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60 results

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Page 1
Clinical impact of additional findings detected by genome-wide non-invasive prenatal testing: Follow-up results of the TRIDENT-2 study.
van Prooyen Schuurman L, Sistermans EA, Van Opstal D, Henneman L, Bekker MN, Bax CJ, Pieters MJ, Bouman K, de Munnik S, den Hollander NS, Diderich KEM, Faas BHW, Feenstra I, Go ATJI, Hoffer MJV, Joosten M, Komdeur FL, Lichtenbelt KD, Lombardi MP, Polak MG, Jehee FS, Schuring-Blom H, Stevens SJC, Srebniak MI, Suijkerbuijk RF, Tan-Sindhunata GM, van der Meij KRM, van Maarle MC, Vernimmen V, van Zelderen-Bhola SL, van Ravesteyn NT, Knapen MFCM, Macville MVE, Galjaard RH; Dutch NIPT consortium. van Prooyen Schuurman L, et al. Among authors: go atji. Am J Hum Genet. 2022 Jun 2;109(6):1140-1152. doi: 10.1016/j.ajhg.2022.04.018. Am J Hum Genet. 2022. PMID: 35659929 Free PMC article.
Chorionic Villus Sampling for Rapid Confirmation of High-Risk NIPT Results for Trisomy 21, 18, and 13.
Srebniak MI, Weerts M, Joosten M, Drost M, Galjaard RJ, van der Schoot V, van den Born M, Knapen MFCM, Prinsen K, Cornette JMJ, DeKoninck PLJ, Papatsonis D, Spaan J, Dijkman A, de Weerd S, Go ATJI, Diderich KEM, Van Opstal D. Srebniak MI, et al. Among authors: go atji. Prenat Diagn. 2025 Jul;45(8):988-993. doi: 10.1002/pd.6837. Epub 2025 Jun 17. Prenat Diagn. 2025. PMID: 40528522 Free PMC article.
The High Diagnostic Yield of Prenatal Exome Sequencing Followed by 3400 Gene Panel Analysis in 629 Ongoing Pregnancies With Ultrasound Anomalies.
Diderich KEM, Bruggenwirth HT, Joosten M, Thurik F, Mijalkovic J, Polak M, Kromosoeto J, Somers-Bolman GM, van den Born M, Drost M, Galjaard RJH, Galjaard S, Hoefsloot LH, Knapen MFCM, van Minkelen R, van der Schoot V, van Slegtenhorst MA, Sleutels F, Stuurman KE, Weerts MJA, Go ATJI, Wilke M, Srebniak MI. Diderich KEM, et al. Among authors: go atji. Prenat Diagn. 2024 Nov;44(12):1444-1450. doi: 10.1002/pd.6676. Epub 2024 Sep 30. Prenat Diagn. 2024. PMID: 39349395
Prenatal cell-free DNA testing of women with pregnancy-associated cancer: a retrospective cross-sectional study.
Heesterbeek CJ, Tjan-Heijnen VCG, Heimovaara JH, Lenaerts L, Lok C, Vriens IJH, Van Opstal D, Boon EMJ, Sie D, de Die-Smulders CEM, Amant F, Macville MVE; Dutch NIPT Consortium. Heesterbeek CJ, et al. Lancet Reg Health Eur. 2024 Aug 7;45:101024. doi: 10.1016/j.lanepe.2024.101024. eCollection 2024 Oct. Lancet Reg Health Eur. 2024. PMID: 39220433 Free PMC article.
Novel biomarkers in preeclampsia.
Smets EM, Visser A, Go AT, van Vugt JM, Oudejans CB. Smets EM, et al. Clin Chim Acta. 2006 Feb;364(1-2):22-32. doi: 10.1016/j.cca.2005.06.011. Epub 2005 Sep 1. Clin Chim Acta. 2006. PMID: 16139262 Review.
Whole-genome array as a first-line cytogenetic test in prenatal diagnosis.
Srebniak MI, Van Opstal D, Joosten M, Diderich KE, de Vries FA, Riedijk S, Knapen MF, Go AT, Govaerts LC, Galjaard RJ. Srebniak MI, et al. Ultrasound Obstet Gynecol. 2015 Apr;45(4):363-72. doi: 10.1002/uog.14745. Ultrasound Obstet Gynecol. 2015. PMID: 25488734 Free article. No abstract available.
60 results