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Are We Ready for Systematic Newborn Genome Sequencing?

Routine sampling and analysis of newborn DNA would enable screening for hundreds of childhood genetic diseases, but also raises concerns about privacy and ethics.

United statesNew yorkUnited kingdomFrance generalNorth carolinaRobert guthriePascal pujolDavid geneviNewborn genomes programmeFrench association of clinical geneticistsUniversity of montpellierCurrent international trialsFrench society of predictiveDijon specialist teamFrench associationClinical geneticists

Don t Keep Parents in the Dark About the Genetic Risks in Their Families

Don t Keep Parents in the Dark About the Genetic Risks in Their Families
reason.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from reason.com Daily Mail and Mail on Sunday newspapers.

United statesLainie friedman rossEllen wright claytonBioethics may be hazardous to your healthBabyseq projectAmerican journalHuman geneticsBioethics may be hazardous

Newborn genome sequencing project identifies unanticipated disease risks

Genomic sequencing of newborns reveals unanticipated genetic risks, prompting actionable medical interventions and potential life-saving care for infants and their families. This study highlights the value of comprehensive sequencing in newborns for early detection and management of genetic conditions.

Priyom boseNational institute of healthAmerican journalHuman geneticsstudyImage creditBabyseq projectNational instituteGenomic sequencingNewborn screening

Large-scale comprehensive sequencing helps downstream medical care in newborns

Researchers who lead the world's first comprehensive sequencing program for newborn infants have published the next chapter in the ongoing study of the BabySeq Project, with new findings on infants and families who have been followed for 3-5 years.

United statesRobertc greenLily ramseyNidhi shahAlan beggsHarvard medical schoolDisease research at boston children hospitalPeople research programManton centerDartmouth health childrenBabyseq projectAmerican journalHuman geneticsMass general brighamBoston childrenStudy corresponding author

Newborn screening project: one in 10 has genetic mutations

Newborn screening project: one in 10 has genetic mutations
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United statesRobertc greenphysicianTiziana moriconiSimone valesiniTina simonielloAlan beggsdirectorDisease research at boston children hospitalDartmouth health childrenPeople research programManton centerHarvard medical schoolWoman hospitalAmerican journalHuman geneticsBabyseq projectBoston children