Publications by authors named "Erica Soster"

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Clinical Laboratory Experience With Prenatal cfDNA Screening in Triplet Pregnancies.
Erica Soster, Brittany Dyr, Samantha Caldwell, Savannah Moore, Eyad Almasri

Prenat Diagn· June 2025

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Clinical outcomes of screen-positive genome-wide cfDNA cases for trisomy 20: results from the global expanded NIPT Consortium.
Erica Soster, Tamara Mossfield, Melody Menezes, Gloudi Agenbag, Marie-Line Dubois

Mol Cytogenet· April 2024

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Prenatal cfDNA Screening for Emanuel Syndrome and Other Unbalanced Products of Conception in Carriers of the Recurrent Balanced Translocation t(11;22): One Laboratory's Retrospective Experience.
Erica Soster, Brittany Dyr, Samantha Caldwell, Amanda Sussman, Hany Magharyous

Genes (Basel)· October 2023

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Laboratory performance of genome-wide cfDNA for copy number variants as compared to prenatal microarray.
Erica Soster, John Tynan, Clare Gibbons, Wendy Meschino, Jenna Wardrop

Mol Cytogenet· June 2023

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Positive cfDNA screening results for 22q11.2 deletion syndrome-Clinical and laboratory considerations.
Erica Soster, Brittany Dyr, Jill Rafalko, Eyad Almasri, Phillip Cacheris

Front Genet· March 2023

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Multisite assessment of the impact of cell-free DNA-based screening for rare autosomal aneuploidies on pregnancy management and outcomes.
Tamara Mossfield, Erica Soster, Melody Menezes, Gloudi Agenbag, Marie-Line Dubois

Front Genet· August 2022

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Application of mosaicism ratio to multifetal gestations.
Jill Rafalko, Samantha Caldwell, Erica Soster, Eyad Almasri, Graham McLennan

PLoS One· October 2021

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Genome-wide cell-free DNA screening: a focus on copy-number variants.
Jill Rafalko, Erica Soster, Samantha Caldwell, Eyad Almasri, Thomas Westover

Genet Med· October 2021

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Three years of clinical experience with a genome-wide cfDNA screening test for aneuploidies and copy-number variants.
Erica Soster, Theresa Boomer, Susan Hicks, Samantha Caldwell, Brittany Dyr

Genet Med· July 2021

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Correction to: Three years of clinical experience with a genome-wide cfDNA screening test for aneuploidies and copy number variants.
Erica Soster, Theresa Boomer, Susan Hicks, Samantha Caldwell, Brittany Dyr

Genet Med· July 2021

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Hydranencephaly in a newborn with a FLVCR2 mutation and prenatal exposure to cocaine.
Erica L Soster, Megan Tucker, Luis F Escobar, Gail H Vance

Birth Defects Res A Clin Mol Teratol· January 2015

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