PubMed for id: 220202

Year	Number of Results
2000	1
2002	4
2005	1
2006	1
2009	1
2010	2
2011	7
2012	3
2013	2
2014	4
2015	2
2016	2
2017	3
2018	2
2020	2
2022	2
2023	1
2024	0

1

OCULAR FEATURES ASSOCIATED WITH MUTATIONS IN ATOH7 GENE OVERLAP THOSE WITH FAMILIAL EXUDATIVE VITREORETINOPATHY.

Naruse S, Kondo H. Naruse S, et al. Retin Cases Brief Rep. 2023 Nov 1;17(6):694-698. doi: 10.1097/ICB.0000000000001267. Retin Cases Brief Rep. 2023. PMID: 35389970

2

Functional Characterization of an In-Frame Deletion in the Basic Domain of the Retinal Transcription Factor ATOH7.

Atac D, Mohn L, Feil S, Maggi K, Haenni D, Seebauer B, Koller S, Berger W. Atac D, et al. Int J Mol Sci. 2022 Jan 19;23(3):1053. doi: 10.3390/ijms23031053. Int J Mol Sci. 2022. PMID: 35162975 Free PMC article.

3

The polymorphisms of ATOH 7, ET-1 and ACE in non-arteritic anterior ischemic optic neuropathy.

Chen T, Ma J, Shan G, Zhong Y. Chen T, et al. Exp Eye Res. 2018 Sep;174:147-151. doi: 10.1016/j.exer.2018.05.021. Epub 2018 May 21. Exp Eye Res. 2018. PMID: 29792847

4

Elevated expression of human bHLH factor ATOH7 accelerates cell cycle progression of progenitors and enhances production of avian retinal ganglion cells.

Zhang XM, Hashimoto T, Tang R, Yang XJ. Zhang XM, et al. Sci Rep. 2018 May 1;8(1):6823. doi: 10.1038/s41598-018-25188-z. Sci Rep. 2018. PMID: 29717171 Free PMC article.

5

The Genetic Causes of Nonsyndromic Congenital Retinal Detachment: A Genetic and Phenotypic Study of Pakistani Families.

Keser V, Khan A, Siddiqui S, Lopez I, Ren H, Qamar R, Nadaf J, Majewski J, Chen R, Koenekoop RK. Keser V, et al. Invest Ophthalmol Vis Sci. 2017 Feb 1;58(2):1028-1036. doi: 10.1167/iovs.16-20281. Invest Ophthalmol Vis Sci. 2017. PMID: 28192794 Free PMC article.

6

A Genome-Wide Association Study of Vertical Cup-Disc Ratio in a Latino Population.

Nannini DR, Torres M, Chen YI, Taylor KD, Rotter JI, Varma R, Gao X. Nannini DR, et al. Invest Ophthalmol Vis Sci. 2017 Jan 1;58(1):87-95. doi: 10.1167/iovs.16-19891. Invest Ophthalmol Vis Sci. 2017. PMID: 28061514 Free PMC article.

7

Analysis of Polymorphism rs1900004 in Atonal bHLH Transcription Factor 7 in Saudi Patients with Primary Open Angle Glaucoma.

Kondkar AA, Mousa A, Azad TA, Sultan T, Almobarak FA, Alawad A, Altuwaijri S, Al-Obeidan SA, Abu-Amero KK. Kondkar AA, et al. Genet Test Mol Biomarkers. 2016 Nov;20(11):715-718. doi: 10.1089/gtmb.2016.0209. Epub 2016 Sep 12. Genet Test Mol Biomarkers. 2016. PMID: 27617586

8

Mutations in ATOH7 gene in patients with nonsyndromic congenital retinal nonattachment and familial exudative vitreoretinopathy.

Kondo H, Matsushita I, Tahira T, Uchio E, Kusaka S. Kondo H, et al. Ophthalmic Genet. 2016 Dec;37(4):462-464. doi: 10.3109/13816810.2015.1120316. Epub 2016 Mar 2. Ophthalmic Genet. 2016. PMID: 26933893 No abstract available.

9

Clarifying the role of ATOH7 in glaucoma endophenotypes.

Venturini C, Nag A, Hysi PG, Wang JJ, Wong TY, Healey PR, Mitchell P, Hammond CJ, Viswanathan AC; Wellcome Trust Case Control Consortium 2, BMES GWAS Group. Venturini C, et al. Br J Ophthalmol. 2014 Apr;98(4):562-6. doi: 10.1136/bjophthalmol-2013-304080. Epub 2014 Jan 23. Br J Ophthalmol. 2014. PMID: 24457358

10

Sequencing analysis of the ATOH7 gene in individuals with optic nerve hypoplasia.

Lim SH, St Germain E, Tran-Viet KN, Staffieri S, Marino M, Dollfus PH, Nading EB, Crowe S, Gole G, Perdomo-Trujillo Y, Haybittel M, Elder J, Pelletier V, Traboulsi E, Mackey D, Young TL. Lim SH, et al. Ophthalmic Genet. 2014 Mar;35(1):1-6. doi: 10.3109/13816810.2012.752017. Epub 2013 Jun 26. Ophthalmic Genet. 2014. PMID: 23802135 Free PMC article.

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