Gu WY - Search Results

1

Genetic variation and molecular profiling of congenital malformations of the female genital tract based on whole-genome sequencing.

Qiu JJ, Chang XY, Zhang N, Guo LP, Wang S, Gu WY, Yin YM, Shi ZW, Hua KQ. Qiu JJ, et al. Among authors: gu wy. World J Pediatr. 2024 Nov;20(11):1179-1195. doi: 10.1007/s12519-024-00839-6. Epub 2024 Sep 9. World J Pediatr. 2024. PMID: 39251565

2

Novel rare genetic variants of familial and sporadic pulmonary atresia identified by whole-exome sequencing.

Xing J, Wang H, Xie Y, Fan T, Cui C, Li Y, Wang S, Gu W, Wang C, Tang H, Liu L. Xing J, et al. Open Life Sci. 2023 May 19;18(1):20220593. doi: 10.1515/biol-2022-0593. eCollection 2023. Open Life Sci. 2023. PMID: 37215497 Free PMC article.

3

Genomic and molecular landscape of homologous recombination deficiency across multiple cancer types.

Shi Z, Chen B, Han X, Gu W, Liang S, Wu L. Shi Z, et al. Sci Rep. 2023 Jun 1;13(1):8899. doi: 10.1038/s41598-023-35092-w. Sci Rep. 2023. PMID: 37264024 Free PMC article.

4

Machine learning for the identification of neoantigen-reactive CD8 + T cells in gastrointestinal cancer using single-cell sequencing.

Sun H, Han X, Du Z, Chen G, Guo T, Xie F, Gu W, Shi Z. Sun H, et al. Br J Cancer. 2024 Jul;131(2):387-402. doi: 10.1038/s41416-024-02737-0. Epub 2024 Jun 7. Br J Cancer. 2024. PMID: 38849478

5

Homozygous GDF2-Related Hereditary Hemorrhagic Telangiectasia in a Chinese Family.

Liu J, Yang J, Tang X, Li H, Shen Y, Gu W, Zhao S. Liu J, et al. Pediatrics. 2020 Aug;146(2):e20191970. doi: 10.1542/peds.2019-1970. Epub 2020 Jul 15. Pediatrics. 2020. PMID: 32669404 Review.

6

Application of Trio-Whole Exome Sequencing in Genetic Diagnosis and Therapy in Chinese Children With Epilepsy.

Jiang T, Gao J, Jiang L, Xu L, Zhao C, Su X, Shen Y, Gu W, Kong X, Yang Y, Gao F. Jiang T, et al. Front Mol Neurosci. 2021 Aug 19;14:699574. doi: 10.3389/fnmol.2021.699574. eCollection 2021. Front Mol Neurosci. 2021. PMID: 34489640 Free PMC article.

7

Prenatal diagnosis of 21 fetuses with balanced chromosomal abnormalities (BCAs) using whole-genome sequencing.

Fu F, Li R, Dang X, Yu Q, Xu K, Gu W, Wang D, Yang X, Pan M, Zhen L, Zhang Y, Li F, Jing X, Li F, Li D, Liao C. Fu F, et al. Front Genet. 2022 Sep 15;13:951829. doi: 10.3389/fgene.2022.951829. eCollection 2022. Front Genet. 2022. PMID: 36186435 Free PMC article.

8

Digenetic inheritance of SLC12A3 and CLCNKB genes in a Chinese girl with Gitelman syndrome.

Kong Y, Xu K, Yuan K, Zhu J, Gu W, Liang L, Wang C. Kong Y, et al. BMC Pediatr. 2019 Apr 18;19(1):114. doi: 10.1186/s12887-019-1498-3. BMC Pediatr. 2019. PMID: 30999883 Free PMC article.

9

Case Report: Novel CA12 Homozygous Variant Causing Isolated Hyperchloridrosis in a Chinese Child With Hyponatremia.

Han M, Peng M, Han Z, Zhu X, Huang Q, Gu W, Guo Y. Han M, et al. Front Pediatr. 2022 Mar 14;10:820707. doi: 10.3389/fped.2022.820707. eCollection 2022. Front Pediatr. 2022. PMID: 35359895 Free PMC article.

10

Early-onset ophthalmoplegia, cervical dyskinesia, and lower extremity weakness due to partial deletion of chromosome 16: A case report.

Xu M, Jiang J, He Y, Gu WY, Jin B. Xu M, et al. Among authors: gu wy. World J Clin Cases. 2022 Sep 16;10(26):9332-9339. doi: 10.12998/wjcc.v10.i26.9332. World J Clin Cases. 2022. PMID: 36159412 Free PMC article.

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