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Featured GeneDx blog posts

How GeneDx Uses AI to Improve Genomic Variant Interpretation Blog Header
AI
From thousands of variants to one answer

Learn how GeneDx uses AI-powered variant prioritization through MIMI Ranker to help clinical teams analyze exome and genome sequencing results, surface clinically relevant variants, and support faster rare disease diagnosis.

Infinity
GeneDx Showcases GeneDx Infinity™ Expansion and New Data Exploration Capabilities at ISPOR 2026

Using GeneDx Infinity™ Data to Study Cardiomyopathy Blog Header
Research Ready
Using GeneDx Infinity™ Data to Advance Cardiomyopathy Research

Neurology
Genetic Testing in Neurology: Evolving Perspectives from AAN 2026 and Beyond

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Savannah’s Story: How Exome Testing Diagnosed CTNNB1 Syndrome
Rare Disease Diagnostics

Savannah’s Story: How Exome Testing Diagnosed CTNNB1 Syndrome

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Patient Stories
Ben’s Story: How Genome Sequencing Diagnosed Labrune Syndrome
Epilepsy

Ben’s Story: How Genome Sequencing Diagnosed Labrune Syndrome

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

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

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

Bodhi’s Story: How Exome Testing Diagnosed Cabezas Syndrome

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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

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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

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

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

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

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

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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

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Research & Innovation