Xu H - Search Results

1

Molecular Mechanisms and Clinical Phenotypes of GJB2 Missense Variants.

Mao L, Wang Y, An L, Zeng B, Wang Y, Frishman D, Liu M, Chen Y, Tang W, Xu H. Mao L, et al. Among authors: xu h. Biology (Basel). 2023 Mar 27;12(4):505. doi: 10.3390/biology12040505. Biology (Basel). 2023. PMID: 37106706 Free PMC article. Review.

2

Genomic determinants of somatic copy number alterations across human cancers.

Zhang Y, Xu H, Frishman D. Zhang Y, et al. Among authors: xu h. Hum Mol Genet. 2016 Mar 1;25(5):1019-30. doi: 10.1093/hmg/ddv623. Epub 2016 Jan 4. Hum Mol Genet. 2016. PMID: 26732428

3

Maternal placenta modulates a deleterious fetal mutation.

Xu H, Pausch H, Venhoranta H, Rutkowska K, Wurmser C, Rieblinger B, Flisikowska T, Frishman D, Zwierzchowski L, Fries R, Andersson M, Kind A, Schnieke A, Flisikowski K. Xu H, et al. Biol Reprod. 2017 Aug 1;97(2):249-257. doi: 10.1093/biolre/iox064. Biol Reprod. 2017. PMID: 28679164

4

Porcine familial adenomatous polyposis model enables systematic analysis of early events in adenoma progression.

Flisikowska T, Stachowiak M, Xu H, Wagner A, Hernandez-Caceres A, Wurmser C, Perleberg C, Pausch H, Perkowska A, Fischer K, Frishman D, Fries R, Switonski M, Kind A, Saur D, Schnieke A, Flisikowski K. Flisikowska T, et al. Among authors: xu h. Sci Rep. 2017 Jul 26;7(1):6613. doi: 10.1038/s41598-017-06741-8. Sci Rep. 2017. PMID: 28747659 Free PMC article.

5

Mechanisms of hearing loss and cell death in the cochlea of connexin mutant mice.

Chen B, Xu H, Mi Y, Jiang W, Guo D, Zhang J, Zhao Y, Tang W. Chen B, et al. Among authors: xu h. Am J Physiol Cell Physiol. 2020 Sep 1;319(3):C569-C578. doi: 10.1152/ajpcell.00483.2019. Epub 2020 Aug 5. Am J Physiol Cell Physiol. 2020. PMID: 32755449 Free article.

6

Perrault syndrome: Clinical report and retrospective analysis.

Pan Z, Xu H, Tian Y, Liu D, Liu H, Li R, Dou Q, Zuo B, Zhai R, Tang W, Lu W. Pan Z, et al. Among authors: xu h. Mol Genet Genomic Med. 2020 Oct;8(10):e1445. doi: 10.1002/mgg3.1445. Epub 2020 Aug 7. Mol Genet Genomic Med. 2020. PMID: 32767731 Free PMC article.

7

Early truncation of the N-terminal variable region of EYA4 gene causes dominant hearing loss without cardiac phenotype.

Mi Y, Liu D, Zeng B, Tian Y, Zhang H, Chen B, Zhang J, Xue H, Tang W, Zhao Y, Xu H. Mi Y, et al. Among authors: xu h. Mol Genet Genomic Med. 2021 Jan;9(1):e1569. doi: 10.1002/mgg3.1569. Epub 2020 Dec 10. Mol Genet Genomic Med. 2021. PMID: 33301229 Free PMC article.

8

Treacher Collins syndrome: Clinical report and retrospective analysis of Chinese patients.

Pan Z, Xu H, Chen B, Tian Y, Zhang L, Zhang S, Liu D, Liu H, Li R, Hu X, Guan J, Tang W, Lu W. Pan Z, et al. Among authors: xu h. Mol Genet Genomic Med. 2021 Feb;9(2):e1573. doi: 10.1002/mgg3.1573. Epub 2020 Dec 17. Mol Genet Genomic Med. 2021. PMID: 33332773 Free PMC article.

9

Auditory Neuropathy Spectrum Disorder (ANSD)-Clinical Characteristics and Pathogenic Variant Analysis of Three Nonsyndromic Deafness Families.

Zhai R, Feng H, Li Q, Lu W, Liu D, Tian Y, Liu H, Li R, Zuo B, Tang W, Xu H, Chen B. Zhai R, et al. Among authors: xu h. Biomed Res Int. 2020 Dec 21;2020:8843539. doi: 10.1155/2020/8843539. eCollection 2020. Biomed Res Int. 2020. PMID: 33426078 Free PMC article.

10

High Genetic Heterogeneity in Chinese Patients With Waardenburg Syndrome Revealed by Next-Generation Sequencing.

Zhang S, Xu H, Tian Y, Liu D, Hou X, Zeng B, Chen B, Liu H, Li R, Li X, Zuo B, Tang R, Tang W. Zhang S, et al. Among authors: xu h. Front Genet. 2021 Jun 4;12:643546. doi: 10.3389/fgene.2021.643546. eCollection 2021. Front Genet. 2021. PMID: 34149797 Free PMC article.

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