A.B.C. Coumans

Bronsgeest, K., Lust, E. E. R., Henneman, L., Crombag, N., Bilardo, C. M., Galjaard, R.-J. H., Sikkel, E., Van Geloven, N., Coumans, A. B. C., Elvan-Taspinar, A., Galjaard, S., Go, A. T. J. I., van Leeuwen, E., Manten, G. T. R., Pajkrt, E., Bekker, M. N., Haak, M. C., & IMITAS Study Group (2026). Dedicated First-Trimester Anomaly Scan in a National Prenatal Screening Program and Timing of Diagnosis: The Prospective IMITAS Cohort Study. Bjog-an International Journal of Obstetrics and Gynaecology, 133(7), 1373-1380. https://doi.org/10.1111/1471-0528.70192

Lust, E. E. R., Bronsgeest, K., Henneman, L., Crombag, N. M. T. H., Bilardo, C. M., Galjaard, R.-J. H., Sikkel, E., Coumans, A. B. C., Elvan-taspinar, A., Galjaard, S., Go, A. T. J. I., Manten, G. T. R., Pajkrt, E., van Leeuwen, E., Haak, M. C., & Bekker, M. N. (2026). Early versus late termination for fetal anomalies: Women's perspectives and psychological impact in a mixed methods study. Acta Obstetricia et Gynecologica Scandinavica, 105(3), 444-454. https://doi.org/10.1111/aogs.70122

Lust, E. E. R., Bronsgeest, K., Henneman, L., Crombag, N., Bilardo, C. M., Galjaard, R.-J. H., Sikkel, E., van der Hout, S., Coumans, A., Elvan-Taspinar, A., Go, A. T. J. I., Galjaard, S., Manten, G. T. R., Pajkrt, E., van Leeuwen, L., Haak, M. C., & Bekker, M. N. (2025). Introduction of a Nationwide First-Trimester Anomaly Scan in the Dutch National Screening Program. Obstetrical & Gynecological Survey, 80(10), 614-616. https://doi.org/10.1097/01.ogx.0001169608.98016.7a

Lust, E. E. R., Bronsgeest, K., Henneman, L., Crombag, N., Bilardo, C. M., Galjaard, R.-J. H., Sikkel, E., van der Hout, S., Coumans, A., Elvan-Taspinar, A., Go, A. T. J. I., Galjaard, S., Manten, G. T. R., Pajkrt, E., van Leeuwen, L., Haak, M. C., & Bekker, M. N. (2025). Introduction of a nationwide first-trimester anomaly scan in the Dutch national screening program. American Journal of Obstetrics and Gynecology, 232(4), 396.e1-396.e19. https://doi.org/10.1016/j.ajog.2024.07.026

Lust, E. E. R., Bronsgeest, K., Henneman, L., Crombag, N. M. T. H., Bilardo, C. M., Galjaard, R. H., Sikkel, E., Coumans, A. B. C., Elvan-taspinar, A., Galjaard, S., Go, A. T. J. I., Manten, G. T. R., Pajkrt, E., Van Leeuwen, E., Haak, M. C., & Bekker, M. N. (2025). Clinical Utility of Nuchal Translucency Measurement in First-Trimester Ultrasound Screening in a Setting With First-Tier NIPT for Aneuploidy Screening. Prenatal Diagnosis. Advance online publication. https://doi.org/10.1002/pd.70047

van Heurn, L. J., Coumans, A., Haak, M. C., van der Kaaij, A., van Heurn, L. W. E., Pajkrt, E., & Derikx, J. P. M. (2023). Prognostic accuracy of factors associated with poor outcome in prenatally diagnosed sacrococcygeal teratoma: A systematic review and meta-analysis. Prenatal Diagnosis, 43(12), 1495-1505. https://doi.org/10.1002/pd.6457

Faas, B. H. W., Westra, D., de Munnik, S. A., van Rij, M., Marcelis, C., Joosten, S., Krapels, I., Vernimmen, V., Heijligers, M., Willemsen, M. H., de Leeuw, N., Rinne, T., Pfundt, R., Smeekens, S. P., Stegmann, S. P. A., Macville, M., Sikkel, E., Coumans, A., Wijnberger, L., ... Feenstra, I. (2023). All-in-one whole exome sequencing strategy with simultaneous copy number variant, single nucleotide variant and absence-of-heterozygosity analysis in fetuses with structural ultrasound anomalies: A 1-year experience. Prenatal Diagnosis, 43(4), 527-543. https://doi.org/10.1002/pd.6314

Noben, L., Lempersz, C., van den Heuvel, E. R., Zhan, Z., Vandenbussche, F. P. H. A., Coumans, A. B. C., Haak, M. C., Vullings, R., Oei, S. G., Clur, S. A. B., & van Laar, J. O. E. H. (2022). The electrical heart axis in fetuses with congenital heart disease, measured with non-invasive fetal electrocardiography. PLOS ONE, 17(10), Article e0275802. https://doi.org/10.1371/journal.pone.0275802

Aukema, S. M., de Geus, C. M., Robben, S. G. F., van Kaam, K. J. A. F., Staal, H. M., Witlox, A. M., de la Haye, N. A. J., Klaassens, M., Coumans, A., Stegmann, A. P. A., Paley, D., & Stumpel, C. T. R. M. (2022). Tibia hemimelia in a patient with CHARGE syndrome: A rare but recurrent phenomenon. American Journal of Medical Genetics Part A, 188(3), 1000-1004. https://doi.org/10.1002/ajmg.a.62600

van Heurn, L. J., Coumans, A. B. C., Derikx, J. P. M., Bekker, M. N., Bilardo, K. M., Duin, L. K., Knapen, M. F. C. M., Pajkrt, E., Sikkel, E., van Heurn, L. W. E., & Oepkes, D. (2021). Factors associated with poor outcome in fetuses prenatally diagnosed with sacrococcygeal teratoma. Prenatal Diagnosis, 41(11), 1430-1438. https://doi.org/10.1002/pd.6026