Connection

Co-Authors

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

4.002
  1. The antagonism of folate receptor by dolutegravir: developmental toxicity reduction by supplemental folic acid. AIDS. 2019 11 01; 33(13):1967-1976.
    View in: PubMed
    Score: 0.734
  2. Autoantibodies to folate receptor during pregnancy and neural tube defect risk. J Reprod Immunol. 2008 Oct; 79(1):85-92.
    View in: PubMed
    Score: 0.340
  3. Investigations into the etiology of neural tube defects. Birth Defects Res C Embryo Today. 2004 Dec; 72(4):330-44.
    View in: PubMed
    Score: 0.261
  4. Dolutegravir-induced neural tube defects in mice are folate responsive. AIDS. 2024 Mar 15; 38(4):439-446.
    View in: PubMed
    Score: 0.248
  5. 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: 0.215
  6. Gene Environment Interactions in the Etiology of Neural Tube Defects. Front Genet. 2021; 12:659612.
    View in: PubMed
    Score: 0.204
  7. Approaches to studying the genomic architecture of complex birth defects. Prenat Diagn. 2020 08; 40(9):1047-1055.
    View in: PubMed
    Score: 0.192
  8. 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: 0.165
  9. Impact of selective serotonin reuptake inhibitors on neural crest stem cell formation. Toxicol Lett. 2017 Nov 05; 281:20-25.
    View in: PubMed
    Score: 0.158
  10. Functional regulation of P-glycoprotein at the blood-brain barrier in proton-coupled folate transporter (PCFT) mutant mice. FASEB J. 2013 Mar; 27(3):1167-75.
    View in: PubMed
    Score: 0.114
  11. 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: 0.112
  12. Autoantibodies to folate receptor alpha during early pregnancy and risk of oral clefts in Denmark. Pediatr Res. 2010 Mar; 67(3):274-9.
    View in: PubMed
    Score: 0.094
  13. 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: 0.080
  14. 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: 0.072
  15. Valproic acid-induced skeletal malformations: associated gene expression cascades. Pharmacogenet Genomics. 2005 Nov; 15(11):787-800.
    View in: PubMed
    Score: 0.070
  16. 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: 0.063
  17. Mapping a chromosomal locus for valproic acid-induced exencephaly in mice. Mamm Genome. 2004 May; 15(5):361-9.
    View in: PubMed
    Score: 0.063
  18. 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: 0.061
  19. Excess folic acid intake increases DNA de novo point mutations. Cell Discov. 2023 Feb 28; 9(1):22.
    View in: PubMed
    Score: 0.058
  20. KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency. Biology (Basel). 2022 Dec 31; 12(1).
    View in: PubMed
    Score: 0.057
  21. CIC missense variants contribute to susceptibility for spina bifida. Hum Mutat. 2022 12; 43(12):2021-2032.
    View in: PubMed
    Score: 0.056
  22. Hypermethylation of PI3K-AKT signalling pathway genes is associated with human neural tube defects. Epigenetics. 2022 Jan-Feb; 17(2):133-146.
    View in: PubMed
    Score: 0.050
  23. FKBP8 variants are risk factors for spina bifida. Hum Mol Genet. 2020 11 04; 29(18):3132-3144.
    View in: PubMed
    Score: 0.049
  24. 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: 0.048
  25. Loss of RAD9B impairs early neural development and contributes to the risk for human spina bifida. Hum Mutat. 2020 04; 41(4):786-799.
    View in: PubMed
    Score: 0.047
  26. 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: 0.045
  27. 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: 0.043
  28. 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: 0.042
  29. 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.
    View in: PubMed
    Score: 0.041
  30. Corrigendum for: Levels of folate receptor autoantibodies in maternal and cord blood and risk of neural tube defects in a Chinese population, 106:685-695 (10.1002/bdra.23517). Birth Defects Res A Clin Mol Teratol. 2016 12; 106(12):1062.
    View in: PubMed
    Score: 0.038
  31. Identification of vascular disruptor compounds by analysis in zebrafish embryos and mouse embryonic endothelial cells. Reprod Toxicol. 2017 06; 70:60-69.
    View in: PubMed
    Score: 0.037
  32. Levels of folate receptor autoantibodies in maternal and cord blood and risk of neural tube defects in a Chinese population. Birth Defects Res A Clin Mol Teratol. 2016 Aug; 106(8):685-95.
    View in: PubMed
    Score: 0.036
  33. Autoantibodies against homocysteinylated protein in a mouse model of folate deficiency-induced neural tube defects. Birth Defects Res A Clin Mol Teratol. 2016 Mar; 106(3):201-7.
    View in: PubMed
    Score: 0.036
  34. 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: 0.029
  35. A mouse model of hereditary folate malabsorption: deletion of the PCFT gene leads to systemic folate deficiency. Blood. 2011 May 05; 117(18):4895-904.
    View in: PubMed
    Score: 0.025
  36. Genetic or nutritional disorders in homocysteine or folate metabolism increase protein N-homocysteinylation in mice. FASEB J. 2009 Jun; 23(6):1721-7.
    View in: PubMed
    Score: 0.022
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.