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2019 4
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Page 1
Genetic correlation between smoking behavior and gastroesophageal reflux disease: insights from integrative multi-omics data.
Yan Z, Xu Y, Li K, Liu L. Yan Z, et al. BMC Genomics. 2024 Jun 27;25(1):642. doi: 10.1186/s12864-024-10536-3. BMC Genomics. 2024. PMID: 38937676 Free PMC article.
Moreover, both smoking behavior and GERD were found to be co-enriched in multiple brain tissues, with GMPPB, RNF123, and RBM6 identified as potential functional genes co-enriched in Cerebellar Hemisphere, Cerebellum, Cortex/Nucleus accumbens in SI and GERD, and SUOX identi …
Moreover, both smoking behavior and GERD were found to be co-enriched in multiple brain tissues, with GMPPB, RNF123, and RBM6 identified as …
Identifying drug targets for neurological and psychiatric disease via genetics and the brain transcriptome.
Baird DA, Liu JZ, Zheng J, Sieberts SK, Perumal T, Elsworth B, Richardson TG, Chen CY, Carrasquillo MM, Allen M, Reddy JS, De Jager PL, Ertekin-Taner N, Mangravite LM, Logsdon B, Estrada K, Haycock PC, Hemani G, Runz H, Smith GD, Gaunt TR; AMP-AD eQTL working group. Baird DA, et al. PLoS Genet. 2021 Jan 8;17(1):e1009224. doi: 10.1371/journal.pgen.1009224. eCollection 2021 Jan. PLoS Genet. 2021. PMID: 33417599 Free PMC article.
From these we identified five genes (ACE, GPNMB, KCNQ5, RERE and SUOX) as attractive drug targets that may warrant follow-up in functional studies and clinical trials, demonstrating the value of this study design for discovering drug targets in neuropsychiatric diseases... …
From these we identified five genes (ACE, GPNMB, KCNQ5, RERE and SUOX) as attractive drug targets that may warrant follow-up in funct …
Identification of Novel T1D Risk Loci and Their Association With Age and Islet Function at Diagnosis in Autoantibody-Positive T1D Individuals: Based on a Two-Stage Genome-Wide Association Study.
Zhu M, Xu K, Chen Y, Gu Y, Zhang M, Luo F, Liu Y, Gu W, Hu J, Xu H, Xie Z, Sun C, Li Y, Sun M, Xu X, Hsu HT, Chen H, Fu Q, Shi Y, Xu J, Ji L, Liu J, Bian L, Zhu J, Chen S, Xiao L, Li X, Jiang H, Shen M, Huang Q, Fang C, Li X, Huang G, Fan J, Jiang Z, Jiang Y, Dai J, Ma H, Zheng S, Cai Y, Dai H, Zheng X, Zhou H, Ni S, Jin G, She JX, Yu L, Polychronakos C, Hu Z, Zhou Z, Weng J, Shen H, Yang T. Zhu M, et al. Diabetes Care. 2019 Aug;42(8):1414-1421. doi: 10.2337/dc18-2023. Epub 2019 May 31. Diabetes Care. 2019. PMID: 31152121
We identified four T1D risk loci reaching genome-wide significance in the Chinese Han population, including two novel loci, rs4320356 near BTN3A1 (odds ratio [OR] 1.26, P = 2.70 10(-8)) and rs3802604 in GATA3 (OR 1.24, P = 2.06 10(-8)), and two previously reported loci, rs1770 in …
We identified four T1D risk loci reaching genome-wide significance in the Chinese Han population, including two novel loci, rs4320356 near B …
Colocalization analysis of polycystic ovary syndrome to identify potential disease-mediating genes and proteins.
Censin JC, Bovijn J, Holmes MV, Lindgren CM. Censin JC, et al. Eur J Hum Genet. 2021 Sep;29(9):1446-1454. doi: 10.1038/s41431-021-00835-8. Epub 2021 Mar 4. Eur J Hum Genet. 2021. PMID: 33664499 Free PMC article.
Through these analyses, we identified seven proteins or genes with evidence of a possibly shared causal variant for almost 30% of known PCOS signals, including follicle stimulating hormone and ERBB3, IKZF4, RPS26, SUOX, ZFP36L2, and C8orf49. Several of these potential effe …
Through these analyses, we identified seven proteins or genes with evidence of a possibly shared causal variant for almost 30% of known PCOS …
Machine learning-based identification and characterization of 15 novel pathogenic SUOX missense mutations.
