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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1978 1
1980 3
1981 3
1982 6
1983 3
1984 9
1985 5
1986 6
1987 2
1988 1
1989 14
1990 9
1991 12
1992 16
1993 13
1994 5
1995 3
1996 3
1999 1
2001 4
2003 3
2004 5
2005 4
2006 1
2007 3
2008 1
2009 1
2012 2
2013 4
2014 4
2015 5
2016 5
2017 2
2018 5
2019 3
2020 3
2021 5
2022 4
2023 9
2024 0

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178 results

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Page 1
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.
Genetic testing: Getting it right.
Paredes DI, Haefeli LM, Okoye O, Capasso JE, Wyman C, Khetan V, Levin AV. Paredes DI, et al. Among authors: capasso je. Oman J Ophthalmol. 2023 Feb 21;16(1):1-3. doi: 10.4103/ojo.ojo_11_23. eCollection 2023 Jan-Apr. Oman J Ophthalmol. 2023. PMID: 37007263 Free PMC article. No abstract available.
Lyonization in ophthalmology.
Wuthisiri W, Lingao MD, Capasso JE, Levin AV. Wuthisiri W, et al. Among authors: capasso je. Curr Opin Ophthalmol. 2013 Sep;24(5):389-97. doi: 10.1097/ICU.0b013e3283641f91. Curr Opin Ophthalmol. 2013. PMID: 23892913 Review.
Genetics of the anterior segment dysgenesis.
Paredes DI, Capasso JE, Wyman CS, Levin AV. Paredes DI, et al. Among authors: capasso je. Taiwan J Ophthalmol. 2023 Jul 18;13(4):500-504. doi: 10.4103/tjo.TJO-D-23-00062. eCollection 2023 Oct-Dec. Taiwan J Ophthalmol. 2023. PMID: 38249510 Free PMC article. Review.
Organophosphate retinopathy.
Pham H, Lingao MD, Ganesh A, Capasso JE, Keep R, Sadagopan KA, Levin AV. Pham H, et al. Among authors: capasso je. Oman J Ophthalmol. 2016 Jan-Apr;9(1):49-51. doi: 10.4103/0974-620X.176101. Oman J Ophthalmol. 2016. PMID: 27013829 Free PMC article.
CNGB1-related rod-cone dystrophy: A mutation review and update.
Nassisi M, Smirnov VM, Solis Hernandez C, Mohand-Saïd S, Condroyer C, Antonio A, Kühlewein L, Kempf M, Kohl S, Wissinger B, Nasser F, Ragi SD, Wang NK, Sparrow JR, Greenstein VC, Michalakis S, Mahroo OA, Ba-Abbad R, Michaelides M, Webster AR, Degli Esposti S, Saffren B, Capasso J, Levin A, Hauswirth WW, Dhaenens CM, Defoort-Dhellemmes S, Tsang SH, Zrenner E, Sahel JA, Petersen-Jones SM, Zeitz C, Audo I. Nassisi M, et al. Among authors: capasso j. Hum Mutat. 2021 Jun;42(6):641-666. doi: 10.1002/humu.24205. Epub 2021 May 16. Hum Mutat. 2021. PMID: 33847019 Free PMC article. Review.
Stargardt misdiagnosis: How ocular genetics helps.
Ibanez MB 4th, de Guimarães TAC, Capasso J, Bello N, Levin AV. Ibanez MB 4th, et al. Among authors: capasso j. Am J Med Genet A. 2021 Mar;185(3):814-819. doi: 10.1002/ajmg.a.62045. Epub 2020 Dec 24. Am J Med Genet A. 2021. PMID: 33369172
Optical Coherence Tomography in Knobloch Syndrome.
Thau A, Tsukikawa M, Wangtiraumnuay N, Capasso J, Affel E, Alnabi WA, Adam M, Alsulaiman SM, Spirn M, Levin AV. Thau A, et al. Among authors: capasso j. Ophthalmic Surg Lasers Imaging Retina. 2019 Aug 1;50(8):e203-e210. doi: 10.3928/23258160-20190806-13. Ophthalmic Surg Lasers Imaging Retina. 2019. PMID: 31415705
Mutations in AGBL5 associated with Retinitis pigmentosa.
Paredes DI, Bello NR, Capasso JE, Procopio R, Levin AV. Paredes DI, et al. Among authors: capasso je. Ophthalmic Genet. 2023 Dec 11:1-6. doi: 10.1080/13816810.2023.2291687. Online ahead of print. Ophthalmic Genet. 2023. PMID: 38078364
Ocular manifestations of Emanuel syndrome.
Saffren BD, Capasso JE, Zanolli M, Levin AV. Saffren BD, et al. Among authors: capasso je. Am J Med Genet A. 2018 Sep;176(9):1964-1967. doi: 10.1002/ajmg.a.40361. Epub 2018 Sep 4. Am J Med Genet A. 2018. PMID: 30178914
178 results