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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) , Pfundt, Rolph, Sanchis-Juan, Alba, van Bokhoven, Hans, van Essen, Anthony, van Ravenswaaij-Arts, Conny, Boycott, Kym M, Kernohan, Kristin D, Dyack, Sarah and Raymond, F Lucy (2018) De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures. AMERICAN JOURNAL OF HUMAN GENETICS, 103 (1). pp. 144-153.

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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) , Bermejo-Rodriguez, Camino ORCID: 0000-0002-7554-1640, Seko, Tomomi, Kugoh, Hiroyuki, Shiraishi, Ken, Sayama, Koji ORCID: 0000-0001-9915-8964, Kimura, Hiroshi ORCID: 0000-0003-0854-083X, Fraser, Peter ORCID: 0000-0002-0041-1227, Narita, Masako ORCID: 0000-0002-9774-4908, Samarajiwa, Shamith A ORCID: 0000-0003-1046-0601 and Narita, Masashi ORCID: 0000-0001-7764-577X (2022) Locus-specific induction of gene expression from heterochromatin loci during cellular senescence. Nature Aging, 2 (1). pp. 31-45.

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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) , Lyons, Scott K, Lynch, Andy G, Kimura, Hiroshi, Ohbayashi, Tetsuya, Tavare, Simon and Narita, Masashi (2015) Phenotype Specific Analyses Reveal Distinct Regulatory Mechanism for Chronically Activated p53. PLOS GENETICS, 11 (3). e1005053-.