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Large-scale targeted sequencing identifies risk genes for neurodevelopmental disorders.
Wang T, Hoekzema K, Vecchio D, Wu H, Sulovari A, Coe BP, Gillentine MA, Wilfert AB, Perez-Jurado LA, Kvarnung M, Sleyp Y, Earl RK, Rosenfeld JA, Geisheker MR, Han L, Du B, Barnett C, Thompson E, Shaw M, Carroll R, Friend K, Catford R, Palmer EE, Zou X, Ou J, Li H, Guo H, Gerdts J, Avola E, Calabrese G, Elia M, Greco D, Lindstrand A, Nordgren A, Anderlid BM, Vandeweyer G, Van Dijck A, Van der Aa N, McKenna B, Hancarova M, Bendova S, Havlovicova M, Malerba G, Bernardina BD, Muglia P, van Haeringen A, Hoffer MJV, Franke B, Cappuccio G, Delatycki M, Lockhart PJ, Manning MA, Liu P, Scheffer IE, Brunetti-Pierri N, Rommelse N, Amaral DG, Santen GWE, Trabetti E, Sedláček Z, Michaelson JJ, Pierce K, Courchesne E, Kooy RF; SPARK Consortium; Nordenskjöld M, Romano C, Peeters H, Bernier RA, Gecz J, Xia K, Eichler EE. Wang T, et al. Among authors: xia k. Nat Commun. 2020 Oct 1;11(1):4932. doi: 10.1038/s41467-020-18723-y. Nat Commun. 2020. PMID: 33004838 Free PMC article.
Genetics of autism spectrum disorders.
Guo H, Hu Z, Zhao J, Xia K. Guo H, et al. Among authors: xia k. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2011 Aug;36(8):703-11. doi: 10.3969/j.issn.1672-7347.2011.08.001. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2011. PMID: 21937793 Review.
New ZNF644 mutations identified in patients with high myopia.
Xiang X, Wang T, Tong P, Li Y, Guo H, Wan A, Xia L, Liu Y, Li Y, Tian Q, Shen L, Cai X, Tian L, Jin X, Xia K, Hu Z. Xiang X, et al. Among authors: xia l, xia k. Mol Vis. 2014 Jun 30;20:939-46. eCollection 2014. Mol Vis. 2014. PMID: 24991186 Free PMC article.
AMPD1 functional variants associated with autism in Han Chinese population.
Zhang L, Ou J, Xu X, Peng Y, Guo H, Pan Y, Chen J, Wang T, Peng H, Liu Q, Tian D, Pan Q, Zou X, Zhao J, Hu Z, Xia K. Zhang L, et al. Among authors: xia k. Eur Arch Psychiatry Clin Neurosci. 2015 Sep;265(6):511-7. doi: 10.1007/s00406-014-0524-6. Epub 2014 Aug 26. Eur Arch Psychiatry Clin Neurosci. 2015. PMID: 25155876
Association of genetic variants of GRIN2B with autism.
Pan Y, Chen J, Guo H, Ou J, Peng Y, Liu Q, Shen Y, Shi L, Liu Y, Xiong Z, Zhu T, Luo S, Hu Z, Zhao J, Xia K. Pan Y, et al. Among authors: xia k. Sci Rep. 2015 Feb 6;5:8296. doi: 10.1038/srep08296. Sci Rep. 2015. PMID: 25656819 Free PMC article.
1,822 results