Nurture is rooted in research and reputation — and we are committed to bringing clarity and collaboration to genomic screening. Below is a collection of resources to explore.
Resources
Resources
Nurture is rooted in research and reputation — and we are committed to bringing clarity and collaboration to genomic screening. Below is a collection of resources to explore.
How Nurture Works
See how Nurture works — from online ordering to genetic counseling support.
What You’ll Learn From Nurture
Learn more about genetics and how Nurture’s service differs from other genetic testing.
Nurture’s Informed Consent
Understand the benefits and limitations of Nurture’s service.
How Genomic Sequencing Works
Go behind the scenes and learn what happens after a sample collection arrives at the lab.
Dr. Robyn R. Heister: Why Genetics Matter
Dr. Robyn R. Heister talks about her son’s journey with a rare genetic disorder and how that led to her profession in genetics.
Nurture Co-founder Dr. Green speaks with CBS News
Dr. Green discusses his ground-breaking research and a mom shares her experience learning of her son’s genetic condition.
Nurture’s Guide to Genetic Counseling
Nurture includes genetic counseling, before and after testing, as part of our service. Understand what genetic counseling is and how it can help.
Nurture screens for 400+ actionable, childhood-onset conditions. See the complete list of conditions that we screen for details.
Review the list of 413 genes included in Nurture’s screening panel.
Nurture is suitable for any family that wants to screen their healthy newborn for genetic risk factors for pediatric-onset conditions. Download to learn more.
You’ve purchased Nurture Genomics | Screening Service for Children — Congratulations! This is your guide to what you can expect next.
ARTICLES
Boston doctor wants more screening for rare genetic conditions in newborn babies
CBS Boston | February 2024
BabySeq Project Unearths Actionable Genetic Variants Impacting Infants, Parents
Genome Web | June 2023
‘We arguably saved their lives’: Newborn DNA-sequencing reveals elevated cancer risks for parents
Stat News | June 2023
Should a baby’s genes be sequenced at birth? Study finds potential life-saving benefits
USA Today | June 2023
Experts Endorse Universal Genomic Screening of Monogenic, Treatable Diseases in Newborns
Genome Web | May 2023
Should All U.S. Newborns Undergo Genomic Testing?
U.S. News & World Report | May 2023
CNN | March 2023
Can Genomic Screening of Newborns Help More Children Born with Rare Diseases?
Columbia University Irving Medical Center News | February 2023
Yahoo | February 2023
By sharing their genetic risks, Hemsworth, Jolie are raising awareness of testing
Chicago Tribune | December 2022
Newborns to get rapid genetic disease diagnosis
BBC News | December 2022
Revealing the hidden impact of whole genome sequencing on the family
New Scientist | August 2022
Genomic Screening of Healthy Newborns Gets More Popular
Medscape | December 2021
The Wilderness of Rare Genetic Diseases and the Parents Navigating It
New York Times | July 2020
PODCASTS
Guest: Dr. Robert Green Topic: Discussing The Future of Genetic Testing, Episode #05
Beyond the Heart | October 2022
The Genetics Podcast | April 2021
Dr Robert Green: A liberating vision of the future
The G Word | October 2021
VIDEOS
When Doctors Don’t Know What’s Wrong
TEDx Talks | January 2020
Genetics 101 — What is Genetics?
National Geographic | July 2018
TEDx Talks | February 2017
Genetic Counseling: How much do you want to know?
TEDx Talks | February 2022
Genomic newborn screening: Are we entering a new era of screening?
Published in Journal of Inherited Metabolic Disease | July 2023
Published in The American Journal of Human Genetics (AJHG) | July 2023
Genomic newborn screening for rare diseases
Published in Nature Reviews Genetics (Nat Rev Genet) | June 2023
Perspectives of Rare Disease Experts on Newborn Genome Sequencing
Published in The Journal of the American Medical Association (JAMA) | May 2023
Newborn Screening Conditions: Early Intervention and Probability of Developmental Delay
Published in Journal of Developmental & Behavioral Pediatrics | April 2023
Published in The American Journal of Medical Genetics (AJMG) | February 2023
Prioritizing the detection of rare pathogenic variants in population screening
Published in Nature Reviews Genetics | January 2023
Published in Frontiers in Genetics | April 2022
Are we prepared to deliver gene-targeted therapies for rare diseases?
Published in The American Journal of Medical Genetics (AJMG) | December 2022
Newborn Sequencing in Genomic Medicine and Public Health (NSIGHT)
Published on NIH National Genome Research Institute website | Archive
