GeneDx presents new evidence advancing genomic newborn screening at ICoNS 2026. Key Takeaway: GeneDx has presented new evidence that supports the advancement of genomic newborn screening at the ICoNS 2026 conference. This development highlights the company's commitment to enhancing healthcare through innovative genomic solutions. The findings could lead to significant improvements in newborn screening practices. Market sentiment analysis. Positive factors. * GeneDx is advancing genomic newborn screening. * New evidence presented at a significant conference. * Potential for improved healthcare outcomes. GAITHERSBURG, md.-(business wire)-genedx presents new evidence advancing genomic newborn screening at ICoNS 2026. Frequently asked questions. What did GeneDx present at ICoNS 2026? GeneDx presented new evidence advancing genomic newborn screening. What is the significance of genomic newborn screening? Genomic newborn screening can enhance healthcare outcomes for infants. Where was the evidence for newborn screening presented? The evidence was presented at the ICoNS 2026 conference.

GeneDx introduces Easy Order at AAP 2026 to simplify genomic testing in everyday Pediatric Care. New tools make genomic testing easier from ordering through results, helping pediatricians confidently integrate genomics into routine care GAITHERSBURG, Md.-(BUSINESS WIRE)-GeneDx, the leader in rare disease diagnosis and improving health through the power of genomic data, today announced it will introduce Easy Order at the 2026 American Academy of Pediatrics (AAP) National Conference & Exhibition, October 2-6 in San Diego. The new streamlined experience makes it faster and simpler for general pediatricians to order ExomeDx(TM) and chromosomal microarray (CMA) and is part of GeneDx's broader effort to simplify genomic testing from ordering through understanding and communicating results. "General pediatricians are often the first to recognize developmental concerns and are uniquely positioned to help families get answers sooner," said Linda Genen, M.D., M.P.H., Chief Medical Officer of GeneDx. Share In 2025, the AAP updated its guidance to recommend exome or genome sequencing as a first-tier test for children with global developmental delay (GDD) or intellectual disability (ID), marking an important shift toward genomic testing in routine pediatric care. GeneDx is focused on helping pediatricians put that guidance into practice by removing barriers across the testing experience. Available through the GeneDx Provider Portal, Easy Order provides a guided workflow that reduces required inputs and helps general pediatricians, including those who may not regularly order genetic testing, submit complete orders with confidence. "General pediatricians are often the first to recognize developmental concerns and are uniquely positioned to help families get answers sooner," said Linda Genen, M.D., M.P.H., Chief Medical Officer of GeneDx. "Making genomic testing part of everyday pediatric care means designing the entire experience for the pediatrician, not just the genetics expert, so they can confidently order the right test, interpret results and talk with families about what those results mean and what comes next." GeneDx is also developing Provider Report Guides that will surface provider-friendly explanations directly within reports, helping non-genetics experts understand results faster, communicate them to families and determine next steps, alongside new educational resources designed to make genetic findings clearer and more actionable. These efforts extend beyond product and education, with GeneDx serving as the implementation partner for the Leveraging Genomic Assessment of Developmental Delay (LEAD) Project, a national initiative advancing earlier genomic testing for children with developmental delay and related neurodevelopmental conditions. At the AAP National Conference & Exhibition, GeneDx will host educational programming focused on integrating exome and genome sequencing into pediatric care, including: * Implementing Recommended Genetic Testing for Patients with GDD or ID: A Practical Guide for Pediatricians - Saturday, October 3, 1:15 p.m. PDT, Product Theater C booth #3020 * Explore the AAP recommendation for exome (+CMA) and genome sequencing as first-line testing options for children with GDD and ID, including how to identify patients who may benefit and how results can help inform more precise care. Learn how GeneDx clinical expertise, resources, and patient support can help pediatric care teams incorporate genetic testing into practice. *This Product Theater is not designated for CME credit and is not sponsored nor endorsed by the American Academy of Pediatrics. * Diagnosis is Action: Why Earlier Answers Matter in Pediatric Care - Saturday, October 3, 2:00 p.m. PDT at the GeneDx booth #1031 * Join Dr. Tommy Martin, Internal Medicine and Pediatrics Physician, and Geraldine Bliss, President and Co-founder of CureSHANK, as they share clinical and family perspectives on the benefits of earlier genetic testing, how a genetic diagnosis can inform more personalized care, and how answers can connect families to condition-specific resources and support. About GeneDx GeneDx's (Nasdaq: WGS) mission is to empower everyone to live their healthiest life through genomics. GeneDx combines unmatched clinical expertise, advanced technology, and the power of GeneDx Infinity(TM)- the world's largest rare disease genomic dataset. This unparalleled foundation powers GeneDx's ExomeDx(TM) and GenomeDx(R) tests - ranked #1 by expert geneticists and granted FDA Breakthrough Device designation - enabling clinicians to deliver precise, fast, and actionable diagnoses. GeneDx Infinity also fuels discovery for biopharma, with the most powerful AI-driven genomic intelligence. A genomics pioneer over the last 25 years, diagnosing more than 4,800 genetic diseases and publishing more than 1,000 research publications, GeneDx is building the network that will drive the future of genomic precision medicine. For more information, visit genedx.com and connect with Business Wire, Inc. on LinkedIn, Facebook, and Instagram. 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A further list and description of risks, uncertainties and other matters can be found in the "Risk Factors" section of its Annual Report on Form 10-K for the fiscal year ended December 31, 2025 and its Quarterly Report on Form 10-Q for the fiscal quarter ended March 31, 2026, filed with the SEC on May 4, 2026, its Quarterly Report on Form 10-Q for the fiscal quarter ended June 30, 2026, filed with the SEC on August 3, 2026 and other documents filed by Business Wire, Inc. from time to time with the SEC. These filings identify and address other important risks and uncertainties that could cause actual events and results to differ materially from those contained in the forward-looking statements. Forward-looking statements speak only as of the date they are made. Readers are cautioned not to put undue reliance on forward-looking statements, and Business Wire, Inc. assume no obligation and do not intend to update or revise these forward-looking statements, whether as a result of new information, future events, or otherwise. Business Wire, Inc. do not give any assurance that Business Wire, Inc. will achieve its expectations. More News From GeneDx GAITHERSBURG, Md.-( BUSINESS WIRE )-GeneDx and Beren Therapeutics Launch NPC GenomeComplete to Improve Diagnosis of Niemann-Pick Disease Type C... GAITHERSBURG, Md.-( BUSINESS WIRE )-Katherine Stueland, CEO of GeneDx, has been named a 2026 Fierce 50 honoree for Health Equity... GAITHERSBURG, Md.-( BUSINESS WIRE )-GeneDx and Seattle Children's show hospital-wide rapid genome sequencing accelerates accurate diagnosis and expands access to answers for children... GeneDx. NASDAQ:WGS Release Summary Release Versions