Author

Lydia Nel

University College London

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 1 Genomics· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 2 Research Focus:differential expression· 2 Organism:human· 2 Approach:statistical model· 2 Research Focus:cell type annotation· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Assay:scRNA-seq· 1

Frequent Co-Authors

Berta CrespoiD· 2 shared Danielle LiptrotiD· 2 shared Gerard S. ConwayiD· 2 shared Ignacio del ValleiD· 2 shared Jenifer P. SuntharalinghamiD· 2 shared John C. AchermanniD· 2 shared Nita SolankyiD· 2 shared Olumide Kayode OgunbiyiiD· 2 shared

Activity by Year

2023-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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2 shared papersGenetics

Berta CrespoORCID

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2 papers

Recent·Most cited

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

Jenifer P. Suntharalingham, Ignacio del Valle, Federica Buonocore, Sinead Mary McGlacken-Byrne, Tony Brooks, Olumide Kayode Ogunbiyi, Danielle Liptrot, Nathan J. Dunton, Gaganjit Kaur Madhan, Kate Metcalfe, Lydia Nel, Abigail R. Marshall, Miho Ishida, Neil James Sebire, Gudrun E. Moore, , John C. Achermann

The paper analyzes the transcriptomic differences in 45,X tissues compared to 46,XX and 46,XY controls during early human fetal and placental development, identifying gene expression changes associated with Turner syndrome.

Communications Biology · Feb 16, 2025Peer-reviewedGenetics

Single-nucleus RNA-sequencing reveals novel potential mechanisms of ovarian insufficiency in 45,X Turner Syndrome

Sinead Mary McGlacken-Byrne, Ignacio del Valle, Theodoros Xenakis, Jenifer P. Suntharalingham, Lydia Nel, Danielle Liptrot, Berta Crespo, Olumide Kayode Ogunbiyi, Paola Niola, Tony Brooks, Nita Solanky, Gerard S. Conway, John C. Achermann

This study uses single-nucleus and bulk RNA sequencing to identify novel pathogenic mechanisms of ovarian insufficiency in Turner Syndrome, beyond X chromosome haploinsufficiency.

bioRxiv · Dec 22, 2023 · PreprintGenomics