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Ito, Yoko, Carss, Keren J, Duarte, Sofia T, Hartley, Taila, Keren, Boris, Kurian, Manju A, Marey, Isabelle, Charles, Perinne, Mendonca, Carla, Nava, Caroline et al (show 9 more authors)
(2018)
De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures.
AMERICAN JOURNAL OF HUMAN GENETICS, 103 (1).
pp. 144-153.
Tomimatsu, Kosuke, Bihary, Dóra, Olan, Ioana, Parry, Aled J ORCID: 0000-0001-5192-3727, Schoenfelder, Stefan, Chan, Adelyne SL, Slater, Guy St C, Ito, Yoko
ORCID: 0000-0003-4578-6126, Rugg-Gunn, Peter J
ORCID: 0000-0002-9601-5949, Kirschner, Kristina
ORCID: 0000-0001-7607-8670 et al (show 10 more authors)
(2022)
Locus-specific induction of gene expression from heterochromatin loci during cellular senescence.
Nature Aging, 2 (1).
pp. 31-45.
Kirschner, Kristina, Samarajiwa, Shamith A, Cairns, Jonathan M, Menon, Suraj, Perez-Mancera, Pedro A, Tomimatsu, Kosuke, Bermejo-Rodriguez, Camino ORCID: 0000-0002-7554-1640, Ito, Yoko, Chandra, Tamir, Narita, Masako et al (show 6 more authors)
(2015)
Phenotype Specific Analyses Reveal Distinct Regulatory Mechanism for Chronically Activated p53.
PLOS GENETICS, 11 (3).
e1005053-.