Parental perspectives regarding the return of genomic research results in neurodevelopmental disorders in South Africa: anticipated impact and preferences by Diedericks, A, Bruwer, Z, Laing, N, Eastman, E, De Vries, J, Newton, CR, Abubakar, A, Robinson, EB, Donald, KA

Principled distillation of UK Biobank phenotype data reveals underlying structure in human variation by Carey, CE, Shafee, R, Wedow, R, Elliott, A, Palmer, DS, Compitello, J, Kanai, M, Abbott, L, Schultz, P, Karczewski, KJ, Bryant, SC, Cusick, CM, Churchhouse, C, Howrigan, DP, King, D, Davey Smith, G, Neale, BM, Walters, RK, Robinson, EB

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders. by Walters, RK, Kosmicki, JA, Grove, J, Samocha, KE, Goldstein, JI, Okbay, A, Bybjerg-Grauholm, J, Werge, T, Hougaard, DM, Taylor, J, iPSYCH-Broad Autism Group, Psychiatric Genomics Consortium Autism Group, Skuse, D, Devlin, B, Anney, R, Sanders, SJ, Bishop, S, Mortensen, PB, Børglum, AD, Smith, GD, Daly, MJ, Robinson, EB

Phenotype and genetic analysis of data collected within the first year of NeuroDev by Kipkemoi, P, Kim, HA, Christ, B, O'Heir, E, Allen, J, Austin-Tse, C, Baxter, S, Brand, H, Bryant, S, Buser, N, de Menil, V, Eastman, E, Murugasen, S, Galvin, A, Kombe, M, Ngombo, A, Mkubwa, B, Mwangi, P, Kipkoech, C, Lovgren, A, MacArthur, DG, Melly, B, Mwangasha, K, Martin, A, Nkambule, LL, Sanchis-Juan, A, Singer-Berk, M, Talkowski, ME, VanNoy, G, van der Merwe, C, Newton, C, O'Donnell-Luria, A, Abubakar, A, Donald, KA, Robinson, EB