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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. Among authors: capasso j. 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.
Genetics for the ophthalmologist.
Sadagopan KA, Capasso J, Levin AV. Sadagopan KA, et al. Among authors: capasso j. Oman J Ophthalmol. 2012 Sep;5(3):144-9. doi: 10.4103/0974-620X.106092. Oman J Ophthalmol. 2012. PMID: 23439654 Free PMC article.
Lyonization in ophthalmology.
Wuthisiri W, Lingao MD, Capasso JE, Levin AV. Wuthisiri W, et al. Curr Opin Ophthalmol. 2013 Sep;24(5):389-97. doi: 10.1097/ICU.0b013e3283641f91. Curr Opin Ophthalmol. 2013. PMID: 23892913 Review.
Ocular manifestations of 22q11.2 microduplication.
Cordovez JA, Capasso J, Lingao MD, Sadagopan KA, Spaeth GL, Wasserman BN, Levin AV. Cordovez JA, et al. Among authors: capasso j. Ophthalmology. 2014 Jan;121(1):392-398. doi: 10.1016/j.ophtha.2013.06.040. Epub 2013 Aug 21. Ophthalmology. 2014. PMID: 23972321
Anirdia-like phenotype caused by 6p25 dosage aberrations.
Sadagopan KA, Liu GT, Capasso JE, Wuthisiri W, Keep RB, Levin AV. Sadagopan KA, et al. Am J Med Genet A. 2015 Mar;167A(3):524-8. doi: 10.1002/ajmg.a.36890. Am J Med Genet A. 2015. PMID: 25691405
Peters anomaly in cri-du-chat syndrome.
Hope WC, Cordovez JA, Capasso JE, Hammersmith KM, Eagle RC, Lall-Trail J, Levin AV. Hope WC, et al. Among authors: capasso je. J AAPOS. 2015 Jun;19(3):277-9. doi: 10.1016/j.jaapos.2015.01.018. J AAPOS. 2015. PMID: 26059676
178 results