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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-.

This list was generated on Thu Jan 26 13:52:53 2023 GMT.