Wang H - Search Results

1

Low blood S-methyl-5-thioadenosine is associated with postoperative delayed neurocognitive recovery.

Zhang L, Mao H, Zhou R, Zhu J, Wang H, Miao Z, Chen X, Yan J, Jiang H. Zhang L, et al. Among authors: wang h. Commun Biol. 2024 Oct 20;7(1):1356. doi: 10.1038/s42003-024-07086-5. Commun Biol. 2024. PMID: 39428444 Free PMC article.

2

Severe Left Atrial Spontaneous Echo Contrast in Nonvalvular Atrial Fibrillation: Clinical Characteristics and Impact on Ischemic Risk Postablation.

Wang H, Xi S, Chen J, Zhao L, Gan T, He B. Wang H, et al. Thromb Haemost. 2023 May;123(5):522-534. doi: 10.1055/a-1983-0516. Epub 2022 Nov 19. Thromb Haemost. 2023. PMID: 36402133

3

Impact of sequential (first- to third-generation) EGFR-TKI treatment on corrected QT interval in NSCLC patients.

Gan T, Chen J, Wang H, Shang C, Xi S, Fan Z, He B, Zhang M, Zhao L. Gan T, et al. Among authors: wang h. Front Oncol. 2024 May 7;14:1330165. doi: 10.3389/fonc.2024.1330165. eCollection 2024. Front Oncol. 2024. PMID: 38774407 Free PMC article.

4

Bioinformatic Analysis Identifies Potential Key Genes in the Pathogenesis of Turner Syndrome.

Wang H, Zhu H, Zhu W, Xu Y, Wang N, Han B, Song H, Qiao J. Wang H, et al. Among authors: wang n. Front Endocrinol (Lausanne). 2020 Mar 6;11:104. doi: 10.3389/fendo.2020.00104. eCollection 2020. Front Endocrinol (Lausanne). 2020. PMID: 32210915 Free PMC article.

5

Phenotypic and biochemical characteristics and molecular basis in 36 Chinese patients with androgen receptor variants.

Zhu H, Yao H, Xu Y, Chen Y, Han B, Wang N, Wang H, Zhang Q, Zhu W, Shi Y, Sun H, Zhao S, Song H, Liu Y, Qiao J. Zhu H, et al. Among authors: wang h, wang n. Orphanet J Rare Dis. 2021 Mar 9;16(1):122. doi: 10.1186/s13023-021-01765-w. Orphanet J Rare Dis. 2021. PMID: 33750429 Free PMC article.

6

Estrogen effects on fetal penile and urethral development in organotypic mouse genital tubercle culture.

Ma LM, Wang Z, Wang H, Li RS, Zhou J, Liu BC, Baskin LS. Ma LM, et al. Among authors: wang h, wang z. J Urol. 2009 Nov;182(5):2511-7. doi: 10.1016/j.juro.2009.07.008. Epub 2009 Sep 17. J Urol. 2009. PMID: 19765770

7

Identification of three novel SRD5A2 mutations in Chinese patients with 5α-reductase 2 deficiency.

Cheng T, Wang H, Han B, Zhu H, Yao HJ, Zhao SX, Zhu WJ, Zhai HL, Chen FG, Song HD, Cheng KX, Liu Y, Qiao J. Cheng T, et al. Among authors: wang h. Asian J Androl. 2019 Nov-Dec;21(6):577-581. doi: 10.4103/aja.aja_113_18. Asian J Androl. 2019. PMID: 31031332 Free PMC article.

8

Inherited Missense Mutation Occurring in Arginine76 of the SRY Gene Does Not Account for Familial 46, XY Sex Reversal.

Wang N, Zhu W, Han B, Wang H, Zhu H, Chen Y, Chen Y, Liu J, Liu Y, Zhao S, Song H, Qiao J. Wang N, et al. Among authors: wang h. J Clin Endocrinol Metab. 2020 May 1;105(5):dgaa109. doi: 10.1210/clinem/dgaa109. J Clin Endocrinol Metab. 2020. PMID: 32140723

9

Next-generation sequencing reveals genetic landscape in 46, XY disorders of sexual development patients with variable phenotypes.

Wang H, Zhang L, Wang N, Zhu H, Han B, Sun F, Yao H, Zhang Q, Zhu W, Cheng T, Cheng K, Liu Y, Zhao S, Song H, Qiao J. Wang H, et al. Among authors: wang n. Hum Genet. 2018 Mar;137(3):265-277. doi: 10.1007/s00439-018-1879-y. Epub 2018 Mar 26. Hum Genet. 2018. PMID: 29582157

10

Somatic mosaicism of androgen receptor gene in an androgen insensitivity syndrome patient conceived through assisted reproduction technique.

Wang H, Zhu H, Wang N, Cheng T, Han B, Zhao S, Song H, Cheng K, Liu Y, Qiao J. Wang H, et al. Among authors: wang n. Mol Genet Genomic Med. 2019 Oct;7(10):e00906. doi: 10.1002/mgg3.906. Epub 2019 Aug 20. Mol Genet Genomic Med. 2019. PMID: 31429517 Free PMC article.

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