S. P. Ponnam, K. Ramesha, S. Tejwani, B. Ramamurthy, C. Kannabiran, "Mutation of the gap junction protein alpha 8 (GJA8) gene causes autosomal recessive cataract", J Med Genet, Vol. 44, No. 7, 2007, pp. e85.
 E. Pras, J. Raz, V. Yahalom, M. Frydman, H. J. Garzozi, E. Pras, J. F. Hejtmancik, "A nonsense mutation in the glucosaminyl (Nacetyl) transferase 2 gene (GCNT2) association with autosomal recessive congenital cat-aracts", Invest Ophthalmol Vis Sci, , Vol. 45, No. 62004, pp. 1940-5.
 N. Smaoui, O. Beltaief, S. BenHamed, R. M'Rad, F. Maazoul, A. Ouertani, H. Chaabouni, J. F. Hejtmancik, "A homozygous splice mutation in the HSF4 gene is associated with an autosomal recessive congenital cataract", Invest Ophthalmol Vis Sci, Vol. 45, No. 8, 2004, pp. 2716-21.
 E. Pras, E. Levy-Nissenbaum, T. Bakhan, H. Lahat, E. Assia, N. Geffen-Carmi, M. Frydman, B. Goldman, E. Pras, "A missense mutation in the LIM2 gene is associated with autosomal recessive presenile cataract in an inbred Iraqi Jewish family", Am J Hum Genet, Vol. 70, No. 5, 2002, pp. 1363-7.
 E. Pras, M. Frydman, E. Levy-Nissenbaum, T. Bakhan, J. Raz, E. I. Assia, B. Goldman, E. Pras, "A nonsense mutation (W9X) in CRYAA causes autosomal recessive cataract in an inbred Jewish Persian family", Invest Ophthalmol Vis Sci, Vol. 41, No. 11, 2000, pp. 3511-5.
 S. A. Riazuddin, A. Yasmeen, W. Yao, Y. V. Sergeev, Q. Zhang, F. Zulfiqar, A. Riaz, S. Riazuddin, J. F. Hejtmancik, "Mutations in betaB3-crystallin associated with autosomal recessive cataract in two Pakistani families", Invest Ophthalmol Vis Sci, Vol. 46, No. 6, 2005, pp. 2100-6.
 D. Cohen, U. Bar-Yosef, J. Levy, L. Gradstein, N. Belfair, R. Ofir, S. Joshua, T. Lifshitz, R. Carmi, O. S. Birk, "Homozygous CRYBB1 deletion mutation underlies autosomal recessive congenital cataract", Invest Ophthalmol Vis Sci, Vol. 48, No. 5, 2007, pp. 2208-13.
 H. Kaul, S. A. Riazuddin, M. Shahid, S. Kousar, N. H. Butt, A. U. Zafar, S. N. Khan, T. Husnain, J. Akram, J. F. Hejtmancik, S. Riazuddin, "Autosomal recessive congenital cataract linked to EPHA2 in a consanguineous Pakistani family", Mol Vis, Vol. 16, 2010, pp. 511-7.
 A. Yasmeen, S. A. Riazuddin, H. Kaul, S. Mohsin, M. Khan, Z. A. Qazi, I. A. Nasir, A. U. Zafar, S. N. Khan, T. Husnain, J. Akram, J. F. Hejtmancik, S. Riazuddin, "Autosomal recessive congenital cataract in consanguineous Pakistani families is associated with mutations in GALK1", Mol Vis, Vol. 16, 2010, pp. 682-8.
 T. Mori, A. Wanaka, A. Taguchi, K. Matsumoto, M. Tohyama, "Differential expressions of the eph family of receptor tyrosine kinase genes (sek, elk, eck) in the developing nervous system of the mouse", Mol Brain Res, Vol. 29, No. 2, 1995, pp. 325–335.
 D. Stambolian, Y. Ai, D. Sidjanin, K. Nesburn, G. Sathe, M. Rosenberg, D. J. Bergsma, "Cloning of the galactokinase cDNA and identification of mutations in two families with cataracts", Nat Genet, Vol. 10, No. 3, 1995, pp. 307-12.
 K. Sasaki, K. Kurata-Miura, M. Ujita, K. Angata, S. Nakagawa, S. Sekine, T. Nishi, M. Fukuda, "Expression cloning of cDNA encoding a human beta-1,3-N-acetyl glucosaminyl transferase that is essential for poly-N-acetyllactosamine synthesis", Proc Natl Acad Sci, Vol. 94, No. 26, 1997, pp. 14294-9.
