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211 results

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Page 1
Using machine learning to identify pediatric ophthalmologists.
Oke I, Elze T, Miller JW, Lorch AC, Ong MS, Wu AC, Hunter DG; IRIS® Registry Analytic Center Consortium. Oke I, et al. Among authors: hunter dg. J AAPOS. 2024 Nov 19:104052. doi: 10.1016/j.jaapos.2024.104052. Online ahead of print. J AAPOS. 2024. PMID: 39566680
Gene identification for ocular congenital cranial motor neuron disorders using human sequencing, zebrafish screening, and protein binding microarrays.
Jurgens JA, Matos Ruiz PM, King J, Foster EE, Berube L, Chan WM, Barry BJ, Jeong R, Rothman E, Whitman MC, MacKinnon S, Rivera-Quiles C, Pratt BM, Easterbrooks T, Mensching FM, Di Gioia SA, Pais L, England EM, de Berardinis T, Magli A, Koc F, Asakawa K, Kawakami K, O'Donnell-Luria A, Hunter DG, Robson CD, Bulyk ML, Engle EC. Jurgens JA, et al. Among authors: hunter dg. bioRxiv [Preprint]. 2024 Sep 15:2024.09.12.612713. doi: 10.1101/2024.09.12.612713. bioRxiv. 2024. PMID: 39314366 Free PMC article. Preprint.
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.
Jurgens JA, Barry BJ, Chan WM, MacKinnon S, Whitman MC, Matos Ruiz PM, Pratt BM, England EM, Pais L, Lemire G, Groopman E, Glaze C, Russell KA, Singer-Berk M, Di Gioia SA, Lee AS, Andrews C, Shaaban S, Wirth MM, Bekele S, Toffoloni M, Bradford VR, Foster EE, Berube L, Rivera-Quiles C, Mensching FM, Sanchis-Juan A, Fu JM, Wong I, Zhao X, Wilson MW, Weisburd B, Lek M; Ocular CCDD Phenotyping Consortium; Brand H, Talkowski ME, MacArthur DG, O'Donnell-Luria A, Robson CD, Hunter DG, Engle EC. Jurgens JA, et al. Among authors: hunter dg. Genet Med. 2024 Jul 17:101216. doi: 10.1016/j.gim.2024.101216. Online ahead of print. Genet Med. 2024. PMID: 39033378 Free article.
Impact of Pediatric Instrument-Based Vision Screening.
Oke I, Hunter DG, Galbraith AA. Oke I, et al. Among authors: hunter dg. JAMA Ophthalmol. 2024 Sep 1;142(9):882. doi: 10.1001/jamaophthalmol.2024.2256. JAMA Ophthalmol. 2024. PMID: 38958990 No abstract available.
Refractive errors in patients with Bardet Biedl syndrome.
Yavuz Saricay L, Baldwin G, Moulton EA, Gonzalez E, Rajabi F, Hunter DG, Fulton AB. Yavuz Saricay L, et al. Among authors: hunter dg. Ophthalmic Genet. 2024 Oct;45(5):435-440. doi: 10.1080/13816810.2024.2357296. Epub 2024 Jul 2. Ophthalmic Genet. 2024. PMID: 38953718
Vision Screening in Children-Reply.
Oke I, Hunter DG, Galbraith AA. Oke I, et al. Among authors: hunter dg. JAMA Ophthalmol. 2024 Jul 1;142(7):687. doi: 10.1001/jamaophthalmol.2024.1867. JAMA Ophthalmol. 2024. PMID: 38842881 No abstract available.
211 results