At the Laboratory of Cellular Genomic Medicine (CGM), we develop and apply innovative technologies to study the genome, epigenome, transcriptome, and other molecular layers at single-cell resolution.
Our research focuses on how these molecular layers interact within individual cells, how they shape cellular identity and function, and how this knowledge can be translated into clinical applications. We are particularly interested in genome and epigenome stability during early human development, with applications in reproductive genetics, preimplantation genetic testing (PGT), non-invasive prenatal testing (NIPT), and equitable reproductive care.
- 🧬 Single-cell genomics and multi-omics
- 🧫 Genome and epigenome stability in early development
- 🧪 PGT and NIPT method development
- 💻 Bioinformatics, AI, and clinical genomics pipelines
- 👶 Reproductive genetics and embryo development
- 🌍 Reproductive literacy, ethics, and equitable access to care
To connect genomic technology, AI, and clinical insight to advance reproductive medicine and improve care from cells to patients.
