Xu H - Search Results

1

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

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

Genome-wide analysis of somatic copy number alterations and chromosomal breakages in osteosarcoma.

Smida J, Xu H, Zhang Y, Baumhoer D, Ribi S, Kovac M, von Luettichau I, Bielack S, O'Leary VB, Leib-Mösch C, Frishman D, Nathrath M. Smida J, et al. Among authors: xu h. Int J Cancer. 2017 Aug 15;141(4):816-828. doi: 10.1002/ijc.30778. Epub 2017 May 25. Int J Cancer. 2017. PMID: 28494505

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

Differentially methylated region in bovine MIMT1 detected by small-scale whole-genome methylation sequencing.

Rutkowska K, Xu H, Flisikowski K. Rutkowska K, et al. Among authors: xu h. J Appl Genet. 2019 Nov;60(3-4):401-404. doi: 10.1007/s13353-019-00519-6. Epub 2019 Aug 30. J Appl Genet. 2019. PMID: 31468362

6

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.

7

An accessible insight into genetic findings for transplantation recipients with suspected genetic kidney disease.

Wang Z, Xu H, Xiang T, Liu D, Xu F, Zhao L, Feng Y, Xu L, Liu J, Fang Y, Liu H, Li R, Hu X, Guan J, Liu L, Feng G, Shen Q, Xu H, Frishman D, Tang W, Guo J, Rao J, Shang W. Wang Z, et al. Among authors: xu l, xu f, xu h. NPJ Genom Med. 2021 Jul 2;6(1):57. doi: 10.1038/s41525-021-00219-3. NPJ Genom Med. 2021. PMID: 34215756 Free PMC article.

8

Identification and Validation of Ikaros (IKZF1) as a Cancer Driver Gene for Marek's Disease Virus-Induced Lymphomas.

Steep A, Hildebrandt E, Xu H, Hearn C, Frishman D, Niikura M, Dunn JR, Kim T, Conrad SJ, Muir WM, Cheng HH. Steep A, et al. Among authors: xu h. Microorganisms. 2022 Feb 9;10(2):401. doi: 10.3390/microorganisms10020401. Microorganisms. 2022. PMID: 35208856 Free PMC article.

9

Missense Variant of Endoplasmic Reticulum Region of WFS1 Gene Causes Autosomal Dominant Hearing Loss without Syndromic Phenotype.

Li J, Xu H, Sun J, Tian Y, Liu D, Qin Y, Liu H, Li R, Neng L, Deng X, Xue B, Yu C, Tang W. Li J, et al. Among authors: xu h. Biomed Res Int. 2021 Mar 4;2021:6624744. doi: 10.1155/2021/6624744. eCollection 2021. Biomed Res Int. 2021. PMID: 34258273 Free PMC article.

10

Identification of key genes in osteosarcoma by meta‑analysis of gene expression microarray.

Sun J, Xu H, Qi M, Zhang C, Shi J. Sun J, et al. Among authors: xu h. Mol Med Rep. 2019 Oct;20(4):3075-3084. doi: 10.3892/mmr.2019.10543. Epub 2019 Jul 31. Mol Med Rep. 2019. PMID: 31432118 Free PMC article.

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