Research from Our Team
Minerva Genomics team members have contributed to the existing literature
Family History and Disease
The Impact of Family History on the Lifetime Prevalence of Disease, Elan Bechor. Orchid Health (2023).
Methods to Validate the Genotyping of Embryos
Xia Y, [...], Bechor E, et al. The first clinical validation of whole-genome screening on standard trophectoderm biopsies of preimplantation embryos, F&S Reports, Volume 5, Issue 1, 2024.
Nathan R. Treff, [...] , Elan Bechor, et. al, Validation of concurrent preimplantation genetic testing for polygenic and monogenic disorders, structural rearrangements, and whole and segmental chromosome aneuploidy with a single universal platform. European Journal of Medical Genetics. Volume 62, Issue 8, 2019.
Disease Risk Reduction through Polygenic Embryo Screening
Treff NR, Eccles J, Lello L, Bechor E, Hsu J, Plunkett K, Zimmerman R, Rana B, Samoilenko A, Hsu S, Tellier LCAM. Utility and First Clinical Application of Screening Embryos for Polygenic Disease Risk Reduction. Front Endocrinol (Lausanne). 2019 Dec 4;10:845. doi: 10.3389/fendo.2019.00845. PMID: 31920964; PMCID: PMC6915076.