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Acta Obstetricia Et Gynecologica Scandinavica|July 21, 2023
A decade of change - lessons learned from prenatal diagnostics in Central Denmark region in 2008-2018Dorte Launholt Lildballe, Naja Becher, Else Marie Vestergaard, et al.
Prenatal Diagnosis|July 8, 2026
Novel and High-Throughput Method of Isolating Single Fetal Cells Using FACS for NIPTRipudaman Singh, Bolette Hestbek Nicolaisen, Mathias Kølvraa, et al.
Prenatal Diagnosis|November 30, 2022
Noninvasive prenatal screening for cystic fibrosis using circulating trophoblasts: Detection of the 50 most common disease-causing variantsLine Dahl Jeppesen, Dorte Launholt Lildballe, Lotte Hatt, et al.
Frontiers in Genetics|April 1, 2022
Cell-Based NIPT Detects 47,XXY Genotype in a Twin PregnancyLine Dahl Jeppesen, Tina Duelund Hjortshøj, Johnny Hindkjær, et al.
Plos One|May 14, 2026
The impact of uncertainty on disclosure of prenatal exome sequencing results: A vignette study among medical studentsJasmijn E Klapwijk, Vyne Van der Schoot, Marike G Polak, et al.
American Journal of Human Genetics|April 15, 2008
Truncation of the Down syndrome candidate gene DYRK1A in two unrelated patients with microcephalyRikke S Møller, Sabine Kübart, Maria Hoeltzenbein, et al.
American Journal of Medical Genetics. Part A|March 23, 2017
Confirmation of CAGSSS syndrome as a distinct entity in a Danish patient with a novel homozygous mutation in IARS2Shahida Moosa, Annette Haagerup, Pernille Axel Gregersen, et al.
Clinical Case Reports|December 28, 2020
Cell-based noninvasive prenatal testing (cbNIPT) detects pathogenic copy number variationsLotte Hatt, Ripudaman Singh, Rikke Christensen, et al.
Placenta|September 16, 2020
First trimester biomarkers for prediction of gestational diabetes mellitusKinneret Tenenbaum-Gavish, Adi Sharabi-Nov, Dana Binyamin, et al.
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