BeginNGS is a novel health care delivery system designed to screen newborns for genetic diseases — and connect their doctors with effective treatment options.
Joined May 2022
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Begin_NGS retweeted
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/sp…
Begin_NGS retweeted
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
Begin_NGS retweeted
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
Begin_NGS retweeted
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
Begin_NGS retweeted
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-c…
Begin_NGS retweeted
Looking back at our 2022 highlights: the launch of our #BeginNGS newborn genomic screening initiative marked a major milestone. More in @sdut: sandiegouniontribune.com/new…
#NewbornScreening #WholeGenomeSequencing
Begin_NGS retweeted
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
Begin_NGS retweeted
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
Begin_NGS retweeted
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-diseas…
Begin_NGS retweeted
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
Begin_NGS retweeted
#RareDisease Newborn Screening, Genetic Testing Varies by State - National Press Foundation | NPF nationalpress.org/topic/newb…, see more tweetedtimes.com/search/%23R…
Begin_NGS retweeted
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-annua…
#RareDisease
Begin_NGS retweeted
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/
Begin_NGS retweeted
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
Begin_NGS retweeted
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-diseas…
Begin_NGS retweeted
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
Begin_NGS retweeted
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
Begin_NGS retweeted
Genomic Newborn Screening Studies Around the World Begin to Take Baby Steps. At the inaugural International Conference on Newborn Sequencing in Boston last week, researchers outlined plans from eight studies in the US, the UK, Europe, and Australia. ow.ly/Q6Sg10476NO
Begin_NGS retweeted
"It's very similar to traditional newborn screening but it's on steroids" Dr. Kingsmore explains about @Begin_NGS diagnostic guidance tool. "It's 12 times as many conditions—12x as many lives saved, organs saved, heartbreak avoided" #precisionmedicine #WGS
ow.ly/8qqj50L6jaK
Begin_NGS retweeted
In this Rare Disease Report, Dr. Stephen Kingsmore, @RadyGenomics and Catherine Nester, RN, @inozyme, speak with @GiulianaGrossi about how the novel diagnostic tool @Begin_NGS will change rare disease medicine.
#PrecisionMedicine #NewbornScreeningAwareness
ow.ly/u7pG50L6YrZ