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Lista de obras de Woong-Yang Park

A Method to Evaluate the Quality of Clinical Gene-Panel Sequencing Data for Single-Nucleotide Variant Detection

artículo científico publicado en 2017

A Preterm Infant with Multiple Anomalies Diagnosed with Atypical CHARGE Syndrome after a Novel CHD7 Variant Confirmed Using Whole-Genome Sequencing

scientific article published on 03 March 2020

A clinical guidance to DFNA22 drawn from a Korean cohort study with an autosomal dominant deaf population: A retrospective cohort study

artículo científico publicado en 2018

A genome-wide association analysis of chromosomal aberrations and Hirschsprung disease

artículo científico publicado en 2016

A genome-wide association study identifies a breast cancer risk variant in ERBB4 at 2q34: results from the Seoul Breast Cancer Study

scientific journal article

A novel likely pathogenic variant in the RAB28 gene in a Korean patient with cone-rod dystrophy.

artículo científico publicado en 2017

ARID1B alterations identify aggressive tumors in neuroblastoma

artículo científico publicado en 2017

ATP1A3 mutations can cause progressive auditory neuropathy: a new gene of auditory synaptopathy

artículo científico publicado en 2017

Absence of Sirt3 aggravates cisplatin nephrotoxicity via enhanced renal tubular apoptosis and inflammation

scholarly article by Dal Kim published in October 2018

Allelic imbalance of somatic mutations in cancer genomes and transcriptomes.

artículo científico publicado en 2017

Alterations in the Transcriptional Programs of Myeloma Cells and the Microenvironment during Extramedullary Progression Affect Proliferation and Immune Evasion

artículo científico publicado en 2019

Alternative polyadenylation of single cells delineates cell types and serves as a prognostic marker in early stage breast cancer

artículo científico publicado en 2019

Analysis of Gene Expression Profile of AGS Cells Stimulated by Helicobacter pylori Adhesion

artículo científico publicado en 2007

Analysis of intrapatient heterogeneity uncovers the microevolution of Middle East respiratory syndrome coronavirus.

artículo científico publicado en 2016

Analyzing Somatic Genome Rearrangements in Human Cancers by Using Whole-Exome Sequencing

artículo científico publicado en 2016

Application of single-cell RNA sequencing in optimizing a combinatorial therapeutic strategy in metastatic renal cell carcinoma.

artículo científico publicado en 2016

Assessment of intratumoral heterogeneity with mutations and gene expression profiles

scientific article published on 16 July 2019

Author Correction: Genetic Characteristics of Korean Patients with Autosomal Dominant Polycystic Kidney Disease by Targeted Exome Sequencing

scientific article published on 02 April 2020

BGN Mutations in X-Linked Spondyloepimetaphyseal Dysplasia.

artículo científico publicado en 2016

Biomarkers Associated with Tumor Heterogeneity in Prostate Cancer

COMP-angiopoietin-1 mitigates changes in lipid droplet size, macrophage infiltration of adipose tissue and renal inflammation in streptozotocin-induced diabetic mice

artículo científico publicado en 2017

Characterization of background noise in capture-based targeted sequencing data

artículo científico publicado en 2017

Circulating tumor DNA shows variable clonal response of breast cancer during neoadjuvant chemotherapy

artículo científico publicado en 2017

Clinical Application of Targeted Deep Sequencing in Solid-Cancer Patients; Utility of Targeted Deep Sequencing for Biomarker-Selected Clinical Trial

artículo científico publicado en 2017

Clinical Relevance of Genomic Changes in Recurrent Pediatric Solid Tumors

Clinical Targeted Next-Generation sequencing Panels for Detection of Somatic Variants in Gliomas

artículo científico publicado en 2019

Clinical characteristics and exploratory genomic analyses of germline BRCA1 or BRCA2 mutations in breast cancer

scientific article published on 17 June 2020

Clinical implications of genomic profiles in metastatic breast cancer with a focus on TP53 and PIK3CA, the most frequently mutated genes

artículo científico publicado en 2017

Comprehensive genetic exploration of skeletal dysplasia using targeted exome sequencing.

