Tapscott, Stephen J.

CTCF-binding sites flank CTG/CAG repeats and form a methylation-sensitive insulator at the DM1 locus

Filippova, G. N., Thienes, C. P., Penn, B. H., Cho, D. H., Hu, Y. J., Moore, J. M., Klesert, T. R., Lobanenkov, V. V., & Tapscott, S. J. (2001) · Nature Genetics

Genetic Neurodegenerative DiseasesGenomics and Chromatin Dynamics

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Pbx Marks Genes for Activation by MyoD Indicating a Role for a Homeodomain Protein in Establishing Myogenic Potential

Berkes, C. A., Bergstrom, D. A., Penn, B. H., Seaver, K. J., Knoepfler, P. S., & Tapscott, S. J. (2004) · Molecular Cell

Muscle Physiology and DisordersGenomics and Chromatin Dynamics

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Facioscapulohumeral muscular dystrophy and DUX4: breaking the silence

van der Maarel, S. M., Tawil, R., & Tapscott, S. J. (2011) · Trends in Molecular Medicine

Muscle Physiology and DisordersGenomic variations and chromosomal abnormalities

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CTCF cis-regulates trinucleotide repeat instability in an epigenetic manner: a novel basis for mutational hot spot determination

Libby, R. T., Hagerman, K. A., Pineda, V. V., Lau, R., Cho, D. H., Baccam, S. L., Axford, M. M., Cleary, J. D., Moore, J. M., Sopher, B. L., et al. (2008) · PLoS Genetics

Genetic Neurodegenerative DiseasesGenetic factors in colorectal cancer

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High frequency of gastrointestinal manifestations in myotonic dystrophy type 1 and type 2

Hilbert, J. E., Barohn, R. J., Clemens, P. R., Luebbe, E. A., Martens, W. B., McDermott, M. P., Parkhill, A. L., Tawil, R., Thornton, C. A., Moxley, R. T., et al. (2017) · Neurology

Genetic Neurodegenerative DiseasesGastrointestinal motility and disorders

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Quantitative proteomics reveals key roles for post-transcriptional gene regulation in the molecular pathology of FSHD

Jagannathan, S., Ogata, Y., Gafken, P. R., Tapscott, S. J., & Bradley, R. K. (2018) · eLife

Muscle Physiology and DisordersGenomics and Rare Diseases

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