Co-Authors
This is a "connection" page, showing publications co-authored by YUNPING LEI and ROBERT CABRERA.
Connection Strength
1.305
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Excess folic acid intake increases DNA de novo point mutations. Cell Discov. 2023 Feb 28; 9(1):22.
Score: 0.224
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KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency. Biology (Basel). 2022 Dec 31; 12(1).
Score: 0.221
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CIC missense variants contribute to susceptibility for spina bifida. Hum Mutat. 2022 12; 43(12):2021-2032.
Score: 0.217
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FKBP8 variants are risk factors for spina bifida. Hum Mol Genet. 2020 11 04; 29(18):3132-3144.
Score: 0.191
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Loss of RAD9B impairs early neural development and contributes to the risk for human spina bifida. Hum Mutat. 2020 04; 41(4):786-799.
Score: 0.180
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Gene Environment Interactions in the Etiology of Neural Tube Defects. Front Genet. 2021; 12:659612.
Score: 0.049
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Hypermethylation of PI3K-AKT signalling pathway genes is associated with human neural tube defects. Epigenetics. 2022 Jan-Feb; 17(2):133-146.
Score: 0.049
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CIC de novo loss of function variants contribute to cerebral folate deficiency by downregulating FOLR1 expression. J Med Genet. 2021 07; 58(7):484-494.
Score: 0.047
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Approaches to studying the genomic architecture of complex birth defects. Prenat Diagn. 2020 08; 40(9):1047-1055.
Score: 0.047
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Gene variants in the folate pathway are associated with increased levels of folate receptor autoantibodies. Birth Defects Res. 2018 07 17; 110(12):973-981.
Score: 0.040
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Formate rescues neural tube defects caused by mutations in Slc25a32. Proc Natl Acad Sci U S A. 2018 05 01; 115(18):4690-4695.
Score: 0.040