We've announced our membership to the Begin_NGS consortium to help improve #NewbornScreening. Eric Crombez, MD, Chief Medical Officer for Gene Therapy at Ultragenyx, shares his perspective on the importance of this program. Read the blog post: ultragenyx.co/3C7XD6l

A big thank you to EveryLife Foundation for their support of Begin_NGS + our mission to end the diagnostic odyssey for neonatal & pediatric #raredisease. Learn more about this advocacy group here: everylifefoundation.org #BeginNGS #WholeGenomeSequencing #NewbornScreening

A new article from Dr. Stephen Kingsmore shares the urgent need for extensive expansion of #NewbornScreening by genomic sequencing, the reasons why early attempts had limited success & how we're working to end the diagnostic & therapeutic odysseys. onlinelibrary.wiley.com/doi/10.1002/aj…

Dr. Kingsmore joined Catherine Nester of Inozyme Pharma on the #RareDisease Report podcast. They discussed the role of #newbornscreening in diagnosing #rarediseases + the impact that Begin_NGS can have on the future of rare disease medicine. #weekendlistening hcplive.com/view/rare-dise…

Welcome to Begin_NGS consortium member, Mahzi Therapeutics! We thank Mahzi for supporting the #BeginNGS pilot program & joining our mission to end the diagnostic odyssey. mahzi.com #RareDisease #RapidPrecisionMedicine #NewbornScreening

Thank you to COMBINEDBrain for its support Begin_NGS. COMBINEDBrain is a non-profit consortium devoted to speeding the path to clinical treatments for people with severe rare genetic, non-verbal, neurodevelopmental disorders. #RareDisease #BeginNGS combinedbrain.org

Want to learn more about Begin_NGS at #ASHG2022? Join Bill Mowrey of Alexion for “A genome sequencing system for universal #newbornscreening, diagnosis, & #precisionmedicine for severe genetic diseases.” Friday, 10/28, 2:45pm ashg.org/meetings/2022-… #RareDisease

#RareDisease Newborn Screening, Genetic Testing Varies by State - National Press Foundation | NPF nationalpress.org/topic/newborn-…, see more tweetedtimes.com/search/%23Rare…

IHTC's Dr. Amy Shapiro discussed Begin_NGS with WISHTV, an initiative she describes as a "quantum leap forward" in newborn screening. bit.ly/3syC0aT #NewbornScreening #WholeGenomeSequencing #RareDisease #RapidPrecisionMedicine

ICYMI: Dr. Stephen Kingsmore & Catherine Nester of Inozyme Pharma were guests on the #RareDisease Report podcast. They discussed the role of #newbornscreening in diagnosing rare diseases + the impact Begin_NGS can have on the future of rare disease medicine. hcplive.com/view/rare-dise…

Welcome to Begin_NGS consortium member Orchard Therapeutics - U.S., a company focused on new treatments that tap into the curative potential of HSC gene therapy. Thx for sharing in the vision to end the diagnostic odyssey. orchard-tx.com #RareDisease #WGS #NewbornScreening

Great blog by APHL about the importance of #WholeGenomeSequencing & maintaining genetic privacy. The #newbornscreening community is adopting processes for request & approval, destruction, storage & documentation to have more transparency. aphlblog.org/the-promise-of… #RareDisease

Looking back at our 2022 highlights: the launch of our #BeginNGS newborn genomic screening initiative marked a major milestone. More in The San Diego Union-Tribune: sandiegouniontribune.com/news/health/st… #NewbornScreening #WholeGenomeSequencing

The annual Frontiers in Pediatric Genomic Medicine Conference is back, both in person and online. This year's theme is "Taking Steps Towards Ending the Diagnostic Odyssey." Mark your calendars for April 19-20, 2023. Registration opens in February. radygenomics.org/frontiers-conf…

Today we’re excited to announce our new partnership with @Plumcare to support @BeginNGS_Greece & Rady Genomics in Greece's new national pioneering newborn sequencing program. bit.ly/3GS29Zb

Our team is looking forward to meeting up with both prospective and founding members of the Begin_NGS consortium at WORLDSymposia tomorrow. It's exciting to be working together to #endthediagnosticodyssey. #genomics #raredisease

In light of #RareDiseaseMonth, we thank our Begin_NGS partner EveryLife Foundation for joining our mission to screen newborns early for genetic diseases — and connect their doctors with effective interventions. Learn more: everylifefoundation.org #RareDisease #genomics

We had an inspiring time convening with the founding & prospective members of the Begin_NGS consortium at #WORLDSymposia. Thank you to all who accompany us in our journey to help end the diagnostic & therapeutic odysseys. #EndTheDiagnosticOdyssey #genomics #raredisease

Since our last Frontiers conference in 2019, there have been major advances in the world of genomic sequencing. At #GenomicFrontiers23, speakers from around the globe will share the latest research in #NewbornScreening & #WholeGenomeSequencing. Register: radygenomics.org/frontiers

Welcome Begin_NGS founding consortium member Sanofi. For 40+ yrs, Sanofi has been a pioneer of science & innovation, rallying its people & resources to help improve the lives of those living with #RareDisease. We thank Sanofi for its #BeginNGS support. sanofi.com/en/your-health…