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Mutation discovery in mice by whole exome sequencing.
Fairfield H, Gilbert GJ, Barter M, Corrigan RR, Curtain M, Ding Y, D'Ascenzo M, Gerhardt DJ, He C, Huang W, Richmond T, Rowe L, Probst FJ, Bergstrom DE, Murray SA, Bult C, Richardson J, Kile BT, Gut I, Hager J, Sigurdsson S, Mauceli E, Di Palma F, Lindblad-Toh K, Cunningham ML, Cox TC, Justice MJ, Spector MS, Lowe SW, Albert T, Donahue LR, Jeddeloh J, Shendure J, Reinholdt LG. Fairfield H, et al. Among authors: huang w. Genome Biol. 2011 Sep 14;12(9):R86. doi: 10.1186/gb-2011-12-9-r86. Genome Biol. 2011. PMID: 21917142 Free PMC article.
Cilia gene mutations cause atrioventricular septal defects by multiple mechanisms.
Burnicka-Turek O, Steimle JD, Huang W, Felker L, Kamp A, Kweon J, Peterson M, Reeves RH, Maslen CL, Gruber PJ, Yang XH, Shendure J, Moskowitz IP. Burnicka-Turek O, et al. Among authors: huang w. Hum Mol Genet. 2016 Jul 15;25(14):3011-3028. doi: 10.1093/hmg/ddw155. Epub 2016 Jun 23. Hum Mol Genet. 2016. PMID: 27340223 Free PMC article.
Corrigendum to "Default mode network connectivity and social dysfunction in children with attention deficit/hyperactivity disorder" [Int. J. Clin. Health Psychol. 23 (4) (2023) 100393].
Fateh AA, Huang W, Hassan M, Zhuang Y, Lin J, Luo Y, Yang B, Zeng H. Fateh AA, et al. Among authors: huang w. Int J Clin Health Psychol. 2024 Apr-Jun;24(2):100460. doi: 10.1016/j.ijchp.2024.100460. Epub 2024 Apr 24. Int J Clin Health Psychol. 2024. PMID: 38699401 Free PMC article.
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