Characterizing the Human Fetal Perimeiotic 45,X Ovary at Single-Cell Resolution
We characterize the human fetal perimeiotic 45,X ovary at single-cell resolution and offer insights into the genomic mechanisms of the ovarian insufficiency phenotype in TS.
Authors
- John C. Achermann (ORCID: https://orcid.org/0000-0001-8787-6272)
- Theodoros Xenakis (ORCID: https://orcid.org/0000-0003-3682-8873)
- Ignacio del Valle (ORCID: https://orcid.org/0000-0003-2595-3652)
- Jenifer P. Suntharalingham (ORCID: https://orcid.org/0000-0002-8897-7697)
- Sinead McGlacken‐Byrne (ORCID: https://orcid.org/0000-0002-4289-0852)
- Paola Niola (ORCID: https://orcid.org/0000-0002-3377-5991)
- Olumide Ogunbiyi (ORCID: https://orcid.org/0000-0001-5208-5526)
- Gerard Conway (ORCID: https://orcid.org/0000-0001-6122-9325)
- Berta Crespo (ORCID: https://orcid.org/0000-0003-0006-009X)
- Nita Solanky (ORCID: https://orcid.org/0000-0001-8304-5543)
- Danielle Liptrot (ORCID: https://orcid.org/0000-0002-2612-0815)
- Tony Brooks
- Lydia Nel
Institutions
- National Health Service (GB)
- Great Ormond Street Hospital for Children NHS Foundation Trust (GB)
- Institute of Child Health (IN)
- University College London (GB)
Publication Details
- Journal
- Journal of the Endocrine Society
- Published
- 2025-05-20
- DOI
- https://doi.org/10.1210/jendso/bvaf094
- Primary Topic
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Wellcome Trust
- Medical Research Centre