Melissa Stosic

Whole-exome sequencing in the evaluation of fetal structural anomalies: a prospective cohort study

Slavé Petrovski, Vimla S. Aggarwal, Jessica L. Giordano et al. · The Lancet · 2019 · 590 citations

Developmental Anomaly, Sequencing, Whole-exome Sequencing +12

Expanding the scope of noninvasive prenatal testing: detection of fetal microdeletion syndromes

Ronald J. Wapner, Joshua Babiarz, Brynn Levy et al. · American Journal of Obstetrics and Gynecology · 2014 · 332 citations

Single-Nucleotide Polymorphism–Based Noninvasive Prenatal Screening in a High-Risk and Low-Risk Cohort

Eugene Pergament, Howard Cuckle, Bernhard Zimmermann et al. · Obstetrics and Gynecology · 2014 · 280 citations · Full text

Clinical experience and follow-up with large scale single-nucleotide polymorphism–based noninvasive prenatal aneuploidy testing

P. Dar, Kirsten J. Curnow, Susan J. Gross et al. · American Journal of Obstetrics and Gynecology · 2014 · 271 citations

Large Scale Single-nucleotide, Genetic Testing, Genetics +16

Detection of triploid, molar, and vanishing twin pregnancies by a single-nucleotide polymorphism–based noninvasive prenatal test

Kirsten J. Curnow, Louise Wilkins‐Haug, Allison Ryan et al. · American Journal of Obstetrics and Gynecology · 2014 · 216 citations