Author

H. Tyynismaa

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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Biochemistry· 1 Cell Biology· 1 Immunology· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Assay:bulk RNA-seq· 1 Research Focus:cell signaling & trafficking· 1 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Research Focus:chromatin & epigenetic regulation· 1 Research Focus:differential expression· 1

Frequent Co-Authors

A. Dhir· 1 shared A. Lepelley· 1 shared A. Raasakka· 1 shared A. Sutinen· 1 shared B. Bader-Meunier· 1 shared B. Callewaert· 1 shared C. Bodemer· 1 shared C. Wouters· 1 shared

Activity by Year

2021-2023 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 29 mutual co-author links

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1 shared paperImmunology

A. Dhir

Mutual co-authors in cluster

Author profile →

3 papers

Recent·Most cited

Small mitochondrial protein NERCLIN regulates cardiolipin homeostasis and mitochondrial ultrastructure.

S. Konovalova, R. Torregrosa-Munumer, P. Manjunath, S. Baral, X. Liu, M. Holopainen, J. Kvist, J. Rajendran, Y. Yang, M. Varjosalo, R. Käkelä, P. Somerharju, H. Tyynismaa

This study identifies NERCLIN as a mitochondrial protein that regulates cardiolipin homeostasis and ultrastructure, with implications for stress-induced mitochondrial adaptation.

Proceedings of the National Academy of Sciences · Jul 25, 2023Peer-reviewedCell Biology

Structural insights into Charcot-Marie-Tooth disease-linked mutations in human GDAP1

A. Sutinen, G. T. T. Nguyen, A. Raasakka, G. Muruganandam, R. Loris, E. Ylikallio, H. Tyynismaa, L. Bartesaghi, S. Ruskamo, P. Kursula

This study investigates the structural and biochemical effects of CMT-linked GDAP1 mutations, finding reduced thermal stability and disrupted interaction networks that may impair neuronal function.

bioRxiv · Feb 18, 2022Biochemistry

Enhanced cGAS-STING-dependent interferon signaling associated with mutations in ATAD3A

A. Lepelley, E. Della Mina, E. Van Nieuwenhove, L. Waumans, S. Fraitag, G. I. Rice, A. Dhir, M.-L. Fremond, M. P. Rodero, L. Seabra, E. Carter, C. Bodemer, D. Buhas, B. Callewaert, P. de Lonlay, , Y. J. Crow

The paper identifies mutations in ATAD3A causing enhanced type I interferon signaling in patients with neurological and autoimmune features.

bioRxiv · Apr 2, 2021Immunology