Co-Authors
This is a "connection" page, showing publications co-authored by RICHARD FINNELL and ROBERT CABRERA.
Connection Strength
4.392
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The antagonism of folate receptor by dolutegravir: developmental toxicity reduction by supplemental folic acid. AIDS. 2019 11 01; 33(13):1967-1976.
Score: 0.704
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Autoantibodies to folate receptor during pregnancy and neural tube defect risk. J Reprod Immunol. 2008 Oct; 79(1):85-92.
Score: 0.326
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Investigations into the etiology of neural tube defects. Birth Defects Res C Embryo Today. 2004 Dec; 72(4):330-44.
Score: 0.250
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Dolutegravir induces FOLR1 expression during brain organoid development. Front Mol Neurosci. 2024; 17:1394058.
Score: 0.241
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Dolutegravir-induced neural tube defects in mice are folate responsive. AIDS. 2024 03 15; 38(4):439-446.
Score: 0.237
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Gene expression profiling within the developing neural tube. Neurochem Res. 2002 Oct; 27(10):1165-80.
Score: 0.215
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Embryonic Hypotaurine Levels Contribute to Strain-Dependent Susceptibility in Mouse Models of Valproate-Induced Neural Tube Defects. Front Cell Dev Biol. 2022; 10:832492.
Score: 0.206
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Gene Environment Interactions in the Etiology of Neural Tube Defects. Front Genet. 2021; 12:659612.
Score: 0.195
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Approaches to studying the genomic architecture of complex birth defects. Prenat Diagn. 2020 08; 40(9):1047-1055.
Score: 0.184
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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: 0.158
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Impact of selective serotonin reuptake inhibitors on neural crest stem cell formation. Toxicol Lett. 2017 Nov 05; 281:20-25.
Score: 0.151
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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.
Score: 0.109
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Transcriptional analyses of two mouse models of spina bifida. Birth Defects Res A Clin Mol Teratol. 2012 Oct; 94(10):782-9.
Score: 0.108
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Association between inhibited binding of folic acid to folate receptor alpha in maternal serum and folate-related birth defects in Norway. Hum Reprod. 2011 Aug; 26(8):2232-8.
Score: 0.098
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Autoantibodies to folate receptor alpha during early pregnancy and risk of oral clefts in Denmark. Pediatr Res. 2010 Mar; 67(3):274-9.
Score: 0.090
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Differentially expressed genes in embryonic cardiac tissues of mice lacking Folr1 gene activity. BMC Dev Biol. 2007 Nov 20; 7:128.
Score: 0.077
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Arsenic-induced gene expression changes in the neural tube of folate transport defective mouse embryos. Neurotoxicology. 2006 Jul; 27(4):547-57.
Score: 0.069
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Valproic acid-induced skeletal malformations: associated gene expression cascades. Pharmacogenet Genomics. 2005 Nov; 15(11):787-800.
Score: 0.067
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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.
Score: 0.060
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Mapping a chromosomal locus for valproic acid-induced exencephaly in mice. Mamm Genome. 2004 May; 15(5):361-9.
Score: 0.060
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Folate regulation of planar cell polarity pathway and F-actin through folate receptor alpha. FASEB J. 2024 01; 38(1):e23346.
Score: 0.059
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Excess folic acid intake increases DNA de novo point mutations. Cell Discov. 2023 Feb 28; 9(1):22.
Score: 0.055
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KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency. Biology (Basel). 2022 Dec 31; 12(1).
Score: 0.055
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CIC missense variants contribute to susceptibility for spina bifida. Hum Mutat. 2022 12; 43(12):2021-2032.
Score: 0.054
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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: 0.048
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FKBP8 variants are risk factors for spina bifida. Hum Mol Genet. 2020 11 04; 29(18):3132-3144.
Score: 0.047
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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: 0.046
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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: 0.045
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Heritable spina bifida in sheep: A potential model for fetal repair of myelomeningocele. J Pediatr Surg. 2020 Mar; 55(3):475-481.
Score: 0.043
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Teratogenicity of valproic acid and its constitutional isomer, amide derivative valnoctamide in mice. Birth Defects Res. 2019 08 15; 111(14):1013-1023.
Score: 0.041
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Combining mouse embryonic stem cells and zebrafish embryos to evaluate developmental toxicity of chemical exposure. Reprod Toxicol. 2018 10; 81:220-228.
Score: 0.040
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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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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.
Score: 0.036
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Identification of vascular disruptor compounds by analysis in zebrafish embryos and mouse embryonic endothelial cells. Reprod Toxicol. 2017 06; 70:60-69.
Score: 0.036
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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.
Score: 0.035
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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.
Score: 0.034
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The transcobalamin receptor knockout mouse: a model for vitamin B12 deficiency in the central nervous system. FASEB J. 2013 Jun; 27(6):2468-75.
Score: 0.028
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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.
Score: 0.024
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Genetic or nutritional disorders in homocysteine or folate metabolism increase protein N-homocysteinylation in mice. FASEB J. 2009 Jun; 23(6):1721-7.
Score: 0.021