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Browsing Tag

newborn screening

6 posts
GGenetics
Building A Future Without Missed Diagnoses
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Building A Future Without Missed Diagnoses

  • October 16, 2025
Despite advances, whole genome sequencing—and with it the promise of early, life-altering therapies—still isn’t a routine part of…
GGenetics
Illumina's constellation tech a star in Genedx pilot
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Illumina’s constellation tech a star in Genedx pilot

  • October 16, 2025
Genedx LLC partnered with Illumina Inc. to test whether Illumina’s constellation map read technology could shed light on…
GGenetics
Study: Feasibility, acceptability and clinical outcomes of the BabyScreen+ genomic newborn screening study. Image Credit: Sergei Drozd / Shutterstock
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How genomic screening in newborns found 16 hidden disorders standard tests overlooked

  • October 14, 2025
By uncovering life-altering genetic conditions before symptoms appear, genomic screening could redefine newborn care if health systems can…
GGenetics
GeneDx to Partner with Florida’s Sunshine Genetics Network, Launching Nation’s First State-Backed Genomic Newborn Screening Program
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GeneDx to Partner with Florida’s Sunshine Genetics Network, Launching Nation’s First State-Backed Genomic Newborn Screening Program

  • October 13, 2025
Florida Institute for Pediatric Rare Diseases and Representative Adam Anderson ushering in a new era of preventative care…
GGenetics
Newborn genomic screening may detect hundreds of additional childhood conditions
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Newborn genomic screening may detect hundreds of additional childhood conditions

  • October 9, 2025
Adding genomic sequencing to newborn blood screening would detect hundreds of additional childhood conditions, providing much earlier diagnosis…
GGenetics
GeneDx to Showcase Pioneering Research Findings at American Society of Human Genetics (ASHG) Annual Meeting
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GeneDx to Showcase Pioneering Research Findings at American Society of Human Genetics (ASHG) Annual Meeting

  • October 8, 2025
With unmatched scale and diversity, GeneDx Infinity™ powers scientific discovery while enabling the most precise clinical rare disease…
Ireland
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