Jared Evans

发表

Target-enrichment sequencing and copy number evaluation in inherited polyneuropathy

E. Thorland, P. Dyck, S. Baheti, 2016, Neurology.

CAP-miRSeq: a comprehensive analysis pipeline for microRNA sequencing data

Zhifu Sun, Sumit Middha, Huihuang Yan, 2014, BMC Genomics.

Patient-specific functional genomics and disease modeling suggest a role for LRP2 in Hypoplastic Left Heart Syndrome

K. Ocorr, R. Bodmer, A. Terzic, 2019, bioRxiv.

A Comprehensive Approach to Sequence-oriented IsomiR annotation (CASMIR): demonstration with IsomiR profiling in colorectal neoplasia

J. Jen, D. Ahlquist, T. Smyrk, 2018, BMC Genomics.

Adipose tissue DNA methylome changes in development of new-onset diabetes after kidney transplantation.

J. Kocher, M. Jensen, V. Somers, 2017, Epigenomics.

Recessive TAF1A mutations reveal ribosomopathy in siblings with end-stage pediatric dilated cardiomyopathy

Jared Evans, J. Maleszewski, T. Olson, 2017, Human molecular genetics.

TNNI 3 K mutation in familial syndrome of conduction system disease , atrial tachyarrhythmia and dilated cardiomyopathy

Michael T. Zimmermann, E. Wieben, M. Zimmermann, 2014 .

Exome Sequencing and Systems Biology Converge to Identify Novel Mutations in the L-Type Calcium Channel, CACNA1C, Linked to Autosomal Dominant Long QT Syndrome

Michael J. Ackerman, Sumit Middha, Jared M. Evans, 2013, Circulation. Cardiovascular genetics.

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

S. Middha, D. Tester, M. Ackerman, 2015, Circulation.

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

M. Frye, G. Jenkins, S. McElroy, 2017, Journal of psychiatric research.

Enhancer of Zeste Homolog 2 Inhibition Stimulates Bone Formation and Mitigates Bone Loss Caused by Ovariectomy in Skeletally Mature Mice*

G. Stein, A. V. van Wijnen, Jared Evans, 2016, The Journal of Biological Chemistry.

Mitochondrial DNA: Hotspot for Potential Gene Modifiers Regulating Hypertrophic Cardiomyopathy

Jared Evans, C. Denning, T. Nelson, 2020, Journal of clinical medicine.

Genetic Association between Hypoplastic Left Heart Syndrome and Cardiomyopathies.

W. Bamlet, Jared Evans, P. O’Leary, 2020, Circulation. Genomic and precision medicine.

Erratum to: RNA sequencing reveals a depletion of collagen targeting microRNAs in Dupuytren’s disease

A. V. van Wijnen, P. Kloen, Jared Evans, 2015, BMC Medical Genomics.

Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndrome

M. de Andrade, Jared Evans, T. Nelson, 2015, Human Genetics.

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

L. Lerman, Hui Tang, A. V. van Wijnen, 2014, Gene.

High‐Resolution Molecular Validation of Self‐Renewal and Spontaneous Differentiation in Clinical‐Grade Adipose‐Tissue Derived Human Mesenchymal Stem Cells

Asha A. Nair, G. Stein, A. Dietz, 2014, Journal of cellular biochemistry.

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

Jared Evans, S. Hayes, M. O'byrne, 2019, Circulation. Genomic and precision medicine.

A Comprehensive Approach to Sequence-oriented IsomiR annotation (CASMIR): demonstration with IsomiR profiling in colorectal neoplasia

J. Jen, D. Ahlquist, T. Smyrk, 2018, BMC Genomics.

HiChIP: a high-throughput pipeline for integrative analysis of ChIP-Seq data

Ying Li, Jared Evans, Jean-Pierre A. Kocher, 2014, BMC Bioinformatics.

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

V. Mootha, E. Schon, A. Terzic, 2016, The EMBO journal.

CAP-miRSeq: a comprehensive analysis pipeline for microRNA sequencing data

J. Kocher, Zhifu Sun, S. Middha, 2014, BMC Genomics.

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

Jared Evans, T. Olson, B. T. Larsen, 2015, Journal of the American Heart Association.

Noncardiac genetic predisposition in sudden infant death syndrome

E. Behr, M. Simpson, D. Tester, 2018, Genetics in Medicine.

Hypoxia‐related microRNA‐210 is a diagnostic marker for discriminating osteoblastoma and osteosarcoma

F. Sim, A. Folpe, M. Yaszemski, 2017, Journal of orthopaedic research : official publication of the Orthopaedic Research Society.

Bioinformatics Strategies for Identifying Regions of Epigenetic Deregulation Associated with Aberrant Transcript Splicing and RNA-editing

Zhiguo Zhang, Jared Evans, Jeong-Heon Lee, 2015, BIOINFORMATICS.

