Author

Clive Hawkins

Royal Stoke University HospitalORCID 0000-0002-5114-232XUnclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Assay:bulk RNA-seq· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:GWAS / association mapping· 1 Assay:GWAS summary statistics· 1 Organism:human· 1

Frequent Co-Authors

Adam SantanielloiD· 1 shared Adrian C. WilliamsiD· 1 shared An GorisiD· 1 shared Anne Haney CrossiD· 1 shared Anne SpurklandiD· 1 shared Antonios BayasiD· 1 shared Ashley Harris BeechamiD· 1 shared Benedicte A. LieiD· 1 shared

Activity by Year

2018-2020 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 36 mutual co-author links

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1 shared paperGenetics

Adam SantanielloORCID

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2 papers

Recent·Most cited

Nicotinamide restricts neural precursor proliferation to enhance catecholaminergic neuronal subtype differentiation from mouse embryonic stem cells

Síle M. Griffin, Mark R. Pickard, Clive Hawkins, Adrian C. Williams, Rosemary A. Fricker

This study shows nicotinamide reduces neural progenitor proliferation and enhances catecholaminergic neuron differentiation from mouse embryonic stem cells.

PLoS ONE · Sep 14, 2020Peer-reviewedNeuroscience

Low frequency and rare coding variation contributes to multiple sclerosis risk

Mitja Mitrovič, Nikolaos A. Patsopoulos, Ashley Harris Beecham, Theresa Dankowski, An Goris, Bénédicte Dubois, Marie Beatrice D'hooghe, Robin Lemmens, Philip Van Damme, Helle Bach Søndergaard, Finn Thorup Sellebjerg, Per Soelberg Sørensen, Henrik Ullum, Lise Wegner Thørner, Thomas Mears Werge, , Hakon H. Hakonarson

The paper identifies low-frequency coding variants contributing to multiple sclerosis risk using a large case-control study.

Cell · Oct 18, 2018Peer-reviewedGenetics