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Expert Review of Molecular Diagnostics Volume 14, 2014 - Issue 5
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Editorial

Introducing WISECONDOR for noninvasive prenatal diagnostics

Roy StraverDelft Bioinformatics Lab, Delft University of Technology, Mekelweg 4, 2628 CD Delft, The Netherlands;Department of Clinical Genetics, VU University Medical Center Amsterdam, van der Boechorststraat 7 (BS7/J377), 1081 BT Amsterdam, The Netherlands
,
Erik A SistermansDepartment of Clinical Genetics, VU University Medical Center Amsterdam, van der Boechorststraat 7 (BS7/J377), 1081 BT Amsterdam, The Netherlands
&
Marcel JT ReindersDelft Bioinformatics Lab, Delft University of Technology, Mekelweg 4, 2628 CD Delft, The NetherlandsCorrespondence[email protected]
Pages 513-515 | Published online: 16 May 2014

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Jean Gekas, Sylvie Langlois, Vardit Ravitsky, François Audibert, David Gradus van den Berg, Hazar Haidar & François Rousseau. (2016) Non-invasive prenatal testing for fetal chromosome abnormalities: review of clinical and ethical issues. The Application of Clinical Genetics 9, pages 15-26.
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Diane Van Opstal & Malgorzata I Srebniak. (2016) Cytogenetic confirmation of a positive NIPT result: evidence-based choice between chorionic villus sampling and amniocentesis depending on chromosome aberration. Expert Review of Molecular Diagnostics 16:5, pages 513-520.
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Articles from other publishers (11)

Mira N. MoufarrejDiana W. Bianchi, Gary M. Shaw, David K. Stevenson & Stephen R. Quake. (2023) Noninvasive Prenatal Testing Using Circulating DNA and RNA: Advances, Challenges, and Possibilities. Annual Review of Biomedical Data Science 6:1, pages 397-418.
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Maria Hammer Moellgaard, Ida Charlotte Bay Lund, Naja Becher, Anne‐Bine Skytte, Lotte Andreasen, Malgorzata Ilona Srebniak & Ida Vogel. (2022) Incidental finding of maternal malignancy in an unusual non‐invasive prenatal test and a review of similar cases. Clinical Case Reports 10:10.
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Amy E. Turriff, Christina M. Annunziata & Diana W. Bianchi. (2022) Prenatal DNA Sequencing for Fetal Aneuploidy Also Detects Maternal Cancer: Importance of Timely Workup and Management in Pregnant Women. Journal of Clinical Oncology 40:22, pages 2398-2401.
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Malgorzata I. Srebniak, Fernanda S. Jehee, Marieke Joosten, Marjan Boter, Walter G. Valk, Robert Helm, Erik A. Sistermans, Els Voorhoeve, Shama Bhola, Mariette J. V. Hoffer, Nicolette Hollander, Merryn V. E. Macville & Diane Opstal. (2021) Non‐invasive prenatal diagnosis for translocation carriers—YES please or NO go?. Acta Obstetricia et Gynecologica Scandinavica 100:11, pages 2036-2043.
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Malgorzata I. Srebniak, Maarten F.C.M. Knapen, Marike Polak, Marieke Joosten, Karin E.M. Diderich, Lutgarde C.P. Govaerts, Marjan Boter, Joan N.R. Kromosoeto, Daniella Aloysia C.M. van Hassel, Gido Huijbregts, Wilfred F.J. van IJcken, Roger Heydanus, Anneke Dijkman, Toon Toolenaar, Femke A.T. de Vries, Jeroen Knijnenburg, Attie T.J.I. Go, Robert-Jan H. Galjaard & Diane Van Opstal. (2017) The influence of SNP-based chromosomal microarray and NIPT on the diagnostic yield in 10,000 fetuses with and without fetal ultrasound anomalies. Human Mutation 38:7, pages 880-888.
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L. Beulen, B. H. W. Faas, I. Feenstra, J. M. G. van Vugt & M. N. Bekker. (2017) Clinical utility of non-invasive prenatal testing in pregnancies with ultrasound anomalies. Ultrasound in Obstetrics & Gynecology 49:6, pages 721-728.
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Tianjiao Chu, Patricia A. Shaw, Suveyda Yeniterzi, Mary Dunkel, Aleksander Rajkovic, W. Allen Hogge, Kimberly D. Bunce & David G. Peters. (2017) Comparative evaluation of the Minimally-Invasive Karyotyping (MINK) algorithm for non-invasive prenatal testing. PLOS ONE 12:3, pages e0171882.
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Annelies Dheedene, Tom Sante, Matthias De Smet, Jean‐François Vanbellinghen, Bernard Grisart, Sarah Vergult, Sandra Janssens & Björn Menten. (2016) Implementation of non‐invasive prenatal testing by semiconductor sequencing in a genetic laboratory. Prenatal Diagnosis 36:8, pages 699-707.
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Kornelia Neveling, Djie Tjwan Thung, Lean Beulen, Wendy van Rens-Buijsman, Ingrid Gomes, Simone van den Heuvel, Hanneke Mieloo, Irma Derks-Prinsen, Ellen Kater-Baats & Brigitte H. W. Faas. (2016) Validation of two-channel sequencing-by-synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations. Prenatal Diagnosis 36:3, pages 216-223.
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S. Drury, M. Hill & L.S. Chitty. 2016. 1 35 .
Wybo Dondorp, Guido de Wert, Yvonne Bombard, Diana W Bianchi, Carsten Bergmann, Pascal Borry, Lyn S Chitty, Florence Fellmann, Francesca Forzano, Alison Hall, Lidewij Henneman, Heidi C Howard, Anneke Lucassen, Kelly Ormond, Borut Peterlin, Dragica Radojkovic, Wolf Rogowski, Maria Soller, Aad Tibben, Lisbeth Tranebjærg, Carla G van El & Martina C Cornel. (2015) Non-invasive prenatal testing for aneuploidy and beyond: challenges of responsible innovation in prenatal screening. European Journal of Human Genetics 23:11, pages 1438-1450.
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