Testimonials

Hear from our community

Discover the real-world impact of Fore Genomics through our library of testimonials. Watch heartfelt videos and browse through photos capturing genuine experiences.

For insights into navigating your child’s health with our services, connect with our parent advocates, whose contact details are available for those who wish to reach out directly.

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Caroline

I wanted to get my daughter screened as my family has a history of genetic disease.

Fore had the most comprehensive genetic health screen I could find and their service was easy to use. Our family was concerned about how confidential and private the process and results would be. We were very pleased that we could order online, collect a sample at home and have a private conversation with a genetic counselor on our results.

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Ashley

My family is focused on healthy living and being able to be proactive about healthcare for our kids is important to us.

I have seen a number of family health solutions and this peaked my interest as something to increase the knowledge of my child’s health. The post-test genetic counseling session was very insightful and the most valuable part of the experience for my family.

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Nick

I work in healthcare and am always looking forthe newest technologies that can help families live healthier lives.

A lot is focused on helping adults and very little focused on helping kids. Understanding DNA and genetic health risk early in life really helps build a lifetime of precisions healthcare. It’s great to see a solution introduced to families directly. I had my questions about how easily the results translate to our pediatrician. It’s been a very smooth process and our pediatrician is receptive to this extra insight.

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Suzanne

From a family with physicians and lots of experience around healthcare solutions, this has been a great preventative care experience.

A wonderful gift to my daughter, for her child. We are happy to have this level of care for our family.

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Mandy

The service was very easy to use.

Everything went as expected without delays. Reports were clear and the information was easy to understand.  The peace of mind that comes with the knowledge of my child’s potential to develop disease is invaluable.

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Morgan

During my pregnancy journey I learned my family had a history of genetic disease.

Once my child was born I knew I needed Fore’s genetic health screen to ensure I was prepared for any potential disease my child may have to face.

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Learning made visual

Streamline your educational journey with our comprehensive video library. From tutorials that simplify complex genetic concepts to deep-dives into our service’s nuances, every visual resource you need is right here, in one convenient location.

Featured Videos

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Genetic Counseling Basics
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Introduction to Genetic Health Screening

Stay informed with the latest discoveries

Keep abreast of the latest advancements in genetics with our selection of research articles. We bring you news and scholarly articles that resonate with both the scientific and healthcare communities, fostering a well-informed approach to children’s genetic health.

Research Articles

1. Actionability of unanticipated monogenic disease risks in newborn genomicscreening: Findings from the BabySeq Project

Published in American Journal of Human Genetics | July 2023

2. Genomic sequencing for newborn screening: current perspectives and challenges

Published in Croatian Medical Journal | 2024 Volumes 65-261

3. From newborn screening to genomic medicine: challenges and suggestions on how to incorporate genomic newborn screening in public health programs

Published in Medzinische Genetik | 2022

4. Newborn genetic screening is highly effective for high-risk infants: A single-centre study in China

Published in Journal of Global Health | October 2023

5. Newborn screening for genetic disorders: Current status and prospects for the future

Published in Pediatric Investigation | October 2022

6. Genomic Sequencing as a First-Tier Screening Test and Outcomes of Newborn Screening

Published in JAMA Network Open | September 2023

7. The key principles behind newborn genome screening

Published in Genomics Education Programme | October 2023

8. Bringing equity to genomic sequencing in newborns: BabySeq 2.0

Published in Bostin Children’s Hospital Answers | October 2023

9. Genome Sequencing for Newborn Screening—An Effective Approach for Tackling Rare Diseases

Published in JAMA Network Open | September 2023

10. Prospective cohort study of genomic newborn screening: BabyScreen+pilot study protocol

Published in BMJ Open | April 2024

11. Genetic newborn screening and digital technologies: A project protocol based on a dual approach to shorten the rare diseases diagnostic path in Europe

Published in PLoS One | November 2023

12. Implications of Genomic Newborn Screening for Infant Mortality

Published in International Journal of Neonatal Screening | February 2023

13. Principles of Genomic Newborn Screening Programs

Published in JAMA Network Open | July 2021

14. The modern face of newborn screening

Published in Pediatrics and Neonatology | November 2022

15. Genomic newborn screening: Are we entering a new era of screening?

Published in Journal of Inherited Metabolic Disease | July 2023

16. Evaluating a Novel Newborn Screening Methodology: Combined Genetic and Biochemical Screenings

Published in Archives of Medical Research | February 2024

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