Featured GeneDx blog posts

GeneDx and Start Genetic Testing Action Day Blog header

Education

GeneDx Joins Start Genetic in Support of Genetic Testing Action Day

GeneDx is proud to partner with Start Genetic in support of Genetic Testing Action Day, a global awareness campaign encouraging more individuals and families to start the conversation about genetic testing and access answers sooner.

NICU

Earlier Genetic Answers Are Changing the NICU Journey

Every NICU clinician has encountered an infant whose condition does not fully align with the expected diagnosis. This article explores key insights from a recent NANNcast conversation with Dr. Linda Genen, Chief Medical Officer at GeneDx and practicing neonatologist, and examines how rapid genome sequencing is helping care teams identify underlying genetic conditions earlier, reduce diagnostic uncertainty, and support more informed care decisions.

Stargardt disease treatment is changing. GeneDx Infinity data is helping researchers - blog header.

Ready for Research Series

Stargardt Disease: Genetic Insights are Powering the Next Generation of Research

The Stargardt disease treatment landscape is changing rapidly. Learn how genetically characterized ABCA4 data within GeneDx Infinity™ is helping researchers identify patients, strengthen clinical trials, and accelerate the development of new therapies.

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Does Ancestry Affect Genetic Testing Results? Insights From a Large Exome Study

Exome

Does Ancestry Affect Genetic Testing Results? Insights From a Large Exome Study

For Carlotta’s Family, Early Intervention Meant Everything

Rare Disease Diagnostics

For Carlotta’s Family, Early Intervention Meant Everything

Why Ordering Exome Sequencing First Matters for Epilepsy Diagnosis

Epilepsy

Why Ordering Exome Sequencing First Matters for Epilepsy Diagnosis

SeqFirst-Neo Study: Rapid Genome Sequencing in the NICU Improves Diagnosis Rates | GeneDx

NICU

SeqFirst-Neo Study: Rapid Genome Sequencing in the NICU Improves Diagnosis Rates | GeneDx

A Rare Disease Diagnosis From the Start: One Family’s Experience With Genome-Based Newborn Screening

Newborn

A Rare Disease Diagnosis From the Start: One Family’s Experience With Genome-Based Newborn Screening

Evelyn’s Story: When a Cerebral Palsy Diagnosis Wasn’t Enough

Cerebral Palsy

Evelyn’s Story: When a Cerebral Palsy Diagnosis Wasn’t Enough

From Dismissed to Diagnosed: A Family’s Journey to an HHT Genetic Diagnosis

Rare Disease Diagnostics

From Dismissed to Diagnosed: A Family’s Journey to an HHT Genetic Diagnosis

Savannah’s Story: How Exome Testing Diagnosed CTNNB1 Syndrome

Rare Disease Diagnostics

Savannah’s Story: How Exome Testing Diagnosed CTNNB1 Syndrome

Ben’s Story: How Genome Sequencing Diagnosed Labrune Syndrome

Epilepsy

Ben’s Story: How Genome Sequencing Diagnosed Labrune Syndrome