Eric D Wieben

Eric D Wieben

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Eric D Wieben

Eric D Wieben

Publications by authors named "Eric D Wieben"

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Autosomal dominant calpainopathy due to heterozygous CAPN3 C.643_663del21.

Muscle Nerve 2018 04 30;57(4):679-683. Epub 2017 Sep 30.

Department of Neurology, Mayo Clinic, 200 First Street SW, Rochester, Minnesota, 55905, USA.

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http://dx.doi.org/10.1002/mus.25970DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5915624PMC
April 2018

Repeat-Associated Non-ATG (RAN) Translation in Fuchs' Endothelial Corneal Dystrophy.

Invest Ophthalmol Vis Sci 2018 04;59(5):1888-1896

Department of Molecular Medicine, The Scripps Research Institute, La Jolla, California, United States.

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http://dx.doi.org/10.1167/iovs.17-23265DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5886103PMC
April 2018

Molecular Modeling and Functional Analysis of Exome Sequencing-Derived Variants of Unknown Significance Identify a Novel, Constitutively Active FGFR2 Mutant in Cholangiocarcinoma.

JCO Precis Oncol 2017 1;2017. Epub 2017 Aug 1.

David L. Marks, Tara L. Hogenson, Anne M. Vrabel, Ashley N. Sigafoos, Ezequiel J. Tolosa, Ryan M. Carr, Stephanie L. Safgren, Elisa Enriquez Hesles, Luciana L. Almada, Paola A. Romecin-Duran, Eriko Iguchi, Aryan Ala'Aldeen, Jean-Pierre A. Kocher, Gavin R. Oliver, Naresh Prodduturi, David W. Mead, Asif Hossain, Norine E. Huneke, Colleen M. Tagtow, Sikander Ailawadhi, Stephen M. Ansell, Michaela S. Banck, Asher A. Chanan-Khan, Ronald S. Go, Thorvardur R. Halfdanarson, Richard W. Joseph, Prashant Kapoor, Aaron S. Mansfield, Amulya A. Nageswara Rao, Grzegorz S. Nowakowski, Animesh Pardanani, Sameer A. Parikh, John C. Cheville, Andrew L. Feldman, Ramesh K. Ramanathan, Steven I. Robinson, Heidi D. Finnes, Jennifer B. McCormick, Robert R. McWilliams, Aminah Jatoi, Mrinal M. Patnaik, Eric D. Wieben, Tammy M. McAllister, Kandelaria M. Rumilla, Sarah E. Kerr, Konstantinos N. Lazaridis, Gianrico Farrugia, Karl J. Clark, Eric W. Klee, and Martin E. Fernandez-Zapico, Mayo Clinic, Rochester; Ernesto Resnik, Bio-Techne, Minneapolis, MN; Sikander Ailawadhi, Asher A. Chanan-Khan, and Richard W. Joseph, Mayo Clinic, Jacksonville, FL; Jan B. Egan, Alan H. Bryce, Estrella M. Carballido, KellyK. Curtis, Chelsea D. Gawryletz, Thai H. Ho,Nathalie Meurice, Ramesh K. Ramanathan, Raoul Tibes, Alvin C. Silva, A. Keith Stewart, and Mitesh J. Borad, Mayo Clinic, Phoenix, AZ; and Eileen J. Kennedy, University of Georgia, Athens, GA.

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http://dx.doi.org/10.1200/PO.17.00018DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6369924PMC
August 2017

Whole 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 Neurol 2016 Feb 6;55:46-51. Epub 2015 Nov 6.

Division of Cardiovascular Diseases, Department of Medicine, Mayo Clinic, Rochester, Minnesota; Department of Pediatric and Adolescent Medicine (Division of Pediatric Cardiology), Mayo Clinic, Rochester, Minnesota; Department of Molecular Pharmacology & Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota. Electronic address:

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http://dx.doi.org/10.1016/j.pediatrneurol.2015.10.014DOI Listing
February 2016

Recessive MYH6 Mutations in Hypoplastic Left Heart With Reduced Ejection Fraction.

Circ Cardiovasc Genet 2015 Aug 17;8(4):564-71. Epub 2015 Jun 17.

