Bjornsson, Hans T.

Intra-individual Change Over Time in DNA Methylation With Familial Clustering

Bjornsson, H. T. (2008) · JAMA

Epigenetics and DNA MethylationGenetic Syndromes and Imprinting

Cited by 702

An integrated epigenetic and genetic approach to common human disease

BJORNSSON, H. (2004) · Trends in Genetics

Epigenetics and DNA MethylationGenetic Associations and Epidemiology

Cited by 448

SNP-specific array-based allele-specific expression analysis

Bjornsson, H. T., Albert, T. J., Ladd-Acosta, C. M., Green, R. D., Rongione, M. A., Middle, C. M., Irizarry, R. A., Broman, K. W., & Feinberg, A. P. (2008) · Genome Research

Genetic Syndromes and ImprintingGene expression and cancer classification

Cited by 68

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

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