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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1998 2
2001 1
2004 2
2005 1
2008 2
2009 1
2010 5
2011 2
2012 1
2013 7
2014 12
2015 7
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2017 9
2018 14
2019 15
2020 10
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2022 5
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2024 1

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Similar articles for PMID: 32817297

101 results

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Page 1
Pathogenic variants in IMPG1 cause autosomal dominant and autosomal recessive retinitis pigmentosa.
Olivier G, Corton M, Intartaglia D, Verbakel SK, Sergouniotis PI, Le Meur G, Dhaenens CM, Naacke H, Avila-Fernández A, Hoyng CB, Klevering J, Bocquet B, Roubertie A, Sénéchal A, Banfi S, Muller A, Hamel CL, Black GC, Conte I, Roosing S, Zanlonghi X, Ayuso C, Meunier I, Manes G. Olivier G, et al. J Med Genet. 2021 Aug;58(8):570-578. doi: 10.1136/jmedgenet-2020-107150. Epub 2020 Aug 17. J Med Genet. 2021. PMID: 32817297
Mutations in IMPG1 cause vitelliform macular dystrophies.
Manes G, Meunier I, Avila-Fernández A, Banfi S, Le Meur G, Zanlonghi X, Corton M, Simonelli F, Brabet P, Labesse G, Audo I, Mohand-Said S, Zeitz C, Sahel JA, Weber M, Dollfus H, Dhaenens CM, Allorge D, De Baere E, Koenekoop RK, Kohl S, Cremers FP, Hollyfield JG, Sénéchal A, Hebrard M, Bocquet B, Ayuso García C, Hamel CP. Manes G, et al. Am J Hum Genet. 2013 Sep 5;93(3):571-8. doi: 10.1016/j.ajhg.2013.07.018. Epub 2013 Aug 29. Am J Hum Genet. 2013. PMID: 23993198 Free PMC article.
SPACR Encoded by IMPG1 Is Essential for Photoreceptor Survival by Interplaying between the Interphotoreceptor Matrix and the Retinal Pigment Epithelium.
Olivier G, Brabet P, Pirot N, Broyon M, Guillou L, Cazevieille C, Sar C, Quiles M, Sarzi E, Pequignot M, Andreo E, Roubertie A, Meunier I, Muller A, Kalatzis V, Manes G. Olivier G, et al. Genes (Basel). 2022 Aug 23;13(9):1508. doi: 10.3390/genes13091508. Genes (Basel). 2022. PMID: 36140676 Free PMC article.
101 results