views on Longer Storage of Neonatal Dried Blood Spots for Specific Secondary Uses

artículo científico publicado en 2015

Neonatal and carrier screening for rare diseases: how innovation challenges screening criteria worldwide

artículo científico publicado en 2020

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

artículo científico publicado en 2015

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations

Opinions of maternity care professionals and other stakeholders about integration of maternity care: a qualitative study in the Netherlands

artículo científico publicado en 2016

Parents' perceived vulnerability and perceived control in preventing Meningococcal C infection: a large-scale interview study about vaccination

artículo científico publicado en 2008

Preconceptional ancestry-based carrier couple screening for cystic fibrosis and haemoglobinopathies: what determines the intention to participate or not and actual participation?

artículo científico publicado en 2009

Preconceptional genetic carrier testing and the commercial offer directly-to-consumers

artículo científico publicado en 2011

Present to future: what the reasons for declining first-trimester combined testing tell us about accepting or declining cell-free DNA testing

artículo científico publicado en 2016

Presenting health risk information in different formats: the effect on participants' cognitive and emotional evaluation and decisions

artículo científico publicado en 2008

Prioritization of future genetics education for general practitioners: a Delphi study

artículo científico publicado en 2012

Public attitudes towards genetic testing revisited: comparing opinions between 2002 and 2010

artículo científico publicado en 2012

Public experiences, knowledge and expectations about medical genetics and the use of genetic information.

artículo científico publicado en 2004

Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics

artículo científico publicado en 2013

Responsible implementation of expanded carrier screening

artículo científico publicado en 2016

Responsible implementation of expanded carrier screening

artículo científico publicado en 2017

Screening for Familial Hypercholesterolemia in Children: What Can We Learn From Adult Screening Programs?

artículo científico publicado en 2015

Stakeholder perspectives on the implementation of genetic carrier screening in a changing landscape

artículo científico publicado en 2017

Sustained effects of online genetics education: a randomized controlled trial on oncogenetics

artículo científico publicado en 2013

The effectiveness of a graphical presentation in addition to a frequency format in the context of familial breast cancer risk communication: a multicenter controlled trial

artículo científico publicado en 2013

Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part I-clinical impact

artículo científico publicado en 2016

Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part II-women's perspectives

scientific article published on 14 October 2016

Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands

artículo científico publicado en 2016

Using family history information to promote healthy lifestyles and prevent diseases; a discussion of the evidence

artículo científico publicado en 2010

Using web-based familial risk information for diabetes prevention: a randomized controlled trial

artículo científico publicado en 2013

What Do Parents of Children with Down Syndrome Think about Non-Invasive Prenatal Testing (NIPT)?

artículo científico publicado en 2016

What do people want to know about NIPT? Content analysis of questions emailed to national NIPT information websites

artículo científico publicado en 2017

With expanded carrier screening, founder populations run the risk of being overlooked

artículo científico publicado en 2017

Women's Experience with Non-Invasive Prenatal Testing and Emotional Well-being and Satisfaction after Test-Results.

artículo científico publicado en 2017

Lista de obras de Lidewij Henneman

A decade of molecular genetic testing for MODY: a retrospective study of utilization in The Netherlands

Attitudes of cystic fibrosis patients and parents toward carrier screening and related reproductive issues

Attitudes of general practitioners and midwives towards ethnicity-based haemoglobinopathy-carrier screening

Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening

Autosomal recessive disease in children of consanguineous parents: inferences from the proportion of compound heterozygotes

Causal beliefs and perceptions of risk for diabetes and cardiovascular disease, The Netherlands, 2007.

Challenges in the care for consanguineous couples: an exploratory interview study among general practitioners and midwives

Changing to NIPT as a first-tier screening test and future perspectives: opinions of health professionals

Comment on Gialluisi et al.

Consanguineous marriage and reproductive risk: attitudes and understanding of ethnic groups practising consanguinity in Western society

Consanguinity and endogamy in the Netherlands: demographic and medical genetic aspects

Design of the BRISC study: a multicentre controlled clinical trial to optimize the communication of breast cancer risks in genetic counselling

Developing a framework for implementation of genetic services: learning from examples of testing for monogenic forms of common diseases

Direct-to-consumer carrier screening for cystic fibrosis via a hospital website: a 6-year evaluation

Do Health Professionals Need Additional Competencies for Stratified Cancer Prevention Based on Genetic Risk Profiling?

