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In Vivo Assessment of Retinal Phenotypes in Axenfeld-Rieger Syndrome.
Untaroiu A, Reis LM, Higgins BP, Walesa A, Zacharias S, Nikezic D, Costakos DM, Carroll J, Semina EV. Untaroiu A, et al. Among authors: reis lm. Invest Ophthalmol Vis Sci. 2024 Apr 1;65(4):20. doi: 10.1167/iovs.65.4.20. Invest Ophthalmol Vis Sci. 2024. PMID: 38587439 Free PMC article.
Genetics of anterior segment dysgenesis disorders.
Reis LM, Semina EV. Reis LM, et al. Curr Opin Ophthalmol. 2011 Sep;22(5):314-24. doi: 10.1097/ICU.0b013e328349412b. Curr Opin Ophthalmol. 2011. PMID: 21730847 Free PMC article. Review.
Axenfeld-Rieger syndrome: more than meets the eye.
Reis LM, Maheshwari M, Capasso J, Atilla H, Dudakova L, Thompson S, Zitano L, Lay-Son G, Lowry RB, Black J, Lee J, Shue A, Kremlikova Pourova R, Vaneckova M, Skalicka P, Jedlickova J, Trkova M, Williams B, Richard G, Bachman K, Seeley AH, Costakos D, Glaser TM, Levin AV, Liskova P, Murray JC, Semina EV. Reis LM, et al. J Med Genet. 2023 Apr;60(4):368-379. doi: 10.1136/jmg-2022-108646. Epub 2022 Jul 26. J Med Genet. 2023. PMID: 35882526 Free PMC article.
Application of genetic approaches to ocular disease.
Ruttum MS, Reis LM, Semina EV. Ruttum MS, et al. Among authors: reis lm. Pediatr Clin North Am. 2006 Aug;53(4):751-65. doi: 10.1016/j.pcl.2006.05.010. Pediatr Clin North Am. 2006. PMID: 16873003 Review.
PITX2 and FOXC1 spectrum of mutations in ocular syndromes.
Reis LM, Tyler RC, Volkmann Kloss BA, Schilter KF, Levin AV, Lowry RB, Zwijnenburg PJ, Stroh E, Broeckel U, Murray JC, Semina EV. Reis LM, et al. Eur J Hum Genet. 2012 Dec;20(12):1224-33. doi: 10.1038/ejhg.2012.80. Epub 2012 May 9. Eur J Hum Genet. 2012. PMID: 22569110 Free PMC article.
162 results