Ross ME - Search Results

1

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. Among authors: ross me. PLoS One. 2013 Jul 26;8(7):e69262. doi: 10.1371/journal.pone.0069262. Print 2013. PLoS One. 2013. PMID: 23922697 Free PMC article.

2

Identification of novel CELSR1 mutations in spina bifida.

Lei Y, Zhu H, Yang W, Ross ME, Shaw GM, Finnell RH. Lei Y, et al. Among authors: ross me. PLoS One. 2014 Mar 14;9(3):e92207. doi: 10.1371/journal.pone.0092207. eCollection 2014. PLoS One. 2014. PMID: 24632739 Free PMC article.

3

Untargeted metabolite profiling of murine embryos to reveal metabolic perturbations associated with neural tube closure defects.

Hansler A, Chen Q, Gray JD, Ross ME, Finnell RH, Gross SS. Hansler A, et al. Among authors: ross me. Birth Defects Res A Clin Mol Teratol. 2014 Aug;100(8):623-32. doi: 10.1002/bdra.23272. Epub 2014 Aug 13. Birth Defects Res A Clin Mol Teratol. 2014. PMID: 25115437 Free PMC article.

4

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. Among authors: ross me. Hum Mutat. 2015 Mar;36(3):342-9. doi: 10.1002/humu.22750. Hum Mutat. 2015. PMID: 25546815 Free PMC article.

5

Metabolite profiling of whole murine embryos reveals metabolic perturbations associated with maternal valproate-induced neural tube closure defects.

Akimova D, Wlodarczyk BJ, Lin Y, Ross ME, Finnell RH, Chen Q, Gross SS. Akimova D, et al. Among authors: ross me. Birth Defects Res. 2017 Jan 30;109(2):106-119. doi: 10.1002/bdra.23583. Birth Defects Res. 2017. PMID: 27860192 Free PMC article.

6

Genomic approaches to the assessment of human spina bifida risk.

Ross ME, Mason CE, Finnell RH. Ross ME, et al. Birth Defects Res. 2017 Jan 30;109(2):120-128. doi: 10.1002/bdra.23592. Birth Defects Res. 2017. PMID: 27883265 Free PMC article. Review.

7

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: ross me. 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.

8

Dominant negative GPR161 rare variants are risk factors of human spina bifida.

Kim SE, Lei Y, Hwang SH, Wlodarczyk BJ, Mukhopadhyay S, Shaw GM, Ross ME, Finnell RH. Kim SE, et al. Among authors: ross me. Hum Mol Genet. 2019 Jan 15;28(2):200-208. doi: 10.1093/hmg/ddy339. Hum Mol Genet. 2019. PMID: 30256984 Free PMC article.

9

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: ross me. Cell Res. 2019 Sep;29(9):776. doi: 10.1038/s41422-019-0201-4. Cell Res. 2019. PMID: 31346254 Free PMC article.

10

Loss of RAD9B impairs early neural development and contributes to the risk for human spina bifida.

Cao X, Tian T, Steele JW, Cabrera RM, Aguiar-Pulido V, Wadhwa S, Bhavani N, Bi P, Gargurevich NH, Hoffman EN, Cai CQ, Marini NJ, Yang W, Shaw GM, Ross ME, Finnell RH, Lei Y. Cao X, et al. Among authors: ross me. Hum Mutat. 2020 Apr;41(4):786-799. doi: 10.1002/humu.23969. Epub 2020 Jan 16. Hum Mutat. 2020. PMID: 31898828 Free PMC article.

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