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Discussion to: Minimally invasive approach associated with lower resource utilization after aortic and mitral valve surgery

JTCVS open, 2023-09, Vol.15, p.81-82

2023

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Socioeconomic status as a predictor of post-operative mortality and outcomes in carotid artery stenting vs. carotid endarterectomy

Frontiers in cardiovascular medicine, 2024-02, Vol.11, p.1286100-1286100

2024

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Enhanced Recovery After Surgery in Cardiac Surgery: Imploring Investigation

The Annals of thoracic surgery, 2023-06, Vol.115 (6), p.1559-1560

2023

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Ambulatory Electrocardiography Monitoring for Early Discharge After Minimally Invasive Valve Surgery

The Journal of surgical research, 2023-12, Vol.292, p.182-189

2023

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Quality of Mitral Valve Surgery Does Not Differ by Hospital Volume in New Jersey

Journal of cardiac surgery, 2023-06, Vol.2023, p.1-7

2023

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Minimally invasive approach associated with lower resource utilization after aortic and mitral valve surgery

JTCVS open, 2023-09, Vol.15, p.72-80

2023

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Minimally invasive approach associated with lower resource utilization after aortic and mitral valve surgeryCentral MessagePerspective

JTCVS open, 2023-09, Vol.15, p.72-80

2023

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

PloS one, 2016-10, Vol.11 (10), p.e0165680-e0165680

2016

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

Experimental and Molecular Medicine, 2021, 53(0), , pp.1-13

2021

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Deciphering intratumor heterogeneity using cancer genome analysis

Human Genetics, 2016-06, Vol.135 (6), p.635-642

2016

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

PloS one, 2019-11, Vol.14 (11), p.e0224227-e0224227

2019

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Downsloping high-frequency hearing loss due to inner ear tricellular tight junction disruption by a novel ILDR1 mutation in the Ig-like domain

PloS one, 2015-02, Vol.10 (2), p.e0116931-e0116931

2015

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

Nature communications, 2017-11, Vol.8 (1), p.1377-10, Article 1377

2017

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

Journal of translational medicine, 2018-11, Vol.16 (1), p.330-330, Article 330

2018

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

Scientific reports, 2017-11, Vol.7 (1), p.16504-11, Article 16504

2017

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

Human mutation, 2020-05, Vol.41 (5), p.913-920

2020

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

Neonatology (Basel, Switzerland), 2020-11, Vol.117 (3), p.374-379

2020

Volltextzugriff (PDF)

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

International journal of molecular sciences, 2017-10, Vol.18 (11), p.2246

2017

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Paired analysis of tumor mutation burden calculated by targeted deep sequencing panel and whole exome sequencing in non-small cell lung cancer

BMB Reports, 2021, 54(7), , pp.386-391

2021

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Lighthouse in the open sea of spastic ataxia; what are the features that should not be missed in SPG11?

Parkinsonism & related disorders, 2021-10, Vol.91, p.181-183

2021

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Clinical characteristics of ataxia-telangiectasia presenting dystonia as a main manifestation

Clinical neurology and neurosurgery, 2020-12, Vol.199, p.106267-106267, Article 106267

2020

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

Journal of clinical medicine, 2020-06, Vol.9 (6), p.2013

2020

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Comprehensive somatic genome alterations of urachal carcinoma

Journal of medical genetics, 2017-08, Vol.54 (8), p.572

2017

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

Scientific reports, 2019-11, Vol.9 (1), p.16952-16952, Article 16952

2019

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Discussion to: Minimally invasive approach associated with lower resource utilization after aortic and mitral valve surgery

Socioeconomic status as a predictor of post-operative mortality and outcomes in carotid artery stenting vs. carotid endarterectomy

Enhanced Recovery After Surgery in Cardiac Surgery: Imploring Investigation

Ambulatory Electrocardiography Monitoring for Early Discharge After Minimally Invasive Valve Surgery

Quality of Mitral Valve Surgery Does Not Differ by Hospital Volume in New Jersey

Minimally invasive approach associated with lower resource utilization after aortic and mitral valve surgery

Minimally invasive approach associated with lower resource utilization after aortic and mitral valve surgeryCentral MessagePerspective

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

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

Deciphering intratumor heterogeneity using cancer genome analysis

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

Downsloping high-frequency hearing loss due to inner ear tricellular tight junction disruption by a novel ILDR1 mutation in the Ig-like domain

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

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

Tumor Genomic Profiling Guides Patients with Metastatic Gastric Cancer to Targeted Treatment: The VIKTORY Umbrella Trial

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

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

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

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

Paired analysis of tumor mutation burden calculated by targeted deep sequencing panel and whole exome sequencing in non-small cell lung cancer

Lighthouse in the open sea of spastic ataxia; what are the features that should not be missed in SPG11?

Clinical characteristics of ataxia-telangiectasia presenting dystonia as a main manifestation

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

Comprehensive somatic genome alterations of urachal carcinoma

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

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