Kaczmarek AT, Bahlmann N, Thaqi B, May P, Schwarz G. Kaczmarek AT, et al. Mol Genet Metab. 2021 Sep-Oct;134(1-2):188-194. doi: 10.1016/j.ymgme.2021.07.011. Epub 2021 Aug 8. Mol Genet Metab. 2021. PMID: 34420858
Isolated sulfite oxidase deficiency (ISOD) is a rare hereditary metabolic disease caused by absence of functional sulfite oxidase (SO) due to mutations of the SUOX gene. SO oxidizes toxic sulfite and sulfite accumulation is associated with neurological disorders, progressi …
Isolated sulfite oxidase deficiency (ISOD) is a rare hereditary metabolic disease caused by absence of functional sulfite oxidase (SO) due t …
High sulfite oxidase expression could predict postoperative biochemical recurrence in patients with prostate cancer.
Kurose H, Naito Y, Akiba J, Kondo R, Ogasawara S, Kusano H, Sanada S, Abe H, Kakuma T, Ueda K, Igawa T, Yano H. Kurose H, et al. Med Mol Morphol. 2019 Sep;52(3):164-172. doi: 10.1007/s00795-018-00214-1. Epub 2019 Jan 10. Med Mol Morphol. 2019. PMID: 30631948
Here, we performed a clinicopathological investigation of SUOX expression in prostate cancer and discussed the usefulness of SUOX expression as a predictor of biochemical recurrence following surgical treatment in prostate cancer. This study was conducted using Tiss …
Here, we performed a clinicopathological investigation of SUOX expression in prostate cancer and discussed the usefulness of SUOX …
Isolated sulfite oxidase deficiency: a founder mutation.
Mhanni AA, Greenberg CR, Spriggs EL, Agatep R, Sisk RR, Prasad C. Mhanni AA, et al. Cold Spring Harb Mol Case Stud. 2020 Dec 17;6(6):a005900. doi: 10.1101/mcs.a005900. Print 2020 Dec. Cold Spring Harb Mol Case Stud. 2020. PMID: 33335014 Free PMC article.
Both patients have a homozygous 4-bp deletion, 1347-1350delTTGT in the sulfite oxidase gene (SUOX), predicting a premature termination of the sulfite oxidase protein leading to absence of the carboxy-terminal third portion of the protein. ...
Both patients have a homozygous 4-bp deletion, 1347-1350delTTGT in the sulfite oxidase gene (SUOX), predicting a premature terminatio …
Investigating the shared genetic links between hypothyroidism and psychiatric disorders: a large-scale genomewide cross-trait analysis.
Chen Y, Zhang Z, Chen Y, Liu P, Yi S, Fan C, Zhao W, Liu J. Chen Y, et al. J Affect Disord. 2025 Jan 15;369:312-320. doi: 10.1016/j.jad.2024.08.202. Epub 2024 Sep 29. J Affect Disord. 2025. PMID: 39353512
Especially, many pleiotropic genes were significantly expressed for multiple pairwise traits, such as BCL11B, RERE, and SUOX. Lastly, the Latent causal variable model (LCV) analysis did not find any causal components in the genetic structure between them. ...
Especially, many pleiotropic genes were significantly expressed for multiple pairwise traits, such as BCL11B, RERE, and SUOX. Lastly, …
Analysis of expression of candidate genes for polycystic ovary syndrome in adult and fetal human and fetal bovine ovaries†.
Liu M, Hummitzsch K, Hartanti MD, Rosario R, Bastian NA, Hatzirodos N, Bonner WM, Irving-Rodgers HF, Laven JSE, Anderson RA, Rodgers RJ. Liu M, et al. Biol Reprod. 2020 Oct 5;103(4):840-853. doi: 10.1093/biolre/ioaa119. Biol Reprod. 2020. PMID: 32678441
ARL14EP, FDFT1, NEIL2, and MAPRE1 were expressed across gestation and not correlated with gestational age as shown previously for THADA, ERBB4, RAD50, C8H9orf3, YAP1, RAB5B, SUOX, and KRR1. LHCGR, because of its unusual bimodal expression pattern, had some unusual correlat …
ARL14EP, FDFT1, NEIL2, and MAPRE1 were expressed across gestation and not correlated with gestational age as shown previously for THADA, ERB …
Identification of a novel SUOX pathogenic variants as the cause of isolated sulfite oxidase deficiency in a Chinese pedigree.
Du P, Hassan RN, Luo H, Xie J, Zhu Y, Hu Q, Yan J, Jiang W. Du P, et al. Mol Genet Genomic Med. 2021 Feb;9(2):e1590. doi: 10.1002/mgg3.1590. Epub 2021 Jan 6. Mol Genet Genomic Med. 2021. PMID: 33405344 Free PMC article.
BACKGROUND: Isolated sulfite oxidase deficiency (ISOD) is a life-threatening rare autosomal recessive disorder caused by pathogenic variants in SUOX (OMIM 606887) gene. The aim of our study was to establish a comprehensive genetic diagnosis strategy for the pathogenicity a …
BACKGROUND: Isolated sulfite oxidase deficiency (ISOD) is a life-threatening rare autosomal recessive disorder caused by pathogenic variants …
22 results