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Dominant Cone Rod Dystrophy, Previously Assigned to a Missense Variant in RIMS1, Is Fully Explained by Co-Inheritance of a Dominant Allele of PROM1.
Martin-Gutierrez MP, Schiff ER, Wright G, Waseem N, Mahroo OA, Michaelides M, Moore AT, Webster AR, Arno G; Genomics England Research Consortium. Martin-Gutierrez MP, et al. Among authors: waseem n. Invest Ophthalmol Vis Sci. 2022 Aug 2;63(9):14. doi: 10.1167/iovs.63.9.14. Invest Ophthalmol Vis Sci. 2022. PMID: 35947379 Free PMC article.
Genome-Wide Association Study Identifies Two Common Loci Associated with Pigment Dispersion Syndrome/Pigmentary Glaucoma and Implicates Myopia in its Development.
Simcoe MJ, Shah A, Fan B, Choquet H, Weisschuh N, Waseem NH, Jiang C, Melles RB, Ritch R, Mahroo OA, Wissinger B, Jorgenson E, Wiggs JL, Garway-Heath DF, Hysi PG, Hammond CJ. Simcoe MJ, et al. Among authors: waseem nh. Ophthalmology. 2022 Jun;129(6):626-636. doi: 10.1016/j.ophtha.2022.01.005. Epub 2022 Jan 11. Ophthalmology. 2022. PMID: 35031440 Free article.
Multicoagulant resistant pseudothrombocytopenia.
Waseem N, Hanif B, Jabbar J. Waseem N, et al. J Pak Med Assoc. 2021 Sep;71(9):2247-2249. doi: 10.47391/JPMA.03-390. J Pak Med Assoc. 2021. PMID: 34580523 Free article.
Mutations in SPATA13/ASEF2 cause primary angle closure glaucoma.
Waseem NH, Low S, Shah AZ, Avisetti D, Ostergaard P, Simpson M, Niemiec KA, Martin-Martin B, Aldehlawi H, Usman S, Lee PS, Khawaja AP, Ruddle JB, Shah A, Sackey E, Day A, Jiang Y, Swinfield G, Viswanathan A, Alfano G, Chakarova C, Cordell HJ, Garway-Heath DF, Khaw PT, Bhattacharya SS, Waseem A, Foster PJ. Waseem NH, et al. PLoS Genet. 2020 Apr 27;16(4):e1008721. doi: 10.1371/journal.pgen.1008721. eCollection 2020 Apr. PLoS Genet. 2020. PMID: 32339198 Free PMC article.
86 results