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Baylor Genetics Baylor Genetics is a joint venture of H.U. Group Holdings and the #1 NIH-funded genetics program at

Baylor Genetics is founded in academics and driven by discovery; we are dedicated to delivering comprehensive answers to the toughest genetic questions.

In a recent study of more than 650 children, Baylor Genetics’ Whole Genome Sequencing provided a genetic diagnosis for n...
10/27/2026

In a recent study of more than 650 children, Baylor Genetics’ Whole Genome Sequencing provided a genetic diagnosis for nearly one-third (31.1%) of patients, with additional diagnoses identified among some patients who previously underwent exome sequencing.

Our latest blog discusses the study findings and clinical value of using genome sequencing earlier in the diagnostic odyssey.

Read the blog to learn more: https://www.baylorgenetics.com/blog/study-highlights-the-clinical-value-of-genome-sequencing-in-children-with-developmental-disorders/

We’re wrapping up ASHG 2026 in Montréal after a great week with the genetics community. We were proud to share research ...
10/23/2026

We’re wrapping up ASHG 2026 in Montréal after a great week with the genetics community. We were proud to share research focused on advancing genomic diagnosis for individuals with rare and complex conditions, including findings across genome sequencing, mitochondrial testing, and novel genomic findings.

Thank you to everyone who visited our booth, attended our presentations, and connected with our team throughout the meeting. If we missed you at , we'd love to connect: https://www.baylorgenetics.com/contact/

Bonjour, Montréal!Baylor Genetics is at presenting research exploring the diagnostic utility of genome sequencing, nov...
10/21/2026

Bonjour, Montréal!

Baylor Genetics is at presenting research exploring the diagnostic utility of genome sequencing, novel findings in developmental and epileptic encephalopathy, and factors that may help optimize clinical mitochondrial testing.

Join us as our team shares findings that highlight the value of advanced genomic technologies in informing diagnosis and clinical decision-making.

Visit booth #500 to connect with our team and learn more about how genomic research is advancing diagnosis for individuals with rare and complex conditions: https://www.baylorgenetics.com/news/baylor-genetics-to-highlight-clinical-and-diagnostic-utility-of-genome-sequencing-at-the-2026-american-society-of-human-genetics-annual-meeting/

10/20/2026

Thank you to everyone who connected with us at in Montréal.

The conversations throughout the meeting highlighted the growing role of genomic testing in helping clinicians uncover answers and inform care for patients with neurological conditions.

We appreciate the opportunity to be part of this year's meeting as an official genetic testing partner of the Child Neurology Society. https://www.baylorgenetics.com/news/baylor-genetics-to-showcase-how-genome-sequencing-is-advancing-pediatric-care-at-the-2026-child-neurology-society-annual-meeting/

We're in Montréal for , joining important conversations around the latest developments in genomic testing for neurologi...
10/15/2026

We're in Montréal for , joining important conversations around the latest developments in genomic testing for neurological disorders.

Stop by booth #500 to meet our team and explore how genomic testing is helping clinicians uncover answers for patients with complex neurological conditions.

We look forward to seeing you! www.baylorgenetics.com/conferences/cns-2026/

Live from in Montréal.Join us for our satellite lunch symposium, From Genome to Diagnosis: The Next Era of Precision N...
10/14/2026

Live from in Montréal.

Join us for our satellite lunch symposium, From Genome to Diagnosis: The Next Era of Precision Neurology. Expert speakers will discuss emerging approaches to genetic diagnosis and the evolving role of genomics in neurology.

Visit Baylor Genetics at booth #500 to learn how advanced genomic technologies are helping expand access to diagnosis and support more informed clinical decision-making:
www.baylorgenetics.com/conferences/cns-2026/

“For children with rare or undiagnosed conditions, every minute spent without a diagnosis can be marked by uncertainty a...
10/12/2026

“For children with rare or undiagnosed conditions, every minute spent without a diagnosis can be marked by uncertainty and missed opportunities for care. At Baylor Genetics, we're committed to changing that.” — Christine Eng, MD, Chief Medical Officer and Chief Quality Officer, Baylor Genetics

At the 2026 Child Neurology Society Annual Meeting, Baylor Genetics will highlight the growing role of genome sequencing in pediatric neurology through a satellite symposium and poster presentations focused on diagnostic yield, clinical utility, and access to testing.

Visit us at booth #500 to connect with our team and learn more about how comprehensive genomic testing and advanced technologies are helping inform precision neurology: https://www.baylorgenetics.com/news/baylor-genetics-to-showcase-how-genome-sequencing-is-advancing-pediatric-care-at-the-2026-child-neurology-society-annual-meeting/

ICoNS 2026 brought together a community of researchers, clinicians, advocates, and policymakers dedicated to the future ...
10/10/2026

ICoNS 2026 brought together a community of researchers, clinicians, advocates, and policymakers dedicated to the future of newborn sequencing.

We were honored to celebrate the launch of Florida's Sunshine Genetics Pilot Program, the first statewide program to offer Whole Genome Sequencing for newborn screening. As a strategic sequencing partner and the lead sequencing provider at launch, Baylor Genetics is proud to support this effort to expand access to genomic newborn screening and help shape the future of pediatric health.

Additionally, our team presented research highlighting how genome sequencing can support the identification of genetic hearing loss and inform earlier care for infants and families.

Learn how this statewide initiative is expanding access to genomic newborn screening and helping shape the future of pediatric health: https://www.baylorgenetics.com/news/baylor-genetics-selected-as-the-lead-sequencing-partner-for-floridas-sunshine-genetics-pilot-program-launch/

Every discovery has the potential to expand our understanding of rare and complex genetic conditions. At ASHG 2026, Bayl...
10/06/2026

Every discovery has the potential to expand our understanding of rare and complex genetic conditions. At ASHG 2026, Baylor Genetics is proud to share research that highlights how comprehensive genomic analysis can uncover novel findings, improve diagnostic insight, and inform clinical testing strategies.

Join our team as we present research highlighting the clinical utility of advanced genomic technologies in improving diagnosis for individuals with complex genetic and neurological conditions.

We look forward to connecting with researchers, clinicians, and genetic healthcare professionals throughout the meeting. Visit us at booth 500 to learn more: www.baylorgenetics.com/conferences/ashg-2026/



American Society of Human Genetics - ASHG [tag]

Thank you to the American Academy of Pediatrics and everyone who connected with us at .The conversations throughout the...
10/06/2026

Thank you to the American Academy of Pediatrics and everyone who connected with us at .

The conversations throughout the meeting reflected the growing role of genome sequencing in pediatric care and the importance of delivering answers for children with complex genetic conditions.

It was a privilege to have Lisa Mullen Salz, MS, LCGC, present research highlighting the impact of genome sequencing across pediatric indications.

If you'd like to continue the conversation or learn more about how genome sequencing can support pediatric diagnosis, connect with our team: https://www.baylorgenetics.com/contact/

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77021

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