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Author Details
Full Name
Naresh Prodduturi
Affiliation
Mayo Clinic
ORCID
Career Start Year
2011
Papers
18
H Index
9
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
35535982
Artificial intelligence for the evaluation of peripheral artery disease using arterial Doppler waveforms to predict abnormal ankle-brachial index.
Vasc Med
2022
34033669
LPCAT1-TERT fusions are uniquely recurrent in epithelioid trophoblastic tumors and positively regulate cell growth.
PLoS One
2021
34267986
Dicom_wsi: A Python Implementation for Converting Whole-Slide Images to Digital Imaging and Communications in Medicine Compliant Files.
J Pathol Inform
2021
33102624
Image-to-image translation for automatic ink removal in whole slide images.
J Med Imaging (Bellingham)
2020
31339943
Robust hierarchical density estimation and regression for re-stained histological whole slide image co-registration.
PLoS One
2019
29559662
Author Correction: UClncR: Ultrafast and comprehensive long non-coding RNA detection from RNA-seq.
Sci Rep
2018
30255803
Indel sensitive and comprehensive variant/mutation detection from RNA sequencing data for precision medicine.
BMC Med Genomics
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
29079769
UClncR: Ultrafast and comprehensive long non-coding RNA detection from RNA-seq.
Sci Rep
2017
29295223
Shiny FHIR: An Integrated Framework Leveraging Shiny R and HL7 FHIR to Empower Standards-Based Clinical Data Applications.
Stud Health Technol Inform
2017
25452597
Circulating atrial natriuretic peptide genetic association study identifies a novel gene cluster associated with stroke in whites.
Circ Cardiovasc Genet
2015
26039248
Chromosome X genomic and epigenomic aberrations and clinical implications in breast cancer by base resolution profiling.
Epigenomics
2015
24325915
Genome-wide association study identifies 25 known breast cancer susceptibility loci as risk factors for triple-negative breast cancer.
Carcinogenesis
2014
25954427
Adverse Drug Event-based Stratification of Tumor Mutations: A Case Study of Breast Cancer Patients Receiving Aromatase Inhibitors.
AMIA Annu Symp Proc
2014
25320007
Nuclear factor of activated T-cell activity is associated with metastatic capacity in colon cancer.
Cancer Res
2014
24876377
PatternCNV: a versatile tool for detecting copy number changes from exome sequencing data.
Bioinformatics
2014
21594272
Relating protein adduction to gene expression changes: a systems approach.
Mol Biosyst
2011
1 - 18 of 18
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2
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Westmead Institute for Medical Research, University of Sydney
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German Cancer Research Center (DKFZ)
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Otto-Friedrich-University Bamberg
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