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Products are filtered by different dates, depending on the combination of live and on-demand components that they contain, and on whether any live components are over or not.
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  • Contains 1 Component(s) Includes a Live Web Event on 10/21/2026 at 12:00 PM (CDT)

    Learn a brief overview of what to expect at the Annual Conference and how to get the most out of your conference experience.

    First-time attendees of the NSGC Annual Conference are invited to join this webinar for an overview of what to expect at the NSGC 45th Annual Conference. Learn more about NSGC membership benefits and programming, receive an overview of sessions to look forward to at this year's conference, and hear from recent graduates about their experience from attending the conference in the past. There will be time for Q&A at the end of the webinar. 

    This event is exclusively for Annual Conference attendees who have registered to attend the First-Time Attendee Workshop and/or the First-Time Attendee Welcome Reception on Tuesday, Nov. 10. 

  • Contains 1 Component(s) Includes a Live Web Event on 09/23/2026 at 12:00 PM (CDT)

    Presented by the NSGC Ophthalmology and Hearing Loss SIG

    Advancements in genomic knowledge and next generation sequencing technologies have resulted in expanded carrier screening creating more equitable opportunities for individuals to learn about their reproductive risks for various genetic conditions including inherited eye and hearing conditions.  For many of the ocular and auditory conditions included in carrier screening panels there are wide spectrums of phenotypic features including age of onset and severity.  In this webinar, we discuss some common carrier screening findings for ocular and auditory conditions and offer strategies for providing a nuanced approach to genetic counseling about ocular and auditory conditions.

    Presented by: 

    NSGC Ophthalmology and Hearing Loss SIG
    1. Shay Guetz-Lindahl, MS, CGC
    2. Emily Place, MS LCGC, Senior Genetic Counselor

    Learning Objectives:

    1. Define the spectrum of presentation of ocular genetic conditions found on carrier screening.
    2. Define the spectrum of presentation of hearing loss genetic conditions on carrier screening.

  • Contains 1 Component(s) Includes a Live Web Event on 09/16/2026 at 12:00 PM (CDT)

    Join authors Misha Rashkin, MS, CGC, and Anya Prince, JD, MPP, for a lively discussion about their recent paper in Journal of Genetic Counseling, “Understanding GINA Through Case Examples: A Guide for U.S.-Based Genetic Counselors.”

    The Genetic Information Nondiscrimination Act (GINA) is a well-known law within the genetic counseling community. Most genetic counselors are familiar with its major provisions, including prohibiting genetic discrimination in health insurance and employment. Nevertheless, clinical scenarios often arise for which genetic counselors were not specifically trained. Anchoring ourselves in clinical case examples, this presentation provides a brief guide to GINA contextualized in specific scenarios where misunderstandings of the law on the part of the genetics professional and patients are likely, focusing on the legal context of the United States.

    Presented By:
    1. Anya Prince, JD
    2. Misha Rashkin, MS, CGC

    Learning Objectives:
    1. Summarize federal and state laws that interact with GINA in ways that can affect genetic counselor patients and families.
    2. Apply GINA and other legal stipulations to specific clinical scenarios.

    Genetic Counselor CEUs:
    This event has been submitted to the National Society of Genetic Counselors (NSGC) for approval of Category 1 CEUs. The American Board of Genetic Counseling (ABGC) accepts CEUs approved by NSGC for purposes of recertification. Approval for the requested CEUs and Contact Hours is currently pending.

    Successful Completion:
    1. Attend live session
    2. Complete evaluation

    Misha Rashkin, MS, CGC

    Misha Rashkin, MS, CGC

    Anya Prince, JD

    Anya Prince, JD

  • Contains 1 Component(s) Includes a Live Web Event on 09/09/2026 at 12:00 PM (CDT)

    Presented by the NSGC Precision Medicine SIG

    This webinar examines how genetic counselors are implementing pharmacogenomics (PGx) testing and counseling across healthcare settings. Over 95% of the population carries clinically significant pharmacogene variants, yet implementation lags behind other genetic testing due to limited workforce training, provider literacy gaps, and high clinical decision support costs. The presenters showcased three primary PGx service delivery models: academic medicine programs (Brigham & Women's Hospital telemedicine clinic and M Health Fairview's Go4PGx Initiative), private practice collaborations between genetic counselors and pharmacists, and laboratory-based models such as Color Health's integration with cancer clinics and research partnerships. Future challenges include managing increasingly complex sequencing-based and polygenic score PGx results while capitalizing on opportunities from long-read genomics and rapid sequencing technologies. Training programs and continuing education must expand to meet growing clinical integration of PGx and establish counselor competency as a hiring differentiator.

