A Survey of Rare Epigenetic Variation in 23,116 Human Genomes Indentifies Disease-Relevant Epivariations and CGG Expansions.
Garg, P., Jadhav, B., Rodriguez, O. L., Patel, N., Martin-Trujillo, A., Jain, M., Ritz, B… & Sharp, A. J. (2020). The American Journal of Human Genetics, 107(4), 654-669.
