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Common variants at 9p21 and 8q22 are associated with increased susceptibility to optic nerve degeneration in glaucoma.
PLoS Genet. 2012;8(4):e1002654. doi: 10.1371/journal.pgen.1002654. Epub 2012 Apr 26.
PLoS Genet. 2012.
PMID: 22570617
Free PMC article.
Mutations in TCF8 cause posterior polymorphous corneal dystrophy and ectopic expression of COL4A3 by corneal endothelial cells.
Krafchak CM, Pawar H, Moroi SE, Sugar A, Lichter PR, Mackey DA, Mian S, Nairus T, Elner V, Schteingart MT, Downs CA, Kijek TG, Johnson JM, Trager EH, Rozsa FW, Mandal MN, Epstein MP, Vollrath D, Ayyagari R, Boehnke M, Richards JE.
Krafchak CM, et al. Among authors: trager eh.
Am J Hum Genet. 2005 Nov;77(5):694-708. doi: 10.1086/497348. Epub 2005 Sep 14.
Am J Hum Genet. 2005.
PMID: 16252232
Free PMC article.
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A locus for posterior polymorphous corneal dystrophy (PPCD3) maps to chromosome 10.
Shimizu S, Krafchak C, Fuse N, Epstein MP, Schteingart MT, Sugar A, Eibschitz-Tsimhoni M, Downs CA, Rozsa F, Trager EH, Reed DM, Boehnke M, Moroi SE, Richards JE.
Shimizu S, et al. Among authors: trager eh.
Am J Med Genet A. 2004 Nov 1;130A(4):372-7. doi: 10.1002/ajmg.a.30267.
Am J Med Genet A. 2004.
PMID: 15384081
Free PMC article.
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Age-related macular degeneration: a high-resolution genome scan for susceptibility loci in a population enriched for late-stage disease.
Abecasis GR, Yashar BM, Zhao Y, Ghiasvand NM, Zareparsi S, Branham KE, Reddick AC, Trager EH, Yoshida S, Bahling J, Filippova E, Elner S, Johnson MW, Vine AK, Sieving PA, Jacobson SG, Richards JE, Swaroop A.
Abecasis GR, et al. Among authors: trager eh.
Am J Hum Genet. 2004 Mar;74(3):482-94. doi: 10.1086/382786. Epub 2004 Feb 16.
Am J Hum Genet. 2004.
PMID: 14968411
Free PMC article.
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Madeline 2.0 PDE: a new program for local and web-based pedigree drawing.
Trager EH, Khanna R, Marrs A, Siden L, Branham KE, Swaroop A, Richards JE.
Trager EH, et al.
Bioinformatics. 2007 Jul 15;23(14):1854-6. doi: 10.1093/bioinformatics/btm242. Epub 2007 May 8.
Bioinformatics. 2007.
PMID: 17488757
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Evaluation of an Algorithm for Identifying Ocular Conditions in Electronic Health Record Data.
Stein JD, Rahman M, Andrews C, Ehrlich JR, Kamat S, Shah M, Boese EA, Woodward MA, Cowall J, Trager EH, Narayanaswamy P, Hanauer DA.
Stein JD, et al. Among authors: trager eh.
JAMA Ophthalmol. 2019 May 1;137(5):491-497. doi: 10.1001/jamaophthalmol.2018.7051.
JAMA Ophthalmol. 2019.
PMID: 30789656
Free PMC article.
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Mutations in a BTB-Kelch protein, KLHL7, cause autosomal-dominant retinitis pigmentosa.
Friedman JS, Ray JW, Waseem N, Johnson K, Brooks MJ, Hugosson T, Breuer D, Branham KE, Krauth DS, Bowne SJ, Sullivan LS, Ponjavic V, Gränse L, Khanna R, Trager EH, Gieser LM, Hughbanks-Wheaton D, Cojocaru RI, Ghiasvand NM, Chakarova CF, Abrahamson M, Göring HH, Webster AR, Birch DG, Abecasis GR, Fann Y, Bhattacharya SS, Daiger SP, Heckenlively JR, Andréasson S, Swaroop A.
Friedman JS, et al. Among authors: trager eh.
Am J Hum Genet. 2009 Jun;84(6):792-800. doi: 10.1016/j.ajhg.2009.05.007.
Am J Hum Genet. 2009.
PMID: 19520207
Free PMC article.
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The Finland-United States investigation of non-insulin-dependent diabetes mellitus genetics (FUSION) study. II. An autosomal genome scan for diabetes-related quantitative-trait loci.
Watanabe RM, Ghosh S, Langefeld CD, Valle TT, Hauser ER, Magnuson VL, Mohlke KL, Silander K, Ally DS, Chines P, Blaschak-Harvan J, Douglas JA, Duren WL, Epstein MP, Fingerlin TE, Kaleta HS, Lange EM, Li C, McEachin RC, Stringham HM, Trager E, White PP, Balow J Jr, Birznieks G, Chang J, Eldridge W.
Watanabe RM, et al.
Am J Hum Genet. 2000 Nov;67(5):1186-200. Epub 2000 Oct 13.
Am J Hum Genet. 2000.
PMID: 11032784
Free PMC article.
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