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The role of Frizzled-4 mutations in familial exudative vitreoretinopathy and Coats disease.
Robitaille JM, Zheng B, Wallace K, Beis MJ, Tatlidil C, Yang J, Sheidow TG, Siebert L, Levin AV, Lam WC, Arthur BW, Lyons CJ, Jaakkola E, Tsilou E, Williams CA, Weaver RG Jr, Shields CL, Guernsey DL. Robitaille JM, et al. Among authors: guernsey dl. Br J Ophthalmol. 2011 Apr;95(4):574-9. doi: 10.1136/bjo.2010.190116. Epub 2010 Nov 21. Br J Ophthalmol. 2011. PMID: 21097938
Mutant frizzled-4 disrupts retinal angiogenesis in familial exudative vitreoretinopathy.
Robitaille J, MacDonald ML, Kaykas A, Sheldahl LC, Zeisler J, Dubé MP, Zhang LH, Singaraja RR, Guernsey DL, Zheng B, Siebert LF, Hoskin-Mott A, Trese MT, Pimstone SN, Shastry BS, Moon RT, Hayden MR, Goldberg YP, Samuels ME. Robitaille J, et al. Among authors: guernsey dl. Nat Genet. 2002 Oct;32(2):326-30. doi: 10.1038/ng957. Epub 2002 Aug 12. Nat Genet. 2002. PMID: 12172548
Severe retinopathy of prematurity associated with FZD4 mutations.
Ells A, Guernsey DL, Wallace K, Zheng B, Vincer M, Allen A, Ingram A, DaSilva O, Siebert L, Sheidow T, Beis J, Robitaille JM. Ells A, et al. Among authors: guernsey dl. Ophthalmic Genet. 2010 Mar;31(1):37-43. doi: 10.3109/13816810903479834. Ophthalmic Genet. 2010. PMID: 20141357
Exfoliation syndrome: clinical and genetic features.
Orr AC, Robitaille JM, Price PA, Hamilton JR, Falvey DM, De Saint-Sardos AG, Pasternak S, Guernsey DL. Orr AC, et al. Among authors: guernsey dl. Ophthalmic Genet. 2001 Sep;22(3):171-85. doi: 10.1076/opge.22.3.171.2223. Ophthalmic Genet. 2001. PMID: 11559859
Genotype/phenotype correlations in aniridia.
Gupta SK, De Becker I, Tremblay F, Guernsey DL, Neumann PE. Gupta SK, et al. Among authors: guernsey dl. Am J Ophthalmol. 1998 Aug;126(2):203-10. doi: 10.1016/s0002-9394(98)00191-3. Am J Ophthalmol. 1998. PMID: 9727514
Mutations in a novel serine protease PRSS56 in families with nanophthalmos.
Orr A, Dubé MP, Zenteno JC, Jiang H, Asselin G, Evans SC, Caqueret A, Lakosha H, Letourneau L, Marcadier J, Matsuoka M, Macgillivray C, Nightingale M, Papillon-Cavanagh S, Perry S, Provost S, Ludman M, Guernsey DL, Samuels ME. Orr A, et al. Among authors: guernsey dl. Mol Vis. 2011;17:1850-61. Epub 2011 Jul 12. Mol Vis. 2011. PMID: 21850159 Free PMC article.
Mutations in centrosomal protein CEP152 in primary microcephaly families linked to MCPH4.
Guernsey DL, Jiang H, Hussin J, Arnold M, Bouyakdan K, Perry S, Babineau-Sturk T, Beis J, Dumas N, Evans SC, Ferguson M, Matsuoka M, Macgillivray C, Nightingale M, Patry L, Rideout AL, Thomas A, Orr A, Hoffmann I, Michaud JL, Awadalla P, Meek DC, Ludman M, Samuels ME. Guernsey DL, et al. Am J Hum Genet. 2010 Jul 9;87(1):40-51. doi: 10.1016/j.ajhg.2010.06.003. Am J Hum Genet. 2010. PMID: 20598275 Free PMC article.
82 results