Author

P. M. Nolan

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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Cell Biology· 1 Physiology· 1

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 2 Approach:experimental assay· 2 Organism:mouse· 2 Assay:bulk RNA-seq· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:differential expression· 1 Research Focus:metabolism & bioenergetics· 1 Assay:proteomics· 1

Frequent Co-Authors

L. Bentley· 2 shared A. G. Wilcox· 1 shared C. Schmidt-Hieber· 1 shared D. Wilson· 1 shared E. Forsythe· 1 shared F. J. Sialana· 1 shared G. Banks· 1 shared G. Lubec· 1 shared

Activity by Year

2019-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 27 mutual co-author links

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2 shared papersPhysiology

L. Bentley

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Author profile →

2 papers

Recent·Most cited

A missense mutation in zinc finger homeobox-3 (ZFHX3) impedes growth and alters metabolism and hypothalamic gene expression in mice.

P. M. Nolan, G. Banks, N. Bourbia, A. G. Wilcox, L. Bentley, L. Moir, L. Kent, R. Hillier, D. Wilson, P. Barrett, R. Dumbell

This study shows that a ZFHX3 mutation in mice reduces body weight, alters metabolism, and changes hypothalamic gene expression related to growth and energy balance.

bioRxiv · May 25, 2022Physiology

Loss of Bardet-Biedl syndrome proteins causes synaptic aberrations in principal neurons

N. Haq, C. Schmidt-Hieber, F. J. Sialana, L. Ciani, J. P. Heller, M. Stewart, L. Bentley, S. Wells, R. J. Rodenburg, P. M. Nolan, E. Forsythe, M. C. Wu, G. Lubec, M. Hausser, P. Beales, S. Christou-Savina

This study shows that loss of Bardet-Biedl syndrome proteins causes synaptic dysfunction in principal neurons, contributing to cognitive impairment in BBS patients.

bioRxiv · Mar 18, 2019Cell Biology