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Jamie Maziarz

Researcher at Yale University

Publications -  30
Citations -  1100

Jamie Maziarz is an academic researcher from Yale University. The author has contributed to research in topics: Stromal cell & Gene. The author has an hindex of 11, co-authored 24 publications receiving 747 citations.

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Genetic Associations with Gestational Duration and Spontaneous Preterm Birth

TL;DR: It is found that variants at the EBF1, EEFSEC, AGTR2, WNT4, ADCY5, and RAP2C loci were associated with gestational duration and variants atThe EBF 1, EE FSEC, and AG TR2 loci with preterm birth.
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Single-cell transcriptomics of the human placenta: inferring the cell communication network of the maternal-fetal interface.

TL;DR: This work studied the cell-cell interactome of fetal placental trophoblast cells and maternal endometrial stromal cells, using single-cell transcriptomics and finds a highly cell-type-specific expression of G-protein-coupled receptors, implying that ligand-receptor profiles could be a reliable tool for cell type identification.
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Embryo implantation evolved from an ancestral inflammatory attachment reaction

TL;DR: The data suggest that implantation in eutherians is derived from an ancestral inflammatory reaction to embryo attachment in the therian ancestor, and the ability to shift from an inflammatory attachment reaction to a noninflammatory period of pregnancy was a key innovation in e Lutherian mammals that allowed an extended period of intimate placentation.
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Genetic Associations with Gestational Duration and Spontaneous Preterm Birth

TL;DR: A genomewide association study in a discovery set of samples obtained from 43,568 women of European ancestry using gestational duration as a continuous trait and term or preterm (<37 weeks) birth as a dichotomous outcome is performed.
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The mammalian decidual cell evolved from a cellular stress response.

TL;DR: It is shown that a novel cell type of eutherians mammals, the decidual stromal cell (DSC), evolved by rewiring an ancestral cellular stress response, and proposed that rewired of cellular stress responses was an important mechanism for the evolution of the eutherian decidUAL cell type.