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Whole-exome sequencing study of hypospadias.
Chen Z, Lei Y, Finnell RH, Ding Y, Su Z, Wang Y, Xie H, Chen F. Chen Z, et al. Among authors: lei y. iScience. 2023 Apr 12;26(5):106663. doi: 10.1016/j.isci.2023.106663. eCollection 2023 May 19. iScience. 2023. PMID: 37168556 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.
Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans.
Lu HC, Tan Q, Rousseaux MW, Wang W, Kim JY, Richman R, Wan YW, Yeh SY, Patel JM, Liu X, Lin T, Lee Y, Fryer JD, Han J, Chahrour M, Finnell RH, Lei Y, Zurita-Jimenez ME, Ahimaz P, Anyane-Yeboa K, Van Maldergem L, Lehalle D, Jean-Marcais N, Mosca-Boidron AL, Thevenon J, Cousin MA, Bro DE, Lanpher BC, Klee EW, Alexander N, Bainbridge MN, Orr HT, Sillitoe RV, Ljungberg MC, Liu Z, Schaaf CP, Zoghbi HY. Lu HC, et al. Among authors: lei y. Nat Genet. 2017 Apr;49(4):527-536. doi: 10.1038/ng.3808. Epub 2017 Mar 13. Nat Genet. 2017. PMID: 28288114 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.
6,720 results