L. Beulen

发表

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

D. Oepkes, B. Faas, K. Lichtenbelt, 2017, Journal of Genetic Counseling.

Electrohysterographic volume conductor modeling

J. Bergmans, C. Rabotti, M. Mischi, 2009 .

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

D. Oepkes, B. Faas, K. Lichtenbelt, 2016, Prenatal diagnosis.

TRIAL BY DUTCH LABORATORIES FOR THE EVALUATION OF NON-INVASIVE PRENATAL TESTING – WOMEN ’ S PERSPECTIVES

D. Oepkes, B. Faas, I. V. Langen, 2016 .

Origin and clinical relevance of chromosomal aberrations other than the common trisomies detected by genome-wide NIPS: results of the TRIDENT study

D. Oepkes, E. Sistermans, M. Weiss, 2017, Genetics in Medicine.

Women's and healthcare professionals' preferences for prenatal testing: a discrete choice experiment

B. Faas, I. Feenstra, J. Grutters, 2015, Prenatal diagnosis.

Clinical utility of non‐invasive prenatal testing in pregnancies with ultrasound anomalies

B. Faas, I. Feenstra, J. V. van Vugt, 2017, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The effect of a decision aid on informed decision-making in the era of non-invasive prenatal testing: a randomised controlled trial

Ilse Feenstra, B. Faas, I. Feenstra, 2016, European Journal of Human Genetics.

The consequences of implementing non-invasive prenatal testing in Dutch national health care: a cost-effectiveness analysis.

B. Faas, I. Feenstra, J. Grutters, 2014, European journal of obstetrics, gynecology, and reproductive biology.

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

J. Hehir-Kwa, B. Faas, D. T. Thung, 2015, Expert review of molecular diagnostics.

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

K. Buysse, I. Janssen, C. Gilissen, 2013, Clinical biochemistry.

Validation of two‐channel sequencing‐by‐synthesis for noninvasive prenatal testing of fetal whole and partial chromosome aberrations

B. Faas, K. Neveling, L. Beulen, 2016, Prenatal diagnosis.

Modeling and Identification of the Electrohysterographic Volume Conductor by High-Density Electrodes

Jan W. M. Bergmans, Chiara Rabotti, S. Guid Oei, 2010, IEEE Transactions on Biomedical Engineering.

Modeling and Identification of the Electrohysterographic Volume Conductor by High-Density Electrodes

J. Bergmans, C. Rabotti, M. Mischi, 2010, IEEE Transactions on Biomedical Engineering.