artículo científico publicado en 2015

Comprehensive genomic profiling of IgM multiple myeloma identifies IRF4 as a prognostic marker.

artículo científico publicado en 2016

Comprehensive somatic genome alterations of urachal carcinoma

artículo científico

Correction: The mutational landscape of ocular marginal zone lymphoma identifies frequent alterations in followed by mutations in and

article

DNA Damage Response and Repair Pathway Alteration and Its Association with Tumor Mutation Burden and Platinum-Based Chemotherapy in Small Cell Lung Cancer

artículo científico publicado en 2019

Deciphering intratumor heterogeneity using cancer genome analysis.

artículo científico publicado en 2016

Discovery of CDH23 as a Significant Contributor to Progressive Postlingual Sensorineural Hearing Loss in Koreans.

artículo científico publicado en 2016

Discovery of actionable genetic alterations with targeted panel sequencing in children with relapsed or refractory solid tumors

artículo científico publicado en 2019

Distinct genomic profile and specific targeted drug responses in adult cerebellar glioblastoma

artículo científico publicado en 2019

Efficacy of BRAF Inhibitors in Asian Metastatic Melanoma Patients: Potential Implications of Genomic Sequencing in BRAF-Mutated Melanoma.

artículo científico publicado en 2016

Elucidation of Novel Therapeutic Targets for Acute Myeloid Leukemias with - Fusion ⬇️

artículo científico

Exome and transcriptome sequencing identifies loss of PDLIM2 in metastatic colorectal cancers.

artículo científico publicado en 2017

Expansion of phenotypic spectrum of MYO15A pathogenic variants to include postlingual onset of progressive partial deafness

artículo científico publicado en 2018

FOXO3a Turns the Tumor Necrosis Factor Receptor Signaling Towards Apoptosis Through Reciprocal Regulation of c-Jun N-Terminal Kinase and NF-κB

scholarly article by Hae-Young Lee et al published January 2008 in Arteriosclerosis, Thrombosis, and Vascular Biology

Forkhead factor, FOXO3a, induces apoptosis of endothelial cells through activation of matrix metalloproteinases.

artículo científico publicado en 2007

Functional catechol-O-methyltransferase gene polymorphism and susceptibility to schizophrenia

artículo científico publicado en 2002

Functional characterization of a novel loss-of-function mutation of PRPS1 related to early-onset progressive nonsyndromic hearing loss in Koreans (DFNX1): Potential implications on future therapeutic intervention.

artículo científico publicado en 2016

Gene expression of AGS cells stimulated with released proteins by Helicobacter pylori

article

Gene expression profiles of human subcutaneous and visceral adipose-derived stem cells.

artículo científico publicado en 2016

Genetic Characteristics of Korean Patients with Autosomal Dominant Polycystic Kidney Disease by Targeted Exome Sequencing

scientific article published on 18 November 2019

Genetic Study in Korean Pediatric Patients with Steroid-Resistant Nephrotic Syndrome or Focal Segmental Glomerulosclerosis

artículo científico publicado en 2020

Genetic and Clinical Characteristics of Phyllodes Tumors of the Breast

artículo científico publicado en 2017

Genetic variants of PARK genes in Korean patients with early-onset Parkinson's disease

artículo científico publicado en 2018

Genome-wide DNA methylation profiles in noncancerous gastric mucosae with regard to Helicobacter pylori infection and the presence of gastric cancer

artículo científico publicado en 2011

Genomic Alterations in Biliary Tract Cancer Using Targeted Sequencing

artículo científico publicado en 2016

Genomic Characterization and Comparison of Multi-Regional and Pooled Tumor Biopsy Specimens

artículo científico publicado en 2016

Genomic alterations of ground-glass nodular lung adenocarcinoma.

artículo científico publicado en 2018

HER2 as a novel therapeutic target for cervical cancer

artículo científico publicado en 2015

Hepatorenal fibrocystic diseases in children

artículo científico publicado en 2015

Highly Concordant Key Genetic Alterations in Primary Tumors and Matched Distant Metastases in Differentiated Thyroid Cancer.

