PubMed (RefSeq) for id: 2462620078

Year	Number of Results
1993	5
1994	1
1998	1
1999	1
2000	2
2002	2
2003	1
2004	4
2005	5
2006	8
2007	8
2008	9
2009	6
2010	16
2011	5
2012	11
2013	10
2014	10
2015	10
2016	13
2017	12
2018	19
2019	13
2020	13
2021	14
2022	20
2023	5
2024	4

1

CHD7 and SOX2 act in a common gene regulatory network during mammalian semicircular canal and cochlear development.

Gao J, Skidmore JM, Cimerman J, Ritter KE, Qiu J, Wilson LMQ, Raphael Y, Kwan KY, Martin DM. Gao J, et al. Proc Natl Acad Sci U S A. 2024 Mar 5;121(10):e2311720121. doi: 10.1073/pnas.2311720121. Epub 2024 Feb 26. Proc Natl Acad Sci U S A. 2024. PMID: 38408234

2

Interaction network of human early embryonic transcription factors.

Gawriyski L, Tan Z, Liu X, Chowdhury I, Malaymar Pinar D, Zhang Q, Weltner J, Jouhilahti EM, Wei GH, Kere J, Varjosalo M. Gawriyski L, et al. EMBO Rep. 2024 Mar;25(3):1589-1622. doi: 10.1038/s44319-024-00074-0. Epub 2024 Jan 31. EMBO Rep. 2024. PMID: 38297188 Free PMC article.

3

Maternal CHD7 gonosomal mosaicism in a fetus with CHARGE syndrome.

Bai T, Shen Y, Yang Y, Dai S, Liu H. Bai T, et al. Am J Med Genet A. 2024 Apr;194(4):e63491. doi: 10.1002/ajmg.a.63491. Epub 2023 Dec 6. Am J Med Genet A. 2024. PMID: 38057991

4

A novel CHD7 variant in a chinese family with CHARGE syndrome.

Shan Y, Yao L, Li L, Gao X, Jiang J. Shan Y, et al. Genes Genomics. 2024 Mar;46(3):379-387. doi: 10.1007/s13258-023-01411-8. Epub 2023 Jun 5. Genes Genomics. 2024. PMID: 37273125

5

Expanding the reproductive organ phenotype of CHD7-spectrum disorder.

Nomakuchi TT, Danowitz M, Stewart B, Leonard J, Izumi K, Krantz I, Kolon TF, Langdon D, Skraban C, Van Batavia J, Zackai E, Jiao K, Linn R, Alexander C, Zaontz M, Vogiatzi MG, Pyle LC. Nomakuchi TT, et al. Am J Med Genet A. 2023 May;191(5):1418-1424. doi: 10.1002/ajmg.a.63148. Epub 2023 Feb 16. Am J Med Genet A. 2023. PMID: 36794641 Free PMC article.

6

The spectrum of cochlear malformations in CHARGE syndrome and insights into the role of the CHD7 gene during embryogenesis of the inner ear.

Lewis MA, Juliano A, Robson C, Clement E, Nash R, Rajput K, D'Arco F. Lewis MA, et al. Neuroradiology. 2023 Apr;65(4):819-834. doi: 10.1007/s00234-023-03118-9. Epub 2023 Jan 30. Neuroradiology. 2023. PMID: 36715725 Review.

7

Chromatin remodeler CHD7 targets active enhancer region to regulate cell type-specific gene expression in human neural crest cells.

Sanosaka T, Okuno H, Mizota N, Andoh-Noda T, Sato M, Tomooka R, Banno S, Kohyama J, Okano H. Sanosaka T, et al. Sci Rep. 2022 Dec 31;12(1):22648. doi: 10.1038/s41598-022-27293-6. Sci Rep. 2022. PMID: 36587182 Free PMC article.

8

CHD7 regulates otic lineage specification and hair cell differentiation in human inner ear organoids.

Nie J, Ueda Y, Solivais AJ, Hashino E. Nie J, et al. Nat Commun. 2022 Nov 17;13(1):7053. doi: 10.1038/s41467-022-34759-8. Nat Commun. 2022. PMID: 36396635 Free PMC article.

9

The Nse5/6-like SIMC1-SLF2 complex localizes SMC5/6 to viral replication centers.

Oravcová M, Nie M, Zilio N, Maeda S, Jami-Alahmadi Y, Lazzerini-Denchi E, Wohlschlegel JA, Ulrich HD, Otomo T, Boddy MN. Oravcová M, et al. Elife. 2022 Nov 14;11:e79676. doi: 10.7554/eLife.79676. Elife. 2022. PMID: 36373674 Free PMC article.

10

HDLBP Promotes Hepatocellular Carcinoma Proliferation and Sorafenib Resistance by Suppressing Trim71-dependent RAF1 Degradation.

Yuan J, Lv T, Yang J, Wu Z, Yan L, Yang J, Shi Y, Jiang L. Yuan J, et al. Cell Mol Gastroenterol Hepatol. 2023;15(2):307-325. doi: 10.1016/j.jcmgh.2022.10.005. Epub 2022 Oct 14. Cell Mol Gastroenterol Hepatol. 2023. PMID: 36244648 Free PMC article.

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