E. Wang

Trisomy 13 detection in the first trimester of pregnancy using a chromosome‐selective cell‐free DNA analysis method

A. Oliphant, C. Struble, K. Nicolaides, 2013, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Gestational age and maternal weight effects on fetal cell‐free DNA in maternal plasma

A. Oliphant, C. Struble, T. Musci, 2013, Prenatal diagnosis.

Clinical performance of non‐invasive prenatal testing (NIPT) using targeted cell‐free DNA analysis in maternal plasma with microarrays or next generation sequencing (NGS) is consistent across multiple controlled clinical studies

R. Stokowski, T. Musci, K. Nicolaides, 2015, Prenatal diagnosis.

Accuracy and reproducibility of fetal‐fraction measurement using relative quantitation at polymorphic loci with microarray

R. Stokowski, M. Schmid, E. Wang, 2018, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

The fetal fraction of cell-free DNA in maternal plasma is not affected by a priori risk of fetal trisomy

C. Struble, T. Musci, M. Norton, 2012, The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.

Non‐invasive risk assessment of fetal sex chromosome aneuploidy through directed analysis and incorporation of fetal fraction

A. Oliphant, C. Struble, T. Musci, 2014, Prenatal diagnosis.

Prenatal Screening for 22q11.2 Deletion Using a Targeted Microarray-Based Cell-Free DNA Test

J. Doshi, R. Stokowski, J. Jani, 2017, Fetal Diagnosis and Therapy.

Selective analysis of cell-free DNA in maternal blood for evaluation of fetal trisomy

Wade A. Barrett, J. Doshi, N. Shen, 2012, Prenatal diagnosis.

Complexity of noninvasive prenatal screening and diagnostic testing for an unbalanced translocation involving chromosomes 5 and 18

J. Foroutan, J. Gebbia, E. Wang, 2014, Prenatal diagnosis.

Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18.

Arnold Oliphant, A. Oliphant, C. Struble, 2012, American journal of obstetrics and gynecology.

Targeted cell‐free DNA analysis with microarray quantitation for assessment of fetal sex and sex chromosome aneuploidy risk

R. Stokowski, K. Nicolaides, M. Schmid, 2018, Ultrasound in obstetrics & gynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology.

Microarray-Based Cell-Free DNA Analysis Improves Noninvasive Prenatal Testing

Craig A. Struble, Paul Ryvkin, Arnold Oliphant, 2014, Fetal Diagnosis and Therapy.

Identifying Robertsonian Translocation Carriers by Microarray-Based DNA Analysis

A. Oliphant, C. Struble, K. Nicolaides, 2016, Fetal Diagnosis and Therapy.

Copy-Number Variation and False Positive Results of Prenatal Screening.

A. Oliphant, E. Wang, C. Kingsley, 2015, The New England journal of medicine.

Noninvasive prenatal detection and selective analysis of cell-free DNA obtained from maternal blood: evaluation for trisomy 21 and trisomy 18.

A. Oliphant, C. Struble, K. Song, 2012, American journal of obstetrics and gynecology.