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Author Details
Full Name
Jean-Pierre A Kocher
Affiliation
Mayo Clinic
ORCID
Career Start Year
1991
Papers
121
H Index
40
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
33990473
Quality Performance of a Transfer Center Reduces Interhospital Transfer and Direct Admission-Related ED Evaluations.
Am J Med Qual
2022
35716010
DNA methylation signature predicts cancer response to demethylation agents from profiling diverse cancer cell lines.
Cancer Commun (Lond)
2022
36271076
CRISPR/Cas9-mediated excision of ALS/FTD-causing hexanucleotide repeat expansion in C9ORF72 rescues major disease mechanisms in vivo and in vitro.
Nat Commun
2022
36008405
In vivo lentiviral vector gene therapy to cure hereditary tyrosinemia type 1 and prevent development of precancerous and cancerous lesions.
Nat Commun
2022
35022670
Telogator: a method for reporting chromosome-specific telomere lengths from long reads.
Bioinformatics
2022
31808791
CpGtools: a python package for DNA methylation analysis.
Bioinformatics
2021
33648520
Determining mutational burden and signature using RNA-seq from tumor-only samples.
BMC Med Genomics
2021
33816122
Elevated Expression of Plasminogen Activator Inhibitor (PAI-1/SERPINE1) is Independent from rs1799889 Genotypes in Arthrofibrosis.
Meta Gene
2021
34550971
Exogene: A performant workflow for detecting viral integrations from paired-end next-generation sequencing data.
PLoS One
2021
34377961
P<sup>2</sup>T<sup>2</sup>: Protein Panoramic annoTation Tool for the interpretation of protein coding genetic variants.
JAMIA Open
2021
34394200
PB-Motif-A Method for Identifying Gene/Pseudogene Rearrangements With Long Reads: An Application to CYP21A2 Genotyping.
Front Genet
2021
34234399
Re-Evaluate Fusion Genes in Prostate Cancer.
Cancer Inform
2021
33975459
Surface Roughness of Titanium Orthopedic Implants Alters the Biological Phenotype of Human Mesenchymal Stromal Cells.
Tissue Eng Part A
2021
32593486
Human Fibrosis: Is There Evidence for a Genetic Predisposition in Musculoskeletal Tissues?
J Arthroplasty
2020
31787246
Combining copy number, methylation markers, and mutations as a panel for endometrial cancer detection via intravaginal tampon collection.
Gynecol Oncol
2020
31797631
Coverage profile correction of shallow-depth circulating cell-free DNA sequencing via multidistance learning.
Pac Symp Biocomput
2020
33213041
A Potential Theragnostic Regulatory Axis for Arthrofibrosis Involving Adiponectin (ADIPOQ) Receptor 1 and 2 (ADIPOR1 and ADIPOR2), TGFβ1, and Smooth Muscle α-Actin (ACTA2).
J Clin Med
2020
32913881
<i>Ex Vivo</i> Cell Therapy by Ectopic Hepatocyte Transplantation Treats the Porcine Tyrosinemia Model of Acute Liver Failure.
Mol Ther Methods Clin Dev
2020
32594533
Aberrant immunohistochemical expression of CD4 as a rare finding in metastatic melanoma.
J Cutan Pathol
2020
30878468
Ccne1 Overexpression Causes Chromosome Instability in Liver Cells and Liver Tumor Development in Mice.
Gastroenterology
2019
31214875
Prognostic subclass of intrahepatic cholangiocarcinoma by integrative molecular-clinical analysis and potential targeted approach.
Hepatol Int
2019
31101622
Recurrent <i>MSC</i> <sup>E116K</sup> mutations in ALK-negative anaplastic large cell lymphoma.
Blood
2019
30704449
Predict drug sensitivity of cancer cells with pathway activity inference.
BMC Med Genomics
2019
28926134
Early genetic aberrations in patients with sporadic colorectal cancer.
Mol Carcinog
2018
30021563
Correction to: the impact of pharmacokinetic gene profiles across human cancers.
BMC Cancer
2018
30016933
HGT-ID: an efficient and sensitive workflow to detect human-viral insertion sites using next-generation sequencing data.
BMC Bioinformatics
2018
30255803
Indel sensitive and comprehensive variant/mutation detection from RNA sequencing data for precision medicine.
BMC Med Genomics
2018
29932737
Improving Single-Nucleotide Polymorphism-Based Fetal Fraction Estimation of Maternal Plasma Circulating Cell-Free DNA Using Bayesian Hierarchical Models.
J Comput Biol
2018
30577744
Detection and visualization of complex structural variants from long reads.
BMC Bioinformatics
2018
30347404
Novel Neural Network Approach to Predict Drug-Target Interactions Based on Drug Side Effects and Genome-Wide Association Studies.
