Lei Y - Search Results

1

Global DNA hypomethylation is associated with NTD-affected pregnancy: A case-control study.

Chen X, Guo J, Lei Y, Zou J, Lu X, Bao Y, Wu L, Wu J, Zheng X, Shen Y, Wu BL, Zhang T. Chen X, et al. Among authors: lei y. Birth Defects Res A Clin Mol Teratol. 2010 Jul;88(7):575-81. doi: 10.1002/bdra.20670. Birth Defects Res A Clin Mol Teratol. 2010. PMID: 20641100

2

VANGL2 mutations in human cranial neural-tube defects.

Lei YP, Zhang T, Li H, Wu BL, Jin L, Wang HY. Lei YP, et al. N Engl J Med. 2010 Jun 10;362(23):2232-5. doi: 10.1056/NEJMc0910820. N Engl J Med. 2010. PMID: 20558380 No abstract available.

3

Identification of novel rare mutations of DACT1 in human neural tube defects.

Shi Y, Ding Y, Lei YP, Yang XY, Xie GM, Wen J, Cai CQ, Li H, Chen Y, Zhang T, Wu BL, Jin L, Chen YG, Wang HY. Shi Y, et al. Among authors: lei yp. Hum Mutat. 2012 Oct;33(10):1450-5. doi: 10.1002/humu.22121. Epub 2012 Jun 19. Hum Mutat. 2012. PMID: 22610794

4

Mutations in the COPII vesicle component gene SEC24B are associated with human neural tube defects.

Yang XY, Zhou XY, Wang QQ, Li H, Chen Y, Lei YP, Ma XH, Kong P, Shi Y, Jin L, Zhang T, Wang HY. Yang XY, et al. Among authors: lei yp. Hum Mutat. 2013 Aug;34(8):1094-101. doi: 10.1002/humu.22338. Epub 2013 May 13. Hum Mutat. 2013. PMID: 23592378

5

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

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

Gene variants in the folate pathway are associated with increased levels of folate receptor autoantibodies.

Dong Y, Wang L, Lei Y, Yang N, Cabrera RM, Finnell RH, Ren A. Dong Y, et al. Among authors: lei y. Birth Defects Res. 2018 Jul 17;110(12):973-981. doi: 10.1002/bdr2.1334. Epub 2018 May 6. Birth Defects Res. 2018. PMID: 29732742 Free PMC article.

8

Threshold for neural tube defect risk by accumulated singleton loss-of-function variants.

Chen Z, Lei Y, Zheng Y, Aguiar-Pulido V, Ross ME, Peng R, Jin L, Zhang T, Finnell RH, Wang H. Chen Z, et al. Among authors: lei y. Cell Res. 2018 Oct;28(10):1039-1041. doi: 10.1038/s41422-018-0061-3. Epub 2018 Jul 5. Cell Res. 2018. PMID: 29976953 Free PMC article. No abstract available.

9

Variants identified in PTK7 associated with neural tube defects.

Lei Y, Kim SE, Chen Z, Cao X, Zhu H, Yang W, Shaw GM, Zheng Y, Zhang T, Wang HY, Finnell RH. Lei Y, et al. Mol Genet Genomic Med. 2019 Apr;7(4):e00584. doi: 10.1002/mgg3.584. Epub 2019 Jan 28. Mol Genet Genomic Med. 2019. PMID: 30689296 Free PMC article.

10

Author Correction: Threshold for neural tube defect risk by accumulated singleton loss-of-function variants.

Chen Z, Lei Y, Zheng Y, Aguiar-Pulido V, Ross ME, Peng R, Jin L, Zhang T, Finnell RH, Wang H. Chen Z, et al. Among authors: lei y. Cell Res. 2019 Sep;29(9):776. doi: 10.1038/s41422-019-0201-4. Cell Res. 2019. PMID: 31346254 Free PMC article.

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