Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

56 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
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.
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. 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.
Corrigendum to "Digenic variants of planar cell polarity genes in human neural tube defect patients." Mol Genet Metab. 2018 May;124(1):94-100. doi:10.1016/j.ymgme.2018.03.005. Epub 2018 Mar 18.
Wang L, Xiao Y, Tian T, Jin L, Lei Y, Finnell RH, Ren A. Wang L, et al. Mol Genet Metab. 2021 Mar;132(3):211. doi: 10.1016/j.ymgme.2021.01.010. Epub 2021 Feb 10. Mol Genet Metab. 2021. PMID: 33582009 No abstract available.
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. 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.
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.
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.
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.
56 results