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Author Details

Jeaneen L Andorf
Institute for Vision Research, Carver College of Medicine, University of Iowa
2000
19
13
PMIDPaper TitleJournal TitlePublished Year
37106000Modeling rod and cone photoreceptor cell survival in vivo using optical coherence tomography.Sci Rep2023
37930186Demonstration of the pathogenicity of a common non-exomic mutation in ABCA4 using iPSC-derived retinal organoids and retrospective clinical data.Hum Mol Genet2023
37221451Propensity of Patient-Derived iPSCs for Retinal Differentiation: Implications for Autologous Cell Replacement.Stem Cells Transl Med2023
33243830Predominance of hyperopia in autosomal dominant Best vitelliform macular dystrophy.Br J Ophthalmol2022
30959774Correction of NR2E3 Associated Enhanced S-cone Syndrome Patient-specific iPSCs using CRISPR-Cas9.Genes (Basel)2019
31106594Development of a Molecularly Stable Gene Therapy Vector for the Treatment of <i>RPGR</i>-Associated X-Linked Retinitis Pigmentosa.Hum Gene Ther2019
28559085Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease.Ophthalmology2017
28619647Using CRISPR-Cas9 to Generate Gene-Corrected Autologous iPSCs for the Treatment of Inherited Retinal Degeneration.Mol Ther2017
24667040An international effort towards developing standards for best practices in analysis, interpretation and reporting of clinical genome sequencing results in the CLARITY Challenge.Genome Biol2014
23308101Union makes strength: a worldwide collaborative genetic and clinical study to provide a comprehensive survey of RD3 mutations and delineate the associated phenotype.PLoS One2013
23918662Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease.Hum Mol Genet2013
18779497Association of a novel mutation in the retinol dehydrogenase 12 (RDH12) gene with autosomal dominant retinitis pigmentosa.Arch Ophthalmol2008
17353431No association between variations in the WDR36 gene and primary open-angle glaucoma.Arch Ophthalmol2007
18024811ABCA4 mutations and discordant ABCA4 alleles in patients and siblings with bull's-eye maculopathy.Br J Ophthalmol2007
18172923Transcript annotation prioritization and screening system (TrAPSS) for mutation screening.J Bioinform Comput Biol2007
15539463Bbs2-null mice have neurosensory deficits, a defect in social dominance, and retinopathy associated with mislocalization of rhodopsin.Proc Natl Acad Sci U S A2004
12215093Variations in the myocilin gene in patients with open-angle glaucoma.Arch Ophthalmol2002
11133845Genomic organization and mutation analysis of the gene encoding lecithin retinol acyltransferase in human retinal pigment epithelium.Invest Ophthalmol Vis Sci2001
10766140Mutation analysis of 3 genes in patients with Leber congenital amaurosis.Arch Ophthalmol2000
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Collaborators

Edwin M Stone
Carver College of Medicine, University of Iowa, USA Institute for Vision Research
Co-authored papers 19
Val C Sheffield
Carver College of Medicine, University of Iowa
Co-authored papers 10
Robert F Mullins
the University of Iowa Carver College of Medicine
Co-authored papers 9
Budd A Tucker
the University of Iowa Carver College of Medicine
Co-authored papers 8
Adam P DeLuca
Institute for Vision Research, Carver College of Medicine, University of Iowa
Co-authored papers 6
Terry A Braun
University of Iowa
Co-authored papers 4
Todd E Scheetz
the University of Iowa Carver College of Medicine
Co-authored papers 4
S Scott Whitmore
Institute for Vision Research, Carver College of Medicine, University of Iowa
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Richard G Weleber
Casey Eye Institute, Oregon Health & Science University
Co-authored papers 2
Byron L Lam
Bascom Palmer Eye Institute
Co-authored papers 2
Gerald A Fishman
University of Illinois at Chicago
Co-authored papers 2
Samuel G Jacobson
Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania
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University of Southampton
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Christopher R Pierson
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Michael F Murray
Yale School of Medicine
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Anne E Kwitek
Medical College of Wisconsin
Co-authored papers 1
Gustavo Glusman
Institute for Systems Biology
Co-authored papers 1
Barry Moore
Utah Center for Genetic Discovery, University of Utah
Co-authored papers 1
Isaac S Kohane
Harvard Medical School
Co-authored papers 1
Matthew S Lebo
Harvard Medical School, Brigham and Women's Hospital
Co-authored papers 1
Peter Freisinger
Hospital Reutlingen
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Abbot F Clark
North Texas Eye Research Institute, University of North Texas Health Science Center
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Bruce E Bray
University of Utah School of Medicine
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Thomas L Casavant
The University of Iowa College of Nursing.
Co-authored papers 1
Shamil R Sunyaev
Harvard Medical School
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The Ohio State University
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