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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2019 | 1 |
2020 | 2 |
2022 | 2 |
2023 | 2 |
2024 | 0 |
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6 results
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Page 1
Causal factors in primary open angle glaucoma: a phenome-wide Mendelian randomisation study.
Sci Rep. 2023 Jun 20;13(1):9984. doi: 10.1038/s41598-023-37144-7.
Sci Rep. 2023.
PMID: 37340071
Free PMC article.
The Role of Genetic Testing in Children Requiring Surgery for Ectopia Lentis.
Musleh M, Bull A, Linton E, Liu J, Waller S, Hardcastle C, Clayton-Smith J, Sharma V, Black GC, Biswas S, Ashworth JL, Sergouniotis PI.
Musleh M, et al.
Genes (Basel). 2023 Mar 25;14(4):791. doi: 10.3390/genes14040791.
Genes (Basel). 2023.
PMID: 37107549
Free PMC article.
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Generation of a human induced pluripotent stem cell line carrying the TYR c.575C>A (p.Ser192Tyr) and c.1205G>A (p.Arg402Gln) variants in homozygous state using CRISPR-Cas9 genome editing.
Liu J, Black GC, Kimber SJ, Sergouniotis PI.
Liu J, et al.
Stem Cell Res. 2022 Oct;64:102880. doi: 10.1016/j.scr.2022.102880. Epub 2022 Jul 30.
Stem Cell Res. 2022.
PMID: 35933957
Free article.
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The contribution of common regulatory and protein-coding TYR variants to the genetic architecture of albinism.
Michaud V, Lasseaux E, Green DJ, Gerrard DT, Plaisant C; UK Biobank Eye and Vision Consortium; Fitzgerald T, Birney E, Arveiler B, Black GC, Sergouniotis PI.
Michaud V, et al.
Nat Commun. 2022 Jul 8;13(1):3939. doi: 10.1038/s41467-022-31392-3.
Nat Commun. 2022.
PMID: 35803923
Free PMC article.
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Variability in Gene Expression is Associated with Incomplete Penetrance in Inherited Eye Disorders.
Green DJ, Sallah SR, Ellingford JM, Lovell SC, Sergouniotis PI.
Green DJ, et al.
Genes (Basel). 2020 Feb 9;11(2):179. doi: 10.3390/genes11020179.
Genes (Basel). 2020.
PMID: 32050448
Free PMC article.
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Clinical utility of genetic testing in 201 preschool children with inherited eye disorders.
Lenassi E, Clayton-Smith J, Douzgou S, Ramsden SC, Ingram S, Hall G, Hardcastle CL, Fletcher TA, Taylor RL, Ellingford JM, Newman WD, Fenerty C, Sharma V, Lloyd IC, Biswas S, Ashworth JL, Black GC, Sergouniotis PI.
Lenassi E, et al.
Genet Med. 2020 Apr;22(4):745-751. doi: 10.1038/s41436-019-0722-8. Epub 2019 Dec 18.
Genet Med. 2020.
PMID: 31848469
Free PMC article.
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