Hum Hered
2018
30482155
A data science approach for the classification of low-grade and high-grade ovarian serous carcinomas.
BMC Genomics
2018
29783934
The impact of pharmacokinetic gene profiles across human cancers.
BMC Cancer
2018
29618619
Prevalent Homozygous Deletions of Type I Interferon and Defensin Genes in Human Cancers Associate with Immunotherapy Resistance.
Clin Cancer Res
2018
29559662
Author Correction: UClncR: Ultrafast and comprehensive long non-coding RNA detection from RNA-seq.
Sci Rep
2018
29267858
Hybrid-denovo: a de novo OTU-picking pipeline integrating single-end and paired-end 16S sequence tags.
Gigascience
2018
27473065
Indel detection from RNA-seq data: tool evaluation and strategies for accurate detection of actionable mutations.
Brief Bioinform
2017
30761385
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
28482068
mTCTScan: a comprehensive platform for annotation and prioritization of mutations affecting drug sensitivity in cancers.
Nucleic Acids Res
2017
28302177
cepip: context-dependent epigenomic weighting for prioritization of regulatory variants and disease-associated genes.
Genome Biol
2017
28376176
Tumor Sequencing and Patient-Derived Xenografts in the Neoadjuvant Treatment of Breast Cancer.
J Natl Cancer Inst
2017
28472449
Exploring genetic associations with ceRNA regulation in the human genome.
Nucleic Acids Res
2017
28423702
Experience with precision genomics and tumor board, indicates frequent target identification, but barriers to delivery.
Oncotarget
2017
28967791
Adipose tissue DNA methylome changes in development of new-onset diabetes after kidney transplantation.
Epigenomics
2017
29079769
UClncR: Ultrafast and comprehensive long non-coding RNA detection from RNA-seq.
Sci Rep
2017
28981748
Linnorm: improved statistical analysis for single cell RNA-seq expression data.
Nucleic Acids Res
2017
29190829
A comprehensive analysis of breast cancer microbiota and host gene expression.
PLoS One
2017
28975018
Comprehensive Genomic Profiling of a Rare Thyroid Follicular Dendritic Cell Sarcoma.
Rare Tumors
2017
29161425
Corrigendum: Linnorm: improved statistical analysis for single cell RNA-seq expression data.
Nucleic Acids Res
2017
28532394
CircularLogo: A lightweight web application to visualize intra-motif dependencies.
BMC Bioinformatics
2017
26210358
VCF-Miner: GUI-based application for mining variants and annotations stored in VCF files.
Brief Bioinform
2016
1 - 50 of 121
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Mark D Robinson
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Wenming Xiao
Human Phenome Institute and Shanghai Cancer Center, Fudan University
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John V Pearson
QIMR Berghofer Medical Research Institute
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Steven J M Jones
University of British Columbia
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Marco A Marra
University of British Columbia
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1993
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Jill P Mesirov
University of California San Diego
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1992
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Aleksandar Milosavljevic
Baylor College of Medicine
Career Start Year
1991
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Elaine R Mardis
The Ohio State University
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row(s) 1 - 30 of 30
Collaborators
Yan W Asmann
Mayo Clinic
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14
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Mayo Clinic
Co-authored papers
11
Chen Wang
Center for Individualized Medicine, Mayo Clinic
Co-authored papers
11
High Seng Chai
Mayo Clinic
Co-authored papers
10
Eric W Klee
Mayo Clinic College of Medicine and Science
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10
Asha A Nair
Mayo Clinic
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9
Michael T Zimmermann
Medical College of Wisconsin
Co-authored papers
8
Terry M Therneau
Mayo Clinic
Co-authored papers
8
Pak C Sham
the University of Hong Kong
Co-authored papers
7
Panwen Wang
Co-authored papers
7
Liewei Wang
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Co-authored papers
7
Naresh Prodduturi
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Co-authored papers
7
Surendra Dasari
Mayo Clinic
Co-authored papers
5
Hongfang Liu
Mayo Clinic
Co-authored papers
5
Eric D Wieben
Mayo Clinic Rochester
Co-authored papers
5
Richard M Weinshilboum
Mayo Clinic
Co-authored papers
5
Shoshana J Wodak
VIB-VUB Center for Structural Biology
Co-authored papers
4
Lewis R Roberts
Co-authored papers
4
Andre J van Wijnen
Co-authored papers
4
Alan H Bryce
Mayo Clinic
Co-authored papers
4
Marianne Rooman
Co-authored papers
3
Xiaoyang Ruan
University of Texas Health Science Center at Houston, Mayo Clinic
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3
Robert W Williams
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3
Gregory A Poland
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3
Kent R Bailey
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