NSGC’s Webinar Series is a timely, year-round series focused on education and other issues impacting the genetic counseling profession. From telemedicine to genetic engineering, and more, these webinars keep you apprised of the latest trends in healthcare and genetics, and how they may affect you and your patients.
Please note that while webinar attendance is free for NSGC members, webinar CEUs must be purchased separately. A link to purchase CEUs will be sent out to all registered live webinar attendees within two days of the live webinar. Webinars can be purchased for CEUs as . NSGC members can view webinar recordings by visiting the .
2026 NSGC Webinar Series
NSGC Webinars take place every other Wednesday from 12:00 pm - 1:00 pm CT unless otherwise noted.
The Mosaic Journey: From Transfer to Term
Wednesday, June 10
12:00-1:00pm CST
Speakers:
Emma Moores, MGC, CGC
Jennifer Kussmann, MS, CGC
Presented by the ART/Infertility SIG
Learning Objectives:
1. Review the background on PGT-A testing with non-euploid results
2. Describe the historical viewpoints and current embryo transfer policies
3. Explain prenatal testing and screening options
4. Use case examples to highlight the challenges in pregnancies with atypical embryos
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From Sequence to Surveillance: Making Sense of Secondary Findings in Inherited Arrhythmia and Cardiomyopathy Genes
Wednesday, June 17
12:00-1:00pm CST
Speakers:
Erin Miller, MS, CGC
Sarah Jurgensmeyer Langas, MS, CGC
Laura Zahavich, MSc, CGC
Presented by the NSGC Cardiogenetics SIG
Learning Objectives:
1. Apply clinical phenotype and family history to guide surveillance strategies for individuals with secondary findings in cardiac disease genes.
2. Identify key molecular, clinical, and family history indicators to guide genetic counseling for patients with secondary findings in genes associated with cardiomyopathy risks.
3. Understand and anticipate implications of secondary findings in inherited arrhythmia genes
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The Evolving Complexity of CFTR Testing and Counseling: A Case-Based Approach
Wednesday, June 24
12:00-1:00pm CST
Speakers:
Emily Calamaro, MGC, CGC
Charlotte Close, MS, CGC
Angel Wooden, MS, CGC
Presented by the NSGC CF and CFTR Spectrum SIG
Learning Objectives:
1. Apply reproductive genetic counseling principles to support family-building for individuals with cystic fibrosis in the era of highly effective CFTR modulator therapies.
2. Compare approaches to preconception/prenatal and newborn screening for cystic fibrosis with respect to potential diagnostic outcomes and associated management recommendations
3. Evaluate clinical and genetic factors associated with cystic fibrosis and CFTR-related conditions and their implications for patient monitoring and counseling
4. Synthesize CFTR variant interpretation resources to inform nuanced genetic counseling about unexpected CFTR findings
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NSGC Live Journal Club: Module 1 of the Journal of Genetic Counseling CEU Series
Tuesday, June 30
4:00-5:00pm CST
Join us for a live discussion on the latest research in genetic counseling by joining the inaugural NSGC Live Journal Club CEU Series. This session will feature presentations from two authors of recent Journal of Genetic Counseling articles featured in the first module of the Journal of Genetic Counseling CEU Program: “Implementing Genetic Screening into Primary Care for Medically Actionable Conditions: Insights From a Precision Health Pilot Program” (Bowler et al., 2025) and “Developing Global Consensus About Core Knowledge and Skills for Genetic Counselor Education” (McEwen et al., 2025), followed by an engaging group discussion with peers and experts.
Pricing:
Members - $35 | Non-members - $50
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Case Based Webinar Series
NSGC is pleased to announce part three of the case based webinar series. Each session will feature four case presentations, each lasting approximately 10-12 minutes, followed by a 10-12 minute Q&A segment. Part III is scheduled for August 12, 2026. The deadline to submit a case for this webinar is July 10, 2026. If you have any questions or would like additional information, please contact Mae Capaldi at mcapaldi@nsgc.org.
Submitting a Case
Please submit a concise and comprehensive case description that includes the following elements:
- The patient’s chief complaint or indication for genetic evaluation.
- Any personal history relevant to this indication, including (when applicable) the onset and progression of symptoms, relevant pathology and age at diagnosis. Include the results of any prior evaluations pertinent to the case, such as imaging, laboratory studies or previous genetic testing.
- Describe the relevant family history, highlighting features that inform genetic risk assessment.
- Present the differential diagnosis, with a brief rationale for each condition considered and an explanation of why the patient’s history raises suspicion for these diagnoses.
- Conclude with the overall assessment and a proposed plan for future testing, noting results if they are already available.
Submit a Case
Past NSGC Webinar Series
Looking for past NSGC webinars? NSGC members can watch recorded webinars in the archives listing below: