• 3 Citations
  • 1 h-Index
20192020

Research output per year

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Fingerprint Dive into the research topics where Meagan Hainlen is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

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Research Output

  • 3 Citations
  • 1 h-Index
  • 2 Article

Deficient histone H3 propionylation by BRPF1-KAT6 complexes in neurodevelopmental disorders and cancer

Yan, K., Rousseau, J., Machol, K., Cross, L. A., Agre, K. E., Gibson, C. F., Goverde, A., Engleman, K. L., Verdin, H., de Baere, E., Potocki, L., Zhou, D., Cadieux-Dion, M., Bellus, G. A., Wagner, M. D., Hale, R. J., Esber, N., Riley, A. F., Solomon, B. D., Cho, M. T. & 12 others, McWalter, K., Eyal, R., Hainlen, M. K., Mendelsohn, B. A., Porter, H. M., Lanpher, B. C., Lewis, A. M., Savatt, J., Thiffault, I., Callewaert, B., Campeau, P. M. & Yang, X. J., Jan 22 2020, In : Science Advances. 6, 4, eaax0021.

Research output: Contribution to journalArticle

Open Access
  • 2 Scopus citations

    MSTO1 mutations cause mtDNA depletion, manifesting as muscular dystrophy with cerebellar involvement

    Care4Rare Canada Consortium, Dec 1 2019, In : Acta Neuropathologica. 138, 6, p. 1013-1031 19 p.

    Research output: Contribution to journalArticle

  • 1 Scopus citations