Chamberlain, Stormy J.

The Murine Polycomb Group Protein Eed Is Required for Global Histone H3 Lysine-27 Methylation

Montgomery, N. D., Yee, D., Chen, A., Kalantry, S., Chamberlain, S. J., Otte, A. P., & Magnuson, T. (2005) · Current Biology

Epigenetics and DNA MethylationGenomics and Chromatin Dynamics

Cited by 345

Induced pluripotent stem cell models of the genomic imprinting disorders Angelman and Prader-Willi syndromes

Chamberlain, S. J., Chen, P.-F., Ng, K. Y., Bourgois-Rocha, F., Lemtiri-Chlieh, F., Levine, E. S., & Lalande, M. (2010) · Proceedings of the National Academy of Sciences

Genetic Syndromes and ImprintingPluripotent Stem Cells Research

Cited by 312

Imprinted expression of UBE3A in non-neuronal cells from a Prader–Willi syndrome patient with an atypical deletion

Martins-Taylor, K., Hsiao, J. S., Chen, P.-F., Glatt-Deeley, H., De Smith, A. J., Blakemore, A. I. F., Lalande, M., & Chamberlain, S. J. (2014) · Human Molecular Genetics

Genetic Syndromes and ImprintingGenomics and Chromatin Dynamics

Cited by 66

RNAs of the human chromosome 15q11-q13 imprinted region

Chamberlain, S. J. (2013) · WIREs RNA

Genetic Syndromes and ImprintingChromosomal and Genetic Variations

Cited by 35

Hyperexcitable phenotypes in induced pluripotent stem cell-derived neurons from patients with 15q11-q13 duplication syndrome, a genetic form of autism

Fink, J. J., Schreiner, J. D., Bloom, J. E., James, J., Baker, D. S., Robinson, T. M., Lieberman, R., Loew, L. M., Chamberlain, S. J., & Levine, E. S. (2021) · Biological Psychiatry

Genetics and Neurodevelopmental DisordersEpilepsy research and treatment

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