Mission Statement
The goal of SERN is to improve health equity and health outcomes in individuals with genetic conditions; reduce morbidity and mortality caused by genetic conditions (including congenital and metabolic disorders); and improve the quality of coordinated and comprehensive genetic services to children and their families.

Meriah Schoen PhD presents Cognitive Variability in Phenylketonuria at 2024 SERGG
41:56
Meriah Schoen PhD presents Cognitive Variability in Phenylketonuria at 2024 SERGG
Ravi Kolhe MD PhD presents The Clinical Impact of Optical Genome Mapping in Oncology Testing
44:07
Ravi Kolhe MD PhD presents The Clinical Impact of Optical Genome Mapping in Oncology Testing
Alan Percy MD presents: Rett syndrome: The Emerging Landscape of Treatment Strategies 2024 SERGG
36:46
Alan Percy MD presents: Rett syndrome: The Emerging Landscape of Treatment Strategies 2024 SERGG
Joseph J Orsini PhD presents: ScreenPlus: Laboratory Challenges and Implementation Strategies
37:54
Joseph J Orsini PhD presents: ScreenPlus: Laboratory Challenges and Implementation Strategies
Dr. Jerry Vockley presents Novel therapies for fatty acid oxidation disorders at SERGG 2024
42:14
Dr. Jerry Vockley presents Novel therapies for fatty acid oxidation disorders at SERGG 2024
Qué son cromosomas y genes Spanish with Spanish Subtitles
6:02
Qué son cromosomas y genes Spanish with Spanish Subtitles
¿Qué son pruebas genéticas Spanish with Spanish Subtitles
7:12
¿Qué son pruebas genéticas Spanish with Spanish Subtitles
Michael B. Bober, MD, PhD - Skeletal Dysplasia: Overview and Emerging Therapies (2013 SERN/SERGG)
56:06
Michael B. Bober, MD, PhD - Skeletal Dysplasia: Overview and Emerging Therapies (2013 SERN/SERGG)
Joe Muenzer PhD- Impact of New Treatment Strategies and Newborn Screening on Hunter Syndrome (2023)
47:36
Joe Muenzer PhD- Impact of New Treatment Strategies and Newborn Screening on Hunter Syndrome (2023)
Lisa Kobrynski MD, MPH - Newborn Screening Severe Combined Immunodeficiency T Cell Lymphopenia (2011
40:14
Lisa Kobrynski MD, MPH - Newborn Screening Severe Combined Immunodeficiency T Cell Lymphopenia (2011
Barry Smith PhD - How to Build Useful Ontologies for Clinical and Translational Research (2011)
1:25:10
Barry Smith PhD - How to Build Useful Ontologies for Clinical and Translational Research (2011)
Gerald Schaefer MD - Clinical Genetic Assessment of the Etiology of Autism (2009 SERN/SERGG Annual)
44:23
Gerald Schaefer MD - Clinical Genetic Assessment of the Etiology of Autism (2009 SERN/SERGG Annual)
Megan Lyon MPH - NCC update (2023 SERN/SERGG Annual Meeting)
20:11
Megan Lyon MPH - NCC update (2023 SERN/SERGG Annual Meeting)
Marilyn M Li, MD - Using Multi-omics Approaches to Inform Precision Cancer Care (2023 SERN/SERGG)
34:43
Marilyn M Li, MD - Using Multi-omics Approaches to Inform Precision Cancer Care (2023 SERN/SERGG)
Molly Ford NSGC - Legislative Update Genetic Counseling Licensure and Medicare Provider Status (2023
23:47
Molly Ford NSGC - Legislative Update Genetic Counseling Licensure and Medicare Provider Status (2023
Bruce Korf MD - The SouthSeq Project (2023 SERN/SERGG Annual Meeting)
35:17
Bruce Korf MD - The SouthSeq Project (2023 SERN/SERGG Annual Meeting)
Bekim Sadikovic, PhD - DNA Methylation Episignatures (2023 SERN/SERGG Annual Meeting)
27:27
Bekim Sadikovic, PhD - DNA Methylation Episignatures (2023 SERN/SERGG Annual Meeting)
Jill Fahrner MD - Mendelian Disorders of the Epigenetic Machinery (2023 SERN/SERGG Annual Meeting)
23:16
Jill Fahrner MD - Mendelian Disorders of the Epigenetic Machinery (2023 SERN/SERGG Annual Meeting)
Loraine Swanson MPH - Blueprint for Change: Implementation Update (2023 SERN/SERGG Annual Meeting)
22:40
Loraine Swanson MPH - Blueprint for Change: Implementation Update (2023 SERN/SERGG Annual Meeting)
2023-01-20 12.00.48 SERN Lunch and Learn 2023
1:08:22
2023-01-20 12.00.48 SERN Lunch and Learn 2023
2022-01-28 12.00.08 SERN Lunch and Learn 99395689679
1:03:52
2022-01-28 12.00.08 SERN Lunch and Learn 99395689679
Behavioral Health and Development in Individuals w Medical Conditions of Known Genetic Origin (2023)
53:29
Behavioral Health and Development in Individuals w Medical Conditions of Known Genetic Origin (2023)
Marzia Pasquali PhD FACMG - GAMT deficiency
58:15
Marzia Pasquali PhD FACMG - GAMT deficiency
Tara Britt - How Policy Impacts Rare Disease (SERN/SERGG 2022)
16:29
Tara Britt - How Policy Impacts Rare Disease (SERN/SERGG 2022)
Hans Andersson MD - What does the 2022 Medical Genetics workforce look like? (2022 SERN/SERGG)
38:44
Hans Andersson MD - What does the 2022 Medical Genetics workforce look like? (2022 SERN/SERGG)
Heidi Wallis: The Role of Families in Advancing Newborn Screening (2022 SERN/SERGG Annual Meeting)
14:07
Heidi Wallis: The Role of Families in Advancing Newborn Screening (2022 SERN/SERGG Annual Meeting)
Gabriella Pridjian MD, MBA - Alternate Therapies for Maternal PKU (2022 SERN/SERGG Annual Meeting)
16:22
Gabriella Pridjian MD, MBA - Alternate Therapies for Maternal PKU (2022 SERN/SERGG Annual Meeting)
Lori Carter Edwards, PhD - Addressing Genetic Conditions (SERN/SERGG 2022)
16:53
Lori Carter Edwards, PhD - Addressing Genetic Conditions (SERN/SERGG 2022)
Christine Matus: Long-term Care Planning for Children with Complex Healthcare Needs (2022 SERN)
33:20
Christine Matus: Long-term Care Planning for Children with Complex Healthcare Needs (2022 SERN)
Megan Lyon, MPH: An Overview of the National Coordinating Center for the Regional Genetics Networks
18:52
Megan Lyon, MPH: An Overview of the National Coordinating Center for the Regional Genetics Networks