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Author Details

Eric D Wieben
Mayo Clinic Rochester
1979
171
50
PMIDPaper TitleJournal TitlePublished Year
35923324Genomic epidemiology reveals the dominance of Hennepin County in transmission of SARS-CoV-2 in Minnesota from 2020-2022.medRxiv2023
37086467εγ-Thalassemia, a New Hemoglobinopathy Category.Clin Chem2023
32735996TCF4-mediated Fuchs endothelial corneal dystrophy: Insights into a common trinucleotide repeat-associated disease.Prog Retin Eye Res2021
33782268Relationship of Body Mass Index With Fuchs Endothelial Corneal Dystrophy Severity and TCF4 CTG18.1 Trinucleotide Repeat Expansion.Cornea2021
33889947Long-read targeted sequencing uncovers clinicopathological associations for C9orf72-linked diseases.Brain2021
34855896Comparison of TCF4 repeat expansion length in corneal endothelium and leukocytes of patients with Fuchs endothelial corneal dystrophy.PLoS One2021
34587219Characterization of a dual media system for culturing primary normal and Fuchs endothelial corneal dystrophy (FECD) endothelial cells.PLoS One2021
34839893Improved Characterization of Complex β-Globin Gene Cluster Structural Variants Using Long-Read Sequencing.J Mol Diagn2021
33435129Identification of Possible Risk Variants of Familial Strabismus Using Exome Sequencing Analysis.Genes (Basel)2021
33444430Disease Expression and Familial Transmission of Fuchs Endothelial Corneal Dystrophy With and Without CTG18.1 Expansion.Invest Ophthalmol Vis Sci2021
33387698Chromosomal Junction Detection from Whole-Genome Sequencing on Formalin-Fixed, Paraffin-Embedded Tumors.J Mol Diagn2021
32224270Transplant chimerism in porcine structural vascularized bone allotransplants.Gene2020
30663199Familial chronic megacolon presenting in childhood or adulthood: Seeking the presumed gene association.Neurogastroenterol Motil2019
31847808Correction to: Recommendations for performance optimizations when using GATK3.8 and GATK4.BMC Bioinformatics2019
31703611Recommendations for performance optimizations when using GATK3.8 and GATK4.BMC Bioinformatics2019
31469403Gene Expression and Missplicing in the Corneal Endothelium of Patients With a TCF4 Trinucleotide Repeat Expansion Without Fuchs' Endothelial Corneal Dystrophy.Invest Ophthalmol Vis Sci2019
31481971Sentieon DNASeq Variant Calling Workflow Demonstrates Strong Computational Performance and Accuracy.Front Genet2019
31276570Amplification-free long-read sequencing of TCF4 expanded trinucleotide repeats in Fuchs Endothelial Corneal Dystrophy.PLoS One2019
30811544Effect of Trinucleotide Repeat Expansion on the Expression of TCF4 mRNA in Fuchs' Endothelial Corneal Dystrophy.Invest Ophthalmol Vis Sci2019
30973406Association of rs613872 and Trinucleotide Repeat Expansion in the TCF4 Gene of German Patients With Fuchs Endothelial Corneal Dystrophy.Cornea2019
28881388Autosomal dominant calpainopathy due to heterozygous CAPN3 C.643_663del21.Muscle Nerve2018
30025114Fuchs' Endothelial Corneal Dystrophy in Patients With Myotonic Dystrophy, Type 1.Invest Ophthalmol Vis Sci2018
29966009Gene expression in the corneal endothelium of Fuchs endothelial corneal dystrophy patients with and without expansion of a trinucleotide repeat in TCF4.PLoS One2018
30038052<i>CDKN2A</i> Germline Rare Coding Variants and Risk of Pancreatic Cancer in Minority Populations.Cancer Epidemiol Biomarkers Prev2018
29671115Utility of DNA, RNA, Protein, and Functional Approaches to Solve Cryptic Immunodeficiencies.J Clin Immunol2018
29599744Myopathy With <i>SQSTM1</i> and <i>TIA1</i> Variants: Clinical and Pathological Features.Front Neurol2018
29677349Repeat-Associated Non-ATG (RAN) Translation in Fuchs' Endothelial Corneal Dystrophy.Invest Ophthalmol Vis Sci2018
29069303A prospective genome-wide study of prostate cancer metastases reveals association of wnt pathway activation and increased cell cycle proliferation with primary resistance to abiraterone acetate-prednisone.Ann Oncol2018
28057009Erratum to: Conserved recurrent gene mutations correlate with pathway deregulation and clinical outcomes of lung adenocarcinoma in never-smokers.BMC Med Genomics2017
30761385Molecular Modeling and Functional Analysis of Exome Sequencing-Derived Variants of Unknown Significance Identify a Novel, Constitutively Active FGFR2 Mutant in Cholangiocarcinoma.JCO Precis Oncol2017
