Our unwavering vision—a world where every child receives timely intervention for any genetic condition.
Our unwavering vision—a world where every child receives timely intervention for any genetic condition.
OUR STORY
Nurturing innovation.
We bridge the gap between knowledge and impact, providing parents and healthcare providers meaningful health insights based on cutting-edge genomic science. Led by clinical geneticists, researchers, and genetic counselors, Nurture puts genomic science into practice. We provide genome sequencing for healthy babies and children, facilitating early diagnosis and timely access to life-changing medical interventions.
Learn About Our Service
OUR STORY
Nurturing innovation.
We bridge the gap between knowledge and impact, providing parents and healthcare providers meaningful health insights based on cutting-edge genomic science. Led by clinical geneticists, researchers, and genetic counselors, Nurture puts genomic science into practice. We provide genome sequencing for healthy babies and children, facilitating early diagnosis and timely access to life-changing medical interventions.
Learn About Our ServiceOUR FOUNDERS
On a mission to help children live their healthiest lives.
Rooted in research.
Nurture was co-founded by Robert Green, MD, MPH, leader of the BabySEQ Project, whose evidence-driven work informs every aspect of Nurture’s service offering. BabySEQ1 was a landmark clinical study looking at newborn genetic risk markers. Later, the study’s findings were used to create a catalog of gene-disease associations, accelerating the real-world application of newborn genomic sequencing (NGS).
See the BabySEQ StudyOUR FOUNDERS
On a mission to help children live their healthiest lives.
Rooted in research.
Nurture was co-founded by Robert Green, MD, MPH, leader of the BabySEQ Project, whose evidence-driven work informs every aspect of Nurture’s service offering. BabySEQ1 was a landmark clinical study looking at newborn genetic risk markers. Later, the study’s findings were used to create a catalog of gene-disease associations, accelerating the real-world application of newborn genomic sequencing (NGS).
See the BabySEQ StudyOUR MEDICAL TEAM
Deep expertise and hands-on
experience to forge a new path forward.
VP of Operations and Certified Genetic Counselor
Genetic counselor and
telehealth operations
Medical Director, Genetics
Assistant Clinical Professor of Pediatrics, Division of Genetics at UCLA Health
Pediatrician and
medical geneticist
Medical Director, Genetics
Assistant Professor of Pediatrics, Division of Human Genetics at CHOP
Pediatrician and rare
genetic disease expert
OUR MEDICAL TEAM
Deep expertise and hands-on
experience to forge a new path forward.
VP of Operations and Certified Genetic Counselor
Genetic counselor and
telehealth operations
Medical Director, Genetics
Assistant Clinical Professor of Pediatrics, Division of Genetics at UCLA Health
Pediatrician and
medical geneticist
Medical Director, Genetics
Assistant Professor of Pediatrics, Division of Human Genetics at CHOP
Pediatrician and rare
genetic disease expert
Navigating genetics
with humility.
We Strive to:
- Close the gap in genomics-supported health
- Move health equity in genomic research forward
- Provide an inclusive and relevant clinical support experience
We are dedicated to advancing genomic science to help all families learn more about their genetic risks and take action so children can live their healthiest lives. Our journey begins with an unwavering vision — a world where every child receives timely intervention for any genetic condition. We recognize the important work ahead of us as we endeavor to see that our service is accessible to and impactful for all. Thank you for taking this first step with us.
Navigating genetics
with humility.
We are dedicated to advancing genomic science to help all families learn more about their genetic risks and take action so children can live their healthiest lives. Our journey begins with an unwavering vision — a world where every child receives timely intervention for any genetic condition. We recognize the important work ahead of us as we endeavor to see that our service is accessible to and impactful for all. Thank you for taking this first step with us.
We Strive to:
- Close the gap in genomics-supported health
- Move health equity in genomic research forward
- Provide an inclusive and relevant clinical support experience
A trusted partner in the pursuit of better health.
To facilitate our groundbreaking work, Nurture has partnered with the innovative team at the Broad Institute of MIT and Harvard, a community of researchers founded in 2004 to fulfill the promise of genetic medicine. Broad Clinical Labs is a CLIA/CAP-accredited laboratory with cutting-edge sequencing tools and methodologies.
A trusted partner in the pursuit of better health.
To facilitate our groundbreaking work, Nurture has partnered with the innovative team at the Broad Institute of MIT and Harvard, a community of researchers founded in 2004 to fulfill the promise of genetic medicine. Broad Clinical Labs is a CLIA/CAP-accredited laboratory with cutting-edge sequencing tools and methodologies.
