SNUBI Research ::   (70 talks satisfying Presenter = 유경훈)
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2019-11:
02 유경훈 Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network     J.Club
21 유경훈   TopicSem

2019-10:
17 유경훈 Influence of CYP2C19 Metabolizer Status on Escitalopram Tolerability and Response in Depressive Disorders  TopicSem
22 유경훈 Influence of CYP2C19 Metabolizer Status on Escitalopram Tolerability and Response in Depressive Disorders  Seminar
24 유경훈 Global Biobank Engine: enabling genotype-phenotype browsing for biobank summary statistics  xMutant

2019-09:
05 유경훈 Influence of CYP2C19 Metabolizer Status on Escitalopram Tolerability and Response in Depressive Disorders  TopicSem
30 유경훈 Pharmacogenomic genotypes define genetic ancestry in patients and enable population-specific genomic implementation  SysBiol

2019-08:
01 유경훈 A robust benchmark for germline structural variant detection  xMutant
10 유경훈 Impact of pharmacogenomics on clinical outcomes in major depressive disorder in the GUIDED trial: A large, patient- and rater-blinded, randomized, controlled study     J.Club
12 유경훈 Standardized Biogeographic Grouping System for Annotating Populations in Pharmacogenetic Research     SysBiol

2019-07:
01 유경훈 Hubble2D6: A deep learning approach for predicting drug metabolic activity  SysBiol
29 유경훈 Influence of CYP2C19 Metabolizer Status on Escitalopram Tolerability and Response in Depressive Disorders  TopicSem

2019-06:
01 유경훈 Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program     J.Club
13 유경훈 A benchmark study of scoring methods for non-coding mutations.  xMutant
20 유경훈 Comparative study of escitalopram according to CPIC guideline (CYP2C19/CYP2D6 Metabolizer Status)  TopicSem

2019-05:
13 유경훈 Comparative study of escitalopram according to CPIC guideline (CYP2C19/CYP2D6 Metabolizer Status)  TopicSem

2019-04:
04 유경훈 Comparative study of escitalopram according to CPIC guideline (CYP2C19 Metabolizer Status)  TopicSem
24 유경훈 VIVA (VIsualization of VAriants): A VCF file visualization tool  xMutant
30 유경훈 Clinical use of current polygenic risk scores may exacerbate health disparities  SysBiol

2019-03:
11 유경훈 Pharmacogenetics of escitalopram response: a candidate gene analysis  TopicSem
23 유경훈 Improved Pathogenic Variant Localization via a Hierarchical Model of Sub-regional Intolerance     J.Club
25 유경훈 DGIdb 3.0: a redesign and expansion of the drug-gene interaction database  SysBiol

2019-02:
16 유경훈 Burden Testing of Rare Variants Identified through Exome Sequencing via Publicly Available Control Data     J.Club

2019-01:
10 유경훈 Drug Targetor: a web interface to investigate the human druggome for over 500 phenotypes  SysBiol
17 유경훈 Pharmacogenetics of escitalopram response: a candidate gene analysis   TopicSem

2018-12:
10 유경훈 Pharmacogenetics of escitalopram response: a candidate gene analysis   TopicSem
11 유경훈 FLASK micro web framework in python  xMutant
18 유경훈 Rare variants in drug target genes contributing to complex diseases, phenome-wide  xMutant
27 유경훈 Pharmacogenetics of escitalopram response: a candidate gene analysis  Seminar

2018-11:
08 유경훈 Subgroup analysis based on antidepressant prescription information of 1000 MDD patients   TopicSem
08 유경훈 Analysis of population-specific pharmacogenomic variants using next-generation sequencing data  SysBiol
24 유경훈 An optimized prediction framework to assess the functional impact of pharmacogenetic variants     J.Club

2018-10:
01 유경훈 Subgroup analysis based on antidepressant prescription information of 1000 MDD patients   TopicSem
23 유경훈 ClinPred: Prediction Tool to Identify Disease-Relevant Nonsynonymous Single-Nucleotide Variants  xMutant
23 유경훈 depression  Seminar

2018-09:
03 유경훈 Subgroup analysis based on antidepressant prescription information of 1000 MDD patients   TopicSem
03 유경훈 depression  Seminar
12 유경훈 depression  Seminar
15 유경훈 Covariate selection for association screening in multiphenotype genetic studies     J.Club
20 유경훈 Integrating rare genetic variants into pharmacogenetic drug response predictions  SysBiol

2018-08:
23 유경훈 depression  Seminar
28 유경훈 SEQSpark: A Complete Analysis Tool for Large-ScaleRare Variant Association Studies  xMutant

2018-07:
02 유경훈 depression  Seminar
05 유경훈 Interpretation of genes related to early response by antidepressant group  SysBiol
24 유경훈 The VAAST Variant Prioritizer (VVP)  xMutant
26 유경훈 Subgroup analysis based on antidepressant prescription information of 1000 MDD patients   TopicSem

2018-06:
23 유경훈 Identification of Misclassified ClinVar Variants via Disease Population Prevalence     J.Club
28 유경훈 Subgroup analysis based on antidepressant prescription information of 1000 MDD patients  TopicSem

2018-05:
12 유경훈 Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression     J.Club
15 유경훈 Patients subgrouping by antidepressant prescription  xMutant
17 유경훈 Review: Ki Database  SysBiol
24 유경훈 Subgroup analysis based on antidepressant prescription information of 1000 MDD patients  TopicSem

2018-04:
19 유경훈 1T Depression Analysis: Patients characterization and subgrouping by prescribed drugs   TopicSem

2018-03:
15 유경훈 1T Depression Analysis: Patients characterization and subgrouping by prescribed drugs  TopicSem
20 유경훈 KRGdb database overview  xMutant
22 유경훈 Sub-group of SIOH patient groups according to drug response record.  SysBiol

2018-01:
04 유경훈 1T Depression Analysis-Patients characterization and subgrouping by prescribed drugs  TopicSem
20 유경훈 Using reference-free compressed data structures to analyze sequencing reads from thousands of human genomes     J.Club
25 유경훈 1T Depression Analysis: Patients characterization and subgrouping by prescribed drugs  TopicSem

2017-11:
25 유경훈 A method to decipher pleiotropy by detecting underlying heterogeneity driven by hidden subgroups applied to autoimmune and neuropsychiatric diseases     J.Club
29 유경훈 1T Depression Analysis: Patients characterization and subgrouping  TopicSem

2017-10:
30 유경훈 1T Depression Analysis: Patients characterization and subgrouping  TopicSem

2017-09:
09 유경훈 The druggable genome and support for target identification and validation in drug development     J.Club
20 유경훈 WXS analysis in 999 Depression patients with Baseline Information  TopicSem

2017-08:
09 유경훈 WXS analysis in 999 Depression patients with Baseline Information  TopicSem

2017-07:
08 유경훈 Semantic prioritization of novel causative genomic variants     J.Club
19 유경훈 Analysis for identifying genes and variants  associated with SIOH in 20 patients.  TopicSem

2017-06:
07 유경훈 Analysis for identifying genes and variants  associated with SIOH in 20 patients.  TopicSem

2017-05:
10 유경훈 Analysis for identifying genes and variants associated with SIOH in 20 patients.  TopicSem

2017-04:
29 유경훈 Whole-genome sequencing identifies common-to-rare variants associated with human blood metabolites     J.Club

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