28412739Retinoic acid receptor alpha drives cell cycle progression and is associated with increased sensitivity to retinoids in T-cell lymphoma.Oncotarget2017
28376176Tumor Sequencing and Patient-Derived Xenografts in the Neoadjuvant Treatment of Breast Cancer.J Natl Cancer Inst2017
28473535Androgen Receptor Variant AR-V9 Is Coexpressed with AR-V7 in Prostate Cancer Metastases and Predicts Abiraterone Resistance.Clin Cancer Res2017
28118661Trinucleotide Repeat Expansion in the Transcription Factor 4 (TCF4) Gene Leads to Widespread mRNA Splicing Changes in Fuchs' Endothelial Corneal Dystrophy.Invest Ophthalmol Vis Sci2017
29178655RYR1 causing distal myopathy.Mol Genet Genomic Med2017
26944241Outcome of Whole Exome Sequencing for Diagnostic Odyssey Cases of an Individualized Medicine Clinic: The Mayo Clinic Experience.Mayo Clin Proc2016
26739101Whole Exome Sequencing and Heterologous Cellular Electrophysiology Studies Elucidate a Novel Loss-of-Function Mutation in the CACNA1A-Encoded Neuronal P/Q-Type Calcium Channel in a Child With Congenital Hypotonia and Developmental Delay.Pediatr Neurol2016
25371537Case-only exome sequencing and complex disease susceptibility gene discovery: study design considerations.J Med Genet2015
26434960Whole-Exome Sequencing of 10 Scientists: Evaluation of the Process and Outcomes.Mayo Clin Proc2015
26296701Exome sequencing reveals frequent deleterious germline variants in cancer susceptibility genes in women with invasive breast cancer undergoing neoadjuvant chemotherapy.Breast Cancer Res Treat2015
26257771How well do whole exome sequencing results correlate with medical findings? A study of 89 Mayo Clinic Biobank samples.Front Genet2015
26695660Mutational Landscapes of Sequential Prostate Metastases and Matched Patient Derived Xenografts during Enzalutamide Therapy.PLoS One2015
26218914Trinucleotide Repeat Expansion in the TCF4 Gene in Fuchs' Endothelial Corneal Dystrophy in Japanese.Invest Ophthalmol Vis Sci2015
26085007Recessive MYH6 Mutations in Hypoplastic Left Heart With Reduced Ejection Fraction.Circ Cardiovasc Genet2015
25985019Common Oncogene Mutations and Novel SND1-BRAF Transcript Fusion in Lung Adenocarcinoma from Never Smokers.Sci Rep2015
25593321RNA toxicity and missplicing in the common eye disease fuchs endothelial corneal dystrophy.J Biol Chem2015
24388019Preemptive genotyping for personalized medicine: design of the right drug, right dose, right time-using genomic data to individualize treatment protocol.Mayo Clin Proc2014
25168903Comprehensive assessment of genetic variants within TCF4 in Fuchs' endothelial corneal dystrophy.Invest Ophthalmol Vis Sci2014
25081206Promoter-proximal transcription factor binding is transcriptionally active when coupled with nucleosome repositioning in immediate vicinity.Nucleic Acids Res2014
25105010Clinical biomarkers of pulmonary carcinoid tumors in never smokers via profiling miRNA and target mRNA.Cell Biosci2014
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Collaborators

Mayo Clinic
Co-authored papers 46
Mayo Clinic
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Mayo Clinic College of Medicine and Science
Co-authored papers 14
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Mayo Clinic
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H. Lee Moffitt Cancer Center and Research Institute
Co-authored papers 7
Mayo Clinic Gastroenterology and Hepatology, Mayo Clinic
Co-authored papers 7
Mayo Clinic
Co-authored papers 6
Mayo Clinic
Co-authored papers 6
Mayo Clinic
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Mayo Clinic
Co-authored papers 6
Center for Individualized Medicine, Mayo Clinic Rochester
Co-authored papers 5
Center for Individualized Medicine, Mayo Clinic
Co-authored papers 5
Mayo Clinic
Co-authored papers 5
Mayo Clinic
Co-authored papers 5
Penn State College of Medicine
Co-authored papers 5
Mayo Clinic
Co-authored papers 4
Mayo Clinic
Co-authored papers 4
Marshfield Clinic Research Institute
Co-authored papers 4
Mayo Clinic
Co-authored papers 4
Mayo Clinic
Co-authored papers 4
Mayo Clinic
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Mayo Clinic
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Mayo Clinic
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Mayo Clinic
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H. Lee Moffitt Cancer Center
Co-authored papers 3
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