| nr |
titel |
auteur |
tijdschrift |
jaar |
jaarg. |
afl. |
pagina('s) |
type |
| 1 |
A Basic Physician Trainee’s Genetic Immersion Experience in Cardiac Genetics
|
Plugge, S.
|
|
|
33 |
S3 |
p. S114
|
artikel
|
| 2 |
A Rare Splice-Site Variant in Cardiac Troponin-T (TNNT2): The Need for Ancestral Diversity in Genomic Reference Datasets
|
Butters, A.
|
|
|
33 |
S3 |
p. S99
|
artikel
|
| 3 |
Australian Healthcare Professionals are Interested in Using Genetics to Inform Personalised Nutrition Intervention for Their Patients Living With Cardiovascular Disease
|
Clarke, E.
|
|
|
33 |
S3 |
p. S102
|
artikel
|
| 4 |
A Validated SCN5A Functional Assay to Adjudicate Variants of Uncertain Significance from the International Brugada Syndrome Genetics Consortia
|
Ma, J.
|
|
|
33 |
S3 |
p. S96
|
artikel
|
| 5 |
Cardiac Medications Causing False-Positive Illicit Drug Results
|
Somma, V.
|
|
|
33 |
S3 |
p. S116
|
artikel
|
| 6 |
Comparison of Apical and Non-Apical HCM: Clinical, Imaging, and Genetic Analysis
|
O'Neill, J.
|
|
|
33 |
S3 |
p. S113
|
artikel
|
| 7 |
Contents Page
|
|
|
|
33 |
S3 |
p. ii-iv
|
artikel
|
| 8 |
Developing a High-Throughput Screening Platform to Understand Disease Mechanisms for Targeted Drug Therapies in Catecholaminergic Ventricular Tachycardia (CPVT)
|
Lim, S.
|
|
|
33 |
S3 |
p. S110
|
artikel
|
| 9 |
Developing a Model of Incomplete Penetrance in Arrhythmogenic Cardiomyopathy Using Patient-Derived Induced Pluripotent Stem Cells
|
Li, S.
|
|
|
33 |
S3 |
p. S109-S110
|
artikel
|
| 10 |
Development and Evaluation of a Support Intervention for Families after Sudden Cardiac Death
|
Yeates, L.
|
|
|
33 |
S3 |
p. S120
|
artikel
|
| 11 |
Development and Outcomes of a Multidisciplinary Inherited Cardiac Clinic in Western Australia
|
Greer, C.
|
|
|
33 |
S3 |
p. S105
|
artikel
|
| 12 |
Disruption of an Atypical U12-type Minor Intron in SCN5A Causes Conduction Disease and Recurrent Ventricular Fibrillation
|
Singer, E.
|
|
|
33 |
S3 |
p. S116
|
artikel
|
| 13 |
Dissecting the Role of Hopx Variants in Cardiac Remodelling and Dysfunction
|
Hanna, A.
|
|
|
33 |
S3 |
p. S106
|
artikel
|
| 14 |
Establishing a Functional Genomics Assay to Assess Clinical Variants in CACNA1C-Related Disorders
|
Tan, C.
|
|
|
33 |
S3 |
p. S117
|
artikel
|
| 15 |
Establishing an Automated Patch Clamp Assay to Assess Both Activity and Adrenergic Responses of KCNQ1 Variants
|
Shen, Q.
|
|
|
33 |
S3 |
p. S115
|
artikel
|
| 16 |
Evaluating the Cost-Effectiveness of Screening for Atrial Fibrillation Based on the Screening Preferences of Healthcare Professionals in Australia
|
Halahakone, U.
|
|
|
33 |
S3 |
p. S105
|
artikel
|
| 17 |
Functional Analysis of an FHOD3 Founder Variant Causing Hypertrophic Cardiomyopathy in the Balkans Population
|
Bagnall, R.
|
|
|
33 |
S3 |
p. S97-S98
|
artikel
|
| 18 |
Genetic and Other Aspects of Sudden Cardiac Death in Schizophrenia
|
Thompson, T.
|
|
|
33 |
S3 |
p. S118
|
artikel
|
| 19 |
Genetic Health in Adolescents with CHD: A Population-Specific Pilot Study
|
O'Malley, B.
|
|
|
33 |
S3 |
p. S112
|
artikel
|
| 20 |
Genetic Landscape of Cardiovascular Disease in the United Arab Emirates
|
Almansoori, G.
|
|
|
33 |
S3 |
p. S96-S97
|
artikel
|
| 21 |
Genetic Screening in Patients With Suspected Heritable Thoracic Aortic Disease in Japan
|
Yagyu, T.
|
|
|
33 |
S3 |
p. S119
|
artikel
|
| 22 |
Growth and Development of a Paediatric Inherited Arrhythmia Clinic
|
Robinson, K.
|
|
|
33 |
S3 |
p. S115
|
artikel
|
| 23 |
Health Professionals’ Preferences of Screening for Atrial Fibrillation in Primary Care—A Discrete Choice Analysis
|
Halahakone, U.
|
|
|
33 |
S3 |
p. S106
|
artikel
|
| 24 |
Hypertrophic Cardiomyopathy in the Adolescent, is it the Mitochondria?
|
Mohammed, A.
|
|
|
33 |
S3 |
p. S111
|
artikel
|
| 25 |
Identification of Four Pathogenic Variants Associated with Marafan and Marafan-Like Syndromes in Four Different Families By Whole Exome Sequencing
|
Almansoori, G.
|
|
|
33 |
S3 |
p. S97
|
artikel
|
| 26 |
Incremental Value in Genetic Testing for Athletes Attending a Specialised Sports Cardiology Clinic
|
Follett, J.
