Featured GeneDx blog posts

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Genome Sequencing for Newborn Screening: First Results From the GUARDIAN Study
Newborn

Genome Sequencing for Newborn Screening: First Results From the GUARDIAN Study

Research & Innovation
Bodhi’s Story: How Exome Testing Diagnosed Cabezas Syndrome
Rare Disease Diagnostics

Bodhi’s Story: How Exome Testing Diagnosed Cabezas Syndrome

Patient Stories
Simon’s Story: How Genetic Testing Diagnosed a Rare Immune Disorder
Rare Disease Diagnostics

Simon’s Story: How Genetic Testing Diagnosed a Rare Immune Disorder

Patient Stories
How Genetic Testing Can Help Identify the Cause of Epilepsy in Children
Epilepsy

How Genetic Testing Can Help Identify the Cause of Epilepsy in Children

Education
Why Year-End Is the Right Time to Order Genetic Testing
Financial

Why Year-End Is the Right Time to Order Genetic Testing

Education
Three Hospitals. Two Surgeries. One Rare Disease Diagnosis: Layla’s Story
Genome

Three Hospitals. Two Surgeries. One Rare Disease Diagnosis: Layla’s Story

Patient Stories
Rare Disease Data for Patient Advocacy Organizations: Introducing GeneDx Discover Snapshot
Rare Disease Diagnostics

Rare Disease Data for Patient Advocacy Organizations: Introducing GeneDx Discover Snapshot

Research & Innovation
Genetic Testing for Unexplained Epilepsy in Adults
Epilepsy

Genetic Testing for Unexplained Epilepsy in Adults

Education
AAP Recommends Exome and Genome Sequencing for Developmental Delay and Intellectual Disability
Genomics

AAP Recommends Exome and Genome Sequencing for Developmental Delay and Intellectual Disability

Education