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Do we care? Reporting of genetic diagnoses in multidisciplinary intellectual disability care: a retrospective chart review.
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- Orphanet Journal of Rare Diseases, 2024, v. 19, n. 1, p. 1, doi. 10.1186/s13023-024-03323-6
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- Article
Rapid exome sequencing as a first-tier test in neonates with suspected genetic disorder: results of a prospective multicenter clinical utility study in the Netherlands.
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- European Journal of Pediatrics, 2023, v. 182, n. 6, p. 2683, doi. 10.1007/s00431-023-04909-1
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- Article
Do Preferred Risk Formats Lead to Better Understanding? A Multicenter Controlled Trial on Communicating Familial Breast Cancer Risks Using Different Risk Formats.
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- Patient Preference & Adherence, 2020, v. 14, p. 333, doi. 10.2147/PPA.S232941
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- Article
Mothers' Views on Longer Storage of Neonatal Dried Blood Spots for Specific Secondary Uses.
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- Public Health Genomics, 2016, v. 19, n. 1, p. 25, doi. 10.1159/000441516
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- Article
Current and Best Practices of Genetic Testing for Maturity Onset Diabetes of the Young: Views of Professional Experts.
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- Public Health Genomics, 2015, v. 18, n. 1, p. 52, doi. 10.1159/000367963
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- Article
Preconception expanded carrier screening: Impact of information presented by text or video on genetic knowledge and attitudes.
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- Journal of Genetic Counseling, 2021, v. 30, n. 2, p. 457, doi. 10.1002/jgc4.1332
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- Article
Experiences of a High-Risk Population with Prenatal Hemoglobinopathy Carrier Screening in a Primary Care Setting: a Qualitative Study.
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- Journal of Genetic Counseling, 2018, v. 27, n. 3, p. 635, doi. 10.1007/s10897-017-0159-7
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- Article
Women's Experience with Non-Invasive Prenatal Testing and Emotional Well-being and Satisfaction after Test-Results.
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- Journal of Genetic Counseling, 2017, v. 26, n. 6, p. 1348, doi. 10.1007/s10897-017-0118-3
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- Article
What Do Parents of Children with Down Syndrome Think about Non-Invasive Prenatal Testing (NIPT)?
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- Journal of Genetic Counseling, 2017, v. 26, n. 3, p. 522, doi. 10.1007/s10897-016-0012-4
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- Article
Consanguinity and Endogamy in the Netherlands: Demographic and Medical Genetic Aspects.
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- Human Heredity, 2014, v. 77, n. 1-4, p. 161, doi. 10.1159/000360761
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- Article
An ESHG–ESHRE survey on the current practice of expanded carrier screening in medically assisted reproduction.
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- Human Reproduction, 2024, v. 39, n. 8, p. 1844, doi. 10.1093/humrep/deae131
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- Article
Preconceptional genetic carrier testing and the commercial offer directly-to-consumers.
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- 2011
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- Publication type:
- journal article
Debating the clinical utility of direct-to-consumer genetic testing for addiction susceptibility.
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- Addiction, 2012, v. 107, n. 12, p. 2076, doi. 10.1111/j.1360-0443.2012.03939.x
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- Article
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
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- European Journal of Human Genetics, 2015, v. 23, n. 11, p. 1438, doi. 10.1038/ejhg.2015.57
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- Article
Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening.
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- European Journal of Human Genetics, 2015, v. 23, n. 11, p. 1592, doi. 10.1038/ejhg.2015.109
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- Article
A decade of molecular genetic testing for MODY: a retrospective study of utilization in The Netherlands.
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- European Journal of Human Genetics, 2015, v. 23, n. 1, p. 29, doi. 10.1038/ejhg.2014.59
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- Article
Attitudes of pregnant women and male partners towards non-invasive prenatal testing and widening the scope of prenatal screening.
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- European Journal of Human Genetics, 2014, v. 22, n. 12, p. 1345, doi. 10.1038/ejhg.2014.32
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- Article
Consanguineous marriage and reproductive risk: attitudes and understanding of ethnic groups practising consanguinity in Western society.
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- European Journal of Human Genetics, 2014, v. 22, n. 4, p. 452, doi. 10.1038/ejhg.2013.167
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- Article
Sustained effects of online genetics education: a randomized controlled trial on oncogenetics.
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- European Journal of Human Genetics, 2014, v. 22, n. 3, p. 310, doi. 10.1038/ejhg.2013.163
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- Article
Comment on Gialluisi et al.
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- European Journal of Human Genetics, 2014, v. 22, n. 2, p. 157, doi. 10.1038/ejhg.2013.152
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- Article
Public attitudes towards genetic testing revisited: comparing opinions between 2002 and 2010.
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- European Journal of Human Genetics, 2013, v. 21, n. 8, p. 793, doi. 10.1038/ejhg.2012.271
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- Article
Parents' views on accepting, declining, and expanding newborn bloodspot screening.
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- PLoS ONE, 2022, v. 17, n. 8, p. 1, doi. 10.1371/journal.pone.0272585
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- Article
Dynamics of reproductive genetic technologies: Perspectives of professional stakeholders.
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- PLoS ONE, 2022, v. 17, n. 6, p. 1, doi. 10.1371/journal.pone.0269719
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- Article
Nationwide implementation of the non-invasive prenatal test: Evaluation of a blended learning program for counselors.
