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Author Details

Lidewij Henneman
location Vrije Universiteit Amsterdam
1997
168
37
Vardit Ravitsky (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
38057584Psychological impact of additional findings detected by genome-wide Non-Invasive Prenatal Testing (NIPT): TRIDENT-2 study.Eur J Hum Genet2024
36097155Societal implications of expanded universal carrier screening: a scoping review.Eur J Hum Genet2023
37754777Attitudes of Patients with Adrenoleukodystrophy towards Sex-Specific Newborn Screening.Int J Neonatal Screen2023
37752446Informed choice and routinization of the second-trimester anomaly scan: a national cohort study in the Netherlands.BMC Pregnancy Childbirth2023
37143173Association between low fetal fraction in cell-free DNA screening and fetal chromosomal aberrations: A systematic review and meta-analysis.Prenat Diagn2023
37269059Current practice of first-trimester ultrasound screening for structural fetal anomalies in developed countries.Prenat Diagn2023
37268964A qualitative study on the perspectives of mothers who had been diagnosed with primary carnitine deficiency through newborn screening of their child.Orphanet J Rare Dis2023
36753831Conditions for autonomous reproductive decision-making in prenatal screening: A mixed methods study.Midwifery2023
36722294Primary care professionals' views on population-based expanded carrier screening: an online focus group study.Fam Pract2023
36740754A cross-country comparison of pregnant women's decision-making and perspectives when opting for non-invasive prenatal testing in the Netherlands and Belgium.Prenat Diagn2023
36575900Non-invasive prenatal testing for everybody or contingent screening?Prenat Diagn2023
36630060Expanded Non-invasive Prenatal Testing (NIPT) : Can the Child's Right to an Open Future Help Set the Scope?J Bioeth Inq2023
36109868Factors involved in the decision to decline prenatal screening with noninvasive prenatal testing (NIPT).Prenat Diagn2023
34385671Routinization of prenatal screening with the non-invasive prenatal test: pregnant women's perspectives.Eur J Hum Genet2022
35803237Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study.Am J Hum Genet2022
35734853Views of patients and parents of children with genetic disorders on population-based expanded carrier screening.Prenat Diagn2022
35727796Dynamics of reproductive genetic technologies: Perspectives of professional stakeholders.PLoS One2022
35499995Nationwide implementation of the non-invasive prenatal test: Evaluation of a blended learning program for counselors.PLoS One2022
35394817Noninvasive Prenatal Test Results Indicative of Maternal Malignancies: A Nationwide Genetic and Clinical Follow-Up Study.J Clin Oncol2022
35690368Patient perspectives on reproductive options for hereditary angioedema: A cross-sectional survey study.J Allergy Clin Immunol Pract2022
35659929Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study.Am J Hum Genet2022
35980961Parents' views on accepting, declining, and expanding newborn bloodspot screening.PLoS One2022
35087185Genetic diagnosis for rare diseases in the Dutch Caribbean: a qualitative study on the experiences and associated needs of parents.Eur J Hum Genet2022
34400811Non-invasive prenatal testing (NIPT) and pregnant women's views on good motherhood: a qualitative study.Eur J Hum Genet2022
32940388Preconception expanded carrier screening: Impact of information presented by text or video on genetic knowledge and attitudes.J Genet Couns2021
33652810Informing Parents about Newborn Screening: A European Comparison Study.Int J Neonatal Screen2021
33848430The Emergence and Global Spread of Noninvasive Prenatal Testing.Annu Rev Genomics Hum Genet2021
33754291Preconception expanded carrier screening: a focus group study with relatives of mucopolysaccharidosis type III patients and the general population.J Community Genet2021
33751485Clinical and community genetics services in the Dutch Caribbean.J Community Genet2021
34915793Economic evaluations of exome and genome sequencing in pediatric genetics: considerations towards a consensus strategy.J Med Econ2021
34426993Low fetal fraction in cell-free DNA testing is associated with adverse pregnancy outcome: Analysis of a subcohort of the TRIDENT-2 study.Prenat Diagn2021
34634131Preconception risk assessment for thalassaemia, sickle cell disease, cystic fibrosis and Tay-Sachs disease.Cochrane Database Syst Rev2021
34692604Expanding Neonatal Bloodspot Screening: A Multi-Stakeholder Perspective.Front Pediatr2021
34505288Non-invasive prenatal test uptake in socioeconomically disadvantaged neighborhoods.Prenat Diagn2021
