Author

Erik Schoenmakers

University of CambridgeORCID 0000-0003-0674-8282Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Biophysics· 1 Developmental Biology· 1 Genetics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Assay:bulk RNA-seq· 2 Research Focus:cell type annotation· 2 Organism:mouse· 2 Approach:statistical model· 2 Approach:biophysical modeling· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1

Frequent Co-Authors

Krishna ChatterjeeiD· 2 shared Adam Kuczynski· 1 shared Albert KoulmaniD· 1 shared Alberto Frangini· 1 shared Alessandra FerrariiD· 1 shared Alexander MörseburgiD· 1 shared Alexandra EfthymiadouiD· 1 shared Beatriz Romartínez-AlonsoiD· 1 shared

Activity by Year

2019-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 25 mutual co-author links

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2 shared papersGenetics

Krishna ChatterjeeORCID

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3 papers

Recent·Most cited

BiophysicsCommunications BiologyPeer-reviewedMar 21, 2025

Extracellular phase separation mediates storage and release of thyroglobulin in the thyroid follicular lumen

Yihan Yao, Nadia A. Erkamp, Tomas Šneideris…·Tuomas P. J. Knowles

The paper investigates thyroglobulin phase separation in thyroid follicles, showing it forms storage depots and reveals a mechanism for hormone homeostasis.

8 citationstop 5%

mousehuman

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GeneticsbioRxivPreprintApr 28, 2024

Damaging mutations in LXRα uncouple lipogenesis from hepatotoxicity and implicate hepatic cholesterol sensing in human liver health

Sam M. Lockhart, Milan Mušo, Ilona Zvetkova…·Stephen O’Rahilly

This study identifies damaging LXRα mutations linked to reduced triglycerides but increased liver enzyme levels and hepatotoxicity, suggesting LXR's role in liver health and cautioning against its inhibition for MASLD treatment.

1 citation

humanmouse

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Developmental BiologyProceedings of the National Academy of SciencesPeer-reviewedOct 18, 2019

Mutations in thyroid hormone receptor α1 cause premature neurogenesis and progenitor cell depletion in human cortical development

Teresa G. Krieger, Carla Moran, Alberto Frangini…·Frederick J. Livesey

This study shows that THRA mutations impair neural progenitor cell proliferation and organisation in human cortical development using patient-derived iPSCs.

42 citations

humanbulk RNA-seq

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