Knapen MFCM - Search Results

1

Prenatal ultrasound finding of atypical genitalia: Counseling, genetic testing and outcomes.

van Bever Y, Groenenberg IAL, Knapen MFCM, Dessens AB, Hannema SE, Wolffenbuttel KP, Diderich KEM, Hoefsloot LH, Srebniak MI, Bruggenwirth HT. van Bever Y, et al. Among authors: knapen mfcm. Prenat Diagn. 2023 Feb;43(2):162-182. doi: 10.1002/pd.6205. Epub 2022 Aug 20. Prenat Diagn. 2023. PMID: 35808910

2

Genomic SNP array as a gold standard for prenatal diagnosis of foetal ultrasound abnormalities.

Srebniak MI, Boter M, Oudesluijs GO, Cohen-Overbeek T, Govaerts LC, Diderich KE, Oegema R, Knapen MF, van de Laar IM, Joosten M, Van Opstal D, Galjaard RJ. Srebniak MI, et al. Mol Cytogenet. 2012 Mar 13;5(1):14. doi: 10.1186/1755-8166-5-14. Mol Cytogenet. 2012. PMID: 22413963 Free PMC article.

3

Another rare prenatal case of post-zygotic mosaic trisomy 17.

de Vries FA, Govaerts LC, Knijnenburg J, Knapen MF, Oudesluijs GG, Lont D, Noomen P, de Graaff K, Srebniak MI, Van Opstal D. de Vries FA, et al. Am J Med Genet A. 2013 May;161A(5):1196-9. doi: 10.1002/ajmg.a.35867. Epub 2013 Mar 20. Am J Med Genet A. 2013. PMID: 23512336 No abstract available.

4

ACTA2 mutation with childhood cardiovascular, autonomic and brain anomalies and severe outcome.

Meuwissen ME, Lequin MH, Bindels-de Heus K, Bruggenwirth HT, Knapen MF, Dalinghaus M, de Coo R, van Bever Y, Winkelman BH, Mancini GM. Meuwissen ME, et al. Am J Med Genet A. 2013 Jun;161A(6):1376-80. doi: 10.1002/ajmg.a.35858. Epub 2013 Apr 23. Am J Med Genet A. 2013. PMID: 23613326

5

Pregnant couples at increased risk for common aneuploidies choose maximal information from invasive genetic testing.

van der Steen SL, Diderich KE, Riedijk SR, Verhagen-Visser J, Govaerts LC, Joosten M, Knapen MF, Van Opstal D, Srebniak MI, Tibben A, Galjaard RJ. van der Steen SL, et al. Clin Genet. 2015 Jul;88(1):25-31. doi: 10.1111/cge.12479. Epub 2014 Oct 28. Clin Genet. 2015. PMID: 25134982

6

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.

7

The Psychological Challenges of Replacing Conventional Karyotyping with Genomic SNP Array Analysis in Prenatal Testing.

Riedijk S, Diderich KE, van der Steen SL, Govaerts LC, Joosten M, Knapen MF, de Vries FA, van Opstal D, Tibben A, Galjaard RJ. Riedijk S, et al. J Clin Med. 2014 Jul 3;3(3):713-23. doi: 10.3390/jcm3030713. J Clin Med. 2014. PMID: 26237473 Free PMC article. Review.

8

Prenatal SNP array testing in 1000 fetuses with ultrasound anomalies: causative, unexpected and susceptibility CNVs.

Srebniak MI, Diderich KE, Joosten M, Govaerts LC, Knijnenburg J, de Vries FA, Boter M, Lont D, Knapen MF, de Wit MC, Go AT, Galjaard RJ, Van Opstal D. Srebniak MI, et al. Eur J Hum Genet. 2016 May;24(5):645-51. doi: 10.1038/ejhg.2015.193. Epub 2015 Sep 2. Eur J Hum Genet. 2016. PMID: 26328504 Free PMC article.

9

False Negative NIPT Results: Risk Figures for Chromosomes 13, 18 and 21 Based on Chorionic Villi Results in 5967 Cases and Literature Review.

Van Opstal D, Srebniak MI, Polak J, de Vries F, Govaerts LC, Joosten M, Go AT, Knapen MF, van den Berg C, Diderich KE, Galjaard RJ. Van Opstal D, et al. PLoS One. 2016 Jan 15;11(1):e0146794. doi: 10.1371/journal.pone.0146794. eCollection 2016. PLoS One. 2016. PMID: 26771677 Free PMC article. Review.

10

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. Ultrasound Obstet Gynecol. 2017 Mar;49(3):342-348. doi: 10.1002/uog.15949. Ultrasound Obstet Gynecol. 2017. PMID: 27102944 Free article.

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