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Journal of Migration and Health|April 27, 2021
Clinical outcomes and risk factors for COVID-19 among migrant populations in high-income countries: A systematic reviewSally E Hayward, Anna Deal, Cherie Cheng, et al.Plos One|April 8, 2017
A tubulin alpha 8 mouse knockout model indicates a likely role in spermatogenesis but not in brain developmentChristine P Diggle, Isabel Martinez-Garay, Zoltan Molnar, et al.Nature Genetics|July 18, 2006
Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 cause Aicardi-Goutières syndrome at the AGS1 locusYanick J Crow, Bruce E Hayward, Rekha Parmar, et al.Nature Genetics|July 31, 2012
Mutations in NMNAT1 cause Leber congenital amaurosis and identify a new disease pathway for retinal degenerationRobert K Koenekoop, Hui Wang, Jacek Majewski, et al.Nature|October 1, 2020
Repeat expansions confer WRN dependence in microsatellite-unstable cancersNiek van Wietmarschen, Sriram Sridharan, William J Nathan, et al.Nature Genetics|July 18, 2006
Mutations in genes encoding ribonuclease H2 subunits cause Aicardi-Goutières syndrome and mimic congenital viral brain infectionYanick J Crow, Andrea Leitch, Bruce E Hayward, et al.American Journal of Human Genetics|September 12, 2007
Clinical and molecular phenotype of Aicardi-Goutieres syndromeGillian Rice, Teresa Patrick, Rekha Parmar, et al.Pageof 17