Erasmus School of Social and Behavioural Sciences
External PhD candidate | Brain & Cognition
More information
Work
- Jasmijn E. Klapwijk, Vyne Van der Schoot, Marike G. Polak, Stina Lou, Ida Vogel, Iris M. Jansen-Bakkeren, Karin E.M. Diderich, Katinka Dijkstra & Sam R. Riedijk (2026) - The impact of uncertainty on disclosure of prenatal exome sequencing results: A vignette study among medical students - PLoS ONE, 21 - doi: 10.1371/journal.pone.0349014 - [link]
- Karin E.M. Diderich, Jasmijn E. Klapwijk, Vyne van der Schoot, Myrthe van den Born, Martina Wilke, Marieke Joosten, Kyra E. Stuurman, Lies H. Hoefsloot, Diane Van Opstal, Hennie T. Brüggenwirth & Malgorzata I. Srebniak (2024) - Response to the comment on Diderich et al. “The role of a multidisciplinary team in managing variants of uncertain clinical significance in prenatal genetic diagnosis” (EJMG 66(10),104844) - European Journal of Medical Genetics, 67 - doi: 10.1016/j.ejmg.2023.104884 - [link]
- Karin E.M. Diderich, Jasmijn E. Klapwijk, Vyne van der Schoot, Myrthe van den Born, Martina Wilke, Marieke Joosten, Kyra E. Stuurman, Lies H. Hoefsloot, Diane Van Opstal, Hennie T. BrĂĽggenwirth & Malgorzata I. Srebniak (2023) - The role of a multidisciplinary team in managing variants of uncertain clinical significance in prenatal genetic diagnosis - European Journal of Medical Genetics, 66 (10) - doi: 10.1016/j.ejmg.2023.104844 - [link]
- Karin E.M. Diderich, Jasmijn E. Klapwijk, Vyne van der Schoot, Hennie T. BrĂĽggenwirth, Marieke Joosten & Malgorzata I. Srebniak (2023) - Challenges and Pragmatic Solutions in Pre-Test and Post-Test Genetic Counseling for Prenatal Exome Sequencing - Application of Clinical Genetics, 16, 89-97 - doi: 10.2147/TACG.S411185 - [link]
- James Buchanan, Melissa Hill, Caroline M. Vass, Jennifer Hammond, Sam Riedijk, Jasmijn E. Klapwijk, Eleanor Harding, Stina Lou, Ida Vogel, Lisa Hui, Charlotta Ingvoldstad-Malmgren, Maria Johansson Soller, Kelly E. Ormond, Mahesh Choolani, Qian Zheng, Lyn S. Chitty & Celine Lewis (2022) - Factors that impact on women's decision-making around prenatal genomic tests: An international discrete choice survey - Prenatal Diagnosis, 42 (7), 934-946 - doi: 10.1002/pd.6159 - [link]
- Jennifer Hammond, Jasmijn E. Klapwijk, Sam Riedijk, Stina Lou, Kelly E. Ormond, Ida Vogel, Lisa Hui, Emma Jane Sziepe, James Buchanan, Charlotta Ingvoldstad-Malmgren, Maria Johansson Soller, Eleanor Harding, Melissa Hill & Celine Lewis (2022) - Assessing women's preferences towards tests that may reveal uncertain results from prenatal genomic testing: Development of attributes for a discrete choice experiment, using a mixed-methods design - PLoS ONE, 17 (1 January) - doi: 10.1371/journal.pone.0261898 - [link]
- Karin E.M. Diderich, Jasmijn E. Klapwijk, Marieke Joosten, Hennie T. BrĂĽggenwirth & Malgorzata I. Srebniak (2022) - Whole-exome sequencing: A changing landscape of prenatal counseling - doi: 10.1016/B978-0-12-823329-0.00001-5 - [link]
- Jasmijn E. Klapwijk, Malgorzata I. Srebniak, Attie T.J.I. Go, Lutgarde C.P. Govaerts, Celine Lewis, Jennifer Hammond, Melissa Hill, Stina Lou, Ida Vogel, Kelly E. Ormond, Karin E.M. Diderich, Hennie T. BrĂĽggenwirth & Sam R. Riedijk (2021) - How to deal with uncertainty in prenatal genomics: A systematic review of guidelines and policies - Clinical Genetics, 100 (6), 647-658 - doi: 10.1111/cge.14010 - [link]
- Celine Lewis, Jennifer Hammond, Jasmijn E. Klapwijk, Eleanor Harding, Stina Lou, Ida Vogel, Emma J. Szepe, Lisa Hui, Charlotta Ingvoldstad-Malmgren, Maria J. Soller, Kelly E. Ormond, Mahesh Choolani, Melissa Hill & Sam Riedijk (2021) - Dealing with uncertain results from chromosomal microarray and exome sequencing in the prenatal setting: An international cross-sectional study with healthcare professionals - Prenatal Diagnosis, 41 (6), 720-732 - doi: 10.1002/pd.5932 - [link]
- J Hammond, Jasmijn Klapwijk, M Hill, S Lou, KE Ormond, Karin Diderich, Sam Riedijk & C Lewis (2021) - Parental experiences of uncertainty following an abnormal fetal anomaly scan: Insights using Han’s taxonomy of uncertainty - Journal of Genetic Counseling, 30 (1), 198-210 - doi: 10.1002/jgc4.1311 - [link]
