Search Results - "van Opstal, D."

Frequency of submicroscopic chromosomal aberrations in pregnancies without increased risk for structural chromosomal aberrations: systematic review and meta‐analysis by Srebniak, M. I., Joosten, M., Knapen, M. F. C. M., Arends, L. R., Polak, M., van Veen, S., Go, A. T. J. I., Van Opstal, D.

“…ABSTRACT Objective To establish, based on a systematic literature review, the frequency of pathogenic submicroscopic chromosomal aberrations in fetuses that…”
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Preimplantation genetic screening reveals a high incidence of aneuploidy and mosaicism in embryos from young women undergoing IVF by Baart, E.B., Martini, E., van den Berg, I., Macklon, N.S., Galjaard, R-J.H., Fauser, B.C.J.M., Van Opstal, D.

“…BACKGROUND: In order to assess the frequency of aneuploidy and mosaicism in embryos obtained from IVF patients aged <38 years, preimplantation genetic…”
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Prenatal and postnatal findings in small‐for‐gestational‐age fetuses without structural ultrasound anomalies at 18–24 weeks by de Wit, M. C., Srebniak, M. I., Joosten, M., Govaerts, L. C. P., Kornelisse, R. F., Papatsonis, D. N. M., de Graaff, K., Knapen, M. F. C. M., Bruggenwirth, H. T., de Vries, F. A. T., Van Veen, S., Van Opstal, D., Galjaard, R. J. H., Go, A. T. J. I.

“…ABSTRACT Objective To assess phenotypic and genotypic characteristics of small‐for‐gestational‐age (SGA) fetuses without structural anomalies at 18–24 weeks'…”
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Choosing between Higher and Lower Resolution Microarrays: do Pregnant Women Have Sufficient Knowledge to Make Informed Choices Consistent with their Attitude? by van der Steen, S. L., Bunnik, E. M., Polak, M. G., Diderich, K. E. M., Verhagen-Visser, J., Govaerts, L. C. P., Joosten, M., Knapen, M. F. C. M., Go, A. T. J. I., Van Opstal, D., Srebniak, M. I., Galjaard, R. J. H., Tibben, A., Riedijk, S. R.

“…Developments in prenatal testing allow the detection of more findings. SNP arrays in prenatal diagnosis (PND) can be analyzed at 0.5 Mb resolution detecting…”
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Fluorescence in situ hybridization analysis of two blastomeres from day 3 frozen–thawed embryos followed by analysis of the remaining embryo on day 5 by Baart, E.B., Van Opstal, D., Los, F.J., Fauser, B.C.J.M., Martini, E.

“…BACKGROUND: Chromosomal mosaicism in human embryos may give rise to false positive or false negative results in preimplantation genetic diagnosis for…”
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FISH analysis of 15 chromosomes in human day 4 and 5 preimplantation embryos: the added value of extended aneuploidy detection by Baart, E. B., van den Berg, I., Martini, E., Eussen, H. J., Fauser, B. C. J. M., Opstal, D. Van

“…Objective Screening for an increased number of chromosomes may improve the detection of abnormal embryos and thus contribute to the capability of…”
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Additional value of prenatal genomic array testing in fetuses with isolated structural ultrasound abnormalities and a normal karyotype: a systematic review of the literature by de wit, M. C., Srebniak, M. I., Govaerts, L. C. P., Van Opstal, D., Galjaard, R. J. H., Go, A. T. J. I.

“…ABSTRACT OBJECTIVE To establish the prevalence of submicroscopic genetic copy number variants (CNVs) in fetuses with a structural ultrasound anomaly…”
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Confined placental mosaicism: Distribution of chromosomally abnormal cells over the term placenta by Eggenhuizen, G.M., van Veen, S., van Koetsveld, N., Go, A.T.J.I., Diderich, K.E.M., Joosten, M., van den Born, M., Srebniak, M.I., Van Opstal, D.

“…Non-invasive prenatal testing (NIPT) investigates placental DNA and may detect confined placental mosaicism (CPM). The aim of this study was to confirm CPM in…”
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Does confined placental mosaicism account for adverse perinatal outcomes in IVF pregnancies? by Jacod, B.C., Lichtenbelt, K.D., Schuring-Blom, G.H., Laven, J.S.E., van Opstal, D., Eijkemans, M.J.C., Macklon, N.S.

