EmilyWhichardScibettaMD

PubMed

• 4 citations
  Novel Use of a Social-Media-Based Survey to Detect Regional Differences in Management of Monochorionic-Diamniotic Twins.
  Ilina D. Pluym, Bettina W. Paek, Martin Walker, Hui Liu, Lorna Kwan, Rashmi Rao, Emily Scibetta, Yalda Afshar, Kerry Holliman, Thalia Wong, Lawrence D. Platt, Christin...> ;American Journal of Perinatology. 2020 Jan 30
• 16 citations
  Ultrasound in Early Pregnancy: Viability, Unknown Locations, and Ectopic Pregnancies.
  Emily Scibetta, Christina S. Han> ;Obstetrics and Gynecology Clinics of North America. 2019 Dec 1
• 25 citations
  Identification of novel PIEZO1 variants using prenatal exome sequencing and correlation to ultrasound and autopsy findings of recurrent hydrops fetalis
  Ilina Datkhaeva, Valerie A. Arboleda, T. Niroshi Senaratne, Gelareh Nikpour, Yipeng Geng, Yalda Afshar, Emily Scibetta, Jeffrey D. Goldstein, Fabiola Quintero-Rivera, ...> ;American Journal of Medical Genetics. Part A. 2018 Dec 1
• 17 citations
  Clinical accuracy of abnormal cell-free fetal DNA results for the sex chromosomes
  Emily Scibetta, Stephanie L. Gaw, Rashmi Rao, Neil S. Silverman, Christina S. Han, Lawrence D. Platt> ;Prenatal Diagnosis. 2017 Aug 24
• 4 citations
  Pseudoamniotic Band Syndrome Post Fetal Thoracoamniotic Shunting for Bilateral Hydrothorax.
  Michelle N. Han, Yalda Afshar, Andrew H. Chon, Emily Scibetta, Rashmi Rao, Cherise Meyerson, Ramen H. Chmait> ;Fetal and Pediatric Pathology. 2017 Apr 28
• 28 citations
  Cell-free DNA screening in clinical practice: abnormal autosomal aneuploidy and microdeletion results
  Stephanie G. Valderramos, Rashmi Rao, Emily Scibetta, Neil S. Silverman, Christina S. Han, Lawrence D. Platt> ;American Journal of Obstetrics and Gynecology. 2016 Nov 1
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Journal Articles

• Identification of Novel PIEZO1 Variants Using Prenatal Exome Sequencing and Correlation to Ultrasound and Autopsy Findings of Recurrent Hydrops Fetalis  
  Yipeng Geng, Emily Scibetta, Valerie A Arboleda, Gelareh Nikpour, Barbara F Crandall, Carla Janzen, Ilina Datkhaeva, Joshua Deignan, American Journal of Medical Genetics Part A