    Presented by: 

    NSGC Precision Medicine SIG

    Learning Objectives:

    1. Explain the clinical relevance and utility of pharmacogenomics (PGx)
    2. Identify barriers to PGx implementation in genetic counseling practice and recognize emerging opportunities to advance the field
    3. Compare genetic counselor roles and responsibilities across academic, private practice, and laboratory-based PGx models

    Hannah Llorin, MS, CGC

    Hannah Llorin, MS, CGC

    Director of Genetic Counseling; Atria Health and Research Institute, Research Fellow; University of Minnesota

    Hannah Llorin, MS, CGC, is a certified genetic counselor and Director of Genetic Counseling at Atria Health and Research Institute in New York, NY. Her work integrates genomic medicine into primary care through clinical and technical strategies that enable genetics to inform routine healthcare decisions. As a GC-FIRST Research Fellow at University of Minnesota, she studies pharmacogenomics implementation and clinical outcomes. Ms. Llorin previously practiced clinically at Brigham and Women's Hospital Center for Fetal Medicine and worked in genetics education at 23andme. She serves on the advisory board for Stanford University's MS Program in Human Genetics and Genetic Counseling, where she is an alumna. She formerly served as executive editor for the National Society of Genetic Counselors' Perspectives in Genetic Counseling, and contributes to national initiatives on inclusive genetic counseling practices.

    Elizabeth Fieg, MS, CGC

    Elizabeth Fieg, MS, CGC

    Clinical Science Liaison; Baylor Genetics

    Elizabeth Fieg is a genetic counselor with experience working in adult medical genetics, endocrine genetics, rare disease research, and pharmacogenomics. Elizabeth is a member of CPIC and previously served in the ClinGen Pharmacogenomics Working Group. She is a clinical science liaison on the medical affairs team at Baylor Genetics and is involved in the Undiagnosed Disease Network (UDN). Elizabeth is an Adjunct Assistant Professor in the Genetic Counseling program at the MGH Institute of Health Professions.

    I am a full time employee of Baylor Genetics. 

    Hetanshi Naik, PhD, MS, CGC

    Hetanshi Naik, PhD, MS, CGC

    Associate Professor and Research Director; Stanford University

    Hetanshi Naik is an Associate Professor in the Department of Genetics and the Research Director of the MS Program in Human Genetics and Genetic Counseling. She is a clinical researcher with expertise in the Porphyrias, lysosomal storage disorders (LSDs), and pharmacogenomics. Her research focuses on developing and evaluating patient reported outcomes (PROs) for genetic disorders and genomic medicine implementation, in particular assessing PROs as outcomes for rare disease trials, pharmacogenomics implementation, and genetic counseling education and processes.

    Jen Eichmeyer, MS, CGC

    Jen Eichmeyer, MS, CGC

    Genetic Counselor; Genetic Support Foundation

    Jen Eichmeyer received her Master's in Genetic Counseling at the University of Texas at Houston in 2002. Jennifer has expertise in creating and developing new clinical genetic services including cancer genetics, telehealth genetic counseling services, and pharmacogenetics. She lectures to multiple genetic counseling training programs on PGx and has been a leader in PGx in the National Society of Genetic Counselors. She established a private practice that served PGx indications and continues to be part of PGx professional organizations such as CPIC and STRIPE.

    Jeri Nichols, MS, PharmD, CGC, CSP

    Jeri Nichols, MS, PharmD, CGC, CSP

    Founder; GenePharmer, LLC, Clinical Pharmacist; University of Missouri Health Care

    Jeri spent 12 years as a genetic counselor focused on prenatal genetics before returning to school to earn her Doctor of Pharmacy degree. Driven by a desire to blend her passion for genetics with her pharmacy training, she launched GenePharmer, LLC. Through this work, Jeri partners with patients and providers to deliver personalized pharmacogenomic guidance.

    Carla McGruder, MS, CGC

    Carla McGruder, MS, CGC

    Senior Genetic Counselor; Color Health

    Carla McGruder, MS, CGC, is a Senior Clinical Genetic Counselor at Color Health, where she leads innovative work in virtual cancer care and risk assessment. Her expertise spans cancer genetics, pharmacogenomics, cardiology, and the integration of clinical care with digital health solutions. She is passionate about expanding access to genetic services and advancing equity in healthcare. In addition to her clinical work, Carla provides educational genetic counseling services through Good Genes Genetic Counseling Services, LLC. She earned her Master of Science in Genetic Counseling from the University of Texas Health Science Center at Houston.