“…BACKGROUND IVF singletons have poorer perinatal outcomes than singletons from spontaneous conceptions. This may be due to the influence of ovarian stimulation…”
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Determination of the parent of origin in nine cases of prenatally detected chromosome aberrations found after intracytoplasmic sperm injection by Van Opstal, D, Los, F J, Ramlakhan, S, Van Hemel, J O, Van Den Ouweland, A M, Brandenburg, H, Pieters, M H, Verhoeff, A, Vermeer, M C, Dhont, M, In't Veld, P A

“…Prenatal cytogenetic analysis of 71 fetuses conceived by intracytoplasmic sperm injection (ICSI) resulted in the detection of nine (12.7%) chromosome…”
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Abnormal non‐invasive prenatal test results concordant with karyotype of cytotrophoblast but not reflecting abnormal fetal karyotype by Srebniak, M. I., Diderich, K. E. M., Noomen, P., Dijkman, A., de Vries, F. A. T., van Opstal, D.

“…ABSTRACT We present a unique case in which non‐invasive and invasive prenatal diagnoses showed abnormal, but discordant, results. A patient with abnormal…”
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P16.04: Prevalence of submicroscopic chromosome aberrations in pregnancies without increased risk for structural chromosome aberrations: a systematic review of the literature by Srebniak, M.I., Joosten, M., Knapen, M., Arends, L., Polak, M., Van Veen, S., Go, A., Van Opstal, D.

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Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing by van der Steen, S.L., Diderich, K.E.M., Riedijk, S.R., Verhagen-Visser, J., Govaerts, L.C.P., Joosten, M., Knapen, M.F.C.M., Van Opstal, D., Srebniak, M.I., Tibben, A., Galjaard, R.J.H.

“…Genomic array detects more pathogenic chromosome aberrations than conventional karyotyping (CK), including genetic variants associated with a susceptibility…”
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The Psychological Impact of Prenatal Diagnosis and Disclosure of Susceptibility Loci: First Impressions of Parents’ Experiences by van der Steen, S. L., Riedijk, S. R., Verhagen-Visser, J., Govaerts, L. C. P., Srebniak, M. I., Van Opstal, D., Joosten, M., Knapen, M. F. C. M., Tibben, A., Diderich, K. E. M., Galjaard, R. J. H.

“…Genomic microarray may detect susceptibility loci (SL) for neurodevelopmental disorders such as autism and epilepsy, with a yet unquantifiable risk for the…”
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Whole‐genome array as a first‐line cytogenetic test in prenatal diagnosis by Srebniak, M. I., Van Opstal, D., Joosten, M., Diderich, K. E. M., de Vries, F. A. T., Riedijk, S., Knapen, M. F. C. M., Go, A. T. J. I., Govaerts, L. C. P., Galjaard, R.‐J. H.

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Frequency of Submicroscopic Chromosomal Aberrations in Pregnancies Without Increased Risk for Structural Chromosomal Aberrations: Systematic Review and Meta-analysis by Srebniak, M I, Joosten, M, Knapen, M. F. C M, Arends, L R, Polak, M, Van Veen, S, Go, A. T. J I, Van Opstal, D

“…(Abstracted from Ultrasound Obstet Gynecol 2018;51:445–452)Chromosomal microarray is currently recommended for women with fetal structural anomalies. However,…”
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EP06.03: Be aware of a diagnostic delay: Rotterdam's experience with NIPT in 1071 high‐risk pregnancies by Diderich, K.E., Srebniak, M.I., Knapen, M., Joosten, M., Govaerts, L., Ijcken, W.F., Go, A., Galjaard, R.J., Van Opstal, D.

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P16.05: The influence of chromosomal microarray and NIPT on the diagnostic yield in 6,811 high‐risk pregnancies without ultrasound anomalies by Srebniak, M.I., Knapen, M., Polak, M., Joosten, M., Diderich, K.E., Govaerts, L., Ijcken, W.F., Heydanus, R., Dijkman, A., Toolenaar, T., de Vries, F.A., Knijnenburg, J., Go, A., Galjaard, R.J., Van Opstal, D.

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SNP array detects chromosome aberrations that we thought do not exist: the first case of an isochromosome Xp (i(X)(p10)) by Srebniak, M. I., Bos, M. J., de Vries, F. A. T., Heydanus, R., Wessels, M. W., Van Opstal, D.

“…What's already known about this topic? Single nucleotide polymorphism (SNP) array detects submicroscopic chromosome aberrations that can be missed by…”
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Prenatal detection and outcome of congenital diaphragmatic hernia (CDH) associated with deletion of chromosome 15q26: Two patients and review of the literature by Klaassens, M., Galjaard, R.J.H., Scott, D.A., Brüggenwirth, H.T., van Opstal, D., Fox, M.V., Higgins, R.R., Cohen-Overbeek, T.E., Schoonderwaldt, E.M., Lee, B., Tibboel, D., de Klein, A.

“…Congenital diaphragmatic hernia (CDH) is a severe birth defect characterized by a defect in the diaphragm with pulmonary hypoplasia and postnatal pulmonary…”
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