Maternal health matters: findings from prenatal genetic screening with implications beyond pregnancy care
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Women's Health
Resources related to women's health needs to support family planning and prenatal testing.
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New Comprehensive Carrier Screening with Horizon Webinar
Overview of new Horizon panels and Natera's tools to streamline carrier screening workflow
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New Comprehensive Carrier Screening with Horizon Webinar - Condensed
Overview of new Horizon panels and Natera's tools to streamline carrier screening workflow
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It's time to screen routinely for 22q11.2 deletion syndrome: new evidence of improved outcomes with prenatal diagnosis
To manage pregnancies at high risk for 22q11.2 deletion syndrome (DS), prenatal and neonatal evaluation after high risk cfDNA screening is needed. Supplemental assessments and early intervention can i
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Carrier Manifestations in Pregnancy
Utility of carrier screening to inform management
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Empower Glossary*
*Some terms can have other meanings in different areas of genetics.
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Impact of high‐risk prenatal screening results for 22q11.2 deletion syndrome on obstetric and neonatal management: Secondary analysis from t
Martin et al. 2023 Prenat. Diagn
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Natera Product Brochure
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Validation of an Enhanced Version of a Single- Nucleotide Polymorphism-Based Noninvasive Prenatal Test for Detection of Fetal Aneuploidies
Ryan A, Hunkapiller N, Banjevic M, et al. Fetal Diagn Ther 2016
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Informatics-based, highly accurate, noninvasive prenatal paternity testing
Ryan A, Baner J, Demko Z, et al. Genet Med 2013
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Letter to the Editor by Megan Hall in response to Munne S.
Saucier J, Merrion K, Mash J, et al. Current Genomics 2013
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Detection of triploid, molar, and vanishing twin pregnancies by a single-nucleotide polymorphismebased noninvasive prenatal test
Curnow KJ, Wilkins-Haug L, Ryan A, et al. Am J Obstet Gynecol 2015
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Validation of a Single-Nucleotide Polymorphism-Based Non-Invasive Prenatal Test in Twin Gestations: Determination of Zygosity, Individual Fe
Norwitz ER, McNeill G, Kalyan A, et al. Journal of Clinical Medicine 2019
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De novo HRAS gene mutation associated with Costello syndrome identified by non-invasive cell-free fetal DNA screening
Nwakalor C, Said-Delgado S, Krinshpun S, et al. Prenatal Diagnosis 2020
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Re: Clinical experience across the fetal-fraction spectrum of a non-invasive prenatal screening approach with low test-failure rate
Jelsema R, Demko ZP, Billing, PR. Ultrasound Obstet Gynecol. 2020
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Estimating the relative frequency of leukodystrophies and recommendations for carrier screening in the era of next-generation sequencing
Schmidt JL, Pizzino A, Nicholl J et al. American Journal of Medical Genetics Part A
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Primary cell-free DNA screening or contingent screening for the common trisomies: a response
Dar P, Norton ME. American Journal of Obstetrics and Gynecology 2022
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Performance of noninvasive prenatal screening for 22q11.2 deletion syndrome in the SMART study
Dar P, Norton ME. American Journal of Obstetrics and Gynecology 2022
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Introduction to Genetic Counseling Roles in Industry
Genetic Counselor Awareness Day 2023
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Patient Medical Records Release Form (Rev 6 - Sept 2023)
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