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Did you mean shengqiang zhao (9 results)?
Multi-omic characterization of genome-wide abnormal DNA methylation reveals diagnostic and prognostic markers for esophageal squamous-cell carcinoma.
Xi Y, Lin Y, Guo W, Wang X, Zhao H, Miao C, Liu W, Liu Y, Liu T, Luo Y, Fan W, Lin A, Chen Y, Sun Y, Ma Y, Niu X, Zhong C, Tan W, Zhou M, Su J, Wu C, Lin D. Xi Y, et al. Among authors: zhao h. Signal Transduct Target Ther. 2022 Feb 25;7(1):53. doi: 10.1038/s41392-022-00873-8. Signal Transduct Target Ther. 2022. PMID: 35210398 Free PMC article.
Computational Methods for Identifying Similar Diseases.
Cheng L, Zhao H, Wang P, Zhou W, Luo M, Li T, Han J, Liu S, Jiang Q. Cheng L, et al. Among authors: zhao h. Mol Ther Nucleic Acids. 2019 Dec 6;18:590-604. doi: 10.1016/j.omtn.2019.09.019. Epub 2019 Sep 28. Mol Ther Nucleic Acids. 2019. PMID: 31678735 Free PMC article. Review.
Genome-wide cell-free DNA methylation analyses improve accuracy of non-invasive diagnostic imaging for early-stage breast cancer.
Liu J, Zhao H, Huang Y, Xu S, Zhou Y, Zhang W, Li J, Ming Y, Wang X, Zhao S, Li K, Dong X, Ma Y, Qian T, Chen X, Xing Z, Zhang Y, Chen H, Liu Z, Pang D, Zhou M, Wu Z, Wang X, Wang X, Wu N, Su J. Liu J, et al. Among authors: zhao h. Mol Cancer. 2021 Feb 19;20(1):36. doi: 10.1186/s12943-021-01330-w. Mol Cancer. 2021. PMID: 33608029 Free PMC article.
Unraveling the genetic architecture of congenital vertebral malformation with reference to the developing spine.
Zhao S, Zhao H, Zhao L, Cheng X, Zheng Z, Wu M, Wen W, Wang S, Zhou Z, Xie H, Ruan D, Li Q, Liu X, Ou C, Li G, Zhao Z, Chen G, Niu Y, Yin X, Hu Y, Zhang X; Deciphering disorders Involving Scoliosis and COmorbidities (DISCO) study; Liu P, Qiu G, Liu W, Zhao C, Wu Z, Zhang J, Wu N. Zhao S, et al. Among authors: zhao h. Nat Commun. 2024 Feb 6;15(1):1125. doi: 10.1038/s41467-024-45442-5. Nat Commun. 2024. PMID: 38321032 Free PMC article.
DrABC: deep learning accurately predicts germline pathogenic mutation status in breast cancer patients based on phenotype data.
Liu J, Zhao H, Zheng Y, Dong L, Zhao S, Huang Y, Huang S, Qian T, Zou J, Liu S, Li J, Yan Z, Li Y, Zhang S, Huang X, Wang W, Li Y, Wang J, Ming Y, Li X, Xing Z, Qin L, Zhao Z, Jia Z, Li J, Liu G, Zhang M, Feng K, Wu J, Zhang J, Yang Y, Wu Z, Liu Z, Ying J, Wang X, Su J, Wang X, Wu N. Liu J, et al. Among authors: zhao h. Genome Med. 2022 Feb 25;14(1):21. doi: 10.1186/s13073-022-01027-9. Genome Med. 2022. PMID: 35209950 Free PMC article.
A genotype-first analysis in a cohort of Mullerian anomaly.
Tian W, Chen N, Ye Y, Ma C, Qin C, Niu Y, Xiaoxin L, Zhao L, Zhao H, Liang Z, Song S, Wang Y, Chen Z, Lin J, Yan Z, Duan J, Zhao S, Zhang TJ, Qiu G, Wu Z, Wu N, Zhu L. Tian W, et al. Among authors: zhao h. J Hum Genet. 2022 Jun;67(6):347-352. doi: 10.1038/s10038-021-00996-w. Epub 2022 Jan 13. J Hum Genet. 2022. PMID: 35022528
CFEA: a cell-free epigenome atlas in human diseases.
Yu F, Li K, Li S, Liu J, Zhang Y, Zhou M, Zhao H, Chen H, Wu N, Liu Z, Su J. Yu F, et al. Among authors: zhao h. Nucleic Acids Res. 2020 Jan 8;48(D1):D40-D44. doi: 10.1093/nar/gkz715. Nucleic Acids Res. 2020. PMID: 31428785 Free PMC article.
95 results