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

Year Number of Results
2016 1
2017 1
2018 4
2019 5
2020 4
2021 8
2022 0
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21 results
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Page 1
MERTK mutation update in inherited retinal diseases.
Audo I, Mohand-Said S, Boulanger-Scemama E, Zanlonghi X, Condroyer C, Démontant V, Boyard F, Antonio A, Méjécase C, El Shamieh S, Sahel JA, Zeitz C. Audo I, et al. Among authors: mejecase c. Hum Mutat. 2018 Jul;39(7):887-913. doi: 10.1002/humu.23431. Epub 2018 May 23. Hum Mutat. 2018. PMID: 29659094 Free article. Review.
Practical guide to genetic screening for inherited eye diseases.
Méjécase C, Malka S, Guan Z, Slater A, Arno G, Moosajee M. Méjécase C, et al. Ther Adv Ophthalmol. 2020 Sep 22;12:2515841420954592. doi: 10.1177/2515841420954592. eCollection 2020 Jan-Dec. Ther Adv Ophthalmol. 2020. PMID: 33015543 Free PMC article. Review.
WDR34, a candidate gene for non-syndromic rod-cone dystrophy.
Solaguren-Beascoa M, Bujakowska KM, Méjécase C, Emmenegger L, Orhan E, Neuillé M, Mohand-Saïd S, Condroyer C, Lancelot ME, Michiels C, Demontant V, Antonio A, Letexier M, Saraiva JP, Lonjou C, Carpentier W, Léveillard T, Pierce EA, Dollfus H, Sahel JA, Bhattacharya SS, Audo I, Zeitz C. Solaguren-Beascoa M, et al. Among authors: mejecase c. Clin Genet. 2021 Feb;99(2):298-302. doi: 10.1111/cge.13872. Epub 2020 Nov 9. Clin Genet. 2021. PMID: 33124039 Free PMC article.
Ocular Phenotype Associated with DYRK1A Variants.
Méjécase C, Way CM, Owen N, Moosajee M. Méjécase C, et al. Genes (Basel). 2021 Feb 5;12(2):234. doi: 10.3390/genes12020234. Genes (Basel). 2021. PMID: 33562844 Free PMC article.
21 results