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Author Details

Todd E Scheetz
the University of Iowa Carver College of Medicine
2000
133
42
PMIDPaper TitleJournal TitlePublished Year
37224920Mutations in EFEMP1 in Patients with Juvenile Open-Angle Glaucoma.Ophthalmol Glaucoma2023
37589989GJA3 Genetic Variation and Autosomal Dominant Congenital Cataracts and Glaucoma Following Cataract Surgery.JAMA Ophthalmol2023
37878301Gene Expression Within a Human Choroidal Neovascular Membrane Using Spatial Transcriptomics.Invest Ophthalmol Vis Sci2023
37645858Polygenic Risk Score Improves Prediction of Primary Open Angle Glaucoma Onset in the Ocular Hypertension Treatment Study.medRxiv2023
37398429GENE EXPRESSION WITHIN A HUMAN CHOROIDAL NEOVASCULAR MEMBRANE USING SPATIAL TRANSCRIPTOMICS.bioRxiv2023
37327471Thrombospondin Mutations and Patients With Primary Congenital Glaucoma in a United States Population.J Glaucoma2023
31764884AUTOIMMUNE RETINOPATHY MIMICKING HERITABLE RETINAL DEGENERATION IN A PATIENT WITH COMMON VARIABLE IMMUNE DEFICIENCY.Retin Cases Brief Rep2022
35181781Choroidal endothelial and macrophage gene expression in atrophic and neovascular macular degeneration.Hum Mol Genet2022
34929400Retinal ciliopathies through the lens of Bardet-Biedl Syndrome: Past, present and future.Prog Retin Eye Res2022
34590675Sensitive quantification of m.3243A>G mutational proportion in non-retinal tissues and its relationship with visual symptoms.Hum Mol Genet2022
33383180Single-cell RNA sequencing in vision research: Insights into human retinal health and disease.Prog Retin Eye Res2021
37672224Genetic Association between <i>MMP9</i> and Choroidal Neovascularization in Age-Related Macular Degeneration.Ophthalmol Sci2021
34251969Clinical albinism score, presence of nystagmus and optic nerves defects are correlated with visual outcome in patients with oculocutaneous albinism.Ophthalmic Genet2021
34157370Automated segmentation of choroidal layers from 3-dimensional macular optical coherence tomography scans.J Neurosci Methods2021
34014299Human photoreceptor cells from different macular subregions have distinct transcriptional profiles.Hum Mol Genet2021
34174832Exome-based investigation of the genetic basis of human pigmentary glaucoma.BMC Genomics2021
34083587Axonopathy precedes cell death in ocular damage mediated by blast exposure.Sci Rep2021
32069977Single-Cell RNA Sequencing in Human Retinal Degeneration Reveals Distinct Glial Cell Populations.Cells2020
32076077Transplantation of iPSC-TM stimulates division of trabecular meshwork cells in human eyes.Sci Rep2020
30816940Myocilin Mutations in Patients With Normal-Tension Glaucoma.JAMA Ophthalmol2019
31712411Single-cell transcriptomics of the human retinal pigment epithelium and choroid in health and macular degeneration.Proc Natl Acad Sci U S A2019
30927186Correlation between electroretinography, foveal anatomy and visual acuity in albinism.Doc Ophthalmol2019
29350691A novel mutation (LEU396ARG) in OPA1 is associated with a severe phenotype in a large dominant optic atrophy pedigree.Eye (Lond)2018
29486162Analysis of 14-3-3 isoforms expressed in photoreceptors.Exp Eye Res2018
28949775Evaluation of sFLT1 protein levels in human eyes with the FLT1 rs9943922 polymorphism.Ophthalmic Genet2018
27790711Transposon mutagenesis identifies candidate genes that cooperate with loss of transforming growth factor-beta signaling in mouse intestinal neoplasms.Int J Cancer2017
28400699LADD syndrome with glaucoma is caused by a novel gene.Mol Vis2017
29457131Keeping an Eye on Bardet-Biedl Syndrome: A Comprehensive Review of the Role of Bardet-Biedl Syndrome Genes in the Eye.Med Res Arch2017
28984711Genomic Organization of TBK1 Copy Number Variations in Glaucoma Patients.J Glaucoma2017
28559085Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease.Ophthalmology2017
27058611De Novo and Rare Variants at Multiple Loci Support the Oligogenic Origins of Atrioventricular Septal Heart Defects.PLoS Genet2016
26564985Molecular response of chorioretinal endothelial cells to complement injury: implications for macular degeneration.J Pathol2016
