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Novel SIX6 mutations cause recessively inherited congenital cataract, microcornea, and corneal opacification with or without coloboma and microphthalmia.
Mol Vis. 2022 May 17;28:57-69. eCollection 2022.
Mol Vis. 2022.
PMID: 35693420
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: farraj la.
Commun Biol. 2021 Mar 1;4(1):266. doi: 10.1038/s42003-021-01784-0.
Commun Biol. 2021.
PMID: 33649486
Free PMC article.
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Gestational diabetes mellitus and macrosomia predispose to diabetes in the Lebanese population.
Ghassibe-Sabbagh M, Mehanna Z, Farraj LA, Salloum AK, Zalloua PA.
Ghassibe-Sabbagh M, et al. Among authors: farraj la.
J Clin Transl Endocrinol. 2019 Feb 20;16:100185. doi: 10.1016/j.jcte.2019.100185. eCollection 2019 Jun.
J Clin Transl Endocrinol. 2019.
PMID: 30899673
Free PMC article.
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