Our Mission
To empower growing families with genetic and epigenetic testing of embryos to support healthy child development. Through molecular solutions, we aim to improve implantation success rates, leveraging a newly discovered human gene.
Our Team
Our team brings decades of experience in molecular genetics and autism spectrum disorder (ASD) research, with a proven track record of groundbreaking discoveries in the field. With deep expertise spanning genetic analysis, epigenetic mechanisms, and neurodevelopmental disorders, our team is uniquely positioned to advance embryo testing technologies for improved in vitro fertilization (IVF) outcomes. Our multidisciplinary approach combines cutting-edge molecular techniques with clinical insights, allowing us to translate complex genetic research into practical solutions for families. Through rigorous scientific investigation and innovative methodologies, we have discovered novel genetic markers that enhance embryo selection processes. This comprehensive understanding of both the molecular foundations of development and the clinical realities of reproductive medicine enables us to develop testing protocols that not only improve implantation success rates but also provide valuable insights for early detection and prevention strategies. Our commitment to scientific excellence and patient-centered care drives our mission to make advanced genetic testing accessible and meaningful for couples pursuing IVF treatment.