34350596Association between low fetal fraction in cell-free DNA testing and adverse pregnancy outcome: A systematic review.Prenat Diagn2021
34155360Couples' experiences with expanded carrier screening: evaluation of a university hospital screening offer.Eur J Hum Genet2021
33191480In memoriam Prof. Dr. Leo P. ten Kate.J Community Genet2021
33074550Neonatal and carrier screening for rare diseases: how innovation challenges screening criteria worldwide.J Community Genet2021
33070266Parents' Perspectives and Societal Acceptance of Implementation of Newborn Screening for SCID in the Netherlands.J Clin Immunol2021
33465829Uptake of fetal aneuploidy screening after the introduction of the non-invasive prenatal test: A national population-based register study.Acta Obstet Gynecol Scand2021
32773775How will new genetic technologies, such as gene editing, change reproductive decision-making? Views of high-risk couples.Eur J Hum Genet2021
32483342Attitudes of relatives of mucopolysaccharidosis type III patients toward preconception expanded carrier screening.Eur J Hum Genet2020
33537639Effect of education and attitude on health professionals' knowledge on prenatal screening.Eur J Midwifery2020
31774570International perspectives on the implementation of reproductive carrier screening.Prenat Diagn2020
32415274Who ever heard of 16p11.2 deletion syndrome? Parents' perspectives on a susceptibility copy number variation syndrome.Eur J Hum Genet2020
32356934Benefit vs potential harm of genome-wide prenatal cfDNA testing requires further investigation and should not be dismissed based on current data.Ultrasound Obstet Gynecol2020
32109999Do Preferred Risk Formats Lead to Better Understanding? A Multicenter Controlled Trial on Communicating Familial Breast Cancer Risks Using Different Risk Formats.Patient Prefer Adherence2020
30563741Attitudes of the general population towards preconception expanded carrier screening for autosomal recessive disorders including inborn errors of metabolism.Mol Genet Metab2019
31781088Dilemma of Reporting Incidental Findings in Newborn Screening Programs for SCID: Parents' Perspective on Ataxia Telangiectasia.Front Immunol2019
31708118TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in the Netherlands.Am J Hum Genet2019
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Collaborators

Pascal Borry
Center for Biomedical Ethics and Law
Co-authored papers 11
Anneke Lucassen
Clinical Ethics, University of Oxford
Co-authored papers 6
A Cecile J W Janssens
Co-authored papers 6
Lyn S Chitty
UCL Institute of Child Health and Great Ormond Street NHS Foundation Trust
Co-authored papers 4
Christi J van Asperen
Leiden University Medical Center
Co-authored papers 4
H??lya Kayserili
Istanbul University
Co-authored papers 3
Annette C Moll
Cancer Center Amsterdam
Co-authored papers 3
Kelly E Ormond
Stanford University School of Medicine
Co-authored papers 3
Peter Heutink
German Center for Neurodegenerative Diseases (DZNE).
Co-authored papers 2
Fowzan S Alkuraya
King Faisal Specialist Hospital and Research Center
Co-authored papers 2
Marielle E van Gijn
University Medical Center Groningen
Co-authored papers 1
Marie-Christine Roy
Universite de Montreal.
Co-authored papers 1
Colleen M McBride
Rollins School of Public Health, Emory University
Co-authored papers 1
Vardit Ravitsky (CM4AI)
The Hastings Center
Co-authored papers 1
Meredith M Regan
Co-authored papers 1
Ben A Oostra
Co-authored papers 1
Muin J Khoury
Centers for Disease Control and Prevention Atlanta GA USA.
Co-authored papers 1
Ewout W Steyerberg
Leiden University Medical Center
Co-authored papers 1
Cornelia M van Duijn
University of Oxford
Co-authored papers 1
Meredith Vanstone
McMaster University
Co-authored papers 1
Wayne W Grody
David Geffen School of Medicine, university of california los angeles
Co-authored papers 1
Nigel G Laing
Harry Perkins Institute of Medical Research, University of Western Australia
Co-authored papers 1
Amira Masri
The University of Jordan
Co-authored papers 1
Tamar Nov-Klaiman
Ben-Gurion University of the Negev
Co-authored papers 1
Olivia M Y Ngan
Centre for Medical Ethics and Law, The University of Hong Kong
Co-authored papers 1
Ainsley J Newson
Sydney Health Ethics, Sydney School of Public Health, The University of Sydney
Co-authored papers 1
Sylvie Langlois
Research Center, Centre Hospitalier Universitaire Sainte-Justine
Co-authored papers 1
Paul D P Pharoah
Center for Cancer Genetic Epidemiology, University of Cambridge
Co-authored papers 1
Hazar Haidar
University of Quebec at Rimouski.
Co-authored papers 1
Patrizia Rizzu
German Center for Neurodegenerative Diseases
Co-authored papers 1
Release 1.2