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Systemic Disease and Ocular Comorbidity Analysis of Geographically Isolated Federally Recognized American Indian Tribes of the Intermountain West.
Hicks PM, Haaland B, Feehan M, Crandall AS, Pettey JH, Nuttall E, Self W, Hartnett ME, Bernstein P, Vitale A, Shakoor A, Shulman JP, Sieminski SF, Kim I, Owen LA, Murtaugh MA, Noyes A, DeAngelis MM. Hicks PM, et al. Among authors: vitale a. J Clin Med. 2020 Nov 7;9(11):3590. doi: 10.3390/jcm9113590. J Clin Med. 2020. PMID: 33171720 Free PMC article.
Genetic Epidemiologic Analysis of Hypertensive Retinopathy in an Underrepresented and Rare Federally Recognized Native American Population of the Intermountain West.
Hicks PM, Melendez SAC, Vitale A, Self W, Hartnett ME, Bernstein P, Morgan DJ, Feehan M, Shakoor A, Kim I, Owen LA, DeAngelis MM. Hicks PM, et al. Among authors: vitale a. J Community Med Public Health. 2019;3(1):152. Epub 2019 Jun 10. J Community Med Public Health. 2019. PMID: 31475247 Free PMC article.
Genetics of age-related macular degeneration (AMD).
DeAngelis MM, Owen LA, Morrison MA, Morgan DJ, Li M, Shakoor A, Vitale A, Iyengar S, Stambolian D, Kim IK, Farrer LA. DeAngelis MM, et al. Among authors: vitale a. Hum Mol Genet. 2017 Aug 1;26(R1):R45-R50. doi: 10.1093/hmg/ddx228. Hum Mol Genet. 2017. PMID: 28854576 Free PMC article. Review.
Genetics of age-related macular degeneration (AMD).
DeAngelis MM, Owen LA, Morrison MA, Morgan DJ, Li M, Shakoor A, Vitale A, Iyengar S, Stambolian D, Kim IK, Farrer LA. DeAngelis MM, et al. Among authors: vitale a. Hum Mol Genet. 2017 Oct 1;26(R2):R246. doi: 10.1093/hmg/ddx343. Hum Mol Genet. 2017. PMID: 28977452 Free PMC article. No abstract available.
ALPK1 missense pathogenic variant in five families leads to ROSAH syndrome, an ocular multisystem autosomal dominant disorder.
Williams LB, Javed A, Sabri A, Morgan DJ, Huff CD, Grigg JR, Heng XT, Khng AJ, Hollink IHIM, Morrison MA, Owen LA, Anderson K, Kinard K, Greenlees R, Novacic D, Nida Sen H, Zein WM, Rodgers GM, Vitale AT, Haider NB, Hillmer AM, Ng PC, Shankaracharya, Cheng A, Zheng L, Gillies MC, van Slegtenhorst M, van Hagen PM, Missotten TOAR, Farley GL, Polo M, Malatack J, Curtin J, Martin F, Arbuckle S, Alexander SI, Chircop M, Davila S, Digre KB, Jamieson RV, DeAngelis MM. Williams LB, et al. Among authors: vitale at. Genet Med. 2019 Sep;21(9):2103-2115. doi: 10.1038/s41436-019-0476-3. Epub 2019 Apr 10. Genet Med. 2019. PMID: 30967659 Free PMC article.
An inherited disorder with splenomegaly, cytopenias, and vision loss.
Tantravahi SK, Williams LB, Digre KB, Creel DJ, Smock KJ, DeAngelis MM, Clayton FC, Vitale AT, Rodgers GM. Tantravahi SK, et al. Am J Med Genet A. 2012 Mar;158A(3):475-81. doi: 10.1002/ajmg.a.34437. Epub 2012 Feb 3. Am J Med Genet A. 2012. PMID: 22307799 Free PMC article.
1,180 results