Jared M Evans

Jared M Evans

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Jared M Evans

Jared M Evans

Publications by authors named "Jared M Evans"

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Rare Missense Variants in TLN1 Are Associated With Familial and Sporadic Spontaneous Coronary Artery Dissection.

Circ Genom Precis Med 2019 Apr 19;12(4):e002437. Epub 2019 Mar 19.

Cardiovascular Genetics Research Laboratory (T.N.T., J.L.T., R.S.S., T.M.O.), Mayo Clinic, Rochester, MN.

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http://dx.doi.org/10.1161/CIRCGEN.118.002437DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6625931PMC
April 2019

Noncardiac genetic predisposition in sudden infant death syndrome.

Genet Med 2019 03 24;21(3):641-649. Epub 2018 Aug 24.

Molecular and Clinical Sciences Research Institute, St George's University of London, London, United Kingdom.

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http://www.nature.com/articles/s41436-018-0131-4
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http://dx.doi.org/10.1038/s41436-018-0131-4DOI Listing
March 2019

Exome-Wide Rare Variant Analyses in Sudden Infant Death Syndrome.

J Pediatr 2018 12 26;203:423-428.e11. Epub 2018 Sep 26.

Department of Cardiovascular Medicine (Division of Heart Rhythm Services), Pediatrics (Division of Pediatric Cardiology), Molecular Pharmacology & Experimental Therapeutics (Windland Smith Rice Sudden Death Genomics Laboratory), Mayo Clinic, Rochester, MN. Electronic address:

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http://dx.doi.org/10.1016/j.jpeds.2018.08.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6394853PMC
December 2018

Cardiac Genetic Predisposition in Sudden Infant Death Syndrome.

J Am Coll Cardiol 2018 03;71(11):1217-1227

Departments of Cardiovascular Medicine (Division of Heart Rhythm Services), Pediatrics (Division of Pediatric Cardiology), and Molecular Pharmacology & Experimental Therapeutics (Windland Smith Rice Sudden Death Genomics Laboratory), Mayo Clinic, Rochester, Minnesota. Electronic address:

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http://dx.doi.org/10.1016/j.jacc.2018.01.030DOI Listing
March 2018

Genomic Triangulation and Coverage Analysis in Whole-Exome Sequencing-Based Molecular Autopsies.

Circ Cardiovasc Genet 2017 Oct;10(5)

From the Department of Molecular Pharmacology and Experimental Therapeutics (G.W.S., D.J.T., M.J.A.), Windland Smith Rice Sudden Death Genomics Laboratory (G.W.S., D.J.T., M.J.A.), Mayo Clinic Graduate School of Biomedical Sciences (G.W.S., D.J.T., M.J.A.), Division of Heart Rhythm Services, Department of Cardiovascular Diseases (D.J.T., M.J.A.), Department of Biomedical Statistics and Informatics (S.N., J.M.E.), and Division of Pediatric Cardiology, Department of Pediatric and Adolescent Medicine (M.J.A.), Mayo Clinic, Rochester, MN.

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http://dx.doi.org/10.1161/CIRCGENETICS.117.001828DOI Listing
October 2017

Diagnostic Yield of Whole Exome Sequencing in Pediatric Dilated Cardiomyopathy.

J Cardiovasc Dev Dis 2017 Aug 8;4(3). Epub 2017 Aug 8.

Division of Pediatric Cardiology, Department of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, MN 55905, USA.

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http://dx.doi.org/10.3390/jcdd4030011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5715713PMC
August 2017

Mitochondrial DNA sequence data reveals association of haplogroup U with psychosis in bipolar disorder.

J Psychiatr Res 2017 01 30;84:221-226. Epub 2016 Sep 30.

Department of Psychiatry and Psychology, Mayo Clinic, Rochester, MN, USA; Department of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.

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http://dx.doi.org/10.1016/j.jpsychires.2016.09.027DOI Listing
January 2017

Natural underlying mtDNA heteroplasmy as a potential source of intra-person hiPSC variability.

EMBO J 2016 09 19;35(18):1979-90. Epub 2016 Jul 19.

Departments of Cardiovascular Diseases, Molecular Pharmacology and Experimental Therapeutics, Division of General Internal Medicine, Division of Pediatric Cardiology, and Transplant Center, Mayo Clinic Center for Regenerative Medicine, Rochester, MN, USA

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http://dx.doi.org/10.15252/embj.201694892DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5282833PMC
September 2016

De novo RRAGC mutation activates mTORC1 signaling in syndromic fetal dilated cardiomyopathy.

Hum Genet 2016 08 27;135(8):909-917. Epub 2016 May 27.

