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Potential psychosocial risks of sequencing newborns

Frankel LA, Pereira S, McGuire AL

Pediatrics January 2016

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From @Genomes2People

Genomes2People @Genomes2People·

“Whole-genome sequencing may be the fastest way to diagnose rare complex diseases, but should it be incorporated into healthy newborn screening?”

Read @CarolineSeydel's "Baby's First Genome" for more on the topic of #WGS & newborn screening.

https://www.genomes2people.org/wp-content/uploads/2022/05/20220425_NatureBiotechnology.pdf

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National Human Genome Research Institute@genome_gov·

When you’re a cell that has to read the genetic code written in DNA so you can produce the molecule you need.

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FrancaFund @FrancaFund·

A concern with genetic testing is that not everyone will share equitably in the associated benefits. While progress has been made towards equity, challenges remain before GCs are reflective of the U.S. population. Visit our blog https://genomes2people.medium.com/ to learn more.
#GCchat

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Genomes2People @Genomes2People·

ICYMI: Reaping the full benefits of personalized medicine requires a cadre of genetic counselors as diverse as our patients. We’re working on it.

Read our latest @Genomes2People blog on Medium on the current state of genetics. https://genomes2people.medium.com/unlocking-a-cosmos-of-diversity-within-the-profession-of-genetic-counseling-b4d6218f8440

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Genomes2People @Genomes2People·

JOIN US: For a #virtual #webinar hosted by @usnews on May 19th @ 12pm EST.

@RobertCGreen will join leading experts to discuss the implementation of genetic screening programs can be incorporated into routine care.

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Research In Translational Genomics and Health Outcomes

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