Faas BH - Search Results

1

Trial by Dutch laboratories for evaluation of non-invasive prenatal testing. Part II-women's perspectives.

van Schendel RV, Page-Christiaens GC, Beulen L, Bilardo CM, de Boer MA, Coumans AB, Faas BH, van Langen IM, Lichtenbelt KD, van Maarle MC, Macville MV, Oepkes D, Pajkrt E, Henneman L; Dutch NIPT Consortium. van Schendel RV, et al. Among authors: faas bh. Prenat Diagn. 2016 Dec;36(12):1091-1098. doi: 10.1002/pd.4941. Epub 2016 Nov 16. Prenat Diagn. 2016. PMID: 27739584 Free PMC article.

2

Fetal anomaly scan potentially will replace routine AFAFP assays for the detection of neural tube defects.

Kooper AJ, de Bruijn D, van Ravenwaaij-Arts CM, Faas BH, Creemers JW, Thomas CM, Smits AP. Kooper AJ, et al. Among authors: faas bh. Prenat Diagn. 2007 Jan;27(1):29-33. doi: 10.1002/pd.1614. Prenat Diagn. 2007. PMID: 17154227

3

Multiplex ligation-dependent probe amplification (MLPA) as a stand-alone test for rapid aneuploidy detection in amniotic fluid cells.

Kooper AJ, Faas BH, Kater-Baats E, Feuth T, Janssen JC, van der Burgt I, Lotgering FK, van Kessel AG, Smits AP. Kooper AJ, et al. Among authors: faas bh. Prenat Diagn. 2008 Nov;28(11):1004-10. doi: 10.1002/pd.2111. Prenat Diagn. 2008. PMID: 18925610

4

2010 Report from the ISPD Special Interest Groups.

Odibo AO, Faas BH, Oepkes D, Leung TY, Shulman L; ISPD Special Interest Groups. Odibo AO, et al. Among authors: faas bh. Prenat Diagn. 2011 Mar;31(3):246-8. doi: 10.1002/pd.2686. Epub 2011 Jan 4. Prenat Diagn. 2011. PMID: 21374639 No abstract available.

5

Non-targeted whole genome 250K SNP array analysis as replacement for karyotyping in fetuses with structural ultrasound anomalies: evaluation of a one-year experience.

Faas BH, Feenstra I, Eggink AJ, Kooper AJ, Pfundt R, van Vugt JM, de Leeuw N. Faas BH, et al. Prenat Diagn. 2012 Apr;32(4):362-70. doi: 10.1002/pd.2948. Prenat Diagn. 2012. PMID: 22467167

6

Summary of the ISPD Preconference Day, June 3, 2012, Miami Beach.

Faas BH, Odibo AO, Cirigliano V, Schielen P, Pergament D, Devers P, Oepkes D, Benn P. Faas BH, et al. Prenat Diagn. 2013 Jan;33(1):1-5. doi: 10.1002/pd.4007. Epub 2012 Nov 7. Prenat Diagn. 2013. PMID: 23132177 No abstract available.

7

Benefits and limitations of whole genome versus targeted approaches for noninvasive prenatal testing for fetal aneuploidies.

Boon EM, Faas BH. Boon EM, et al. Among authors: faas bh. Prenat Diagn. 2013 Jun;33(6):563-8. doi: 10.1002/pd.4111. Prenat Diagn. 2013. PMID: 23613171 Review.

8

Position statement from the Aneuploidy Screening Committee on behalf of the Board of the International Society for Prenatal Diagnosis.

Benn P, Borell A, Chiu R, Cuckle H, Dugoff L, Faas B, Gross S, Johnson J, Maymon R, Norton M, Odibo A, Schielen P, Spencer K, Huang T, Wright D, Yaron Y. Benn P, et al. Prenat Diagn. 2013 Jul;33(7):622-9. doi: 10.1002/pd.4139. Epub 2013 May 21. Prenat Diagn. 2013. PMID: 23616385 No abstract available.

9

Reliable noninvasive prenatal testing by massively parallel sequencing of circulating cell-free DNA from maternal plasma processed up to 24h after venipuncture.

Buysse K, Beulen L, Gomes I, Gilissen C, Keesmaat C, Janssen IM, Derks-Willemen JJ, de Ligt J, Feenstra I, Bekker MN, van Vugt JM, Geurts van Kessel A, Vissers LE, Faas BH. Buysse K, et al. Among authors: faas bh. Clin Biochem. 2013 Dec;46(18):1783-6. doi: 10.1016/j.clinbiochem.2013.07.020. Epub 2013 Aug 8. Clin Biochem. 2013. PMID: 23933476

10

Detecting fetal subchromosomal aberrations by MPS: an unexpected discrepancy between amniocyte DNA and ccffDNA.

Buysse K, de Ligt J, Janssen IM, van Bon BW, Gomes I, Hehir-Kwa J, Eggink AJ, van Vugt JM, Vissers LE, Geurts van Kessel A, Faas BH. Buysse K, et al. Among authors: faas bh. Prenat Diagn. 2014 Apr;34(4):402-5. doi: 10.1002/pd.4312. Epub 2014 Feb 6. Prenat Diagn. 2014. PMID: 24391091 No abstract available.

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