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Discordant NIPT and ultrasound results from vanishing twin pregnancy. Case studies in NIPT

Discordant NIPT and ultrasound results from vanishing twin pregnancy. Case studies in NIPT

Bowdoin Su, Nudelman M, Stosic M, et al. Contemporary OB/GYN

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Detection of complete molar pregnancy by single-nucleotide polymorphism-based non-invasive prenatal testing

Simon AL, Su B, Demko Z, et al. Ultrasound Obstet Gynecol
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A national referral laboratory's experience with the implementation of SNP-based non-invasive prenatal screening for fetal aneuploidy

Santamaria R, Bermejo B, Cigarran S, et al. J Fetal Med

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Clinical Validation of a SNP-based Prenatal Cell-free DNA Screening Test for Fetal RHD Status in a Large US Cohort

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Fetal RhD NIPT: A new testing option to inform care for RhD alloimmunized patients and those at risk

Natera™'s Fetal RhD NIPT (noninvasive prenatal testing) is now available. The test is backed by the largest clinical validation study for fetal RhD in the US to date, and demonstrated 100 percent sens

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2 months ago
Clinical Validation of a SNP-based Prenatal Cell-free DNA Screening Test for Fetal RHD Status in a Large US Cohort

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Natera at ACOG Annual Clinical & Scientific Meeting

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5 months ago
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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Compassionate Care Application - Spanish

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Carrier Manifestations in Pregnancy

Utility of carrier screening to inform management

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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

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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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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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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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NSGC Annual Conference Flyer 2023

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Noninvasive prenatal testing: the future is now

Norwitz ER, Levy B. Rev Obstet Gynecol

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The tests described have been developed and their performance characteristics determined by the CLIA-certified laboratory performing the test. The tests have not been cleared or approved by the US Food and Drug Administration (FDA). CAP accredited, ISO 13485 certified, and CLIA certified. © 2024 Natera, Inc. All Rights Reserved.