The importance of information and support following a suspected second‐trimester anomaly that is later discarded: A qualitative study of women's experiences by Lina Thirup, Puk Sandager, Ida Vogel, Stina Lou

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Danish Sonographers’ Experiences of the Introduction of “Moderate Risk” in Prenatal Screening for Down Syndrome by Anne Møller, Ida Vogel, Olav Bjørn Petersen, Stina Lou

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Parental experience of the diagnostic process and its role in the decision to terminate pregnancy due to fetal abnormality; A qualitative interview study by Maiken Fabricius Damm, Dorte Hvidtjoern, Puk Sandager, Ida Vogel, Christina Prinds, Stina Lou

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Impact of a prenatal screening program on the Down syndrome phenotype: An interrupted time series analysis by Ellen Hollands Steffensen, Lars Henning Pedersen, Stina Lou, Ida Vogel, The Danish Cytogenetic Central Registry Study Group

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A decade of change – lessons learned from prenatal diagnostics in Central Denmark region in 2008–2018 by Dorte Launholt Lildballe, Naja Becher, Else Marie Vestergaard, Rikke Christensen, Stina Lou, Puk Sandager, Lars Henning Pedersen, Kasper Gadsbøll, Olav Bjørn Petersen, Ida Vogel

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Maternal age and the risk of fetal aneuploidy: A nationwide cohort study of more than 500 000 singleton pregnancies in Denmark from 2008 to 2017 by Line Elmerdahl Frederiksen, Sofie Møller Ølgaard, Laura Roos, Olav Bjørn Petersen, Line Rode, Tanja Hartwig, Charlotte Kvist Ekelund, the Danish Central Cytogenetics Registry Study Group, Ida Vogel

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