2013

• Ng, W., Pasutto, F., Bardakjian, T., Wilson, M., Watson, G., Schneider, A., Mackey, D., Grigg, J., Zenker, M., Jamieson, R. (2013), A puzzle over several decades: eye anomalies with FRAS1 and STRA6 mutations in the same family. Clinical Genetics. 83(2), 162-168. [Abstract]
• Grigg, J., Jamieson, R. (2013), Phakomatoses. In: Pediatric Ophthalmology and Strabismus 4th Ed. (pp.675-690).United Kingdom, USA: Elsevier Ltd.
• Jamieson, R., Grigg, J. (2013), Clinical embryology and development of the eye. In: Pediatric Ophthalmology and Strabismus 4th Ed. (pp.6-15).United Kingdom, USA: Elsevier Ltd.

2012

• Cederquist, G., Luchniak, A., Tischfield, M., Peeva, M., Song, Y., Menezes, M., Chan, W., Andrews, C., Chew, S., Jamieson, R., Gomes, L., Flaherty, M., Grant, P., Gupta, M., Engle, E. (2012), An inherited TUBB2B mutation alters a kinesin-binding site and causes polymicrogyria, CFEOM and axon dysinnervation. Human Molecular Genetics. 21(26), 5484-5499. [Abstract]
• Léger, S., Balguerie, X., Goldenberg, A., Drouin-Garraud, V., Cabot, A., Amstutz-Montadert, I., Young, P., Joly, P., Bodereau, V., Holder-Espinasse, M., Jamieson, R., Krause, A., Chen, H., Baumann, C., Nunes, L., Dollfus, H., Goossens, M., Pingault, V. (2012), Novel and recurrent non-truncating mutations of the MITF basic domain: genotypic and phenotypic variations in Waardenburg and Tietz syndromes. European Journal of Human Genetics. 20(5), 584-587. [Abstract]
• Chang, J., Jang, J., Jamieson, R., Grigg, J. (2012), Long-Term Follow-Up Study of Autosomal Dominant Optic Atrophy in an Australian Population. Asia-Pacific Journal of Ophthalmology. 1(2), 88-90.

2011

• Stark, Z., Storen, R., Bennetts, B., Savarirayan, R., Jamieson, R. (2011), Isolated hypogonadotropic hypogonadism with SOX2 mutation and anophthalmia/microphthalmia in offspring. European Journal of Human Genetics. 19(7), 753-756. [Abstract]

2010

• Weaving, L., Mihelec, M., Storen, R., Sosic, D., Grigg, J., Tam, P., Jamieson, R. (2010), Twist2: Role in Corneal Stromal Keratocyte Proliferation and Corneal Thickness. Investigative ophthalmology & visual science. 51(11), 5561-70. [Abstract]
• Tischfield, M., Baris, H., Wu, C., Rudolph, G., Van Maldergem, L., He, W., Chan, W., Andrews, C., Demer, J., Robertson, R., Mackey, D., Ruddle, J., Bird, T., Gottlob, I., Pieh, C., Traboulsi, E., Pomeroy, S., Hunter, D., Soul, J., Newlin, A., Sabol, L., Doherty, E., de Uzcátegui, C., de Uzcátegui, N., Collins, M., Sener, E., Wabbels, B., Hellebrand, H., Meitinger, T., de Berardinis, T., Magli, A., Schiavi, C., Pastore-Trossello, M., Koc, F., Wong, A., Levin, A., Geraghty, M., Descartes, M., Flaherty, M., Jamieson, R., Møller, H., Meuthen, I., Callen, D., Kerwin, J., Lindsay, S., Meindl, A., Gupta, M., Pellman, D., Engle, E. (2010), Human TUBB3 mutations perturb microtubule dynamics, kinesin interactions, and axon guidance. Cell. 140(1), 74-87. [Abstract]

2009

• Mihelec, M., Abraham, P., Gibson, K., Krowka, R., Susman, R., Storen, R., Chen, Y., Donald, J., Tam, P., Grigg, J., Flaherty, M., Gole, G., Jamieson, R. (2009), Novel SOX2 partner-factor domain mutation in a four-generation family. European journal of human genetics : EJHG. 17(11), 1417-22. [Abstract]
• Sharan, S., Swamy, B., Taranath, D., Jamieson, R., Yu, T., Wargon, O., Grigg, J. (2009), Port-wine vascular malformations and glaucoma risk in Sturge-Weber syndrome. Journal of the American Association for Pediatric Ophthalmology and Strabismus. 13(4), 374-378. [Abstract]
• Flaherty, M., Balachandran, C., Jamieson, R., Engle, E. (2009), Congenital fibrosis of the extraocular muscles type 1, distinctive conjunctival changes and intrapapillary disc colobomata. Ophthalmic Genetics. 30(2), 91-95. [Abstract]
• Sharan, S., Swamy, B., Taranath, D., Jamieson, R., Yu, T., Wargon, O., Grigg, J. (2009), Port-wine vascular malformations and glaucoma risk in Sturge-Weber syndrome. Journal of American Association for Pediatric Ophthalmology and Strabismus. 13, 374-378. [Abstract]

2008

• Mihelec, M., St Heaps, L., Flaherty, M., Billson, F., Rudduck, C., Tam, P., Grigg, J., Peters, G., Jamieson, R. (2008), Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucoma. Twin Research and Human Genetics. 11(4), 412-421. [Abstract]
• Lewis, S., Khoo, P., De Young, R., Steiner, K., Wilcock, C., Mukhopadhyay, M., Westphal, H., Jamieson, R., Robb, L., Tam, P. (2008), Dkk1 and Wnt3 interact to control head morphogenesis in the mouse. Development (Cambridge). 135(10), 1791-1801. [Abstract]

2007

• Swamy, B., Billson, F., Martin, F., Donaldson, C., Hing, S., Smith, J., Jamieson, R., Grigg, J. (2007), Secondary glaucoma after paediatric cataract surgery. The British journal of ophthalmology. 91(12), 1627-30. [Abstract]
• Jamieson, R., Farrar, N., Stewart, K., Perveen, R., Mihelec, M., Carette, M., Grigg, J., McAvoy, J., Lovicu, F., Tam, P., Scambler, P., Lloyd, I., Donnai, D., Black, G. (2007), Characterization of a familial t(16;22) balanced translocation associated with congenital cataract leads to identification of a novel gene, TMEM114, expressed in the lens and disrupted by the translocation. Human mutation. 28(10), 968-977. [Abstract]
• Arvind, H., Hunyor, A., McClellan, K., Billson, F., Grigg, J., Jamieson, R. (2007), Management of intraoperative tilting of the scleral-fixated intraocular lens in classical aniridia. The British Journal of Ophthalmology. , 1247-1248. [Abstract]
• Perveen, R., Favor, J., Jamieson, R., Ray, D., Black, G. (2007), A heterozygous c-Maf transactivation domain mutation causes congenital cataract and enhances target gene activation. Human Molecular Genetics. 16(9), 1030-1038. [Abstract]
• Palmer, S., Tay, E., Santucci, N., Cuc Bach, T., Hook, J., Lemckert, F., Jamieson, R., Gunnning, P., Hardeman, E. (2007), Expression of Gtf2ird1, the Williams syndrome-associated gene, during mouse development. Gene expression patterns : GEP. 7, 396-404. [Abstract]
• van Heyningen, V., Williamson, K., Mackey, D., Kearns, L., Hewitt, A., Jamieson, R. (2007), PAX6 mutations may be associated with high myopia. OPHTHALMIC GENETICS. 28(3), 179-182. [Abstract]