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Page 1
Impact of Race on the Outcomes of Retinoblastoma Treated With Primary Enucleation: A Global Study of 1426 Patients.
Kaliki S, Vempuluru VS, Ahmad A, Berry JL, Diaz-Coronado R, Eiger-Moscovich M, Fabian ID, Grossniklaus H, Baker Hubbard G 3rd, Mohammad M, Pe'er J, Reddy MA, Sagoo MS, Shields CL, Staffieri SE, Tanabe M, Ushakova T, Yousef YA; High‐Risk Retinoblastoma Collaborative Study Group. Kaliki S, et al. Among authors: staffieri se. Clin Exp Ophthalmol. 2024 Dec 28. doi: 10.1111/ceo.14488. Online ahead of print. Clin Exp Ophthalmol. 2024. PMID: 39731391
Neovascular Glaucoma as a Predictor of Retinoblastoma High-Risk Histopathology in an International Multicentre Study.
Negretti GS, Ushakova T, Yuri S, Vladimir P, Berry JL, Pike S, Shields CL, Hubbard GB 3rd, Eiger-Moscovich M, Pe'er J, Staffieri SE, Elder JE, McKenzie JD, Ahmad A, Hussain M, Casavilca-Zambrano S, Alarcon-Leon S, Yousef YA, Mohammad M, Tanabe M, Arazi M, Fabian ID, Goldstein S, Kaliki S, Sagoo MS, Reddy MA. Negretti GS, et al. Among authors: staffieri se. Retina. 2024 Nov 20. doi: 10.1097/IAE.0000000000004340. Online ahead of print. Retina. 2024. PMID: 39622251
Treatment Outcomes and Definition Inconsistencies in High-Risk Unilateral Retinoblastoma.
Arazi M, Baum A, Casavilca-Zambrano S, Alarcon-Leon S, Diaz-Coronado R, Ahmad A, Mushtaq A, Hussain M, Ushakova T, Yuri S, Vladimir P, Shields CL, Eagle RC Jr, Berry JL, Pike S, Brown B, Roy SR, Huque F, Fabian I, Frenkel S, Eiger-Moscovich M, Pe'er J, Hubbard GB 3rd, Olson TA, Grossniklaus H, Reddy MA, Sagoo MS, Staffieri SE, Elder JE, McKenzie JD, Tanabe M, Kaliki S, Fabian ID. Arazi M, et al. Among authors: staffieri se. Am J Ophthalmol. 2024 Dec;268:399-408. doi: 10.1016/j.ajo.2024.09.023. Epub 2024 Sep 25. Am J Ophthalmol. 2024. PMID: 39332513
High-Risk Histopathological Features of Retinoblastoma following Primary Enucleation: A Global Study of 1426 Patients from 5 Continents.
Kaliki S, Vempuluru VS, Bakal KR, Dorji S, Tanna V, Shields CN, Fallon SJ, Raval V, Ahmad A, Mushtaq A, Hussain M, Yousef YA, Mohammad M, Roy SR, Huque F, Tatiana U, Yuri S, Vladimir P, Zambrano SC, Alarcón-León S, Valdiviezo-Zapata C, Vargas-Martorellet M, Gutierrez-Chira C, Buitrago M, Ortiz JS, Diaz-Coronado R, Tripathy D, Rath S, Patil G, Berry JL, Pike S, Brown B, Tanabe M, Frenkel S, Eiger-Moscovich M, Pe'er J, Shields CL, Eagle RC Jr, Laiton A, Velasco AM, Vega K, DeSimone J, Bejjanki KM, Kapoor AG, Venkataraman A, Bryant V, Reddy MA, Sagoo MS, Hubbard GB 3rd, Azarcon CP, Olson TA, Grossniklaus H, Rolfe O, Staffieri SE, O'Day R, Mathew AA, Elder JE, McKenzie JD, Fabian ID, Shemesh R, Vishnevskia-Dai V, Ali MH, Jakati S, Mishra DK, Reddy Palkonda VA. Kaliki S, et al. Among authors: staffieri se. Retina. 2024 Aug 14;44(12):2105-15. doi: 10.1097/IAE.0000000000004250. Online ahead of print. Retina. 2024. PMID: 39151183 Free PMC article.
Integrating Genetics in Glaucoma Screening.
Mackey DA, Bigirimana D, Staffieri SE. Mackey DA, et al. Among authors: staffieri se. J Glaucoma. 2024 Aug 1;33(Suppl 1):S49-S53. doi: 10.1097/IJG.0000000000002425. Epub 2024 Aug 19. J Glaucoma. 2024. PMID: 39149951 Free PMC article. Review.
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. Genet Med. 2024 Jul 17:101216. doi: 10.1016/j.gim.2024.101216. Online ahead of print. Genet Med. 2024. PMID: 39033378 Free article.
Making glaucoma genetic studies more diverse.
Mackey DA, Staffieri SE. Mackey DA, et al. Among authors: staffieri se. Cell. 2024 Jan 18;187(2):273-275. doi: 10.1016/j.cell.2023.12.023. Cell. 2024. PMID: 38242084
Noncoding variants alter GATA2 expression in rhombomere 4 motor neurons and cause dominant hereditary congenital facial paresis.
Tenney AP, Di Gioia SA, Webb BD, Chan WM, de Boer E, Garnai SJ, Barry BJ, Ray T, Kosicki M, Robson CD, Zhang Z, Collins TE, Gelber A, Pratt BM, Fujiwara Y, Varshney A, Lek M, Warburton PE, Van Ryzin C, Lehky TJ, Zalewski C, King KA, Brewer CC, Thurm A, Snow J, Facio FM, Narisu N, Bonnycastle LL, Swift A, Chines PS, Bell JL, Mohan S, Whitman MC, Staffieri SE, Elder JE, Demer JL, Torres A, Rachid E, Al-Haddad C, Boustany RM, Mackey DA, Brady AF, Fenollar-Cortés M, Fradin M, Kleefstra T, Padberg GW, Raskin S, Sato MT, Orkin SH, Parker SCJ, Hadlock TA, Vissers LELM, van Bokhoven H, Jabs EW, Collins FS, Pennacchio LA, Manoli I, Engle EC. Tenney AP, et al. Among authors: staffieri se. Nat Genet. 2023 Jul;55(7):1149-1163. doi: 10.1038/s41588-023-01424-9. Epub 2023 Jun 29. Nat Genet. 2023. PMID: 37386251 Free PMC article.
Is the disease risk and penetrance in Leber hereditary optic neuropathy actually low?
Mackey DA, Ong JS, MacGregor S, Whiteman DC, Craig JE, Lopez Sanchez MIG, Kearns LS, Staffieri SE, Clarke L, McGuinness MB, Meteoukki W, Samuel S, Ruddle JB, Chen C, Fraser CL, Harrison J, Howell N, Hewitt AW. Mackey DA, et al. Among authors: staffieri se. Am J Hum Genet. 2023 Jan 5;110(1):170-176. doi: 10.1016/j.ajhg.2022.11.014. Epub 2022 Dec 23. Am J Hum Genet. 2023. PMID: 36565701 Free PMC article.
52 results