From the Cardiovascular Genetics Research Laboratory (J.L.T., T.M.O.), Division of Pediatric Cardiology, Department of Pediatric and Adolescent Medicine (M.Y.Q., P.W.O'L., T.M.O.), Division of Cardiovascular Diseases, Department of Internal Medicine (T.M.O.), Departments of Health Sciences Research and Biomedical Statistics and Informatics (M.T.Z., J.M.E.), Medical Genome Facility (B.W.E., E.D.W.), and Department of Biochemistry and Molecular Biology (E.D.W.), Mayo Clinic, Rochester, MN.

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http://dx.doi.org/10.1161/CIRCGENETICS.115.001070DOI Listing
August 2015

How well do whole exome sequencing results correlate with medical findings? A study of 89 Mayo Clinic Biobank samples.

Front Genet 2015 24;6:244. Epub 2015 Jul 24.

Center for Individualized Medicine, Mayo Clinic Rochester, MN, USA ; Department of Laboratory Medicine and Pathology, Mayo Clinic Rochester, MN, USA.

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http://dx.doi.org/10.3389/fgene.2015.00244DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4513238PMC
August 2015

Case-only exome sequencing and complex disease susceptibility gene discovery: study design considerations.

J Med Genet 2015 Jan 4;52(1):10-6. Epub 2014 Nov 4.

Department of Health Sciences Research, Mayo Clinic, Rochester, Minnesota, USA.

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http://dx.doi.org/10.1136/jmedgenet-2014-102697DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4503357PMC
January 2015

TNNI3K mutation in familial syndrome of conduction system disease, atrial tachyarrhythmia and dilated cardiomyopathy.

Hum Mol Genet 2014 Nov 11;23(21):5793-804. Epub 2014 Jun 11.

Cardiovascular Genetics Research Laboratory, Division of Pediatric Cardiology, Department of Pediatric and Adolescent Medicine,

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http://dx.doi.org/10.1093/hmg/ddu297DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4189907PMC
November 2014

Novel de novo heterozygous FGFR1 mutation in two siblings with Hartsfield syndrome: a case of gonadal mosaicism.

Am J Med Genet A 2014 Sep 28;164A(9):2356-9. Epub 2014 May 28.

Department of Medical Genetics, Mayo Clinic, Rochester, Minnesota.

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http://dx.doi.org/10.1002/ajmg.a.36621DOI Listing
September 2014

Promoter-proximal transcription factor binding is transcriptionally active when coupled with nucleosome repositioning in immediate vicinity.

Nucleic Acids Res 2014 Sep 31;42(15):9602-11. Epub 2014 Jul 31.

GNR Center for Genome Informatics, Institute of Genomics and Integrative Biology, Delhi, India Proteomics and Structural Biology Unit, Institute of Genomics and Integrative Biology, Delhi, India

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http://dx.doi.org/10.1093/nar/gku596DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4150765PMC
September 2014

PredictSNP: robust and accurate consensus classifier for prediction of disease-related mutations.

PLoS Comput Biol 2014 Jan 16;10(1):e1003440. Epub 2014 Jan 16.

Loschmidt Laboratories, Department of Experimental Biology and Research Centre for Toxic Compounds in the Environment, Faculty of Science, Masaryk University, Brno, Czech Republic ; Center of Biomolecular and Cellular Engineering, International Centre for Clinical Research, St. Anne's University Hospital Brno, Brno, Czech Republic.

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http://dx.doi.org/10.1371/journal.pcbi.1003440DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3894168PMC
January 2014

Serine hydroxymethyltransferase 1 and 2: gene sequence variation and functional genomic characterization.

J Neurochem 2012 Mar 6;120(6):881-90. Epub 2012 Feb 6.

Division of Clinical Pharmacology, Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota, USA.

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http://dx.doi.org/10.1111/j.1471-4159.2012.07646.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3296836PMC
March 2012

Hereditary hyperferritinemia-cataract syndrome in two large multigenerational American families.

J AAPOS 2011 Aug;15(4):356-61

College of Medicine, Mayo Clinic and Mayo Foundation, Rochester, Minnesota 55905, USA.

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http://dx.doi.org/10.1016/j.jaapos.2011.03.020DOI Listing
August 2011

Myosin individualized: single nucleotide polymorphisms in energy transduction.

BMC Genomics 2010 Mar 15;11:172. Epub 2010 Mar 15.

Department of Biochemistry and Molecular Biology, Mayo Clinic Rochester, 200 First Street SW, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1186/1471-2164-11-172DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2848645PMC
March 2010

3' tag digital gene expression profiling of human brain and universal reference RNA using Illumina Genome Analyzer.

BMC Genomics 2009 Nov 16;10:531. Epub 2009 Nov 16.

Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo Clinic, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1186/1471-2164-10-531DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2781828PMC
November 2009

Human S-adenosylhomocysteine hydrolase: common gene sequence variation and functional genomic characterization.

J Neurochem 2009 Sep 8;110(6):1806-17. Epub 2009 Jul 8.

Division of Clinical Pharmacology, Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic-Mayo Medical School, Rochester, Minnesota 55905, USA.

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http://dx.doi.org/10.1111/j.1471-4159.2009.06276.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2838417PMC
September 2009

Human glucocorticoid receptor alpha gene (NR3C1) pharmacogenomics: gene resequencing and functional genomics.

J Clin Endocrinol Metab 2009 Aug 12;94(8):3072-84. Epub 2009 May 12.

Division of Clinical Pharmacology, Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.

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https://academic.oup.com/jcem/article-lookup/doi/10.1210/jc.
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http://dx.doi.org/10.1210/jc.2008-2109DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2730876PMC
August 2009

Cytosolic 5'-nucleotidase III (NT5C3): gene sequence variation and functional genomics.

Pharmacogenet Genomics 2009 Aug;19(8):567-76

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, Rochester, Minnesota 55905, USA.

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http://dx.doi.org/10.1097/FPC.0b013e32832c14b8DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2763634PMC
August 2009

Sequence variations of the human MPDZ gene and association with alcoholism in subjects with European ancestry.

Alcohol Clin Exp Res 2009 Apr 21;33(4):712-21. Epub 2009 Jan 21.

Department of Psychiatry and Psychology, Mayo Clinic, Rochester, Minnesota 55905, USA.

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http://dx.doi.org/10.1111/j.1530-0277.2008.00888.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2819379PMC
April 2009

Human betaine-homocysteine methyltransferase (BHMT) and BHMT2: common gene sequence variation and functional characterization.

Mol Genet Metab 2008 Jul 23;94(3):326-35. Epub 2008 May 23.

Division of Clinical Pharmacology, Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, 200 First Street SW, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1016/j.ymgme.2008.03.013DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2515933PMC
July 2008

Dok-7 myasthenia: phenotypic and molecular genetic studies in 16 patients.

Ann Neurol 2008 Jul;64(1):71-87

Department of Neurology and Neuromuscular Research Laboratory, Mayo Clinic, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1002/ana.21408DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2570015PMC
July 2008

Proteasome beta subunit pharmacogenomics: gene resequencing and functional genomics.

Clin Cancer Res 2008 Jun;14(11):3503-13

Division of Clinical Pharmacology, Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic, 200 First Street Southwest, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1158/1078-0432.CCR-07-5150DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2778274PMC
June 2008

Glutathione s-transferase p1: gene sequence variation and functional genomic studies.

Cancer Res 2008 Jun;68(12):4791-801

Division of Clinical Pharmacology, Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Medical School-Mayo Clinic, Rochester, Minnesota, USA.

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http://dx.doi.org/10.1158/0008-5472.CAN-07-6724DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2490824PMC
June 2008

Glutathione S-transferase T1 and M1: gene sequence variation and functional genomics.

Clin Cancer Res 2007 Dec;13(23):7207-16

Division of Clinical Pharmacology, Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, Rochester, Minnesota 55905, USA.

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http://clincancerres.aacrjournals.org/cgi/doi/10.1158/1078-0
Publisher Site
http://dx.doi.org/10.1158/1078-0432.CCR-07-0635DOI Listing
December 2007

Human hydroxysteroid sulfotransferase SULT2B1 pharmacogenomics: gene sequence variation and functional genomics.

J Pharmacol Exp Ther 2007 Aug 11;322(2):529-40. Epub 2007 May 11.

Division of Clinical Pharmacology, Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1124/jpet.107.122895DOI Listing
August 2007

Glutathione S-transferase omega 1 and omega 2 pharmacogenomics.

Drug Metab Dispos 2006 Jul 25;34(7):1237-46. Epub 2006 Apr 25.

Division of Clinical Pharmacology, Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1124/dmd.106.009613DOI Listing
July 2006

Human methylenetetrahydrofolate reductase pharmacogenomics: gene resequencing and functional genomics.

Pharmacogenet Genomics 2006 Apr;16(4):265-77

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1097/01.fpc.0000194423.20393.08DOI Listing
April 2006

Human arsenic methyltransferase (AS3MT) pharmacogenetics: gene resequencing and functional genomics studies.

