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The TFAP2A-IRF6-GRHL3 genetic pathway is conserved in neurulation.
Kousa YA, Zhu H, Fakhouri WD, Lei Y, Kinoshita A, Roushangar RR, Patel NK, Agopian AJ, Yang W, Leslie EJ, Busch TD, Mansour TA, Li X, Smith AL, Li EB, Sharma DB, Williams TJ, Chai Y, Amendt BA, Liao EC, Mitchell LE, Bassuk AG, Gregory S, Ashley-Koch A, Shaw GM, Finnell RH, Schutte BC. Kousa YA, et al. Among authors: lei y. Hum Mol Genet. 2019 May 15;28(10):1726-1737. doi: 10.1093/hmg/ddz010. Hum Mol Genet. 2019. PMID: 30689861 Free PMC article.
Identification of novel CELSR1 mutations in spina bifida.
Lei Y, Zhu H, Yang W, Ross ME, Shaw GM, Finnell RH. Lei Y, et al. PLoS One. 2014 Mar 14;9(3):e92207. doi: 10.1371/journal.pone.0092207. eCollection 2014. PLoS One. 2014. PMID: 24632739 Free PMC article.
Rare LRP6 variants identified in spina bifida patients.
Lei Y, Fathe K, McCartney D, Zhu H, Yang W, Ross ME, Shaw GM, Finnell RH. Lei Y, et al. Hum Mutat. 2015 Mar;36(3):342-9. doi: 10.1002/humu.22750. Hum Mutat. 2015. PMID: 25546815 Free PMC article.
New Techniques for the Study of Neural Tube Defects.
Lei Y, Finnell RH. Lei Y, et al. Adv Tech Biol Med. 2016 Feb;4(1):157. doi: 10.4172/2379-1764.1000157. Epub 2015 Dec 26. Adv Tech Biol Med. 2016. PMID: 27066597 Free PMC article.
Genetic analysis of Wnt/PCP genes in neural tube defects.
Chen Z, Lei Y, Cao X, Zheng Y, Wang F, Bao Y, Peng R, Finnell RH, Zhang T, Wang H. Chen Z, et al. Among authors: lei y. BMC Med Genomics. 2018 Apr 4;11(1):38. doi: 10.1186/s12920-018-0355-9. BMC Med Genomics. 2018. PMID: 29618362 Free PMC article.
Formate rescues neural tube defects caused by mutations in Slc25a32.
Kim J, Lei Y, Guo J, Kim SE, Wlodarczyk BJ, Cabrera RM, Lin YL, Nilsson TK, Zhang T, Ren A, Wang L, Yuan Z, Zheng YF, Wang HY, Finnell RH. Kim J, et al. Among authors: lei y. Proc Natl Acad Sci U S A. 2018 May 1;115(18):4690-4695. doi: 10.1073/pnas.1800138115. Epub 2018 Apr 16. Proc Natl Acad Sci U S A. 2018. PMID: 29666258 Free PMC article.
7,205 results