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NSGC Webinar Series

 

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 individual webinars, or as the full 2026 package. NSGC members can view webinar recordings by visiting the 2026 Webinar Series members archive.

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 CT 

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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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:

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