Publications related to PRECISE

A comprehensive human embryo reference tool using single-cell RNA-sequencing data.
Nat Methods 2025 Jan;22(1):193-206

Clinical-grade whole genome sequencing-based haplarithmisis enables all forms of preimplantation genetic testing.
Nat Commun 2024 Sep;15(1):7164

BinDel: Detecting Clinically Relevant Fetal Genomic Microdeletions Using Low-Coverage Whole-Genome Sequencing-Based NIPT.
Prenat Diagn 2025 Mar;45(3):352-361

Prevalence of chromosomal alterations in first-trimester spontaneous pregnancy loss.
Nat Med 2023 Dec;29(12):3233-3242

Nipocalimab in Early-Onset Severe Hemolytic Disease of the Fetus and Newborn.
N Engl J Med 2024 Aug;391(6):526-537

An exploratory open-label multicentre phase I/II trial evaluating the safety and efficacy of postnatal or prenatal and postnatal administration of allogeneic expanded fetal mesenchymal stem cells for the treatment of severe osteogenesis imperfecta in infants and fetuses: the BOOSTB4 trial protocol.
BMJ Open 2024 Jun;14(6):e079767

In vitro fertilization does not increase the incidence of de novo copy number alterations in fetal and placental lineages.
Nat Med 2019 Nov;25(11):1699-1705

Single-Cell RNA-Seq Reveals Lineage and X Chromosome Dynamics in Human Preimplantation Embryos.
Cell 2016 May;165(4):1012-26