Skip to Main Content

Author Details

Terry A Braun
University of Iowa
1999
61
30
PMIDPaper TitleJournal TitlePublished Year
37086329Assessing variants of uncertain significance implicated in hearing loss using a comprehensive deafness proteome.Hum Genet2023
34964109A splice site mutation in the TSEN2 causes a new syndrome with craniofacial and central nervous system malformations, and atypical hemolytic uremic syndrome.Clin Genet2022
33727600Creation and validation of models to predict response to primary treatment in serous ovarian cancer.Sci Rep2021
33650152Presacral neuroendocrine tumors associated with the Currarino syndrome.Am J Med Genet A2021
31619506A <i>TFAP2C</i> Gene Signature Is Predictive of Outcome in HER2-Positive Breast Cancer.Mol Cancer Res2020
31937620Gene Expression Signatures Identify Novel Therapeutics for Metastatic Pancreatic Neuroendocrine Tumors.Clin Cancer Res2020
30721156RABL6A inhibits tumor-suppressive PP2A/AKT signaling to drive pancreatic neuroendocrine tumor growth.J Clin Invest2019
31327459Structural Insights into Hearing Loss Genetics from Polarizable Protein Repacking.Biophys J2019
31208324Machine learning with the TCGA-HNSC dataset: improving usability by addressing inconsistency, sparsity, and high-dimensionality.BMC Bioinformatics2019
29154080Changes in gene expression in small bowel neuroendocrine tumors associated with progression to metastases.Surgery2018
30245029Genomic Landscape and Mutational Signatures of Deafness-Associated Genes.Am J Hum Genet2018
29486723Genomics of NSCLC patients both affirm PD-L1 expression and predict their clinical responses to anti-PD-1 immunotherapy.BMC Cancer2018
29649990Correction to: Genomics of NSCLC patients both affirm PD-L1 expression and predict their clinical responses to anti-PD-1 immunotherapy.BMC Cancer2018
28068412A Comparison of Gene Expression Profiles between Glucocorticoid Responder and Non-Responder Bovine Trabecular Meshwork Cells Using RNA Sequencing.PLoS One2017
28559085Clinically Focused Molecular Investigation of 1000 Consecutive Families with Inherited Retinal Disease.Ophthalmology2017
28030643Targeted Sequencing of FKBP5 in Suicide Attempters with Bipolar Disorder.PLoS One2016
26530094Audioprofile Surfaces: The 21st Century Audiogram.Ann Otol Rhinol Laryngol2016
25363634Heterozygous deep-intronic variants and deletions in ABCA4 in persons with retinal dystrophies and one exonic ABCA4 variant.Hum Mutat2015
25554686Esophageal cancer in a family with hamartomatous tumors and germline PTEN frameshift and SMAD7 missense mutations.Cancer Genet2015
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
25446321Transcriptomic analysis across nasal, temporal, and macular regions of human neural retina and RPE/choroid by RNA-Seq.Exp Eye Res2014
25262649Utilizing ethnic-specific differences in minor allele frequency to recategorize reported pathogenic deafness variants.Am J Hum Genet2014
25123904Cordova: web-based management of genetic variation data.Bioinformatics2014
24807808CEP290 gene transfer rescues Leber congenital amaurosis cellular phenotype.Gene Ther2014
24767545Optic nerve crush induces spatial and temporal gene expression patterns in retina and optic nerve of BALB/cJ mice.Mol Neurodegener2014
23280582AudioGene: predicting hearing loss genotypes from phenotypes to guide genetic screening.Hum Mutat2013
24265543Altered gene expression in dry age-related macular degeneration suggests early loss of choroidal endothelial cells.Mol Vis2013
23918662Non-exomic and synonymous variants in ABCA4 are an important cause of Stargardt disease.Hum Mol Genet2013
23991284Patient-specific iPSC-derived photoreceptor precursor cells as a means to investigate retinitis pigmentosa.Elife2013
23804846Advancing genetic testing for deafness with genomic technology.J Med Genet2013
23800383Progressive morphological changes and impaired retinal function associated with temporal regulation of gene expression after retinal ischemia/reperfusion injury in mice.Mol Neurodegener2013
23508994Prioritization of retinal disease genes: an integrative approach.Hum Mutat2013
23500522Exon-level expression profiling of ocular tissues.Exp Eye Res2013
23536807A genome-wide association study for primary open angle glaucoma and macular degeneration reveals novel Loci.PLoS One2013
22770688Informatics methods to enable sharing of quantitative imaging research data.Magn Reson Imaging2012
22975204Prediction of cochlear implant performance by genetic mutation: the spiral ganglion hypothesis.Hear Res2012
23055945Calpain-5 mutations cause autoimmune uveitis, retinal neovascularization, and photoreceptor degeneration.PLoS Genet2012
23158174Differentiation of small bowel and pancreatic neuroendocrine tumors by gene-expression profiling.Surgery2012
22785243Using the phenome and genome to improve genetic diagnosis for deafness.Otolaryngol Head Neck Surg2012
20981449Genome-wide analysis of copy number variants in age-related macular degeneration.Hum Genet2011
21520338DFNA8/12 caused by TECTA mutations is the most identified subtype of nonsyndromic autosomal dominant hearing loss.Hum Mutat2011
21310917Copy number variations and primary open-angle glaucoma.Invest Ophthalmol Vis Sci2011
21841894Multi-granularity Parallel Computing in a Genome-Scale Molecular Evolution Application.J Supercomput2009
18363168Evidence for a novel x-linked modifier locus for leber hereditary optic neuropathy.Ophthalmic Genet2008
18172923Transcript annotation prioritization and screening system (TrAPSS) for mutation screening.J Bioinform Comput Biol2007
16671097Genome-wide identification of pseudogenes capable of disease-causing gene conversion.Hum Mutat2006
16983098Regulation of gene expression in the mammalian eye and its relevance to eye disease.Proc Natl Acad Sci U S A2006
16395665Prioritizing regions of candidate genes for efficient mutation screening.Hum Mutat2006
16606853Homozygosity mapping with SNP arrays identifies TRIM32, an E3 ubiquitin ligase, as a Bardet-Biedl syndrome gene (BBS11).Proc Natl Acad Sci U S A2006
16636656Protein expression in a transformed trabecular meshwork cell line: proteome analysis.Mol Vis2006
  • 1 - 50 of 61