artículo científico publicado en 2016

Highly dense, optically inactive silica microbeads for the isolation and identification of circulating tumor cells

artículo científico

Hippo-mediated suppression of IRS2/AKT signaling prevents hepatic steatosis and liver cancer

artículo científico publicado en 2018

Hspa4 (HSP70) is involved in the radioadaptive response: results from mouse splenocytes.

artículo científico publicado en 2002

Identification and Clinical Implications of Novel MYO15A Mutations in a Non-consanguineous Korean Family by Targeted Exome Sequencing

artículo científico publicado en 2015

Identification of Distinct Tumor Subpopulations in Lung Adenocarcinoma via Single-Cell RNA-seq

artículo científico publicado en 2015

Identification of Driving ALK Fusion Genes and Genomic Landscape of Medullary Thyroid Cancer

artículo científico publicado en 2015

Identification of Pathogenic Variants in the CHM Gene in Two Korean Patients With Choroideremia

artículo científico publicado en 2017

Identification of the PROM1 Mutation p.R373C in a Korean Patient With Autosomal Dominant Stargardt-like Macular Dystrophy.

artículo científico publicado en 2017

Identifying SYNE1 ataxia and extending the mutational spectrum in Korea

artículo científico publicado en 2018

Immune signature of metastatic breast cancer: Identifying predictive markers of immunotherapy response

artículo científico publicado en 2017

Immune subtyping of extranodal NK/T-cell lymphoma: a new biomarker and an immune shift during disease progression

scientific article published on 25 October 2019

Impact of Genetic Variants on the Individual Potential for Body Fat Loss.

artículo científico publicado en 2018

Inertial-ordering-assisted droplet microfluidics for high-throughput single-cell RNA-sequencing

artículo científico publicado en 2018

Integrated genomic approaches identify upregulation of SCRN1 as a novel mechanism associated with acquired resistance to erlotinib in PC9 cells harboring oncogenic EGFR mutation

artículo científico publicado en 2016

Integrative Radiogenomics Approach for Risk Assessment of Post-Operative Metastasis in Pathological T1 Renal Cell Carcinoma: A Pilot Retrospective Cohort Study

artículo científico publicado en 2020

Integrative radiogenomic analysis for multicentric radiophenotype in glioblastoma

artículo científico publicado en 2016

Intron retention is a widespread mechanism of tumor-suppressor inactivation.

artículo científico publicado en 2015

Korean Variant Archive (KOVA): a reference database of genetic variations in the Korean population.

artículo científico publicado en 2017

Lineage-dependent gene expression programs influence the immune landscape of colorectal cancer

artículo científico publicado en 2020

Linking transcriptional and genetic tumor heterogeneity through allele analysis of single-cell RNA-seq data

artículo científico publicado en 2018

Local exposure of 849 MHz and 1763 MHz radiofrequency radiation to mouse heads does not induce cell death or cell proliferation in brain

artículo científico publicado en 2008

Molecular Characterization of Colorectal Signet-Ring Cell Carcinoma Using Whole-Exome and RNA Sequencing

scientific article published on 07 May 2018

Molecular Evolution Patterns in Metastatic Lymph Nodes Reflect the Differential Treatment Response of Advanced Primary Lung Cancer.

artículo científico publicado en 2016

Molecular breakdown: a comprehensive view of anaplastic lymphoma kinase (ALK)-rearranged non-small cell lung cancer

artículo científico publicado en 2017

Molecular characterization of colorectal cancer patients and concomitant patient-derived tumor cell establishment

scientific article published on 20 February 2016

Mutational and phenotypic spectrum of OTOF-related auditory neuropathy in Koreans: eliciting reciprocal interaction between bench and clinics

Neuronal Elav-like (Hu) proteins regulate RNA splicing and abundance to control glutamate levels and neuronal excitability

artículo científico publicado en 2012

Nonlinear tumor evolution from dysplastic nodules to hepatocellular carcinoma

artículo científico publicado en 2016

Novel KCNQ4 variants in different functional domains confer genotype- and mechanism-based therapeutics in patients with nonsyndromic hearing loss

scientific article published in 2021

Obesity and genetic polymorphism of ERCC2 and ERCC4 as modifiers of risk of breast cancer.

