PubMed (OMIM) for id: 220202

Year	Number of Results
1938	1
1954	1
1965	1
1973	2
1976	1
1978	1
1979	1
1987	1
1995	1
1998	3
2000	2
2001	2
2002	1
2011	3
2012	2
2024	0

1

ATOH7 mutations cause autosomal recessive persistent hyperplasia of the primary vitreous.

Prasov L, Masud T, Khaliq S, Mehdi SQ, Abid A, Oliver ER, Silva ED, Lewanda A, Brodsky MC, Borchert M, Kelberman D, Sowden JC, Dattani MT, Glaser T. Prasov L, et al. Hum Mol Genet. 2012 Aug 15;21(16):3681-94. doi: 10.1093/hmg/dds197. Epub 2012 May 29. Hum Mol Genet. 2012. PMID: 22645276 Free PMC article.

2

Next generation sequencing identifies mutations in Atonal homolog 7 (ATOH7) in families with global eye developmental defects.

Khan K, Logan CV, McKibbin M, Sheridan E, Elçioglu NH, Yenice O, Parry DA, Fernandez-Fuentes N, Abdelhamed ZI, Al-Maskari A, Poulter JA, Mohamed MD, Carr IM, Morgan JE, Jafri H, Raashid Y, Taylor GR, Johnson CA, Inglehearn CF, Toomes C, Ali M. Khan K, et al. Hum Mol Genet. 2012 Feb 15;21(4):776-83. doi: 10.1093/hmg/ddr509. Epub 2011 Nov 7. Hum Mol Genet. 2012. PMID: 22068589 Free PMC article.

3

Genetic heterogeneity for recessively inherited congenital cataract microcornea with corneal opacity.

Khan K, Al-Maskari A, McKibbin M, Carr IM, Booth A, Mohamed M, Siddiqui S, Poulter JA, Parry DA, Logan CV, Hashmi A, Sahi T, Jafri H, Raashid Y, Johnson CA, Markham AF, Toomes C, Rice A, Sheridan E, Inglehearn CF, Ali M. Khan K, et al. Invest Ophthalmol Vis Sci. 2011 Jun 16;52(7):4294-9. doi: 10.1167/iovs.10-6776. Invest Ophthalmol Vis Sci. 2011. PMID: 21474777 Free PMC article.

4

Deletion of a remote enhancer near ATOH7 disrupts retinal neurogenesis, causing NCRNA disease.

Ghiasvand NM, Rudolph DD, Mashayekhi M, Brzezinski JA 4th, Goldman D, Glaser T. Ghiasvand NM, et al. Nat Neurosci. 2011 May;14(5):578-86. doi: 10.1038/nn.2798. Epub 2011 Mar 27. Nat Neurosci. 2011. PMID: 21441919 Free PMC article.

5

ABLATIO FALCIFORMIS CONGENITA (RETINAL FOLD).

Weve H. Weve H. Br J Ophthalmol. 1938 Aug;22(8):456-70. doi: 10.1136/bjo.22.8.456. Br J Ophthalmol. 1938. PMID: 18169555 Free PMC article. No abstract available.

6

[Familial inflammatory pseudoglioma with consanguineous parents].

[No authors listed] [No authors listed] J Genet Hum. 1954 Mar;3(1):82-5. J Genet Hum. 1954. PMID: 13184107 Undetermined Language. No abstract available.

7

Molecular characterization and mapping of ATOH7, a human atonal homolog with a predicted role in retinal ganglion cell development.

Brown NL, Dagenais SL, Chen CM, Glaser T. Brown NL, et al. Mamm Genome. 2002 Feb;13(2):95-101. doi: 10.1007/s00335-001-2101-3. Mamm Genome. 2002. PMID: 11889557 Free PMC article.

8

Locus for autosomal recessive nonsyndromic persistent hyperplastic primary vitreous.

Khaliq S, Hameed A, Ismail M, Anwar K, Leroy B, Payne AM, Bhattacharya SS, Mehdi SQ. Khaliq S, et al. Invest Ophthalmol Vis Sci. 2001 Sep;42(10):2225-8. Invest Ophthalmol Vis Sci. 2001. PMID: 11527934

9

Math5 is required for retinal ganglion cell and optic nerve formation.

Brown NL, Patel S, Brzezinski J, Glaser T. Brown NL, et al. Development. 2001 Jul;128(13):2497-508. doi: 10.1242/dev.128.13.2497. Development. 2001. PMID: 11493566 Free PMC article.

10

Genetic fine mapping of the gene for nonsyndromic congenital retinal nonattachment.

Ghiasvand NM, Fleming TP, Helms C, Avisa A, Donis-Keller H. Ghiasvand NM, et al. Am J Med Genet. 2000 May 29;92(3):220-3. Am J Med Genet. 2000. PMID: 10817658

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