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Genes|October 28, 2023
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 ExperienceErica Soster, Brittany Dyr, Samantha Caldwell, et al.
Frontiers in Genetics|March 27, 2023
Positive cfDNA screening results for 22q11.2 deletion syndrome-Clinical and laboratory considerationsErica Soster, Brittany Dyr, Jill Rafalko, et al.
American Journal of Obstetrics and Gynecology|April 11, 2021
Obesity and no call results: optimal timing of cell-free DNA testing and redrawMaeve K Hopkins, Nathanael Koelper, Samantha Caldwell, et al.
Prenatal Diagnosis|March 8, 2021
Not all low fetal fraction cell-free DNA screening failures are at increased risk for aneuploidySamantha Caldwell, Eyad Almasri, Lindsey Schmidt, et al.
Genetics in Medicine : Official Journal of the American College of Medical Genetics|March 18, 2021
Three years of clinical experience with a genome-wide cfDNA screening test for aneuploidies and copy-number variantsErica Soster, Theresa Boomer, Susan Hicks, et al.
Prenatal Diagnosis|May 9, 2025
Clinical Laboratory Experience With Prenatal cfDNA Screening in Triplet PregnanciesErica Soster, Brittany Dyr, Samantha Caldwell, et al.
Plos One|August 9, 2019
A new era in aneuploidy screening: cfDNA testing in >30,000 multifetal gestations: Experience at one clinical laboratoryBrittany Dyr, Theresa Boomer, Eyad A Almasri, et al.
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