J. Yao

ORCID: 0000-0001-8974-4265
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About
Contact & Profiles
Research Areas
  • Cardiac Valve Diseases and Treatments
  • Cardiac Structural Anomalies and Repair
  • Cardiomyopathy and Myosin Studies
  • Infective Endocarditis Diagnosis and Management
  • Cardiovascular Issues in Pregnancy
  • Cardiac pacing and defibrillation studies
  • Cardiac Imaging and Diagnostics
  • Cardiac Arrhythmias and Treatments
  • Cardiovascular Effects of Exercise
  • Cardiac electrophysiology and arrhythmias
  • Viral Infections and Immunology Research
  • Aortic Disease and Treatment Approaches
  • Congenital Heart Disease Studies
  • Cardiovascular Syncope and Autonomic Disorders
  • Pulmonary Hypertension Research and Treatments
  • Health and Medical Research Impacts
  • Energy Harvesting in Wireless Networks
  • Pharmaceutical Economics and Policy
  • Liver Disease and Transplantation
  • Connective tissue disorders research
  • Atrial Fibrillation Management and Outcomes
  • Advanced X-ray and CT Imaging
  • Coronary Artery Anomalies
  • Smart Grid Energy Management
  • Health Systems, Economic Evaluations, Quality of Life

The Royal Melbourne Hospital
2017-2024

The University of Sydney
2022

The University of Melbourne
2019

Zhejiang University
2018

Washington University in St. Louis
2017

Baylor College of Medicine
2017

Wuhan Union Hospital
2016

The University of Texas Health Science Center at San Antonio
2015

Pathogenic desmoplakin (DSP) gene variants are associated with the development of a distinct form arrhythmogenic cardiomyopathy known as DSP cardiomyopathy. Patients harbouring these at high risk for sustained ventricular arrhythmia (VA), but existing tools individualized arrhythmic assessment have proven unreliable in this population.

10.1093/eurheartj/ehae409 article EN cc-by-nc European Heart Journal 2024-07-16

Wireless energy sharing is a novel convenient alternative to charge IoT devices. In this demo paper, we present peer-to-peer wireless platform. The platform enables users exchange wirelessly with nearby allows send and receive wirelessly. consists of (i) mobile application that monitors synchronizes the transfer among two devices (ii) backend register providers consumers store their transactions. developed framework collection real dataset. A set preliminary experiments has been conducted on...

10.1109/percomworkshops53856.2022.9767478 article EN 2022 IEEE International Conference on Pervasive Computing and Communications Workshops and other Affiliated Events (PerCom Workshops) 2022-03-21

A 32-year-old male with severe aortic stenosis (AS) and regurgitation (AR) due to a partial-fusion bicuspid valve an annulus area of 917mm2 was admitted cardiogenic shock. Transthoracic echocardiography (TTE) demonstrated mean gradient (MG) 73mmHg, peak (PG) 108mmHg, (AVA) 0.4cm2 eccentric AR. Left ventricular ejection fraction (LVEF) 16%. Following Heart Team review, the patient deemed unsuitable for surgical replacement (SAVR), upfront left-ventricular assist device (LVAD) or...

10.1016/j.crmic.2024.100011 article EN cc-by Cardiovascular Revascularization Medicine Interesting Cases 2024-02-23

Enterprise searches require users to have complex knowledge of queries, configurations, and metadata, rendering it difficult for them access information as needed. Most go-to-market (GTM) platforms utilize advanced search, an interface that enables filter queries by various fields using categories or keywords, which, historically, however, has proven be exceedingly cumbersome, are faced with seemingly hundreds options, fields, buttons. Consequently, querying natural language long been ideal,...

10.48550/arxiv.2411.05048 preprint EN arXiv (Cornell University) 2024-11-06

To examine long-term outcomes after tetralogy of Fallot (TOF) repair. Single-centre retrospective study 293 patients aged ≥16 years with previous TOF repair at a median age 2.6 (IQR:1.1–5.1 years). Surgical approach was trans-atrial (51% (149/293)), right ventriculotomy (34% (101/293)) and unknown (15%, 43/293). After adult centre follow-up 9 (IQR:3.9–15.5 years, max 40), survival excellent (n = 284, 97%). Age-adjusted 99%, 95%, 83% 20, 40, 60 age, respectively. Over half required ≥1...

10.1016/j.ijcchd.2021.100147 article EN cc-by-nc-nd International Journal of Cardiology Congenital Heart Disease 2021-05-12

Palmoplantar keratoderma (PPK) is a keratinizing disorder that can occur as an isolated phenomenon or in association with various systemic abnormalities. A woman PPK was found through cascade genetic testing to have heterozygous deletion chromosome region 6p25.1p24.3 loss of the DSP gene. Subsequent cardiac investigations revealed arrhythmogenic right ventricular cardiomyopathy (ARVC).

10.1016/j.jdcr.2020.06.025 article EN cc-by-nc-nd JAAD Case Reports 2020-06-20

Dilated cardiomyopathy (DCM) is a common cause of heart failure, ventricular arrhythmias, and sudden cardiac death (SCD).1 Current DCM guidelines recommend implantable cardioverter-defibrillator (ICD) insertion for prevention SCD when left ejection fraction (LVEF) less than 35%.2,3 However, can occur in those with relatively preserved LVEF1 also recovered LVEF.4 There significant phenotypic heterogeneity it has been proposed that certain subtypes predispose to arrhythmias independent LVEF.

10.1016/j.hrcr.2020.05.004 article EN cc-by-nc-nd HeartRhythm Case Reports 2020-05-20
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