    Rissa Hall, MS, CGC

    Rissa Hall, MS, CGC

    Genetic Counselor; M Health Fairview

  • Contains 4 Component(s), Includes Contact Hours

    In this interactive session, expert genetic counselors will walk through challenging cases that highlight evolving genetic knowledge, nuanced risk assessment, and the counseling strategies needed to support patients facing difficult decisions.

    Join us for an engaging, case-based webinar that brings the realities of genetic counseling into focus through complex, real-world clinical scenarios. In this interactive session, expert genetic counselors will walk through challenging cases that highlight evolving genetic knowledge, nuanced risk assessment, and the counseling strategies needed to support patients facing difficult decisions.

    Presented by:

    1. Chenery Lowe, ScM, CGC, PhD
    2. Lauren Puryear, MS, CGC
    3. Brittany Sears, PhD, MSPH, LCGC

    Learning Objectives:

    1. Identify patient’s stated and unstated goals for genetic testing.
    2. Design a genetic testing strategy that meets both patient’s stated and unstated goals.
    3. Identify strategies to navigate ethical conflicts regarding personal autonomy, disclosure timelines, and parental authority when managing genetic testing without assent in pediatric populations.
    4. Determine ethically permissible options for reproductive decisions informed by reproductive, disability, and professional ethics frameworks

    Genetic Counselor CEUs: 

    The National Society of Genetic Counselors (NSGC) has authorized the National Society of Genetic Counselors (NSGC) to offer up to .1 CEUs or 1 Category 1 contact hour for the activity, Case Based Webinar - Part III. The American Board of Genetic Counseling (ABGC) will accept CEUs earned by participating in this program for the purposes of genetic counselor recertification.

    Successful Completion: 

    1. View recording
    2. Pass quiz
    3. Complete evaluation

  • Contains 15 Product(s)

    This all-inclusive package offers access to the full set of 24 webinars from NSGC’s 2026 Webinar Series, complete with CEUs. Please note that webinars will be added to this package as they are released.

    This all-inclusive package offers access to the full set of 24 webinars from NSGC’s 2026 Webinar Series, complete with CEUs. Please note that webinars will be added to this package as they are released.

    To purchase the 2026 NSGC Webinar Series Full Package, click the blue "Register Now" button next to the package title. Do not register for the individual components included in the package.

    Genetic Counselor CEUs:
    The National Society of Genetic Counselors (NSGC) has authorized the National Society of Genetic Counselors (NSGC) to offer up to 2.4 CEUs or 24 Category 1 contact hours for the 2026 NSGC Webinar Series Full Package. The American Board of Genetic Counseling (ABGC) will accept CEUs earned by participating in this program for the purposes of genetic counselor recertification.

  • Contains 4 Product(s)

    This package includes four specialized, in-depth educational session recordings from the NSGC 43rd Annual Conference.

    This package includes four specialized, in-depth educational session recordings from the NSGC 43rd Annual Conference.

    To purchase NSGC 43rd Annual Conference Pre-Conference Symposia Package, click the blue "Register Now" button next to the package title. Do not register for the individual components included in the package.

    Genetic Counselor CEUs:

    The National Society of Genetic Counselors (NSGC) has authorized the National Society of Genetic Counselors (NSGC) to offer up to 2.0 CEUs or 20 Category 1 contact hours for the activity, NSGC 43rd Annual Conference Pre-Conference Symposia Package. The American Board of Genetic Counseling (ABGC) will accept CEUs earned by participating in this program for the purposes of genetic counselor recertification.

  • Contains 36 Product(s)

    This package includes the most comprehensive set of recordings from the NSGC 43rd Annual Conference: pre-conference symposia, plenary sessions, educational breakout sessions, and on-demand sessions.

    This package includes the most comprehensive set of recordings from the NSGC 43rd Annual Conference: pre-conference symposia, plenary sessions, educational breakout sessions, and on-demand sessions.

    To purchase the NSGC 43rd Annual Conference Complete Sessions Package, click the blue "Register Now" button next to the package title. Do not register for the individual components included in the package.

    Genetic Counselor CEUs:

    The National Society of Genetic Counselors (NSGC) has authorized the National Society of Genetic Counselors (NSGC) to offer up to 5.91 CEUs or 59.1 Category 1 contact hours for the activity, NSGC 43rd Annual Conference Complete Sessions Package. The American Board of Genetic Counseling (ABGC) will accept CEUs earned by participating in this program for the purposes of genetic counselor recertification.

