Research output

Identification of rare de novo epigenetic variations in congenital disorders

Research output: Contribution to journalArticleAcademicpeer-review

Associated researcher

  • 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.
  • Maciel, P.
  • Buxbaum, J. D.
  • Gelb, B. D.
  • Sharp, A. J.

Associated organisations

    Research areas

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

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