Compound heterozygous NOTCH1 mutations underlie impaired cardiogenesis in a patient with hypoplastic left heart syndrome

Timothy J. Nelson, M. de Andrade, Jared Evans, 2015, Human Genetics.

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

Michael T. Zimmermann, E. Wieben, M. de Andrade, 2014, Human molecular genetics.

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

D. Tester, M. Ackerman, Jared Evans, 2017, Circulation. Cardiovascular genetics.

Diagnostic Yield of Whole Exome Sequencing in Pediatric Dilated Cardiomyopathy

Jared Evans, T. Olson, Pamela A. Long, 2017, Journal of cardiovascular development and disease.

Cardiac Genetic Predisposition in Sudden Infant Death Syndrome.

E. Behr, M. Simpson, D. Tester, 2018, Journal of the American College of Cardiology.

Exome‐Wide Rare Variant Analyses in Sudden Infant Death Syndrome

E. Behr, M. Simpson, D. Tester, 2018, The Journal of pediatrics.

Building a Research-Quality Copy Number Variation Data Repository for Translational Research

Chen Wang, Jared Evans, Guoqian Jiang, 2018, Poly/DMAH@VLDB.

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

S. Middha, Jared Evans, A. Prasad, 2014, European journal of heart failure.

Pediatric Dilated Cardiomyopathy‐Associated LRRC10 (Leucine‐Rich Repeat–Containing 10) Variant Reveals LRRC10 as an Auxiliary Subunit of Cardiac L‐Type Ca2+ Channels

Marites T Woon, T. Kamp, Youngsook Lee, 2018, Journal of the American Heart Association.

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

Jared Evans, T. Olson, Pamela A. Long, 2015, American journal of medical genetics. Part A.

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

Jared Evans, Steven N. Hart, Naresh Prodduturi, 2014, Bioinform..

Clinical Perspective on P 2060

S. Middha, D. Tester, M. Ackerman, 2014 .

Histone Deacetylase Inhibition Promotes Osteoblast Maturation by Altering the Histone H4 Epigenome and Reduces Akt Phosphorylation*

Y. Li, S. Middha, A. V. van Wijnen, 2013, The Journal of Biological Chemistry.

Patient-specific genomics and cross-species functional analysis implicate LRP2 in hypoplastic left heart syndrome

K. Ocorr, R. Bodmer, A. Terzic, 2020, eLife.

Non-Cardiac Genetic Predisposition in Sudden Infant Death Syndrome Short Title: Gray –Non-Cardiac SIDS-Susceptibility Genes

E. Behr, M. Simpson, D. Tester, 2018 .

Recessive MYH6 Mutations in Hypoplastic Left Heart With Reduced Ejection Fraction

Eric D Wieben, Michael T. Zimmermann, Jeanne L Theis, 2015, Circulation. Cardiovascular genetics.

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

M. Zimmermann, Jared Evans, T. Olson, 2016, Human Genetics.

Breast cancer chemoprevention pharmacogenomics: Deep sequencing and functional genomics of the ZNF423 and CTSO genes

Erin E. Carlson, D. Schaid, S. Scherer, 2017, npj Breast Cancer.

Custom Gene Capture and Next‐Generation Sequencing to Resolve Discordant ALK Status by FISH and IHC in Lung Adenocarcinoma

Sarah H. Johnson, J. Jen, Zhifu Sun, 2016, Journal of thoracic oncology : official publication of the International Association for the Study of Lung Cancer.

Association of mitochondrial DNA copy number with self-rated health status

J. Cerhan, J. Olson, G. Jenkins, 2018, The application of clinical genetics.

The Development of an Infrastructure to Facilitate the Use of Whole Genome Sequencing for Population Health

Nephi A. Walton, David P. Taylor, K. Stefánsson, 2022, Journal of personalized medicine.

Breast cancer chemoprevention pharmacogenomics: Deep sequencing and functional genomics of the ZNF423 and CTSO genes

Krishna R. Kalari, Erin E. Carlson, D. Schaid, 2017, npj Breast Cancer.

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

Michael T. Zimmermann, Jared Evans, T. Olson, 2016, Human Genetics.

Cardiac Genetic Predisposition in Sudden Infant Death Syndrome.

E. Behr, M. Simpson, D. Tester, 2018, Journal of the American College of Cardiology.

Noncardiac genetic predisposition in sudden infant death syndrome

E. Behr, M. Simpson, D. Tester, 2018, Genetics in Medicine.

Noncardiac genetic predisposition in sudden infant death syndrome. Genetics in Medicine

E. Behr, M. Simpson, D. Tester, 2018 .

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

V. Mootha, E. Schon, A. Terzic, 2016, The EMBO journal.

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

S. Middha, D. Tester, B. Eckloff, 2015, Circulation.