Impact of the COVID-19 Pandemic on Family Wellbeing in the Context of Neurodevelopmental Disorders by Rizzo R, Karlov L, Maugeri N, DiSilvestre S, Eapen V

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Comprehensive rare variant analysis via whole-genome sequencing to determine the molecular pathology of inherited retinal disease by Carss, K, Arno, G, Erwood, M, Stephens, J, Sanchis-Juan, A, Hull, S, Megy, K, Grozeva, D, Dewhurst, E, Malka, S, Plagnol, V, Penkett, C, Stirrups, K, Rizzo, R, Wright, G, Josifova, D, Bitner-Glindzicz, M, Scott, R, Clement, E, Allen, L, Armstrong, R, Brady, A, Carmichael, J, Chitre, M, Henderson, R, Hurst, J, Maclaren, R, Murphy, E, Paterson, J, Rosser, E, Thompson, D, Wakeling, E, Ouwehand, W, Michaelides, M, Moore, A, Nihr-Bioresource Rare Diseases Consortium, Webster, A, Raymond, F