Cardiovascular Genetics Research Laboratory, Mayo Clinic, Rochester MN.

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http://dx.doi.org/10.1007/s00439-016-1685-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4947566PMC
August 2016

Target-enrichment sequencing and copy number evaluation in inherited polyneuropathy.

Neurology 2016 05 13;86(19):1762-71. Epub 2016 Apr 13.

From the Departments of Neurology, Peripheral Nerve Division (W.W., P.J.D., C.J.K.), Department of Health Science Research (C.W., S.B., J.M.E.), Laboratory Medicine and Pathology (D.B.D., E.C.T., P.A.L., Y.W., C.J.K.), Medical Genome Facility (B.W.E., Y.W.), and Medical Genetics (C.J.K., D.B.D.), Mayo Clinic, Rochester, MN; Department of Neurology (W.W.), China-Japan Friendship Hospital, Beijing, China; and Department of Neurology (S.S.S.), Perelman School of Medicine, University of Pennsylvania, Philadelphia.

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http://dx.doi.org/10.1212/WNL.0000000000002659DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4862246PMC
May 2016

Exome Sequencing Identifies Pathogenic and Modifier Mutations in a Child With Sporadic Dilated Cardiomyopathy.

J Am Heart Assoc 2015 Dec 9;4(12). Epub 2015 Dec 9.

Cardiovascular Genetics Research Laboratory, Mayo Clinic, Rochester, MN (P.A.L., T.M.O.) Division of Pediatric Cardiology, Department of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, MN (T.M.O.) Division of Cardiovascular Diseases, Department of Internal Medicine, Mayo Clinic, Rochester, MN (T.M.O.).

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http://dx.doi.org/10.1161/JAHA.115.002443DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4845292PMC
December 2015

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

Homozygous/Compound Heterozygous Triadin Mutations Associated With Autosomal-Recessive Long-QT Syndrome and Pediatric Sudden Cardiac Arrest: Elucidation of the Triadin Knockout Syndrome.

Circulation 2015 Jun 28;131(23):2051-60. Epub 2015 Apr 28.

From Department of Molecular Pharmacology & Experimental Therapeutics, Windland Smith Rice Sudden Death Genomics Laboratory (H.M.A., D.J.T., M.L.W., M.J.A.), Department of Medicine/Division of Cardiovascular Diseases (D.J.T., M.L.W., M.J.A.), Medical Genome Facility (B.W.E.), and Department of Pediatrics/Division of Pediatric Cardiology (M.J.A.), Mayo Clinic, Rochester, MN; and Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Mayo College of Medicine, Rochester, MN (S.M., J.M.E.).

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http://dx.doi.org/10.1161/CIRCULATIONAHA.115.015397DOI Listing
June 2015

Exome sequencing establishes diagnosis of Alström syndrome in an infant presenting with non-syndromic dilated cardiomyopathy.

Am J Med Genet A 2015 Apr 23;167A(4):886-90. Epub 2015 Feb 23.

Mayo Graduate School, Molecular Pharmacology and Experimental Therapeutics Track, Mayo Clinic, Rochester, Minnesota; Cardiovascular Genetics Research Laboratory, Mayo Clinic, Rochester, Minnesota.

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http://dx.doi.org/10.1002/ajmg.a.36994DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4518724PMC
April 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

MicroRNA and mRNA cargo of extracellular vesicles from porcine adipose tissue-derived mesenchymal stem cells.

Gene 2014 Nov 23;551(1):55-64. Epub 2014 Aug 23.

Division of Nephrology and Hypertension, Mayo Clinic, Rochester, MN, United States. Electronic address:

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http://dx.doi.org/10.1016/j.gene.2014.08.041DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4174680PMC
November 2014

PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data.

Bioinformatics 2014 Sep 29;30(18):2678-80. Epub 2014 May 29.

Division of Biomedical Statistics and Informatics, Department of Health Sciences Research, Division of Epidemiology, Department of Health Sciences Research, Division of Hematology, Department of Internal Medicine, Mayo Clinic, 200 First Street SW, Rochester, MN 55905 and Department of Health Sciences Research, Mayo Clinic, 4500 San Pablo Road South, Jacksonville, FL 32224, USA.

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http://dx.doi.org/10.1093/bioinformatics/btu363DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4155258PMC
September 2014

Characterizing genetic variation of adrenergic signalling pathways in Takotsubo (stress) cardiomyopathy exomes.

Eur J Heart Fail 2014 Sep 8;16(9):942-9. Epub 2014 Aug 8.

Mayo Medical School, Mayo Clinic, Rochester, MN, USA.

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http://dx.doi.org/10.1002/ejhf.145DOI Listing
September 2014