Author

M. Fex

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

Signature Assays, Organisms & Methods

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Research Focus:cell type annotation· 1 Approach:genetic perturbation / CRISPR· 1 Organism:human· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

A. Mamidi· 1 shared A. Rosengren· 1 shared A. Soltanian· 1 shared F. Roberts· 1 shared H. Mulder· 1 shared H. Semb· 1 shared J. P. M. C. M. Cunha· 1 shared K. Yektay Farahmand· 1 shared

Activity by Year

2024-2024 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperCell Biology

A. Mamidi

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1 paper

Recent·Most cited

Modelling genetic risk of β-cell dysfunction in human induced pluripotent stem cells from patients carrying the MTNR1B risk variant.

T. Singh, S. Kalamajski, J. P. M. C. M. Cunha, S. Hladkou, F. Roberts, S. Gheibi, A. Soltanian, K. Yektay Farahmand, O. Ekstrom, A. Mamidi, P. W. Franks, A. Rosengren, H. Semb, H. Mulder, M. Fex

This study uses hiPSC and hESC to model the MTNR1B risk variant's effect on β-cell function, finding increased MTNR1B protein and melatonin sensitivity in G-allele carriers.

bioRxiv · Jul 19, 2024 · PreprintCell Biology