Featured GeneDx blog posts

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From discovery to diagnosis: Canadian collaborations deliver new answers for rare disease patients
Clinical Research

From discovery to diagnosis: Canadian collaborations deliver new answers for rare disease patients

Research & Innovation
canadian-rare-disease-research-collaborations
Expanding rapid genome sequencing beyond the ICU: What a new Seattle Children’s Study means for pediatric care
Rapid Genome Sequencing

Expanding rapid genome sequencing beyond the ICU: What a new Seattle Children’s Study means for pediatric care

Research & Innovation
rapid-genome-sequencing-beyond-icu-pediatric-care
GeneDx launches Easy Order for ExomeDx™ with CMA in the provider portal
Exome

GeneDx launches Easy Order for ExomeDx™ with CMA in the provider portal

News
easy-order-exomedx-cma-provider-portal
Exome-to-Genome Reflex Ordering Is Now Available in Epic Aura
Exome

Exome-to-Genome Reflex Ordering Is Now Available in Epic Aura

News
epic-aura-exome-to-genome-reflex-ordering
Strengthening health plan collaboration to improve claims accuracy and patient access
Payor

Strengthening health plan collaboration to improve claims accuracy and patient access

News
clinical-billing-integrity-genetic-testing
Translating clinical guidance into coverage policy
Exome

Translating clinical guidance into coverage policy

Education
prenatal-exome-genome-sequencing-coverage-policy
New SMFM guidance advances the role of prenatal genomic sequencing
Payor

New SMFM guidance advances the role of prenatal genomic sequencing

Education
smfm-guidance-prenatal-genomic-sequencing
Expanding the availability of exome testing for children with developmental delays and epilepsy
Exome

Expanding the availability of exome testing for children with developmental delays and epilepsy

News
exome-testing-developmental-delay-epilepsy
Maxwell's story: How genetic testing turned uncertainty into a roadmap for action
Rare Disease Diagnostics

Maxwell's story: How genetic testing turned uncertainty into a roadmap for action

Patient Stories
slc6a1-genetic-diagnosis-maxwells-story