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78 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.
Etiology and Prognosis of Severe Ventriculomegaly Diagnosed at Late Gestation.
Dall'Asta A, van Oostrum NHM, Basheer SN, Paramasivam G, Ghi T, Galli L, Groenenberg IA, Tangi A, Accorsi P, Echevarria M, Angeles Rodríguez Perez M, Albaiges Baiget G, Prefumo F, Frusca T, Go AT, Lees CC. Dall'Asta A, et al. Among authors: go at. Ultraschall Med. 2018 Dec;39(6):675-689. doi: 10.1055/a-0627-7173. Epub 2018 Jul 5. Ultraschall Med. 2018. PMID: 29975968 Free article. English.
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.
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.
Prenatal and postnatal findings in small-for-gestational-age fetuses without structural ultrasound anomalies at 18-24 weeks.
de Wit MC, Srebniak MI, Joosten M, Govaerts LC, Kornelisse RF, Papatsonis DN, de Graaff K, Knapen MF, Bruggenwirth HT, de Vries FA, Van Veen S, Van Opstal D, Galjaard RJ, Go AT. de Wit MC, et al. Among authors: go at. Ultrasound Obstet Gynecol. 2017 Mar;49(3):342-348. doi: 10.1002/uog.15949. Ultrasound Obstet Gynecol. 2017. PMID: 27102944 Free article.
Introduction of a nationwide first-trimester anomaly scan in the Dutch national screening program.
Lust EER, Bronsgeest K, Henneman L, Crombag N, Bilardo CM, Galjaard RH, Sikkel E, van der Hout S, Coumans A, Elvan-Taşpınar A, Go ATJI, Galjaard S, Manten GTR, Pajkrt E, van Leeuwen L, Haak MC, Bekker MN. Lust EER, et al. Among authors: go atji. Am J Obstet Gynecol. 2025 Apr;232(4):396.e1-396.e19. doi: 10.1016/j.ajog.2024.07.026. Epub 2024 Jul 25. Am J Obstet Gynecol. 2025. PMID: 39067498 Free article.
A novel family illustrating the mild phenotypic spectrum of TUBB2B variants.
Dekker J, Diderich KEM, Schot R, Husen SC, Dremmen MHG, Go ATJI, Weerts MJA, van Slegtenhorst MA, Mancini GMS. Dekker J, et al. Among authors: go atji. Eur J Paediatr Neurol. 2021 Nov;35:35-39. doi: 10.1016/j.ejpn.2021.09.007. Epub 2021 Sep 15. Eur J Paediatr Neurol. 2021. PMID: 34592644 Free article.
78 results