PubMed ID: 25794026 Author(s): Costin BR, Plesec TP, Kopplin LJ, Chundury RV, McBride JM, Levine MR, Perry JD. Regional variations in orbicularis oculi histology. Ophthalmic Plast Reconstr Surg. 2015 Jul-Aug;31(4):325-7. doi: 10.1097/IOP.0000000000000430. PMID 25794026 Journal: …
Laura Kopplin
Biological response modifiers in the treatment of noninfectious uveitis.
PubMed ID: 25730617 Author(s): Kopplin LJ, Shifera AS, Suhler EB, Lin P. Biological response modifiers in the treatment of noninfectious uveitis. Int Ophthalmol Clin. 2015 Spring;55(2):19-36. doi: 10.1097/IIO.0000000000000060. Review. PMID 25730617 Journal: International Ophthalmology Clinics, …
Relationship of Fuchs endothelial corneal dystrophy severity to central corneal thickness.
PubMed ID: 22491913 Author(s): Kopplin LJ, Przepyszny K, Schmotzer B, Rudo K, Babineau DC, Patel SV, Verdier DD, Jurkunas U, Iyengar SK, Lass JH; Fuchs’ Endothelial Corneal Dystrophy Genetics Multi-Center Study Group. Relationship of Fuchs …
A multicenter study to map genes for Fuchs endothelial corneal dystrophy: baseline characteristics and heritability.
PubMed ID: 22045388 Author(s): Louttit MD, Kopplin LJ, Igo RP Jr, Fondran JR, Tagliaferri A, Bardenstein D, Aldave AJ, Croasdale CR, Price MO, Rosenwasser GO, Lass JH, Iyengar SK; FECD Genetics Multi-Center Study Group. A …
Differing roles for TCF4 and COL8A2 in central corneal thickness and fuchs endothelial corneal dystrophy.
PubMed ID: 23110055 Author(s): Igo RP Jr, Kopplin LJ, Joseph P, Truitt B, Fondran J, Bardenstein D, Aldave AJ, Croasdale CR, Price MO, Rosenwasser M, Lass JH, Iyengar SK; FECD Genetics Multi-center Study Group. Differing …
A 32 kb critical region excluding Y402H in CFH mediates risk for age-related macular degeneration.
PubMed ID: 22022419 Author(s): Sivakumaran TA, Igo RP Jr, Kidd JM, Itsara A, Kopplin LJ, Chen W, Hagstrom SA, Peachey NS, Francis PJ, Klein ML, Chew EY, Ramprasad VL, Tay WT, Mitchell P, Seielstad M, …
Genome-wide association identifies SKIV2L and MYRIP as protective factors for age-related macular degeneration.
PubMed ID: 20861866 Author(s): Kopplin LJ, Igo RP Jr, Wang Y, Sivakumaran TA, Hagstrom SA, Peachey NS, Francis PJ, Klein ML, SanGiovanni JP, Chew EY, Pauer GJ, Sturgill GM, Joshi T, Tian L, Xi Q, …
Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing.
PubMed ID: 16188589 Author(s): Tester DJ, Kopplin LJ, Will ML, Ackerman MJ. Spectrum and prevalence of cardiac ryanodine receptor (RyR2) mutations in a cohort of unrelated patients referred explicitly for long QT syndrome genetic testing. …
Pathogenesis of unexplained drowning: new insights from a molecular autopsy.
PubMed ID: 15887426 Author(s): Tester DJ, Kopplin LJ, Creighton W, Burke AP, Ackerman MJ. Pathogenesis of unexplained drowning: new insights from a molecular autopsy. Mayo Clin Proc. 2005 May;80(5):596-600. PMID 15887426 Journal: Mayo Clinic Proceedings, …