van der Schoot CE - Search Results

1

Absolute first trimester cell-free DNA levels and their associations with adverse pregnancy outcomes.

Thurik FF, Lamain-de Ruiter M, Javadi A, Kwee A, Woortmeijer H, Page-Christiaens GC, Franx A, van der Schoot CE, Koster MP. Thurik FF, et al. Among authors: van der schoot ce. Prenat Diagn. 2016 Dec;36(12):1104-1111. doi: 10.1002/pd.4940. Epub 2016 Nov 10. Prenat Diagn. 2016. PMID: 27734510

2

Earliest gestational age for fetal sexing in cell-free maternal plasma.

Rijnders RJ, Van Der Luijt RB, Peters ED, Goeree JK, Van Der Schoot CE, Ploos Van Amstel JK, Christiaens GC. Rijnders RJ, et al. Among authors: van der schoot ce, van der luijt rb. Prenat Diagn. 2003 Dec 30;23(13):1042-4. doi: 10.1002/pd.750. Prenat Diagn. 2003. PMID: 14691988

3

Use of bi-allelic insertion/deletion polymorphisms as a positive control for fetal genotyping in maternal blood: first clinical experience.

Page-Christiaens GC, Bossers B, VAN DER Schoot CE, DE Haas M. Page-Christiaens GC, et al. Among authors: van der schoot ce. Ann N Y Acad Sci. 2006 Sep;1075:123-9. doi: 10.1196/annals.1368.016. Ann N Y Acad Sci. 2006. PMID: 17108201

4

Reliability of fetal sex determination using maternal plasma.

Scheffer PG, van der Schoot CE, Page-Christiaens GCML, Bossers B, van Erp F, de Haas M. Scheffer PG, et al. Among authors: van erp f, van der schoot ce. Obstet Gynecol. 2010 Jan;115(1):117-126. doi: 10.1097/AOG.0b013e3181c3c938. Obstet Gynecol. 2010. PMID: 20027043

5

Noninvasive fetal blood group genotyping of rhesus D, c, E and of K in alloimmunised pregnant women: evaluation of a 7-year clinical experience.

Scheffer PG, van der Schoot CE, Page-Christiaens GC, de Haas M. Scheffer PG, et al. Among authors: van der schoot ce. BJOG. 2011 Oct;118(11):1340-8. doi: 10.1111/j.1471-0528.2011.03028.x. Epub 2011 Jun 14. BJOG. 2011. PMID: 21668766

6

Noninvasive fetal genotyping of human platelet antigen-1a.

Scheffer PG, Ait Soussan A, Verhagen OJ, Page-Christiaens GC, Oepkes D, de Haas M, van der Schoot CE. Scheffer PG, et al. Among authors: van der schoot ce. BJOG. 2011 Oct;118(11):1392-5. doi: 10.1111/j.1471-0528.2011.03039.x. Epub 2011 Jul 12. BJOG. 2011. PMID: 21749627

7

Noninvasive prenatal blood group and HPA-1a genotyping: the current European experience.

van der Schoot CE, Thurik FF, Veldhuisen B, de Haas M. van der Schoot CE, et al. Transfusion. 2013 Nov;53(11 Suppl 2):2834-6. doi: 10.1111/trf.12411. Epub 2013 Sep 4. Transfusion. 2013. PMID: 24004336 No abstract available.

8

Analysis of false-positive results of fetal RHD typing in a national screening program reveals vanishing twins as potential cause for discrepancy.

Thurik FF, Ait Soussan A, Bossers B, Woortmeijer H, Veldhuisen B, Page-Christiaens GC, de Haas M, van der Schoot CE. Thurik FF, et al. Among authors: van der schoot ce. Prenat Diagn. 2015 Aug;35(8):754-60. doi: 10.1002/pd.4600. Epub 2015 May 19. Prenat Diagn. 2015. PMID: 25855535

9

Haemolytic disease of the fetus and newborn.

de Haas M, Thurik FF, Koelewijn JM, van der Schoot CE. de Haas M, et al. Among authors: van der schoot ce. Vox Sang. 2015 Aug;109(2):99-113. doi: 10.1111/vox.12265. Epub 2015 Apr 20. Vox Sang. 2015. PMID: 25899660 Review.

10

Frequency and characterization of known and novel RHD variant alleles in 37 782 Dutch D-negative pregnant women.

Stegmann TC, Veldhuisen B, Bijman R, Thurik FF, Bossers B, Cheroutre G, Jonkers R, Ligthart P, de Haas M, Haer-Wigman L, van der Schoot CE. Stegmann TC, et al. Among authors: van der schoot ce. Br J Haematol. 2016 May;173(3):469-79. doi: 10.1111/bjh.13960. Epub 2016 Mar 27. Br J Haematol. 2016. PMID: 27018217 Free article.

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