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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 11 more authors)
(2018)
De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures.
AMERICAN JOURNAL OF HUMAN GENETICS, 103 (1).
144 - 153.
Kirschner, Kristina, Samarajiwa, Shamith A, Cairns, Jonathan M, Menon, Suraj, Perez-Mancera, Pedro A, Tomimatsu, Kosuke, Bermejo-Rodriguez, Camino, 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).