Results from myGeneHistory are automatically saved into your MyriadPro account where you’ll be able to order Myriad genetics tests quickly and easily. We make genetic testing simple for your patients and your practice, Commitment to Providing Broad Patient Access. We support patients and healthcare providers throughout the genetic screening process, with pre-test education, billing support, clear results reporting, and post-test education. 21, 18, and 13 and the Option for Classification of Sex Chromosome Status. A. Myriad, the Myriad logo, MyriadPro, the MyriadPro logo, Myriad myRisk Hereditary Cancer, the Myriad myRisk Hereditary Cancer logo, Myriad myPath Melanoma, the Myriad myPath Melanoma logo, Myriad myPlan Lung Cancer, the Myriad myPlan Lung Cancer logo, BRACAnalysis, the BRACAnalysis logo, COLARIS, the COLARIS logo, COLARIS AP, the COLARIS AP logo, MELARIS, the MELARIS logo, PANEXIA, the PANEXIA logo, Prolaris, the Prolaris logo, ResultsNow, the ResultsNow logo, Myriad Promise, and the Myriad Promise logo are either trademarks or registered trademarks of Myriad Genetics, Inc. in the United States and other jurisdictions. Doi/abs/10.1002/pd.5603. Consults. × New Screenings Results Feature! The Myriad myRisk ® Hereditary Cancer test is a 35-gene panel that identifies an elevated risk for eight hereditary cancers: Myriad myRisk captures more mutation carriers than BRAC Analysis ® and COLARIS ® combined. © 2020 Myriad, the Myriad logo, MyriadPro, the MyriadPro logo, Myriad myRisk Hereditary Cancer, the Myriad myRisk Hereditary Cancer logo, Myriad myPath Melanoma, the Myriad myPath Melanoma logo, Myriad myPlan Lung Cancer, the Myriad myPlan Lung Cancer logo, BRACAnalysis, the BRACAnalysis logo, COLARIS, the COLARIS logo, COLARIS AP, the COLARIS AP logo, MELARIS, the MELARIS logo, PANEXIA, the PANEXIA logo, Prolaris, the Prolaris logo, ResultsNow, the ResultsNow logo, Myriad Promise, and the Myriad Promise logo are either trademarks or registered trademarks of Myriad Genetics, Inc. in the United States and other jurisdictions. This results in a lower false-positive rate and false-negative rate.5. Access online resources including educational videos and webinars on topics such as hereditary cancer screening. We deliver screening and testing results effectively and thoroughly so you can focus on care plans. Terms of Use | Notice of Privacy Practices | Privacy Policy, Myriad does not sell your personal information. Twin-twin transfusion syndrome. The Myriad Prequel Prenatal Screen is a noninvasive prenatal screen that uses cell-free DNA (cfDNA) to determine if a pregnancy is at an increased risk for common chromosome abnormalities, such as Down syndrome. cfDNA screening has been shown to be superior to methods that use maternal age, ultrasound, and serum screening. Terms of Use | Notice of Privacy Practices | Privacy Policy, Myriad does not sell your personal information. Myriad myRisk Enhanced With riskScore . When your patients utilize our on-demand or scheduled Patient Education service, you’ll receive detailed notes from the consult. We provide consults from patient educators, who are genetic counselors, tailored to help your patient understand their results. Myriad Complete is a proprietary suite of services to help your patients through the genetic testing process, each designed to assist you as you determine the best care plan for your patient’s individual needs. (2019) Clinical experience across the fetal-fraction spectrum for a noninvasive prenatal screen with low test-failure. The Myriad Prequel Prenatal Screen is a noninvasive prenatal screen that uses cell-free DNA (cfDNA) to determine if a pregnancy is at an increased risk for common chromosome abnormalities, such as Down syndrome. Noninvasive prenatal screening for patients with high body mass index: Evaluating the impact of a customized whole genome sequencing workflow on sensitivity and residual risk. 163: screening for fetal aneuploidy. For best results and to ensure all MyriadPro functionality is working properly, we recommend using the latest versions of Firefox, Chrome, Safari, or Internet Explorer. Copyright 2020 ©Myriad Women’s Health, Inc.All rights reserved.Myriad does not sell your personal data. Once completed, the consult is documented and a summary is sent back to you, their ordering provider. Fetal, Learn more about individualized PPV and residual risk >, Statement on Nondiscrimination and Accessibility. Every