Jenifer P. Suntharalingham

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

Last Updated: 09/26/2026

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Found 24 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

Characterizing the Human Fetal Perimeiotic 45,X Ovary at Single-Cell Resolution.

Characterizing the Human Fetal Perimeiotic 45,X Ovary at Single-Cell Resolution.

Journal: Journal of the Endocrine Society

Published: November 25, 2024

A Tiered Approach to Exome Sequencing Analysis in Early-Onset Primary Ovarian Insufficiency.

A Tiered Approach to Exome Sequencing Analysis in Early-Onset Primary Ovarian Insufficiency.

Journal: The Journal of clinical endocrinology and metabolism

Published: November 21, 2024

Characterization of Turner Syndrome-associated Diabetes Mellitus.

Characterization of Turner Syndrome-associated Diabetes Mellitus.

Journal: The Journal of clinical endocrinology and metabolism

Published: February 28, 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

Analysis of genetic variability in Turner syndrome linked to long-term clinical features.

Analysis of genetic variability in Turner syndrome linked to long-term clinical features.

Journal: Frontiers in endocrinology

Published: May 22, 2023

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

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

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

Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiency.

Pathogenic variants in RNPC3 are associated with hypopituitarism and primary ovarian insufficiency.

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

Published: April 10, 2021

Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years' Experience in the UK.

Genetic Analysis of Pediatric Primary Adrenal Insufficiency of Unknown Etiology: 25 Years' Experience in the UK.

Journal: Journal of the Endocrine Society

Published: March 19, 2021

Showing 1-12 of 24

Last Updated: 09/26/2026