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Meta-Analysis of Differentially Expressed Genes in the Substantia Nigra in Parkinson's Disease Supports Phenotype-Specific Transcriptome Changes

Frontiers in neuroscience, 2020-12, Vol.14, p.596105-596105

2020

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Global Analysis of the Human RNA Degradome Reveals Widespread Decapped and Endonucleolytic Cleaved Transcripts

International journal of molecular sciences, 2020-09, Vol.21 (18), p.6452

2020

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RelCurator: a text mining-based curation system for extracting gene–phenotype relationships specific to neurodegenerative disorders

Genes & Genomics, 2023, 45(8), , pp.1025-1036

2023

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Accuracy of Machine Learning Using the Montreal Cognitive Assessment for the Diagnosis of Cognitive Impairment in Parkinson’s Disease

Journal Of Movement Disorders, 2022, 15(2), , pp.132-139

2022

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PhenGenVar: A User-Friendly Genetic Variant Detection and Visualization Tool for Precision Medicine

Journal of personalized medicine, 2022-06, Vol.12 (6), p.959

2022

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The Korea‐Vietnam trade and the bilateral exchange rate: Asymmetric evidence from commodity trade data

Australian economic papers, 2023-03, Vol.62 (1), p.124-148

2023

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The burden of rare damaging variants in hereditary atypical parkinsonism genes is increased in patients with Parkinson’s disease

Neurobiology of aging, 2021-04, Vol.100, p.118.e5-118.e13

2021

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Extraction of Informative Genes from Multiple Microarray Data Integrated by Rank-Based Approach

IEICE Transactions on Information and Systems, 2011/04/01, Vol.E94.D(4), pp.841-854

2011

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2314-PUB: No Clinical Factors, Except Baseline HbA1c, Can Predict Glycemic Response to Dulaglutide: Real-World Data in Korean Patients

Diabetes (New York, N.Y.), 2019-06, Vol.68 (Supplement_1)

2019

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1247-P: Mildly Elevated Triglyceride Levels Are Associated with Increased Risk for Major Adverse Cardiovascular Events in Statin-Naïve Rheumatoid Arthritis Patients—A Nationwide Cohort Study

Diabetes (New York, N.Y.), 2023-06, Vol.72 (Supplement_1), p.1

2023

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The Protein-Protein Interaction Network of Hereditary Parkinsonism Genes Is a Hierarchical Scale-Free Network

Yonsei Medical Journal, 2022, 63(8), , pp.724-734

2022

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RelCurator: a text mining-based curation system for extracting gene–phenotype relationships specific to neurodegenerative disorders

Genes & genomics, 2023-08, p.1025-1036

2023

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Synthesis and Reactivity of a Mononuclear Manganese(II) Complex Having Pseudo-Seven Coordination Environment

Bulletin of the Korean Chemical Society, 2009, 30(3), , pp.679-682

2009

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Effect of polygenic load on striatal dopaminergic deterioration in Parkinson disease

Neurology, 2019-08, Vol.93 (7), p.e665

2019

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GAAP: A Genome Assembly + Annotation Pipeline

BioMed research international, 2019, Vol.2019, p.4767354-12

2019

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A Case of Endobronchial Osteochondromatous Hamartoma Removed Using Flexible Bronchoscopy

Archivos de bronconeumología (English ed.), 2012-11, Vol.48 (11), p.427-428

2012

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A computational method for detecting copy number variations using scale-space filtering

BMC bioinformatics, 2013-02, Vol.14 (1), p.57-57, Article 57

2013

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ExCNVSS: A Noise-Robust Method for Copy Number Variation Detection in Whole Exome Sequencing Data

BioMed research international, 2017-01, Vol.2017, p.9631282-11

2017

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Comparing Montreal Cognitive Assessment Performance in Parkinson’s Disease Patients: Age- and Education-Adjusted Cutoffs vs. Machine Learning

Journal of movement disorders, 2024-04, Vol.17 (2), p.171-180

2024

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Dysregulation of the causative genes for hereditary parkinsonism in the midbrain in Parkinson's disease

Movement disorders, 2017-08, Vol.32 (8), p.1211-1220

2017

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WebPORD: a web-based pipeline of RNA degradome

International journal of data mining and bioinformatics, 2019, Vol.22 (3), p.216

2019

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Draft Genome of Toxocara canis, a Pathogen Responsible for Visceral Larva Migrans

Korean journal of parasitology, 2016-12, Vol.54 (6), p.751-758

2016

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WebPORD: a web-based pipeline of RNA degradome

International journal of data mining and bioinformatics, 2019, Vol.22 (3), p.216

2019

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An efficient noise reduction method for copy number variations detection from whole exome sequencing data

2016 International Conference on High Performance Computing & Simulation (HPCS), 2016, p.1027-1028

2016

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Detection of copy number variation using scale space filtering

2011 Annual International Conference of the IEEE Engineering in Medicine and Biology Society, 2011, Vol.2011, p.5555-5558

2011

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Meta-Analysis of Differentially Expressed Genes in the Substantia Nigra in Parkinson's Disease Supports Phenotype-Specific Transcriptome Changes

Global Analysis of the Human RNA Degradome Reveals Widespread Decapped and Endonucleolytic Cleaved Transcripts

RelCurator: a text mining-based curation system for extracting gene–phenotype relationships specific to neurodegenerative disorders

Accuracy of Machine Learning Using the Montreal Cognitive Assessment for the Diagnosis of Cognitive Impairment in Parkinson’s Disease

PhenGenVar: A User-Friendly Genetic Variant Detection and Visualization Tool for Precision Medicine

The Korea‐Vietnam trade and the bilateral exchange rate: Asymmetric evidence from commodity trade data

The burden of rare damaging variants in hereditary atypical parkinsonism genes is increased in patients with Parkinson’s disease

Extraction of Informative Genes from Multiple Microarray Data Integrated by Rank-Based Approach

2314-PUB: No Clinical Factors, Except Baseline HbA1c, Can Predict Glycemic Response to Dulaglutide: Real-World Data in Korean Patients

1247-P: Mildly Elevated Triglyceride Levels Are Associated with Increased Risk for Major Adverse Cardiovascular Events in Statin-Naïve Rheumatoid Arthritis Patients—A Nationwide Cohort Study

The Protein-Protein Interaction Network of Hereditary Parkinsonism Genes Is a Hierarchical Scale-Free Network

RelCurator: a text mining-based curation system for extracting gene–phenotype relationships specific to neurodegenerative disorders

Synthesis and Reactivity of a Mononuclear Manganese(II) Complex Having Pseudo-Seven Coordination Environment

Effect of polygenic load on striatal dopaminergic deterioration in Parkinson disease

GAAP: A Genome Assembly + Annotation Pipeline

A Case of Endobronchial Osteochondromatous Hamartoma Removed Using Flexible Bronchoscopy

A computational method for detecting copy number variations using scale-space filtering

ExCNVSS: A Noise-Robust Method for Copy Number Variation Detection in Whole Exome Sequencing Data

Comparing Montreal Cognitive Assessment Performance in Parkinson’s Disease Patients: Age- and Education-Adjusted Cutoffs vs. Machine Learning

Dysregulation of the causative genes for hereditary parkinsonism in the midbrain in Parkinson's disease

WebPORD: a web-based pipeline of RNA degradome

Draft Genome of Toxocara canis, a Pathogen Responsible for Visceral Larva Migrans

WebPORD: a web-based pipeline of RNA degradome

An efficient noise reduction method for copy number variations detection from whole exome sequencing data

Detection of copy number variation using scale space filtering

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