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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.

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’s Conditions List

Nurture screens for 400+ actionable, childhood-onset conditions. See the complete list of conditions that we screen for details.

Nurture’s Gene List

Review the list of 413 genes included in Nurture’s screening panel.

Nurture’s Clinicians Sheet

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.

What To Expect Next

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

100,000 newborn babies will have their genomes sequenced in the UK. It could have big implications for child medicine

CNN | March 2023

Can Genomic Screening of Newborns Help More Children Born with Rare Diseases?

Columbia University Irving Medical Center News | February 2023

It takes an average of 8 years for a rare disease patient to get diagnosed. Why is it so hard to get life-altering genetic testing in the U.S.?

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

VIDEOS

When Doctors Don’t Know What’s Wrong

TEDx Talks | January 2020

Genetics 101 — What is Genetics?

National Geographic | July 2018

What Is Genetic Counseling?

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

Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project

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

Moving away from one disease at a time: Screening, trial design, and regulatory implications of novel platform technologies

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

Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study

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