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2011 1
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2013 2
2014 1
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2024 2

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Page 1
Multi-faceted epigenetic dysregulation of gene expression promotes esophageal squamous cell carcinoma.
Cao W, Lee H, Wu W, Zaman A, McCorkle S, Yan M, Chen J, Xing Q, Sinnott-Armstrong N, Xu H, Sailani MR, Tang W, Cui Y, Liu J, Guan H, Lv P, Sun X, Sun L, Han P, Lou Y, Chang J, Wang J, Gao Y, Guo J, Schenk G, Shain AH, Biddle FG, Collisson E, Snyder M, Bivona TG. Cao W, et al. Among authors: xu h. Nat Commun. 2020 Jul 22;11(1):3675. doi: 10.1038/s41467-020-17227-z. Nat Commun. 2020. PMID: 32699215 Free PMC article.
PKHD1L1, A Gene Involved in the Stereocilia Coat, Causes Autosomal Recessive Nonsyndromic Hearing Loss.
Redfield SE, De-la-Torre P, Zamani M, Wang H, Khan H, Morris T, Shariati G, Karimi M, Kenna MA, Seo GH, Xu H, Lu W, Naz S, Galehdari H, Indzhykulian AA, Shearer AE, Vona B. Redfield SE, et al. Among authors: xu h. medRxiv [Preprint]. 2023 Dec 19:2023.10.08.23296081. doi: 10.1101/2023.10.08.23296081. medRxiv. 2023. PMID: 37873491 Free PMC article. Updated. Preprint.
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.
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
64 results