J Biol Chem 2006 Mar 6;281(11):7364-73. Epub 2006 Jan 6.

Division of Clinical Pharmacology, Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Clinic College of Medicine, 200 First Street SW, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1074/jbc.M512227200DOI Listing
March 2006

Human phenylethanolamine N-methyltransferase pharmacogenomics: gene re-sequencing and functional genomics.

J Neurochem 2005 Dec 8;95(6):1766-76. Epub 2005 Nov 8.

Department of Molecular Pharmacology & Experimental Therapeutics, Mayo Clinic College of Medicine, Rochester, Minnesota, USA.

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http://doi.wiley.com/10.1111/j.1471-4159.2005.03453.x
Publisher Site
http://dx.doi.org/10.1111/j.1471-4159.2005.03453.xDOI Listing
December 2005

Human aromatase: gene resequencing and functional genomics.

Cancer Res 2005 Dec;65(23):11071-82

Department of Medical Oncology, Mayo Clinic College of Medicine, Rochester, Minnesota 55905, USA.

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http://dx.doi.org/10.1158/0008-5472.CAN-05-1218DOI Listing
December 2005

Human SULT1A3 pharmacogenetics: gene duplication and functional genomic studies.

Biochem Biophys Res Commun 2004 Sep;321(4):870-8

Department of Molecular Pharmacology, Mayo Clinic College of Medicine, Mayo Foundation, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1016/j.bbrc.2004.07.038DOI Listing
September 2004

Human catecholamine sulfotransferase (SULT1A3) pharmacogenetics: functional genetic polymorphism.

J Neurochem 2003 Nov;87(4):809-19

Department of Molecular Pharmacology & Experimental Therapeutics, Mayo Medical School-Mayo Clinic, Rochester, Minnesota 55905, USA.

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http://dx.doi.org/10.1046/j.1471-4159.2003.02027.xDOI Listing
November 2003

Human estrogen sulfotransferase (SULT1E1) pharmacogenomics: gene resequencing and functional genomics.

Br J Pharmacol 2003 Aug;139(8):1373-82

Department of Molecular Pharmacology & Experimental Therapeutics, Mayo Medical School-Mayo Clinic-Mayo Foundation, Rochester, MN 55905, U.S.A.

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http://dx.doi.org/10.1038/sj.bjp.0705369DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1573968PMC
August 2003

Pharmacogenetics of human 3'-phosphoadenosine 5'-phosphosulfate synthetase 1 (PAPSS1): gene resequencing, sequence variation, and functional genomics.

Biochem Pharmacol 2003 Jun;65(11):1787-96

Department of Molecular Pharmacology and Experimental Therapeutics, Mayo Medical School-Mayo Clinic-Mayo Foundation, Rochester, MN 55905, USA.

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http://dx.doi.org/10.1016/s0006-2952(03)00104-7DOI Listing
June 2003

Primer on medical genomics. Part VII: The evolving concept of the gene.

Authors:
Eric D Wieben

Mayo Clin Proc 2003 May;78(5):580-7

Department of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, Minn 55905, USA.

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http://dx.doi.org/10.4065/78.5.580DOI Listing
May 2003

Primer on medical genomics. Part IV: Expression proteomics.

Mayo Clin Proc 2002 Nov;77(11):1185-96

Division of Hematology and Internal Medicine, Mayo Clinic, Rochester, Minn 55905, USA.

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http://dx.doi.org/10.4065/77.11.1185DOI Listing
November 2002

Primer on medical genomics. Part III: Microarray experiments and data analysis.

Mayo Clin Proc 2002 Sep;77(9):927-40

Division of Hematology and Internal Medicine, Mayo Clinic, Rochester, Minn 55905, USA.

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http://dx.doi.org/10.4065/77.9.927DOI Listing
September 2002

Primer on medical genomics part I: History of genetics and sequencing of the human genome.

Mayo Clin Proc 2002 Aug;77(8):773-82

Division of Laboratory Genetics, Mayo Clinic, Rochester, Minn 55905, USA.

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http://dx.doi.org/10.4065/77.8.773DOI Listing
August 2002

Primer on medical genomics part II: Background principles and methods in molecular genetics.

Mayo Clin Proc 2002 Aug;77(8):785-808

Division of Hematology and Internal Medicine, Mayo Clinic, Rochester, Minn 55905, USA.

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http://dx.doi.org/10.4065/77.8.785DOI Listing
August 2002