Connection

Co-Authors

This is a "connection" page, showing publications co-authored by ROBERT CABRERA and BOGDAN WLODARCZYK.
Connection Strength

2.316
  1. The teratogenic effects of sertraline in mice. Birth Defects Res. 2020 08; 112(13):1014-1024.
    View in: PubMed
    Score: 0.720
  2. Transcriptional analyses of two mouse models of spina bifida. Birth Defects Res A Clin Mol Teratol. 2012 Oct; 94(10):782-9.
    View in: PubMed
    Score: 0.431
  3. Dolutegravir-induced neural tube defects in mice are folate responsive. AIDS. 2024 03 15; 38(4):439-446.
    View in: PubMed
    Score: 0.238
  4. Gene Environment Interactions in the Etiology of Neural Tube Defects. Front Genet. 2021; 12:659612.
    View in: PubMed
    Score: 0.196
  5. Teratogenicity of valproic acid and its constitutional isomer, amide derivative valnoctamide in mice. Birth Defects Res. 2019 08 15; 111(14):1013-1023.
    View in: PubMed
    Score: 0.164
  6. Arsenic-induced gene expression changes in the neural tube of folate transport defective mouse embryos. Neurotoxicology. 2006 Jul; 27(4):547-57.
    View in: PubMed
    Score: 0.069
  7. Folate regulation of planar cell polarity pathway and F-actin through folate receptor alpha. FASEB J. 2024 01; 38(1):e23346.
    View in: PubMed
    Score: 0.059
  8. Excess folic acid intake increases DNA de novo point mutations. Cell Discov. 2023 Feb 28; 9(1):22.
    View in: PubMed
    Score: 0.055
  9. CIC missense variants contribute to susceptibility for spina bifida. Hum Mutat. 2022 12; 43(12):2021-2032.
    View in: PubMed
    Score: 0.054
  10. Embryonic Hypotaurine Levels Contribute to Strain-Dependent Susceptibility in Mouse Models of Valproate-Induced Neural Tube Defects. Front Cell Dev Biol. 2022; 10:832492.
    View in: PubMed
    Score: 0.052
  11. FKBP8 variants are risk factors for spina bifida. Hum Mol Genet. 2020 11 04; 29(18):3132-3144.
    View in: PubMed
    Score: 0.047
  12. 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.
    View in: PubMed
    Score: 0.047
  13. Heritable spina bifida in sheep: A potential model for fetal repair of myelomeningocele. J Pediatr Surg. 2020 Mar; 55(3):475-481.
    View in: PubMed
    Score: 0.043
  14. Combining mouse embryonic stem cells and zebrafish embryos to evaluate developmental toxicity of chemical exposure. Reprod Toxicol. 2018 10; 81:220-228.
    View in: PubMed
    Score: 0.040
  15. Formate rescues neural tube defects caused by mutations in Slc25a32. Proc Natl Acad Sci U S A. 2018 05 01; 115(18):4690-4695.
    View in: PubMed
    Score: 0.040
  16. The transcobalamin receptor knockout mouse: a model for vitamin B12 deficiency in the central nervous system. FASEB J. 2013 Jun; 27(6):2468-75.
    View in: PubMed
    Score: 0.028
  17. Differentially expressed genes in embryonic cardiac tissues of mice lacking Folr1 gene activity. BMC Dev Biol. 2007 Nov 20; 7:128.
    View in: PubMed
    Score: 0.019
  18. Folate-regulated changes in gene expression in the anterior neural tube of folate binding protein-1 (Folbp1)-deficient murine embryos. Neurochem Res. 2004 Jun; 29(6):1105-12.
    View in: PubMed
    Score: 0.015
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.