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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 Infinityâ„¢ Expansion and New Data Exploration Capabilities at ISPOR 2026

Using GeneDx Infinityâ„¢ Data to Study Cardiomyopathy Blog Header
Research Ready
Using GeneDx Infinityâ„¢ Data to Advance Cardiomyopathy Research

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

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Genetic Testing for Unexplained Epilepsy in Adults
Epilepsy

Genetic Testing for Unexplained Epilepsy in Adults

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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

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Education
What Is the Diagnostic Odyssey — And How Can We End It?
Genomics

What Is the Diagnostic Odyssey — And How Can We End It?

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Education
Genomic Testing Reduces Healthcare Costs and Improves Outcomes
Genomics

Genomic Testing Reduces Healthcare Costs and Improves Outcomes

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Research & Innovation
Autism Research Breakthrough: 230 New Genes Linked to Autism
Autism

Autism Research Breakthrough: 230 New Genes Linked to Autism

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Research & Innovation
Rare Disease Day: Moving Beyond Awareness to Action
Education

Rare Disease Day: Moving Beyond Awareness to Action

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Education