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- PLoS ONE, 2022, v. 17, n. 5, p. 1, doi. 10.1371/journal.pone.0267865
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- Article
Perspectives of pregnant women on broadening the scope of noninvasive prenatal testing from screening for foetal aneuploidies to prediction of adverse pregnancy outcomes: A qualitative study.
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- Prenatal Diagnosis, 2024, v. 44, n. 9, p. 1033, doi. 10.1002/pd.6621
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- Article
Current practice of first‐trimester ultrasound screening for structural fetal anomalies in developed countries.
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- Prenatal Diagnosis, 2023, v. 43, n. 7, p. 873, doi. 10.1002/pd.6389
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- Article
Association between low fetal fraction in cell‐free DNA screening and fetal chromosomal aberrations: A systematic review and meta‐analysis.
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- Prenatal Diagnosis, 2023, v. 43, n. 7, p. 838, doi. 10.1002/pd.6366
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- Article
Non‐invasive prenatal testing for everybody or contingent screening?
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- Prenatal Diagnosis, 2023, v. 43, n. 4, p. 443, doi. 10.1002/pd.6296
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- Article
Factors involved in the decision to decline prenatal screening with noninvasive prenatal testing (NIPT).
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- Prenatal Diagnosis, 2023, v. 43, n. 4, p. 467, doi. 10.1002/pd.6242
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- Article
A cross‐country comparison of pregnant women's decision‐making and perspectives when opting for non‐invasive prenatal testing in the Netherlands and Belgium.
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- Prenatal Diagnosis, 2023, v. 43, n. 3, p. 294, doi. 10.1002/pd.6329
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- Article
Views of patients and parents of children with genetic disorders on population-based expanded carrier screening.
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- 2022
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- Publication type:
- journal article
Non‐invasive prenatal test uptake in socioeconomically disadvantaged neighborhoods.
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- Prenatal Diagnosis, 2021, v. 41, n. 11, p. 1395, doi. 10.1002/pd.6043
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- Article
Low fetal fraction in cell‐free DNA testing is associated with adverse pregnancy outcome: Analysis of a subcohort of the TRIDENT‐2 study.
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- Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1296, doi. 10.1002/pd.6034
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- Article
Association between low fetal fraction in cell‐free DNA testing and adverse pregnancy outcome: A systematic review.
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- Prenatal Diagnosis, 2021, v. 41, n. 10, p. 1287, doi. 10.1002/pd.6028
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- Article
International perspectives on the implementation of reproductive carrier screening.
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- 2020
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- Publication type:
- journal article
What do people want to know about NIPT? Content analysis of questions emailed to national NIPT information websites.
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- 2017
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- Publication type:
- letter
Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part II-women's perspectives.
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- 2016
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- Publication type:
- journal article
Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part I-clinical impact.
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- 2016
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- Publication type:
- journal article
Present to future: what the reasons for declining first-trimester combined testing tell us about accepting or declining cell-free DNA testing.
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- 2016
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- Publication type:
- journal article
Changing to NIPT as a first-tier screening test and future perspectives: opinions of health professionals.
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- 2015
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- Publication type:
- journal article
NIPT-based screening for Down syndrome and beyond: what do pregnant women think?
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- Prenatal Diagnosis, 2015, v. 35, n. 6, p. 598, doi. 10.1002/pd.4579
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- Publication type:
- Article
Genetic Screening—Emerging Issues.
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- Genes, 2024, v. 15, n. 5, p. 581, doi. 10.3390/genes15050581
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- Article
Prioriteit voor implementatie van genetische testen met bewezen klinisch nut.
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- TSG: Tijdschrift Voor Gezondheidswetenschappen, 2013, v. 91, n. 2, p. 84, doi. 10.1007/s12508-013-0029-0
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- Article
Attitudes of general practitioners and midwives towards ethnicity-based haemoglobinopathy-carrier screening.
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- European Journal of Human Genetics, 2012, v. 20, n. 11, p. 1112, doi. 10.1038/ejhg.2012.72
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- Article
Preconceptional ancestry-based carrier couple screening for cystic fibrosis and haemoglobinopathies: what determines the intention to participate or not and actual participation?
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- European Journal of Human Genetics, 2009, v. 17, n. 8, p. 999, doi. 10.1038/ejhg.2009.1
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- Article
Challenges in the care for consanguineous couples: an exploratory interview study among general practitioners and midwives.
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- BMC Family Practice, 2012, v. 13, n. 1, p. 105, doi. 10.1186/1471-2296-13-105
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- Article
Genetic educational needs and the role of genetics in primary care: a focus group study with multiple perspectives.
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- BMC Family Practice, 2011, v. 12, n. 1, p. 5, doi. 10.1186/1471-2296-12-5
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- Publication type:
- Article
Parents' Perspectives and Societal Acceptance of Implementation of Newborn Screening for SCID in the Netherlands.
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- Journal of Clinical Immunology, 2021, v. 41, n. 1, p. 99, doi. 10.1007/s10875-020-00886-4
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- Article
Uptake of prenatal diagnostic testing for retinoblastoma compared to other hereditary cancer syndromes in the Netherlands.
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- Familial Cancer, 2017, v. 16, n. 2, p. 271, doi. 10.1007/s10689-016-9943-z
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- Article
Informing family members of individuals with Lynch syndrome: a guideline for clinical geneticists.
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- Familial Cancer, 2013, v. 12, n. 2, p. 319, doi. 10.1007/s10689-013-9636-9
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- Publication type:
- Article