|
|
|
33 |
S3 |
p. S104
|
artikel
|
| 27 |
Infantile Aortopathy: Case Report and a Genetics-Focused Literature Review
|
Tan, L.
|
|
|
33 |
S3 |
p. S117
|
artikel
|
| 28 |
Initial Findings and Reflections of the Australian Genomics Cardiovascular Disorders Flagship
|
McGaughran, J.
|
|
|
33 |
S3 |
p. S110-S111
|
artikel
|
| 29 |
Limitations of Whole Exome Sequencing Panels: Subsequent Identification of a Missed Pathogenic Large Deletion in Desmoplakin (DSP)
|
Haqqani, H.
|
|
|
33 |
S3 |
p. S107
|
artikel
|
| 30 |
MYBPC3 and MYH7 Penetrance in Hypertrophic Cardiomyopathy (HCM): A Systematic Review
|
Tran, J.
|
|
|
33 |
S3 |
p. S118
|
artikel
|
| 31 |
NSW HEARTS: The NSW Inherited Cardiomyopathy Cohort Study—Clinical and Demographic Characteristics of Participant to Date
|
Catto, L.
|
|
|
33 |
S3 |
p. S100
|
artikel
|
| 32 |
Perceptions of South Asian Australians Towards Genetic Testing for Cardiovascular Disease
|
Nathan, V.
|
|
|
33 |
S3 |
p. S111
|
artikel
|
| 33 |
Polygenic Informed Treatment Selection in Hypertension
|
Reay, W.
|
|
|
33 |
S3 |
p. S114
|
artikel
|
| 34 |
Polygenic Risk, Aspirin and the Primary Prevention of Cardiovascular Disease
|
Yu, C.
|
|
|
33 |
S3 |
p. S96
|
artikel
|
| 35 |
Postmortem Genetic Testing Following Sudden Cardiac Death Using a Cardiomyopathy and Arrhythmia Next-Generation Sequencing Panel
|
Zilliacus, E.
|
|
|
33 |
S3 |
p. S120
|
artikel
|
| 36 |
Prenatal and Maternal Contributors to Disease Severity in Congenital Heart Disease
|
Blue, G.
|
|
|
33 |
S3 |
p. S98-S99
|
artikel
|
| 37 |
Rare Genetic Variants in Heart Failure with Preserved Ejection Fraction (HFpEF)
|
Gorrie, N.
|
|
|
33 |
S3 |
p. S104-S105
|
artikel
|
| 38 |
Study Protocol for Follow Up of Survivors of Young Sudden Cardiac Arrest in Victoria With Regard to All-Cause Mortality, Implantable Cardioverter Defibrillator Insertion and Detection of Ventricular Arrhythmia
|
Fahy, L.
|
|
|
33 |
S3 |
p. S103
|
artikel
|
| 39 |
Survivability of Young Sudden Cardiac Arrest by Aetiology: Insights From a State-Wide Adjudicated Cardiac Arrest Registry
|
Fahy, L.
|
|
|
33 |
S3 |
p. S103-S104
|
artikel
|
| 40 |
The Benefits and Challenges of Implementing MBS Items for Cardiac Testing
|
Cox, K.
|
|
|
33 |
S3 |
p. S102-S103
|
artikel
|
| 41 |
The CHD Severity Classification System: Development of a Tool to Assist With Disease Stratification for CHD Research
|
O'Malley, B.
|
|
|
33 |
S3 |
p. S113
|
artikel
|
| 42 |
The Clinical and Genetic Characteristics and Long Term Follow Up of Survivors of Sudden Cardiac Arrest in a Tertiary Hospital
|
Cheung, L.
|
|
|
33 |
S3 |
p. S100-S102
|
artikel
|
| 43 |
The Experiences, Values and Goals of Patients in Australia Living with Obstructive Hypertrophic Cardiomyopathy: In-Depth Patient Interviews
|
Fifer, S.
|
|
|
33 |
S3 |
p. S107-S108
|
artikel
|
| 44 |
The Impact of Maternal Genetic Testing During Pregnancy on Management of Women With Inherited Cardiac Diseases: A Systematic Review
|
Wan, A.
|
|
|
33 |
S3 |
p. S119
|
artikel
|
| 45 |
The Use of Social and Media Advertisement in Direct-to-Participant Recruitment: NSW HEARTS Inherited Cardiomyopathy Cohort Study
|
Baker, A.
|
|
|
33 |
S3 |
p. S98
|
artikel
|
| 46 |
This abstract has been withdrawn.
|
|
|
|
33 |
S3 |
p. S107
|
artikel
|
| 47 |
Tiered Analysis of Australian Genomics Cardiovascular Genetic Disorders Flagship Genomes Increases the Diagnostic Yield of Genetic Testing
|
Chang, Y.
|
|
|
33 |
S3 |
p. S95
|
artikel
|
| 48 |
Title Page
|
|
|
|
33 |
S3 |
p. i
|
artikel
|
| 49 |
Validating Institutional Coding for Paediatric Hypertrophic Cardiomyopathy—A Single Centre Study
|
Scarfe, G.
|
|
|
33 |
S3 |
p. S108
|
artikel
|
| 50 |
Yield of Diagnostic Genetic Testing in a Multidisciplinary Genetic Heart Disease Clinic with Access to Medicare Rebatable Cardiac Testing
|
Nowak, N.
|
|
|
33 |
S3 |
p. S112
|
artikel
|
| 51 |
Young Sudden Cardiac Arrest in New South Wales: A Data Linkage Study
|
Leslie, F.
|
|
|
33 |
S3 |
p. S109
|
artikel
|
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