Gudrun E. Moore

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

Last Updated: 09/26/2026

Save publications for later

Sign Up

Not sure about your diagnosis?

Check Your Symptoms

Found 53 publications

Valproic Acid Confers Functional Pluripotency to Human Amniotic Fluid Stem Cells in a Transgene-free Approach.

Valproic Acid Confers Functional Pluripotency to Human Amniotic Fluid Stem Cells in a Transgene-free Approach.

Journal: Molecular therapy : the journal of the American Society of Gene Therapy

Published: August 09, 2024

The transcriptomic landscape of monosomy X (45,X) during early human fetal and placental development.

The transcriptomic landscape of monosomy X (45,X) during early human fetal and placental development.

Journal: Communications biology

Published: February 08, 2024

Emerging phenotypes linked to variants in SAMD9 and MIRAGE syndrome.

Emerging phenotypes linked to variants in SAMD9 and MIRAGE syndrome.

Journal: Frontiers in endocrinology

Published: May 26, 2022

Tissue- and ethnicity-independent hypervariable DNA methylation states show evidence of establishment in the early human embryo.

Tissue- and ethnicity-independent hypervariable DNA methylation states show evidence of establishment in the early human embryo.

Journal: Nucleic acids research

Published: December 16, 2021

Inherited duplications of PPP2R3B predispose to nevi and melanoma via a C21orf91-driven proliferative phenotype.

Inherited duplications of PPP2R3B predispose to nevi and melanoma via a C21orf91-driven proliferative phenotype.

Journal: Genetics in medicine : official journal of the American College of Medical Genetics

Published: May 13, 2020

Rare CNVs provide novel insights into the molecular basis of GH and IGF-1 insensitivity.

Rare CNVs provide novel insights into the molecular basis of GH and IGF-1 insensitivity.

Journal: European journal of endocrinology

Published: May 05, 2020

Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations.

Diverse species-specific phenotypic consequences of loss of function sorting nexin 14 mutations.

Journal: Scientific reports

Published: November 15, 2019

Phenotype of genetically confirmed Silver-Russell syndrome beyond childhood.

Phenotype of genetically confirmed Silver-Russell syndrome beyond childhood.

Journal: Journal of medical genetics

Published: September 06, 2019

Exome sequencing identifies variants in FKBP4 that are associated with recurrent fetal loss in humans.

Exome sequencing identifies variants in FKBP4 that are associated with recurrent fetal loss in humans.

Journal: Human molecular genetics

Published: July 02, 2019

Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family.

Disruption of FOXF2 as a Likely Cause of Absent Uvula in an Egyptian Family.

Journal: Journal of dental research

Published: March 28, 2019

Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene PTDSS1 in skeletal cell lineages.

Analysis of transgenic zebrafish expressing the Lenz-Majewski syndrome gene PTDSS1 in skeletal cell lineages.

Journal: F1000Research

Published: February 19, 2019

Analysis of CDKN1C in fetal growth restriction and pregnancy loss.

Analysis of CDKN1C in fetal growth restriction and pregnancy loss.

Journal: F1000Research

Published: January 23, 2019

Showing 1-12 of 53

Last Updated: 09/26/2026