Begin_NGS

#BeginNGS is designed to screen #newborns for genetic diseases, connect doctors with effective treatment options & end the diagnostic odyssey. Through rapid #WholeGenomeSequencing, #raredisease can be diagnosed before symptoms appear. #NewbornScreening begin-ngs.org/?utm_source=li…

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…

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

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

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

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

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

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…

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

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

Welcome to @Begin_NGS consortium member @orchard_tx, 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

ICYMI: Dr. Stephen Kingsmore & Catherine Nester of @inozyme 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…

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

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

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

Thank you to @combined_brain 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

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

Dr. Kingsmore joined Catherine Nester of @inozyme 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…

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…

A big thank you to @EveryLifeOrg 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

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