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

Year Number of Results
1997 2
1998 3
1999 2
2000 3
2001 2
2004 4
2005 2
2006 2
2007 1
2009 1
2011 2
2012 2
2013 3
2014 3
2015 2
2016 4
2017 1
2018 2
2019 3
2020 2
2021 2
2024 0

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44 results

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Page 1
Genetics in Keratoconus: where are we?
Bykhovskaya Y, Margines B, Rabinowitz YS. Bykhovskaya Y, et al. Eye Vis (Lond). 2016 Jun 27;3:16. doi: 10.1186/s40662-016-0047-5. eCollection 2016. Eye Vis (Lond). 2016. PMID: 27350955 Free PMC article. Review.
Update on the genetics of keratoconus.
Bykhovskaya Y, Rabinowitz YS. Bykhovskaya Y, et al. Exp Eye Res. 2021 Jan;202:108398. doi: 10.1016/j.exer.2020.108398. Epub 2020 Dec 13. Exp Eye Res. 2021. PMID: 33316263
Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases.
Iglesias AI, Mishra A, Vitart V, Bykhovskaya Y, Höhn R, Springelkamp H, Cuellar-Partida G, Gharahkhani P, Bailey JNC, Willoughby CE, Li X, Yazar S, Nag A, Khawaja AP, Polašek O, Siscovick D, Mitchell P, Tham YC, Haines JL, Kearns LS, Hayward C, Shi Y, van Leeuwen EM, Taylor KD; Blue Mountains Eye Study—GWAS group; Bonnemaijer P, Rotter JI, Martin NG, Zeller T, Mills RA, Souzeau E, Staffieri SE, Jonas JB, Schmidtmann I, Boutin T, Kang JH, Lucas SEM, Wong TY, Beutel ME, Wilson JF; NEIGHBORHOOD Consortium; Wellcome Trust Case Control Consortium 2 (WTCCC2); Uitterlinden AG, Vithana EN, Foster PJ, Hysi PG, Hewitt AW, Khor CC, Pasquale LR, Montgomery GW, Klaver CCW, Aung T, Pfeiffer N, Mackey DA, Hammond CJ, Cheng CY, Craig JE, Rabinowitz YS, Wiggs JL, Burdon KP, van Duijn CM, MacGregor S. Iglesias AI, et al. Among authors: bykhovskaya y. Nat Commun. 2018 May 14;9(1):1864. doi: 10.1038/s41467-018-03646-6. Nat Commun. 2018. PMID: 29760442 Free PMC article.
Association of Genetic Variation With Keratoconus.
McComish BJ, Sahebjada S, Bykhovskaya Y, Willoughby CE, Richardson AJ, Tenen A, Charlesworth JC, MacGregor S, Mitchell P, Lucas SEM, Mills RA, Mackey DA, Li X, Wang JJ, Jensen RA, Rotter JI, Taylor KD, Hewitt AW, Rabinowitz YS, Baird PN, Craig JE, Burdon KP. McComish BJ, et al. Among authors: bykhovskaya y. JAMA Ophthalmol. 2020 Feb 1;138(2):174-181. doi: 10.1001/jamaophthalmol.2019.5293. JAMA Ophthalmol. 2020. PMID: 31855235 Free PMC article.
PPIP5K2 and PCSK1 are Candidate Genetic Contributors to Familial Keratoconus.
Khaled ML, Bykhovskaya Y, Gu C, Liu A, Drewry MD, Chen Z, Mysona BA, Parker E, McNabb RP, Yu H, Lu X, Wang J, Li X, Al-Muammar A, Rotter JI, Porter LF, Estes A, Watsky MA, Smith SB, Xu H, Abu-Amero KK, Kuo A, Shears SB, Rabinowitz YS, Liu Y. Khaled ML, et al. Among authors: bykhovskaya y. Sci Rep. 2019 Dec 18;9(1):19406. doi: 10.1038/s41598-019-55866-5. Sci Rep. 2019. PMID: 31852976 Free PMC article.
A multi-ethnic genome-wide association study implicates collagen matrix integrity and cell differentiation pathways in keratoconus.
Hardcastle AJ, Liskova P, Bykhovskaya Y, McComish BJ, Davidson AE, Inglehearn CF, Li X, Choquet H, Habeeb M, Lucas SEM, Sahebjada S, Pontikos N, Lopez KER, Khawaja AP, Ali M, Dudakova L, Skalicka P, Van Dooren BTH, Geerards AJM, Haudum CW, Faro VL, Tenen A, Simcoe MJ, Patasova K, Yarrand D, Yin J, Siddiqui S, Rice A, Farraj LA, Chen YI, Rahi JS, Krauss RM, Theusch E, Charlesworth JC, Szczotka-Flynn L, Toomes C, Meester-Smoor MA, Richardson AJ, Mitchell PA, Taylor KD, Melles RB, Aldave AJ, Mills RA, Cao K, Chan E, Daniell MD, Wang JJ, Rotter JI, Hewitt AW, MacGregor S, Klaver CCW, Ramdas WD, Craig JE, Iyengar SK, O'Brart D, Jorgenson E, Baird PN, Rabinowitz YS, Burdon KP, Hammond CJ, Tuft SJ, Hysi PG. Hardcastle AJ, et al. Among authors: bykhovskaya y. Commun Biol. 2021 Mar 1;4(1):266. doi: 10.1038/s42003-021-01784-0. Commun Biol. 2021. PMID: 33649486 Free PMC article.
Maternally inherited nonsyndromic hearing loss.
Friedman RA, Bykhovskaya Y, Sue CM, DiMauro S, Bradley R, Fallis-Cunningham R, Paradies N, Pensak ML, Smith RJ, Groden J, Li XC, Fischel-Ghodsian N. Friedman RA, et al. Among authors: bykhovskaya y. Am J Med Genet. 1999 Jun 4;84(4):369-72. doi: 10.1002/(sici)1096-8628(19990604)84:4<369::aid-ajmg12>3.0.co;2-v. Am J Med Genet. 1999. PMID: 10340654
TSC1 Mutations in Keratoconus Patients With or Without Tuberous Sclerosis.
Bykhovskaya Y, Fardaei M, Khaled ML, Nejabat M, Salouti R, Dastsooz H, Liu Y, Inaloo S, Rabinowitz YS. Bykhovskaya Y, et al. Invest Ophthalmol Vis Sci. 2017 Dec 1;58(14):6462-6469. doi: 10.1167/iovs.17-22819. Invest Ophthalmol Vis Sci. 2017. PMID: 29261847 Free PMC article.
Differential Expression of Coding and Long Noncoding RNAs in Keratoconus-Affected Corneas.
Khaled ML, Bykhovskaya Y, Yablonski SER, Li H, Drewry MD, Aboobakar IF, Estes A, Gao XR, Stamer WD, Xu H, Allingham RR, Hauser MA, Rabinowitz YS, Liu Y. Khaled ML, et al. Among authors: bykhovskaya y. Invest Ophthalmol Vis Sci. 2018 Jun 1;59(7):2717-2728. doi: 10.1167/iovs.18-24267. Invest Ophthalmol Vis Sci. 2018. PMID: 29860458 Free PMC article.
44 results