 D. S. Mackay, O. B. Boskovska, H. L. Knopf, K. J. Lampi, A. Shiels, "A nonsense mutation in CRYBB1 associated with autosomal dominant cataract linked to human chromosome 22q", Am J Hum Genet, Vol. 71, No. 5, 2002, pp. 1216–1221.
  E. Meyer, F. Rahman, J. Owens, S. Pasha, N. V. Morgan, R. C. Trembath, E. M. Stone, A. T. Moore, E. R. Maher, "Initiation codon mutation in betaB1-crystallin (CRYBB1) associated with autosomal recessive nuclear pulverulent cataract", Mol Vis, Vol. 15, 2009, pp. 1014-9.
 A. C. Ionides, V. Berry, D. S. Mackay, A. T. Moore, S. S. Bhattacharya, A. Shiels, "A locus for autosomal dominant posterior polar cataract on chromosome 1p", Hum Mol Genet, Vol. 6, No. 1, 1997, pp. 47-51.
 W. He, C. M. Tuck-Muller, J. E. Martínez, S. Li, E. R. Rowley, W. Wertelecki, "Molecular cha-racterization of a ring chromosome 16 from a patient with bila-teral cataracts", Am J Med Genet, Vol. 107, No. 1, 2002, pp. 12-7.
 P. Finelli, P. Cavalli, D. Giardino, Gottardi G, F. Natacci, S. Savasta, L. Larizza, "FISH characterization of a supernumerary r(1)(::cen-->q22::q22-->sq21::) chromosome associated with multiple anomalies and bilateral cataracts", Am J Med Genet, Vol. 104, No. 2, 2001, pp. 157-64.
 D. Dilli, S. S. Oguz, U. Dilmen, E. S. Cakar, Z. O. Tunay, O. Tok, M. A. Acar, "Congenital cataract with de novo balanced reciprocal t(3;13) (q23;q12) translocation in a newborn", J Perinat Med, Vol. 37, No. 6, 2009, pp. 717-9.
 N. I. Herath, M. D. Spanevello, S. Sabesan, T. Newton, M. Cummings, S. Duffy, D. Lincoln, G. Boyle, P. G. Parsons, A. W. Boyd, "Over-expression of Eph and ephrin genes in advanced ovarian cancer: ephrin gene expression correlates with shortened survival", BMC Cancer, Vol. 6, No. , 2006, pp. 144.
 G. Jun, H. Guo, B. E. Klein, R. Klein, J. J. Wang, P. Mitchell, H. Miao, K. E. Lee, T. Joshi, M. Buck, P. Chugha, D. Bardenstein, A. P. Klein, J. E. Bailey-Wilson, X. Gong, T. D. Spector, T. Andrew, C. J. Hammond, R. C. Elston, S. K. Iyengar, B. Wang, "EPHA2 is associated with age-related cortical cataract in mice and humans", PLoS Genet, Vol. 5, No. 7, 2009, pp. e1000584.
 Y. S. Shin-Buehring, L. Stuempfig, E. Pouget, P. Rahm, J. Schaub, "Characterization of galactose-1-phosphate uridyl-transferase and galactokinase in human organs from the fetus and adult", Clin Chim Acta, Vol. 112, No. 3, 1981, pp. 257-65.
 L. C. Yu, Y. C. Twu, M. L. Chou, M. E. Reid, A. R. Gray, J. M. Moulds, C. Y. Chang, M. Lin, "The molecular genetics of the human I locus and molecular background explain the partial association of the adult i phenotype with congenital cataracts", Blood, Vol. 101, No. 6, 2003, pp. 2081–2088.
 N. Inaba, T. Hiruma, A. Togayachi, H. Iwasaki, X. H. Wang, Y. Furukawa, R. Sumi, T. Kudo, K. Fujimura, T. Iwai, M. Gotoh, M. Nakamura, H. Narimatsu, "A novel I-branching beta-1,6-N acetyl glucosaminyl transferase involved in human blood group I antigen expression", Blood, Vol. 101, No. 7, 2003, pp. 2870–2876.
 C. E. Willoughby, A. Shafiq, W. Ferrini, L. L. Chan, G. Billingsley, M. Priston, C. Mok, A. Chandna, S. Kaye, E. Héon, "CRYBB1 mutation associated with congenital cataract and microcornea", Mol Vis, Vol. 11, 2005, pp. 587-93.
 J. Wang, X. Ma, F. Gu, N. P. Liu, X. L. Hao, K. J. Wang, N. L. Wang, S. Q. Zhu, "A missense mutation S228P in the CRYBB1 gene causes autosomal dominant congenital cataract", Chin Med J, Vol. 120, No. 9, 2007, pp. 820-4.