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Publications indexed to the term Iris

FacultyTitle
2A novel FOXF1 mutation associated with alveolar capillary dysplasia and coexisting colobomas and hemihyperplasia. (Geddes GC, Dimmock DP, Hehir DA, Helbling DC, Kirkpatrick E, Loomba R, Southern J, Waknitz M, Scharer G, Konduri GG) J Perinatol 2015 Feb;35(2):155-7       5 Citations
1The zygomaticomaxillary complex fracture - an anthropometric appraisal of surgical outcomes. (Raschke GF, Rieger UM, Bader RD, Schaefer O, Guentsch A, Hagemeister C, Schultze-Mosgau S) J Craniomaxillofac Surg 2013 Jun;41(4):331-7       21 Citations
1Bevacizumab in glaucoma: a review. (Ichhpujani P, Ramasubramanian A, Kaushik S, Pandav SS) Can J Ophthalmol 2007 Dec;42(6):812-5    
1Occult intraocular foreign body: ultrasound biomicroscopy holds the key. (Kaushik S, Ichhpujani P, Ramasubramanian A, Pandav SS) Int Ophthalmol 2008 Feb;28(1):71-3       19 Citations
1Morphogenesis of the anterior segment in the zebrafish eye. (Soules KA, Link BA) BMC Dev Biol 2005 Jun 28;5:12       140 Citations
1A novel mutation in the PITX2 gene in a family with Axenfeld-Rieger syndrome. (Brooks BP, Moroi SE, Downs CA, Wiltse S, Othman MI, Semina EV, Richards JE) Ophthalmic Genet 2004 Mar;25(1):57-62       26 Citations
1Development of the avian iris and ciliary body: mechanisms of cellular differentiation during the smooth-to-striated muscle transition. (Link BA, Nishi R) Dev Biol 1998 Nov 01;203(1):163-76       26 Citations
1Development of the avian iris and ciliary body: the role of activin and follistatin in coordination of the smooth-to-striated muscle transition. (Link BA, Nishi R) Dev Biol 1998 Jul 15;199(2):226-34       17 Citations
1Mutation in the RIEG1 gene in patients with iridogoniodysgenesis syndrome. (Kulak SC, Kozlowski K, Semina EV, Pearce WG, Walter MA) Hum Mol Genet 1998 Jul;7(7):1113-7       121 Citations
2Autosomal dominant iris hypoplasia is caused by a mutation in the Rieger syndrome (RIEG/PITX2) gene. (Alward WL, Semina EV, Kalenak JW, Héon E, Sheth BP, Stone EM, Murray JC) Am J Ophthalmol 1998 Jan;125(1):98-100       129 Citations
1Activin A and follistatin expression in developing targets of ciliary ganglion neurons suggests a role in regulating neurotransmitter phenotype. (Darland DC, Link BA, Nishi R) Neuron 1995 Oct;15(4):857-66       46 Citations
1Linkage of autosomal dominant iris hypoplasia to the region of the Rieger syndrome locus (4q25). (Héon E, Sheth BP, Kalenak JW, Sunden SL, Streb LM, Taylor CM, Alward WL, Sheffield VC, Stone EM) Hum Mol Genet 1995 Aug;4(8):1435-9       61 Citations
1Rebleeding in experimental traumatic hyphema treated with intraocular tissue plasminogen activator. (Williams DF, Han DP, Abrams GW) Arch Ophthalmol 1990 Feb;108(2):264-6       29 Citations