Nadjeda Moreno

UCL Great Ormond Street Institute Of Child Health
London, ENG WC1N1EH, United Kingdom

Last Updated: 09/26/2026

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Found 10 publications

Transcriptomic sex differences in early human fetal brain development.

Transcriptomic sex differences in early human fetal brain development.

Journal: Communications biology

Published: December 22, 2024

Mapping the anatomical and transcriptional landscape of early human fetal ovary development.

Mapping the anatomical and transcriptional landscape of early human fetal ovary development.

Journal: Scientific reports

Published: November 28, 2024

Multi-Omics Identification of Extracellular Components of the Fetal Monkey and Human Neocortex.

Multi-Omics Identification of Extracellular Components of the Fetal Monkey and Human Neocortex.

Journal: Proteomics

Published: November 13, 2024

Expression of Neurotrophins and Its Receptors During Fetal Development in the Human Cochlea.

Expression of Neurotrophins and Its Receptors During Fetal Development in the Human Cochlea.

Journal: International journal of molecular sciences

Published: October 25, 2024

Multi-omics identification of extracellular components of the fetal monkey and human neocortex.

Multi-omics identification of extracellular components of the fetal monkey and human neocortex.

Journal: bioRxiv : the preprint server for biology

Published: October 10, 2024

An integrated single-cell analysis of human adrenal cortex development.

An integrated single-cell analysis of human adrenal cortex development.

Journal: JCI insight

Published: December 19, 2022

Visualization of macrophage subsets in the development of the fetal human inner ear.

Visualization of macrophage subsets in the development of the fetal human inner ear.

Journal: Frontiers in immunology

Published: June 09, 2022

Recessive PRDM13 mutations cause fatal perinatal brainstem dysfunction with cerebellar hypoplasia and disrupt Purkinje cell differentiation.

Recessive PRDM13 mutations cause fatal perinatal brainstem dysfunction with cerebellar hypoplasia and disrupt Purkinje cell differentiation.

Journal: American journal of human genetics

Published: November 16, 2021

Pathogenic variants in the human m6A reader YTHDC2 are associated with primary ovarian insufficiency.

Pathogenic variants in the human m6A reader YTHDC2 are associated with primary ovarian insufficiency.

Journal: JCI insight

Published: September 08, 2021

ZSWIM7 Is Associated With Human Female Meiosis and Familial Primary Ovarian Insufficiency.

ZSWIM7 Is Associated With Human Female Meiosis and Familial Primary Ovarian Insufficiency.

Journal: The Journal of clinical endocrinology and metabolism

Published: May 27, 2021

Showing 1-10 of 10

Last Updated: 09/26/2026