report includes the myRIsk Genetic Result and a personalized myRisk Medical Management Tool based on professional society guidelines. We provide consults from patient educators, who are genetic counselors, tailored to help address any questions your patients may have. We support patients and healthcare providers throughout the genetic screening process, with pre-test education, billing support, clear results reporting, and post-test education. total patient education consults performed, patient educators who are trained as genetic counselors with an average of 10+ years of experience, Myriad Women's Health, Inc.180 Kimball WaySouth San Francisco, CA 94080, Prenatal (Foresight & Prequel) support:Phone: 888.268.6795Hereditary Cancer (myRisk) support:Phone: 800.469.7423. The Myriad myRisk report provides recommendations for managing patients with either positive or negative genetic results. Myriad myRisk ® Hereditary Cancer Test. For test results and management options, please visit the provider resource center. Hancock et al. Patient Educators are also available to answer any questions your practice may have about Myriad Women’s Health screening. These curated resources were designed to reflect best practices and to help your patients easily understand the process of genetic testing with Myriad Women’s Health. In the past, family history screening has been too complex and time consuming. Norton, M. et al Cell free DNA analysis for noninvasive examination of trisomy. Since 1991, Myriad has invested more than a billion dollars to enhance the world’s collective scientific understanding of disease through collaborative research, outreach and education and to translate that knowledge into molecular and companion diagnostic tools that save and improve the lives of the patients we serve. Once completed, the patient and you will be informed if they meet guidelines for genetic testing. ... We deliver screening and testing results effectively and thoroughly so you can focus on care plans. Prequel can now provide individual fetal sex information for twins, in addition to singletons. Myriad Women’s Health provides a comprehensive patient education experience to ensure patients thoroughly understand the genetic screening and process. myGeneHistory – an online family history questionnaire provides accurate patient identification based on guidelines from NCCN, USPSTF, and ASBrS. Common aneuploidies: Trisomy 21, Trisomy 18, Trisomy 13.Optional analysis of sex chromosomes (which includes the ability to determine fetal sex for singletons and twins), microdeletions, and expanded aneuploidies. Blending both genetic test status and personal cancer family history, the Myriad myRisk® hereditary cancer panel represents the next generation of hereditary cancer risk testing. What Is riskScore? Blending both genetic test status and personal cancer family history, Myriad myRisk hereditary cancer panel represents the next generation of hereditary cancer risk testing. All interactions we have with your patients are documented and summarized for you so you’re kept up-to-date and are prepared for their next visit. Patients input personal and family history into myGeneHistory. Review of Myriad Genetics reproductive testing reports. Maternal age and gestation age-specific risks for chromosomal defects. In addition to offering accurate hereditary cancer test results, Myriad myRisk® includes riskScore for eligible women to provide more comprehensive breast cancer risk assessment. Review clinical research and insights from our latest publications and presentations at national conferences. Our electronic patient identification tools help determine if patients may be appropriate for testing. Am J, W, Henry G, Nicolaides KH. Statement on Nondiscrimination and Accessibility, Patient education from certified genetic counselors. Myriad is dedicated, above all else, to improving patient care through pioneering research and the development of innovative molecular diagnostic tests. If so, your healthcare professional will draw a small amount of your blood or take a saliva sample and send it to Myriad Genetic Laboratories for analysis. If you’d like us to, we can take them through a comprehensive follow-up to ensure all of their questions are answered. Learn about the benefits of myGeneHistory and how to implement it into your practice. “Myriad believes that a patient’s genetic information is private and confidential.