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Wang, Mohan; Salter, Patrick S.; Payne, Frank P.; Shipley, Adrian; Dyson, Igor N.; Lui, Tongyu; Wang, 1tao; Zhang, Kaihui; Zhang, Jian; Jia, Zhitai; Morris, Stephen M.; Booth, Martin J.; Fells, Julian A. J.

Wang, Mohan; Salter, Patrick S.; Payne, Frank P.; Shipley, Adrian; Morris, Stephen M.; Booth, Martin J.; Fells, Julian A. J.

Austin J. Gallagher; Jacob W. Brownscombe; Nourah A. Alsudairy; Andrew B. Casagrande; Chuancheng Fu; Lucy Harding; S. David Harris; Neil Hammerschlag; Wells Howe; Antonio Delgado Huertas; Sami Kattan; Andrew S. Kough; Andre Musgrove; Nicholas L. Payne; Adrian Phillips; Brendan D. Shea; Oliver N. Shipley; U. Rashid Sumaila; Mohammad S. Hossain; Carlos M. Duarte

Nature Communications, Vol 13, Iss 1, Pp 1-10 (2022)

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JOURNAL OF LIGHTWAVE TECHNOLOGY; AUG 15 2024, 42 16, p5629-p5638, 10p.

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Circulation. Nov 21, 2017 136(21):2022-2033

Abby L. Braitman; Anna M. Petrey; Jennifer L. Shipley; Rachel Ayala Guzman; Emily Renzoni; Alison Looby; Adrian J. Bravo

Alcohol Clin Exp Res (Hoboken)

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Sci Adv
Digital.CSIC. Repositorio Institucional del CSIC
instname
Science Advances, vol 8, iss 33
Science Advances (2375-2548) (American Association for the Advancement of Science (AAAS)), 2022-08, Vol. 8, N. 33, P. eabo1754 (19p.)

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Wong; Nicholas Wood; Yvette Wood; Christopher Geoffrey Woods; Emma R. Woodward; Sarita Workman; Stephen J. Wort; Katherine Yates; Nigel Yeatman; Patrick F. K. Yong; Timothy Young; Ping Yu; Patrick Yu-Wai-Man; Eliska Zlamalova

Nature
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Ito, Yoko; Carss, Keren; Duarte, Sofia; Hartley, Taila; Keren, Boris; Kurian, Manju; Marey, Isabelle; Charles, Perinne; Mendonça, Carla; Nava, Caroline; Pfundt, Rolph; Sanchis-Juan, Alba; van Bokhoven, Hans; van Essen, Anthony; van Ravenswaaij-Arts, Conny; Boycott, Kym; Kernohan, Kristin; Dyack, Sarah; Raymond, F. 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Terry; Johnson, Sally; Levine, Adam; Wong, Edwin K.S.; Tan, Rhea; Mackenzie, Alex; Majewski, Jacek; Brudno, Michael; Bulman, Dennis; Dyment, David

Am J Hum Genet
NIHR BioResource & Care4Rare Canada Consortium 2018, 'De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures', American journal of human genetics, vol. 103, no. 1, pp. 144-153. https://doi.org/10.1016/j.ajhg.2018.06.001
American Journal of Human Genetics, 103, 1, pp. 144-153
Ito, Y, Carss, K J, Duarte, S T, Hartley, T, Keren, B, Kurian, M A, Marey, I, Charles, P, Mendonca, C, Nava, C, Pfundt, R, Sanchis-Juan, A, van Bokhoven, H, van Essen, A, van Ravenswaaij-Arts, C, Koziell, A, Boycott, K M & Kernohan, K D & Dyack, S & Raymond, F L 2018, ' De Novo Truncating Mutations in WASF1 Cause Intellectual Disability with Seizures. ', American Journal of Human Genetics, vol. 103, no. 1, pp. 144-153 . https://doi.org/10.1016/j.ajhg.2018.06.001

Hu, Qirui ; Shifren, Adrian ; Sens, Carla ; Choi, Jiwon ; Szabo, Zoltan ; Starcher, Barry C. ; Knutsen, Russell H. ; Shipley, J. Michael ; Davis, Elaine C. ; Mecham, Robert P. ; Urban, Zsolt

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