26507665North Carolina Macular Dystrophy Is Caused by Dysregulation of the Retinal Transcription Factor PRDM13.Ophthalmology2016
26530094Audioprofile Surfaces: The 21st Century Audiogram.Ann Otol Rhinol Laryngol2016
26474494Quantitative measurement of retinal ganglion cell populations via histology-based random forest classification.Exp Eye Res2016
26494905Hypomorphic mutations in TRNT1 cause retinitis pigmentosa with erythrocytic microcytosis.Hum Mol Genet2016
26283021RetFM-J, an ImageJ-based module for automated counting and quantifying features of nuclei in retinal whole-mounts.Exp Eye Res2016
27881886Tank-Binding Kinase 1 (<i>TBK1</i>) Gene and Open-Angle Glaucomas (An American Ophthalmological Society Thesis).Trans Am Ophthalmol Soc2016
27759018Corrigendum: Automated Axon Counting in Rodent Optic Nerve Sections with AxonJ.Sci Rep2016
27707548Glaucoma Risk Alleles in the Ocular Hypertension Treatment Study.Ophthalmology2016
27537365Correction: A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus).PLoS One2016
27480506A targeted sequencing study of glutamatergic candidate genes in suicide attempters with bipolar disorder.Am J Med Genet B Neuropsychiatr Genet2016
27149523A Mutation in LTBP2 Causes Congenital Glaucoma in Domestic Cats (Felis catus).PLoS One2016
27226405Automated Axon Counting in Rodent Optic Nerve Sections with AxonJ.Sci Rep2016
27275741SQSTM1 Mutations and Glaucoma.PLoS One2016
27060491A Homozygous Nme7 Mutation Is Associated with Situs Inversus Totalis.Hum Mutat2016
25581579Heterozygous triplication of upstream regulatory sequences leads to dysregulation of matrix metalloproteinase 19 in patients with cavitary optic disc anomaly.Hum Mutat2015
26392740Novel TMEM98 mutations in pedigrees with autosomal dominant nanophthalmos.Mol Vis2015
26106909Microarray Determination of the Expression of Drug Transporters in Humans and Animal Species Used for the Investigation of Nasal Absorption.Mol Pharm2015
26193923Stereo Photo Measured ONH Shape Predicts Development of POAG in Subjects With Ocular Hypertension.Invest Ophthalmol Vis Sci2015
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Collaborators

Carver College of Medicine, University of Iowa, USA Institute for Vision Research
Co-authored papers 49
The University of Iowa College of Nursing.
Co-authored papers 48
Carver College of Medicine, University of Iowa
Co-authored papers 30
the University of Iowa Carver College of Medicine
Co-authored papers 27
Institute for Vision Research, Carver College of Medicine, University of Iowa
Co-authored papers 26
University of Iowa
Co-authored papers 24
the University of Iowa Carver College of Medicine
Co-authored papers 16
Institute for Vision Research, Carver College of Medicine, University of Iowa
Co-authored papers 11
University of Iowa
Co-authored papers 11
Co-authored papers 8
Washington State University College of Veterinary Medicine
Co-authored papers 7
Shiley Eye Institute, university of california san diego
Co-authored papers 7
Einhorn Clinical Research Center, New York Eye and Ear Infirmary of Mount Sinai
Co-authored papers 5
Medical College of Wisconsin
Co-authored papers 4
University of Iowa Carver College of Medicine
Co-authored papers 4
University of Minnesota
Co-authored papers 4
Institute for Vision Research, Carver College of Medicine, University of Iowa
Co-authored papers 4
Co-authored papers 4
Baylor College of Medicine
Co-authored papers 4
North Texas Eye Research Institute, University of North Texas Health Science Center
Co-authored papers 4
Veterans Affairs Medical Center
Co-authored papers 3
Iowa State University, Mayo Clinic, Nationwide Children's Hospital, The Ohio State University College of Medicine, University of Iowa, Washington University in Saint Louis
Co-authored papers 3
Genomics Research Center
Co-authored papers 3
Vanderbilt University Medical Center, Tennessee Vanderbilt Genetics Institute
Co-authored papers 3
The Stephen A. Wynn Institute for Vision Research
Co-authored papers 3
University of Missouri School of Medicine
Co-authored papers 2
Co-authored papers 2
University of Illinois at Chicago
Co-authored papers 2
Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania
Co-authored papers 2
Co-authored papers 2