Co-Authors
This is a "connection" page, showing publications co-authored by RICHARD FINNELL and YUNPING LEI.
Connection Strength
7.453
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New myotonic dystrophy type 1 mouse model. Cell Res. 2020 02; 30(2):99-100.
Score: 0.747
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Variants identified in PTK7 associated with neural tube defects. Mol Genet Genomic Med. 2019 04; 7(4):e00584.
Score: 0.696
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New Techniques for the Study of Neural Tube Defects. Adv Tech Biol Med. 2016 Feb; 4(1).
Score: 0.562
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Rare LRP6 variants identified in spina bifida patients. Hum Mutat. 2015 Mar; 36(3):342-9.
Score: 0.531
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Identification of novel CELSR1 mutations in spina bifida. PLoS One. 2014; 9(3):e92207.
Score: 0.497
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Mutations in planar cell polarity gene SCRIB are associated with spina bifida. PLoS One. 2013; 8(7):e69262.
Score: 0.475
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Gene-environment interactions underlying the etiology of neural tube defects. Curr Top Dev Biol. 2023; 152:193-220.
Score: 0.454
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Excess folic acid intake increases DNA de novo point mutations. Cell Discov. 2023 Feb 28; 9(1):22.
Score: 0.231
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KDM6B Variants May Contribute to the Pathophysiology of Human Cerebral Folate Deficiency. Biology (Basel). 2022 Dec 31; 12(1).
Score: 0.228
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CIC missense variants contribute to susceptibility for spina bifida. Hum Mutat. 2022 12; 43(12):2021-2032.
Score: 0.224
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Gene Environment Interactions in the Etiology of Neural Tube Defects. Front Genet. 2021; 12:659612.
Score: 0.204
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Somatic and de novo Germline Variants of MEDs in Human Neural Tube Defects. Front Cell Dev Biol. 2021; 9:641831.
Score: 0.201
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Maternal Hypertension-Related Genotypes and Congenital Heart Defects. Am J Hypertens. 2021 02 18; 34(1):82-91.
Score: 0.201
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FKBP8 variants are risk factors for spina bifida. Hum Mol Genet. 2020 11 04; 29(18):3132-3144.
Score: 0.197
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Approaches to studying the genomic architecture of complex birth defects. Prenat Diagn. 2020 08; 40(9):1047-1055.
Score: 0.192
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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: 0.186
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Whole-Exome Sequencing Identifies Damaging de novo Variants in Anencephalic Cases. Front Neurosci. 2019; 13:1285.
Score: 0.184
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Dominant negative GPR161 rare variants are risk factors of human spina bifida. Hum Mol Genet. 2019 01 15; 28(2):200-208.
Score: 0.174
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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: 0.165
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Analysis of archived residual newborn screening blood spots after whole genome amplification. BMC Genomics. 2015 Aug 13; 16:602.
Score: 0.137
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Exome-wide assessment of isolated biliary atresia: A report from the National Birth Defects Prevention Study using child-parent trios and a case-control design to identify novel rare variants. Am J Med Genet A. 2023 06; 191(6):1546-1556.
Score: 0.058
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Systems biology analysis of human genomes points to key pathways conferring spina bifida risk. Proc Natl Acad Sci U S A. 2021 12 21; 118(51).
Score: 0.053
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Actuation enhances patterning in human neural tube organoids. Nat Commun. 2021 05 27; 12(1):3192.
Score: 0.051
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Author Correction: Threshold for neural tube defect risk by accumulated singleton loss-of-function variants. Cell Res. 2021 Apr; 31(4):488.
Score: 0.051
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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: 0.050
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Correction to: Genetic analysis of Wnt/PCP genes in neural tube defects. BMC Med Genomics. 2021 Jan 27; 14(1):29.
Score: 0.050
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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: 0.048
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DVL mutations identified from human neural tube defects and Dandy-Walker malformation obstruct the Wnt signaling pathway. J Genet Genomics. 2020 06 20; 47(6):301-310.
Score: 0.048
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Rare copy number variations of planar cell polarity genes are associated with human neural tube defects. Neurogenetics. 2020 07; 21(3):217-225.
Score: 0.048
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Somatic mutations in planar cell polarity genes in neural tissue from human fetuses with neural tube defects. Hum Genet. 2020 Oct; 139(10):1299-1314.
Score: 0.047
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Genome-wide association study in Chinese cohort identifies one novel hypospadias risk associated locus at 12q13.13. BMC Med Genomics. 2019 12 19; 12(1):196.
Score: 0.046
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Author Correction: Threshold for neural tube defect risk by accumulated singleton loss-of-function variants. Cell Res. 2019 Sep; 29(9):776.
Score: 0.045
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The TFAP2A-IRF6-GRHL3 genetic pathway is conserved in neurulation. Hum Mol Genet. 2019 05 15; 28(10):1726-1737.
Score: 0.044
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Maternal genetic markers for risk of celiac disease and their potential association with neural tube defects in offspring. Mol Genet Genomic Med. 2019 06; 7(6):e688.
Score: 0.044
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Maternal Lactase Polymorphism (rs4988235) Is Associated with Neural Tube Defects in Offspring in the National Birth Defects Prevention Study. J Nutr. 2019 02 01; 149(2):295-303.
Score: 0.044
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Threshold for neural tube defect risk by accumulated singleton loss-of-function variants. Cell Res. 2018 10; 28(10):1039-1041.
Score: 0.042
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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: 0.041
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Genetic analysis of Wnt/PCP genes in neural tube defects. BMC Med Genomics. 2018 04 04; 11(1):38.
Score: 0.041
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Digenic variants of planar cell polarity genes in human neural tube defect patients. Mol Genet Metab. 2018 05; 124(1):94-100.
Score: 0.041
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Disruption of the ATXN1-CIC complex causes a spectrum of neurobehavioral phenotypes in mice and humans. Nat Genet. 2017 Apr; 49(4):527-536.
Score: 0.038
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Planar cell polarity genes Celsr1 and Vangl2 are necessary for kidney growth, differentiation, and rostrocaudal patterning. Kidney Int. 2016 12; 90(6):1274-1284.
Score: 0.037