Do consanguineous parents of a child affected by an autosomal recessive disease have more DNA identical-by-descent than similarly-related parents with healthy offspring? Design of a case-control study

Do people from the Jewish community prefer ancestry-based or pan-ethnic expanded carrier screening?

Effect of comprehensive oncogenetics training interventions for general practitioners, evaluated at multiple performance levels

Effectiveness of oncogenetics training on general practitioners' consultation skills: a randomized controlled trial

Ethnic differences and parental beliefs are important for overweight prevention and management in children: a cross-sectional study in the Netherlands

Ethnicity, educational level and attitudes contribute to parental intentions about genetic testing for child obesity

Evaluation of cystic fibrosis carrier screening programs according to genetic screening criteria

Factors for successful implementation of population-based expanded carrier screening: learning from existing initiatives

Family history of diabetes: exploring perceptions of people at risk in the Netherlands

Fatalistic responses to different types of genetic risk information: exploring the role of self-malleability

Genetic educational needs and the role of genetics in primary care: a focus group study with multiple perspectives

How does a simple enquiry compare to a detailed family history questionnaire to identify coronary heart disease or diabetic familial risk?

How will new genetic technologies, such as gene editing, change reproductive decision-making? Views of high-risk couples

Impact of communicating familial risk of diabetes on illness perceptions and self-reported behavioral outcomes: a randomized controlled trial

Implementing non-invasive prenatal testing for aneuploidy in a national healthcare system: global challenges and national solutions

International perspectives on the implementation of reproductive carrier screening

Lay perceptions of predictive testing for diabetes based on DNA test results versus family history assessment: a focus group study

Maternal Plasma DNA and RNA Sequencing for Prenatal Testing

Mothers' Views on Longer Storage of Neonatal Dried Blood Spots for Specific Secondary Uses

Neonatal and carrier screening for rare diseases: how innovation challenges screening criteria worldwide

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening

Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. Summary and recommendations

Opinions of maternity care professionals and other stakeholders about integration of maternity care: a qualitative study in the Netherlands

Parents' perceived vulnerability and perceived control in preventing Meningococcal C infection: a large-scale interview study about vaccination

Preconceptional ancestry-based carrier couple screening for cystic fibrosis and haemoglobinopathies: what determines the intention to participate or not and actual participation?

Preconceptional genetic carrier testing and the commercial offer directly-to-consumers

Present to future: what the reasons for declining first-trimester combined testing tell us about accepting or declining cell-free DNA testing

Presenting health risk information in different formats: the effect on participants' cognitive and emotional evaluation and decisions

Prioritization of future genetics education for general practitioners: a Delphi study

Public attitudes towards genetic testing revisited: comparing opinions between 2002 and 2010

Public experiences, knowledge and expectations about medical genetics and the use of genetic information.

Reflecting on earlier experiences with unsolicited findings: points to consider for next-generation sequencing and informed consent in diagnostics

Responsible implementation of expanded carrier screening

Responsible implementation of expanded carrier screening

Screening for Familial Hypercholesterolemia in Children: What Can We Learn From Adult Screening Programs?

Stakeholder perspectives on the implementation of genetic carrier screening in a changing landscape

Sustained effects of online genetics education: a randomized controlled trial on oncogenetics

The effectiveness of a graphical presentation in addition to a frequency format in the context of familial breast cancer risk communication: a multicenter controlled trial

Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part I-clinical impact

Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part II-women's perspectives

Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands

Using family history information to promote healthy lifestyles and prevent diseases; a discussion of the evidence

Using web-based familial risk information for diabetes prevention: a randomized controlled trial

What Do Parents of Children with Down Syndrome Think about Non-Invasive Prenatal Testing (NIPT)?

What do people want to know about NIPT? Content analysis of questions emailed to national NIPT information websites

With expanded carrier screening, founder populations run the risk of being overlooked

Women's Experience with Non-Invasive Prenatal Testing and Emotional Well-being and Satisfaction after Test-Results.