Identification of rare de novo epigenetic variations in congenital disorders

Mafalda Barbosa, Ricky S. Joshi, Paras Garg, Alejandro Martin-Trujillo, Nihir Patel, Bharati Jadhav, Corey T. Watson, William Gibson, Kelsey Chetnik, Chloe Tessereau, Hui Mei, Silvia De Rubeis, Jennifer Reichert, Fatima Lopes, Lisenka E. L. M. Vissers, Tjitske Kleefstra, Dorothy E. Grice, Lisa Edelmann, Gabriela Soares, Patricia MacielHan G. Brunner, Joseph D. Buxbaum, Bruce D. Gelb, Andrew J. Sharp*

*Corresponding author for this work

Research output: Contribution to journalArticleAcademicpeer-review

Original languageEnglish
Article number2064
Number of pages11
JournalNature Communications
Volume9
DOIs
Publication statusPublished - 25 May 2018

Keywords

  • EPIGENOME-WIDE ASSOCIATION
  • DNA METHYLATION
  • LYNCH SYNDROME
  • CGG-REPEAT
  • GENOME ANALYSIS
  • HEART-DISEASE
  • GENE
  • EPIMUTATIONS
  • INDIVIDUALS
  • MUTATIONS

Cite this

Barbosa, M., Joshi, R. S., Garg, P., Martin-Trujillo, A., Patel, N., Jadhav, B., Watson, C. T., Gibson, W., Chetnik, K., Tessereau, C., Mei, H., De Rubeis, S., Reichert, J., Lopes, F., Vissers, L. E. L. M., Kleefstra, T., Grice, D. E., Edelmann, L., Soares, G., ... Sharp, A. J. (2018). Identification of rare de novo epigenetic variations in congenital disorders. Nature Communications, 9, [2064]. https://doi.org/10.1038/s41467-018-04540-x