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Human Molecular Genetics 183
Showing records 1 to 25 | Display only abstracts in Human Molecular Genetics from IGR 24-4123061 Genetic correlation between circulating cytokines and risk of three ophthalmic diseases: a bidirectional two-sample Mendelian randomization study
Zhang X
Human Molecular Genetics 2024; 33: 1241-1249 (IGR: 25-1)
122960 Lack of evidence for GWAS signals of exfoliation glaucoma working via monogenic loss-of-function mutation in the nearest gene
Meyer KJ; Fingert JH
Human Molecular Genetics 2024; 0: (IGR: 25-1)
123061 Genetic correlation between circulating cytokines and risk of three ophthalmic diseases: a bidirectional two-sample Mendelian randomization study
Fu Q
Human Molecular Genetics 2024; 33: 1241-1249 (IGR: 25-1)
122960 Lack of evidence for GWAS signals of exfoliation glaucoma working via monogenic loss-of-function mutation in the nearest gene
Anderson MG
Human Molecular Genetics 2024; 0: (IGR: 25-1)
123061 Genetic correlation between circulating cytokines and risk of three ophthalmic diseases: a bidirectional two-sample Mendelian randomization study
Cai Y; Li X; Chen L; Jiang Y; Chen Y
Human Molecular Genetics 2024; 33: 1241-1249 (IGR: 25-1)
117042 High throughput functional profiling of genes at intraocular pressure loci reveals distinct networks for glaucoma
Greatbatch CJ; Lu Q; Hung S; Hung S; Barnett AJ; Wing K; Wing K; Liang H; Han X; Zhou T; Siggs OM; Mackey DA; Cook AL; Senabouth A; Liu GS; Craig JE; Macgregor S; Powell JE; Hewitt AW
Human Molecular Genetics 2024; 33: 739-751 (IGR: 24-4)
112540 Lysyl oxidase-like 1-antisense 1 (LOXL1-AS1) lncRNA differentially regulates gene and protein expression, signaling and morphology of human ocular cells
Schmitt HM; Hake KM; Hake KM; Perkumas KM; Lê BM; Suarez MF; Suarez MF; De
Ieso ML; De
Ieso ML; Rahman RS; Johnson WM; Gomez-Caraballo M; Ashley-Koch AE; Hauser MA; Stamer WD
Human Molecular Genetics 2023; 32: 3053-3062 (IGR: 24-3)
109396 Rare protective variants and glaucoma-relevant cell stressors modulate Angiopoietin-like 7 expression
Aboobakar IF; Collantes ERA; Hauser MA; Stamer WD; Wiggs JL
Human Molecular Genetics 2023; 32: 2523-2531 (IGR: 24-1/2)
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Guggenheim JA
Human Molecular Genetics 2022; 31: 1909-1919 (IGR: 22-4)
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Cui X; Kim HJ
Human Molecular Genetics 2022; 31: 2438-2451 (IGR: 22-4)
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Clark R; Cui J
Human Molecular Genetics 2022; 31: 1909-1919 (IGR: 22-4)
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Cheng CH; Jenny LA
Human Molecular Genetics 2022; 31: 2438-2451 (IGR: 22-4)
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Terry L; Patasova K
Human Molecular Genetics 2022; 31: 1909-1919 (IGR: 22-4)
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
De Carvalho Junior JRL; Chang YJ
Human Molecular Genetics 2022; 31: 2438-2451 (IGR: 22-4)
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Haarman AEG
Human Molecular Genetics 2022; 31: 1909-1919 (IGR: 22-4)
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Kong Y
Human Molecular Genetics 2022; 31: 2438-2451 (IGR: 22-4)
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Musolf AM; Verhoeven VJM
Human Molecular Genetics 2022; 31: 1909-1919 (IGR: 22-4)
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Hsu CW; Huang IW; Huang IW
Human Molecular Genetics 2022; 31: 2438-2451 (IGR: 22-4)
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Klaver CCW; Bailey-Wilson JE
Human Molecular Genetics 2022; 31: 1909-1919 (IGR: 22-4)
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Ragi SD; Lin CS
Human Molecular Genetics 2022; 31: 2438-2451 (IGR: 22-4)
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Hysi PG
Human Molecular Genetics 2022; 31: 1909-1919 (IGR: 22-4)
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Li X
Human Molecular Genetics 2022; 31: 2438-2451 (IGR: 22-4)
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Williams C
Human Molecular Genetics 2022; 31: 1909-1919 (IGR: 22-4)
98900 Long-term vitamin a supplementation in a preclinical mouse model for RhoD190N-associated retinitis pigmentosa
Sparrow JR
Human Molecular Genetics 2022; 31: 2438-2451 (IGR: 22-4)
98509 Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia
Human Molecular Genetics 2022; 31: 1909-1919 (IGR: 22-4)
