Faas, Brigitte H. W.

Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

Jacquemont, S., Reymond, A., Zufferey, F., Harewood, L., Walters, R. G., Kutalik, Z., Martinet, D., Shen, Y., Valsesia, A., Beckmann, N. D., et al. (2011) · Nature

Genomic variations and chromosomal abnormalitiesGenome Rearrangement Algorithms

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TRIDENT-2: National Implementation of Genome-wide Non-invasive Prenatal Testing as a First-Tier Screening Test in The Netherlands

van der Meij, K. R. M., Sistermans, E. A., Macville, M. V. E., Stevens, S. J. C., Bax, C. J., Bekker, M. N., Bilardo, C. M., Boon, E. M. J., Boter, M., Diderich, K. E. M., et al. (2019) · The American Journal of Human Genetics

Prenatal Screening and DiagnosticsGenomics and Rare Diseases

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Women’s Experience with Non-Invasive Prenatal Testing and Emotional Well-being and Satisfaction after Test-Results

van Schendel, R. V., Page‐Christiaens, G. C. M. L., Beulen, L., Bilardo, C. M., de Boer, M. A., Coumans, A. B. C., Faas, B. H. W., van Langen, I. M., Lichtenbelt, K. D., van Maarle, M. C., et al. (2017) · Journal of Genetic Counseling

Prenatal Screening and DiagnosticsMaternal Mental Health During Pregnancy and Postpartum

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Increased cerebrospinal fluid chitotriosidase index in patients with multiple sclerosis

Verbeek, M. M., Notting, E. A., Faas, B., Claessens-Linskens, R., & Jongen, P. J. H. (2010) · Acta Neurologica Scandinavica

Multiple Sclerosis Research StudiesLysosomal Storage Disorders Research

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Implementation of whole genome massively parallel sequencing for noninvasive prenatal testing in laboratories

Thung, D. T., Beulen, L., Hehir-Kwa, J., & Faas, B. H. (2015) · Expert Review of Molecular Diagnostics

Prenatal Screening and DiagnosticsGenomics and Rare Diseases

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