Reynisdottir, Tinna
University of Iceland
2 papers on CoChatORCID 0000-0001-5148-4744
Most cited papers
- Verified
Missense variants causing Wiedemann-Steiner syndrome preferentially occur in the KMT2A-CXXC domain and are accurately classified using AlphaFold2
Reynisdottir, T., Anderson, K., Boukas, L., & Bjornsson, H. T. (2022) · PLoS Genetics
Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders
Cited by 15
- Verified
Missense variants causing Wiedemann-Steiner syndrome preferentially occur in the KMT2A-CXXC domain and are accurately classified using AlphaFold2
Reynisdottir, T., Anderson, K. J., Boukas, L., & Bjornsson, H. T. (2022) · PLOS Genetics
Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders
Cited by 15
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