Myriad Genetics provides the following resources in select languages:

Spanish

Descargar materiales educativos seleccionados del paciente en Espanyol

pdfForesight Carrier Screen Patient Brochure (Folleto para el paciente de detección de portador de Foresight)
pdfForesight Carrier Screen Fundamental Patient Brochure (Folleto para el paciente fundamental de detección de portador de Foresight)
pdfForesight Carrier Screen CF/SMA Only Patient Brochure (Folleto para el paciente solo de CF/SMA de detección de portador de Foresight)
pdfPrequel Prenatal Screen Patient Brochure (Folleto para el paciente de detección prenatal de Prequel)
pdfMyRisk Patient Brochure (Guía del paciente para el cáncer hereditario y las pruebas genéticas)

French

Télécharger des documents d'information du patient en français

pdfForesight Carrier Screen Patient Brochure (Brochure du patient sur le dépistage du statut de porteur Foresight)
pdfForesight Carrier Screen Fundamental Patient Brochure (Brochure du patient sur le dépistage du statut de porteur fondamental Foresight)
pdfForesight Carrier Screen CF/SMA Only Patient Brochure (Brochure du patient sur le dépistage du statut de porteur Foresight pour la mucoviscidose et l’amyotrophie spinale uniquement)
pdfPrequel Prenatal Screen Patient Brochure (Brochure du patient sur le dépistage prénatal Prequel)

Portuguese

Transferir os materiais educativos para o doente selecionados em português

pdfForesight Carrier Screen Patient Brochure (Folheto informativo para o doente do Foresight Carrier Screen)
pdfForesight Carrier Screen Fundamental Patient Brochure (Folheto informativo para o doente do Foresight Carrier Screen Fundamental)
pdfForesight Carrier Screen CF/SMA Only Patient Brochure (Folheto informativo para o doente do Foresight Carrier Screen CF/SMA Only)
pdfPrequel Prenatal Screen Patient Brochure (Folheto informativo para o doente do Prequel Prenatal Screen)

Chinese

下载特定患者教育宣传资料的简体中文版

pdfForesight Carrier Screen Patient Brochure (Foresight 携带者筛查患者手册)
pdfForesight Carrier Screen Fundamental Patient Brochure (Foresight 携带者基本筛查患者手册)
pdfForesight Carrier Screen CF/SMA Only Patient Brochure (Foresight CF/SMA 携带者筛查患者手册)
pdfPrequel Prenatal Screen Patient Brochure (Prequel 产前筛查患者手册)
pdfMyRisk Patient Brochure

Arabic

تنزيل المواد التعليمية المحددة للمريض باللغة [العربية]

pdfForesight Carrier Screen Patient Brochure (نشرة المريض الخاصة بفحص فحص Foresight لحاملي الأمراض الموروثة)
pdfForesight Carrier Screen Fundamental Patient Brochure (نشرة المريض الخاصة بأساسيات فحص فحص Foresight لحاملي الأمراض الموروثة)
pdfForesight Carrier Screen CF/SMA Only Patient Brochure (نشرة المريض الخاصة بفحص فحص Foresight لحاملي الأمراض الموروثة الخاص بالتليف الكيسي/الضمور العضلي نخاعي المنشأ)
pdfPrequel Prenatal Screen Patient Brochure (نشرة المريض الخاصة بفحص فحص Prequel السابق للولادة)
Myriad Genetics

We Create Human Understanding

OUR MISSION IS TO ENSURE EVERY WOMAN HAS ACCESS TO TRANSFORMATIVE GENETIC INSIGHTS.

OUR VISION IS A WORLD IN WHICH GENETIC INSIGHTS ARE A VITAL PART OF WOMENS WELLNESS – AS MAINSTREAM AS A MAMMOGRAM OR AN ULTRASOUND.

OUR STORY

In this rapidly-changing healthcare environment, providers are asked to do exponentially more, in less time and with less support – yet, they are still striving to give patients the best care possible.

In the moments that matter, Myriad Genetics offers a personal and thoughtful genetic insights experience for healthcare providers and the women who rely on them, with the highest level of rigor, intention, and humanity. 

Keeping real people at the center of everything we do, we give reliable and actionable results, provide one-on-one support, and have designed a workflow to make the patient’s experience easier.  

WE ARE MYRIAD GENETICS.
HUMAN. UNDERSTANDING.
AND, WITH YOU EVERY STEP OF THE WAY.

Our Approach

Our genetic screens and tests provide actionable information, empowering women and their families to make critical and timely healthcare decisions, whether they’re thinking about starting a family or evaluating risk for cancer.

Rigor

Proven test performance for confident decision-making

 

Our next generation sequencing platform is scientifically validated to provide industry-leading sensitivities and specificities. This empowers clinicians to provide the best care for patients based on their results.

Intention

Support at every step so clinicians can provide better patient care

 

Your patient is our purpose. From pre-test education to post-test support, we partner with you to integrate genetic screening and testing seamlessly into your clinic’s existing workflow so that you can better care for your patients.

Humanity

Comprehensive patient assistance to improve access and affordability

 

We are committed to making genetic screening and testing accessible for all patients who can benefit so that they can make informed choices about their health, their families, and their futures, regardless of their financial situation.

OUR PRODUCTS & SERVICES

Myriad MyRiskTM Hereditary Cancer Test

Help patients get ahead of cancer with our hereditary cancer test

Learn More

Myriad Foresight® Carrier Screen

Identify couples at risk to pass down serious, prevalent, clinically-actionable inherited conditions

Learn More

Myriad PrequelTM Prenatal Screen

Get reliable results the first time with our noninvasive prenatal screening

Learn More

Myriad CompleteTM

Myriad Complete is a proprietary suite of services to help integrate genetic testing into your practice, each designed to help the patient through the genetic testing and screening process while providing you the tools you need to determine the best care plan for your patient’s individual needs. We support patients and healthcare providers throughout the genetic screening process, with pre-test education, billing support, clear results reporting, and post-test consults.

2M+

patient results delivered

55+

peer-reviewed publications*
*fiscal years 2018 and 2018 November YTD

100K+

consults performed by our Patient Educators, who are board-certified genetic counselors

250+

million lives in-network

We Are Myriad Genetics

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