Author

Thomas H. Müller

Bayer (Germany)ORCID 0000-0001-9017-4781Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Signature Assays, Organisms & Methods

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Organism:human· 2 Research Focus:differential expression· 1 Assay:electronic health records· 1 Approach:experimental assay· 1 Research Focus:protein structure prediction· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Caroline Fiona WrightiD· 2 shared Janina SörmanniD· 2 shared Karin E. J. RödströmiD· 2 shared Peter ProksiD· 2 shared Stephen J. TuckeriD· 2 shared Thibault R. H. Jouen-TachoireiD· 2 shared Alice GardhamiD· 1 shared Alistair A. MathieiD· 1 shared

Activity by Year

2022-2026 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 41 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Caroline Fiona WrightORCID

Mutual co-authors in cluster

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2 papers

Recent·Most cited

Genetic & Genomic MedicineThe Journal of General PhysiologyPeer-reviewedJul 11, 2026

Equivalent Gain-of-Function Variants in KCNK3 and KCNK9 and their Contribution to Distinct TASK K2P Channelopathies

Kate M. Crowther, Thibault R. H. Jouen-Tachoire, Peter Proks…·Stephen J. Tucker

The paper identifies equivalent gain-of-function variants in KCNK3 and KCNK9 that cause distinct channelopathies and investigates their functional effects on homomeric and heteromeric TASK channels.

1 citation

humanelectronic health records

𝕏 PostBluesky

Genetic & Genomic MedicineNature GeneticsPeer-reviewedOct 1, 2022

Defective X-gating caused by de novo gain-of-function mutations in KCNK3 underlies a developmental disorder with sleep apnea

Janina Sörmann, Marcus Schewe, Peter Proks…·Stephen J. Tucker

The paper identifies de novo gain-of-function mutations in KCNK3 causing a developmental disorder with sleep apnea by disrupting X-gating of TASK-1 channels.

30 citations

human

𝕏 PostBluesky