artículo científico publicado en 2005

PHLI-seq: constructing and visualizing cancer genomic maps in 3D by phenotype-based high-throughput laser-aided isolation and sequencing

artículo científico publicado en 2018

POLD1 variants leading to reduced polymerase activity can cause hearing loss without syndromic features

artículo científico publicado en 2020

Paired whole exome and transcriptome analyses for the Immunogenomic changes during concurrent chemoradiotherapy in esophageal squamous cell carcinoma

scholarly article by Sehhoon Park et al published 16 May 2019 in Journal for Immunotherapy of Cancer

Pan-Cancer Analysis of Alternative Lengthening of Telomere Activity

artículo científico publicado en 2020

Paradoxical delay of senescence upon depletion of BRCA2 in telomerase-deficient worms

scientific article published on 07 September 2016

Paraneoplastic neuromyelitis optica associated with ANNA-1 antibodies in invasive thymoma

artículo científico publicado en 2014

Patient-Derived Xenograft Models of Epithelial Ovarian Cancer for Preclinical Studies.

artículo científico publicado en 2017

Performance evaluation of commercial library construction kits for PCR-based targeted sequencing using a unique molecular identifier

Pharmacogenomic analysis of patient-derived tumor cells in gynecologic cancers

scientific article published on 26 November 2019

Practical approach to determine sample size for building logistic prediction models using high-throughput data

artículo científico publicado en 2014

Precision medicine approaches to lung adenocarcinoma with concomitant MET and HER2 amplification

artículo científico publicado en 2017

Predicting multi-class responses to preoperative chemoradiotherapy in rectal cancer patients

artículo científico publicado en 2016

Preferential Infiltration of Unique Vγ9Jγ2-Vδ2 T Cells Into Glioblastoma Multiforme

Prevalence and detection of low-allele-fraction variants in clinical cancer samples.

artículo científico publicado en 2017

RNA-seq Reveals Transcriptomic Differences in Inflamed and Noninflamed Intestinal Mucosa of Crohn's Disease Patients Compared with Normal Mucosa of Healthy Controls

artículo científico publicado en 2017

Rare Mechanism of Acquired Resistance to Osimertinib in Korean Patients with EGFR-mutated Non-small Cell Lung Cancer.

artículo científico publicado en 2018

Recurrent mutations of MAPK pathway genes in multiple myeloma but not in amyloid light-chain amyloidosis.

artículo científico publicado en 2016

Refinement of Molecular Diagnostic Protocol of Auditory Neuropathy Spectrum Disorder: Disclosure of Significant Level of Etiologic Homogeneity in Koreans and Its Clinical Implications

artículo científico publicado en 2015

Risk stratification of triple-negative breast cancer with core gene signatures associated with chemoresponse and prognosis

artículo científico publicado en 2019

Role of HER2 mutations in refractory metastatic breast cancers: targeted sequencing results in patients with refractory breast cancer

artículo científico publicado en 2015

SIDR: simultaneous isolation and parallel sequencing of genomic DNA and total RNA from single cells

artículo científico publicado en 2017

SIRT1 induces the adipogenic differentiation of mouse embryonic stem cells by regulating RA-induced RAR expression via NCOR1 acetylation

scientific article published on 17 March 2020

Single-cell RNA sequencing demonstrates the molecular and cellular reprogramming of metastatic lung adenocarcinoma

artículo científico publicado en 2020

Single-cell RNA sequencing of human nail unit defines RSPO4 onychofibroblasts and SPINK6 nail epithelium

artículo científico publicado en 2021

Single-cell RNA sequencing reveals the tumor microenvironment and facilitates strategic choices to circumvent treatment failure in a chemorefractory bladder cancer patient

artículo científico publicado en 2020

Single-cell RNA-Seq unveils tumor microenvironment

artículo científico publicado en 2017

Single-cell RNA-seq enables comprehensive tumour and immune cell profiling in primary breast cancer

artículo científico publicado en 2017

Single-cell mRNA sequencing identifies subclonal heterogeneity in anti-cancer drug responses of lung adenocarcinoma cells

artículo científico publicado en 2015

Skeletal overgrowth syndrome caused by overexpression of C-type natriuretic peptide in a girl with balanced chromosomal translocation, t(1;2)(q41;q37.1).