Recommended Authors

Moorfields Eye Hospital, UK UCL Institute of Ophthalmology, University College London
Career Start Year 2014
Number of shared co-authors 11
Institute of Molecular and Clinical Ophthalmology Basel (IOB)
Career Start Year 2014
Number of shared co-authors 2
Baylor College of Medicine
Career Start Year 2012
Number of shared co-authors 9
Instituto de Genetica Medica y Molecular (INGEMM), Hospital Universitario La Paz
Career Start Year 2008
Number of shared co-authors 0
Center for Data-Driven Discovery in Biomedicine, Children's Hospital of Philadelphia
Career Start Year 2007
Number of shared co-authors 7
National Human Genome Research Institute, National Institutes of Health
Career Start Year 2007
Number of shared co-authors 9
Children's Cancer Institute, Lowy Cancer Research Centre
Career Start Year 2006
Number of shared co-authors 1
Institute for Genomic Medicine, Nationwide Children's Hospital
Career Start Year 2005
Number of shared co-authors 10
Sanford School of Medicine, University of South Dakota
Career Start Year 2005
Number of shared co-authors 1
Regeneron Pharmaceuticals Inc.
Career Start Year 2004
Number of shared co-authors 8
Boston Children's Hospital, Seoul National University, Seoul National University Hospital
Career Start Year 2003
Number of shared co-authors 8
Columbia University
Career Start Year 2002
Number of shared co-authors 7
Mayo Clinic College of Medicine and Science
Career Start Year 2001
Number of shared co-authors 3
University of Washington
Career Start Year 2001
Number of shared co-authors 11
Broad Institute of MIT and Harvard
Career Start Year 2001
Number of shared co-authors 23
HudsonAlpha Institute for Biotechnology
Career Start Year 1999
Number of shared co-authors 14
Institute of Molecular and Clinical Ophthalmology Basel (IOB)
Career Start Year 1997
Number of shared co-authors 8
William Harvey Research Institute, Queen Mary University of London
Career Start Year 1997
Number of shared co-authors 13
University of Washington
Career Start Year 1997
Number of shared co-authors 8
University of Oxford
Career Start Year 1996
Number of shared co-authors 6
William Harvey Research Institute, Queen Mary University of London
Career Start Year 1996
Number of shared co-authors 9
William Harvey Research Institute, Queen Mary University of London
Career Start Year 1995
Number of shared co-authors 21
Heersink School of Medicine, The University of Alabama at Birmingham
Career Start Year 1995
Number of shared co-authors 7
University of Michigan ann arbor
Career Start Year 1995
Number of shared co-authors 1
university of california los angeles
Career Start Year 1993
Number of shared co-authors 14
David Geffen School of Medicine, University of California los angeles
Career Start Year 1992
Number of shared co-authors 1
Manchester University Hospitals NHS Foundation Trust, St Mary's Hospital
Career Start Year 1991
Number of shared co-authors 9
Baylor College of Medicine
Career Start Year 1988
Number of shared co-authors 27
Baylor College of Medicine
Career Start Year 1987
Number of shared co-authors 33
National Human Genome Research Institute, National Institutes of Health
Career Start Year 1985
Number of shared co-authors 7

Collaborators

The University of Iowa College of Nursing.
Co-authored papers 32
Carver College of Medicine, University of Iowa, USA Institute for Vision Research
Co-authored papers 24
the University of Iowa Carver College of Medicine
Co-authored papers 24
Carver College of Medicine, University of Iowa
Co-authored papers 23
Institute for Vision Research, Carver College of Medicine, University of Iowa
Co-authored papers 14
the University of Iowa Carver College of Medicine
Co-authored papers 9
North Texas Eye Research Institute, University of North Texas Health Science Center
Co-authored papers 8
Washington State University College of Veterinary Medicine
Co-authored papers 7
Co-authored papers 7
the University of Iowa Carver College of Medicine
Co-authored papers 5
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 5
Co-authored papers 4
Institute for Vision Research, Carver College of Medicine, University of Iowa
Co-authored papers 4
Institute for Vision Research, Carver College of Medicine, University of Iowa
Co-authored papers 3
Cleveland Institute for Computational Biology, Case Western Reserve University
Co-authored papers 3
University of Iowa Carver College of Medicine
Co-authored papers 3
Scheie Eye Institute, Perelman School of Medicine, University of Pennsylvania
Co-authored papers 3
Oregon Health & Science University
Co-authored papers 3
Cellworks Group Inc.
Co-authored papers 2
Korea Institute of Oriental Medicine
Co-authored papers 2
Casey Eye Institute, Oregon Health & Science University
Co-authored papers 2
North Texas Eye Research Institute, University North Texas Health Science Center
Co-authored papers 2
Vanderbilt University Medical Center, Tennessee Vanderbilt Genetics Institute
Co-authored papers 2
Co-authored papers 2
Maine Medical Center Research Institute
Co-authored papers 2
Co-authored papers 2
University of Pennsylvania
Co-authored papers 2
Cleveland Clinic.
Co-authored papers 2
Baylor College of Medicine
Co-authored papers 2
The Ohio State University
Co-authored papers 2