The China Neonatal Genomes Project

Launched by CHILDREN'S HOSPITAL OF FUDAN UNIVERSITY · Apr 28, 2019

Keywords

ClinConnect Summary

The China Neonatal Genomes Project is an important study that aims to understand the genetic makeup of newborns in China. Over the next five years, researchers plan to conduct genetic testing on 100,000 babies to create a comprehensive database that can help identify and manage hereditary diseases—conditions that can be passed down from parents to their children. By establishing standards for testing these genetic conditions, the project hopes to improve how we understand and treat genetic diseases in newborns, as well as enhance the training for professionals who provide genetic counseling to families.

To participate in this study, babies must be less than 28 days old and have parents of Chinese origin. It's essential that the baby's parents or guardians agree to take part by providing informed consent. Participants can expect a simple blood sample to be taken for genetic testing, which will help researchers gather valuable information. If you're interested in this study, it's important to note that it does not include babies from certain backgrounds or those who cannot provide a blood sample. This project is a step towards better understanding and addressing genetic diseases in newborns, ultimately aiming to improve health outcomes for future generations.

Gender

ALL

Eligibility criteria

• Inclusion Criteria:
• • 1. Both parents are of Chinese origin;
• • 2. Postnatal age less than 28 days;
• • 3. Can be retained to at least 1ml venous blood sample;
• • 4. Biological parent or guardian's informed consent.
• Exclusion Criteria:
• • 1. the nationality of one of the parents is not the Han nationality or other national minorities;
• • 2. reluctance of parents to use genetic sequencing data for subsequent research;
• • 3. parents under 18 years of age or incapacitated for decision-making;
• • 4. subjects older than 28 days.
• • 5. multiple pregnancies;
• • 6. lack of access to biological samples from which DNA can be extracted;
• • 7. failure to sign informed consent