  • Contains 4 Component(s), Includes Contact Hours

    Attendees will gain practical knowledge to support evidence-based genetic counseling, educate referring providers on current testing recommendations, and incorporate genome sequencing into clinical practice to improve diagnostic outcomes for pediatric patients.

    Genetic testing for pediatric neurodevelopmental disorders has evolved rapidly, with genome sequencing now recognized as a first-tier diagnostic test in updated professional guidelines. This webinar will review the evidence driving this shift, compare historical and current testing approaches, discuss practical considerations for implementation, including insurance coverage and test selection, and highlight clinical cases in which genome sequencing identified diagnoses that would likely have been missed by previous first-tier technologies. Attendees will gain practical knowledge to support evidence-based genetic counseling, educate referring providers on current testing recommendations, and incorporate genome sequencing into clinical practice to improve diagnostic outcomes for pediatric patients.

    Presented by: 

    NSGC Pediatrics and Clinical Genetics SIG
    Emily Muth, MS, CGC
    Jillian Kirk, MS, CGC

    Learning Objectives:

    1. Describe recent changes in professional guidelines supporting genome sequencing as a first-tier diagnostic test for pediatric patients with neurodevelopmental conditions.
    2. Apply evidence from clinical case examples to identify scenarios in which genome sequencing can provide diagnoses that would likely be missed using older testing strategies.
    3. Discuss practical considerations for implementing genome sequencing in clinical practice, including insurance coverage, test selection, and genetic counseling implications.
    4. Describe how provider education on current genetic testing recommendations can facilitate earlier diagnosis of neurodevelopmental conditions, improving access and promoting equitable care. 

    Genetic Counselor CEUs: 

    The National Society of Genetic Counselors (NSGC) has authorized the National Society of Genetic Counselors (NSGC) to offer up to .1 CEUs or 1 Category 1 contact hour for the activity, From First-Tier Then to First-Tier Now: Implementing Genome Sequencing for Pediatric Neurodevelopmental Disorders. The American Board of Genetic Counseling (ABGC) will accept CEUs earned by participating in this program for the purposes of genetic counselor recertification.

    Successful Completion: 

    1. View recording
    2. Pass quiz
    3. Complete evaluation

  • Contains 4 Component(s), Includes Contact Hours

    This webinar explores the evolving genetic counseling landscapes in Hong Kong and the Dominican Republic, highlighting both opportunities and challenges in expanding access to care.

    This webinar explores the evolving genetic counseling landscapes in Hong Kong and the Dominican Republic, highlighting both opportunities and challenges in expanding access to care. The first half provides an overview of genetic counseling in Hong Kong, including training pathways, service delivery, genetic testing infrastructure, and barriers to workforce development and patient access. The second half offers a first-hand perspective on establishing a genetic counseling practice in the Dominican Republic, examining legal and certification challenges, clinical practice across reproductive and pediatric settings, and obstacles to genetic testing. Participants will gain insight into how genetic counseling is delivered in two distinct healthcare systems and the practical realities of advancing the profession in emerging regions. The session concludes with a call for global collaboration, advocacy, and resource sharing to strengthen genetic counseling services worldwide.

    Presented by: 

    NSGC International SIG
    Yoyo (Wing Yiu) Chu, MGenCoun, FHGSA (Genetic Counselling)
    Camila M. Marranzini, MS, GC

    Learning Objectives:

    1. Summarize the education, training pathways, and professional roles of genetic counselors in Hong Kong, including available programs and integration within public and private healthcare systems.
    2. Describe the regulatory framework, minimum practice requirements, and certification barriers affecting genetic counselors in the Dominican Republic, including challenges related to international credentialing systems (ABGC, EBMG).
    3. Analyze structural and systemic barriers to genetic testing access in both Hong Kong and the Dominican Republic, including cost, insurance coverage, infrastructure limitations, and disparities compared to higher-resource settings.
    4. Evaluate how cultural, religious, and socioeconomic factors influence the delivery of genetic counseling and clinical practice adaptations in resource-limited settings.

    Genetic Counselor CEUs: 

    The National Society of Genetic Counselors (NSGC) has authorized the National Society of Genetic Counselors (NSGC) to offer up to .1 CEUs or 1 Category 1 contact hour for the activity, Voices from the Field: Genetic Counseling in Hong Kong and the Dominican Republic. The American Board of Genetic Counseling (ABGC) will accept CEUs earned by participating in this program for the purposes of genetic counselor recertification.

    Successful Completion: 

    1. View recording
    2. Pass quiz
    3. Complete evaluation