Lei Y - Search Results

1

Genome-wide association study in Chinese cohort identifies one novel hypospadias risk associated locus at 12q13.13.

Chen Z, Lin X, Lei Y, Chen H, Finnell RH, Wang Y, Xu J, Lu D, Xie H, Chen F. Chen Z, et al. Among authors: lei y. BMC Med Genomics. 2019 Dec 19;12(1):196. doi: 10.1186/s12920-019-0642-0. BMC Med Genomics. 2019. PMID: 31856834 Free PMC article.

2

Functional characterization of a promoter polymorphism in APE1/Ref-1 that contributes to reduced lung cancer susceptibility.

Lu J, Zhang S, Chen D, Wang H, Wu W, Wang X, Lei Y, Wang J, Qian J, Fan W, Hu Z, Jin L, Shen H, Huang W, Wei Q, Lu D. Lu J, et al. Among authors: lei y. FASEB J. 2009 Oct;23(10):3459-69. doi: 10.1096/fj.09-136549. Epub 2009 Jun 18. FASEB J. 2009. PMID: 19541747

3

Mutations in planar cell polarity gene SCRIB are associated with spina bifida.

Lei Y, Zhu H, Duhon C, Yang W, Ross ME, Shaw GM, Finnell RH. Lei Y, et al. PLoS One. 2013 Jul 26;8(7):e69262. doi: 10.1371/journal.pone.0069262. Print 2013. PLoS One. 2013. PMID: 23922697 Free PMC article.

4

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.

5

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.

6

Analysis of archived residual newborn screening blood spots after whole genome amplification.

Cantarel BL, Lei Y, Weaver D, Zhu H, Farrell A, Benstead-Hume G, Reese J, Finnell RH. Cantarel BL, et al. Among authors: lei y. BMC Genomics. 2015 Aug 13;16(1):602. doi: 10.1186/s12864-015-1747-2. BMC Genomics. 2015. PMID: 26268606 Free PMC article.

7

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.

8

Planar cell polarity genes Celsr1 and Vangl2 are necessary for kidney growth, differentiation, and rostrocaudal patterning.

Brzóska HŁ, d'Esposito AM, Kolatsi-Joannou M, Patel V, Igarashi P, Lei Y, Finnell RH, Lythgoe MF, Woolf AS, Papakrivopoulou E, Long DA. Brzóska HŁ, et al. Among authors: lei y. Kidney Int. 2016 Dec;90(6):1274-1284. doi: 10.1016/j.kint.2016.07.011. Epub 2016 Sep 2. Kidney Int. 2016. PMID: 27597235 Free PMC article.

9

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.

10

Digenic variants of planar cell polarity genes in human neural tube defect patients.

Wang L, Xiao Y, Tian T, Jin L, Lei Y, Finnell RH, Ren A. Wang L, et al. Among authors: lei y. Mol Genet Metab. 2018 May;124(1):94-100. doi: 10.1016/j.ymgme.2018.03.005. Epub 2018 Mar 18. Mol Genet Metab. 2018. PMID: 29573971 Free PMC article.

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