artículo científico publicado en 2015

Spatiotemporal genomic architecture informs precision oncology in glioblastoma

artículo científico publicado en 2017

Stretch-activated atrial natriuretic peptide secretion in atria with heat shock protein 70 overexpression

artículo científico publicado en 2003

Strong founder effect of p.P240L in CDH23 in Koreans and its significant contribution to severe-to-profound nonsyndromic hearing loss in a Korean pediatric population

artículo científico publicado en 2015

TERT promoter mutations and long-term survival in patients with thyroid cancer

artículo científico publicado en 2016

TP53 alteration determines the combinational cytotoxic effect of doxorubicin and an antioxidant NAC.

artículo científico publicado en 2017

TP53-dependence on the effect of doxorubicin and Src inhibitor combination therapy

scientific article published on 01 August 2018

Targeted Exome Sequencing Provided Comprehensive Genetic Diagnosis of Congenital Anomalies of the Kidney and Urinary Tract

scientific article published on 10 March 2020

Targeted Exome Sequencing of Deafness Genes After Failure of Auditory Phenotype-Driven Candidate Gene Screening

artículo científico publicado en 2015

Targeted deep sequencing of gastric marginal zone lymphoma identified alterations of TRAF3 and TNFAIP3 that were mutually exclusive for MALT1 rearrangement.

artículo científico publicado en 2018

Targeted disruption of hsp70.1 sensitizes to osmotic stress

artículo científico publicado en 2002

The Analysis of A Frequent TMPRSS3 Allele Containing P.V116M and P.V291L in A Cis Configuration among Deaf Koreans

artículo científico publicado en 2017

The Effect of Globus Pallidus Interna Deep Brain Stimulation on a Dystonia Patient with the GNAL Mutation Compared to Patients with DYT1 and DYT6.

artículo científico publicado en 2019

The effect of androgen receptor expression on clinical characterization of metastatic breast cancer

scientific article published on 02 January 2017

The minimal amount of starting DNA for Agilent's hybrid capture-based targeted massively parallel sequencing

artículo científico publicado en 2016

The mutational landscape of ocular marginal zone lymphoma identifies frequent alterations in TNFAIP3 followed by mutations in TBL1XR1 and CREBBP.

artículo científico publicado en 2017

The use of FNA samples for whole-exome sequencing and detection of somatic mutations in breast cancer surgical specimens.

artículo científico

Transformation to Small Cell Lung Cancer of Pulmonary Adenocarcinoma: Clinicopathologic Analysis of Six Cases

scientific article published on 10 May 2016

Tumor Heterogeneity Predicts Metastatic Potential in Colorectal Cancer

artículo científico publicado en 2017

Tumor-promoting macrophages prevail in malignant ascites of advanced gastric cancer

artículo científico publicado en 2020

Type 1 Sialidosis Patient With a Novel Deletion Mutation in the NEU1 Gene: Case Report and Literature Review

scientific article published on 01 June 2019

Unraveling of Enigmatic Hearing-Impaired GJB2 Single Heterozygotes by Massive Parallel Sequencing: DFNB1 or Not?

scientific article published on April 2016

Utility of targeted deep sequencing for detecting circulating tumor DNA in pancreatic cancer patients

artículo científico publicado en 2018

Vertical Magnetic Separation of Circulating Tumor Cells for Somatic Genomic-Alteration Analysis in Lung Cancer Patients

artículo científico publicado en 2016

Whole-exome sequencing reveals diverse modes of inheritance in sporadic mild to moderate sensorineural hearing loss in a pediatric population

artículo científico publicado en 2015

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