» Authors » Jamie I Vandenberg

Jamie I Vandenberg

Explore the profile of Jamie I Vandenberg including associated specialties, affiliations and a list of published articles. Areas
Snapshot
Articles 116
Citations 2511
Followers 0
Related Specialties
Top 10 Co-Authors
Published In
Affiliations
Soon will be listed here.
Recent Articles
1.
Ng C, ONeill M, Padigepati S, Ting Y, Facio F, Vatta M, et al.
medRxiv . 2025 Feb; PMID: 39974038
Rare missense variants are often classified as variants of uncertain significance (VUS) due to insufficient evidence for classification. These ambiguous findings create anxiety and frequently lead to inappropriate workup, colloquially...
2.
Aljassar R, Shen Q, Albash B, Vandenberg J, Ebrahim M, Ng C
Genet Med Open . 2024 Dec; 2:101868. PMID: 39669639
Functional investigation of genetic variants found in long QT syndrome can provide evidence that is needed to confirm the genetic diagnosis and establish the cause of the condition. We performed...
3.
Santiago C, Blekkenhorst L, Hsu M, Mirabito Colafella K, Calkin A, Nicholls S, et al.
Heart Lung Circ . 2024 Nov; 34(1):95-101. PMID: 39550291
In 2023, a joint National Cardiovascular Workforce Sustainability Summit was convened by the Australian Cardiovascular Alliance (ACvA), the Cardiac Society of Australia and New Zealand, and the National Heart Foundation...
4.
ONeill M, Ng C, Aizawa T, Sala L, Bains S, Winbo A, et al.
Circulation . 2024 Sep; 150(23):1869-1881. PMID: 39315434
Background: Long QT syndrome is a lethal arrhythmia syndrome, frequently caused by rare loss-of-function variants in the potassium channel encoded by . Variant classification is difficult, often because of lack...
5.
La Gerche A, Paratz E, Bray J, Jennings G, Page G, Timbs S, et al.
Heart Lung Circ . 2024 Sep; 33(11):1507-1522. PMID: 39306551
Sudden cardiac arrest (SCA) represents a major cause of premature mortality globally, with enormous impact and financial cost to victims, families, and communities. SCA prevention should be considered a health...
6.
Elliott A, Middeldorp M, McMullen J, Fatkin D, Thomas L, Gwynne K, et al.
Heart Lung Circ . 2024 Sep; 33(11):1523-1532. PMID: 39244450
Atrial fibrillation (AF) is highly prevalent in the Australian community, ranking amongst the highest globally. The consequences of AF are significant. Stroke, dementia and heart failure risk are increased substantially,...
7.
Balaji P, Liulu X, Sivakumar S, Chong J, Kizana E, Vandenberg J, et al.
Int J Radiat Oncol Biol Phys . 2024 Sep; 121(1):75-89. PMID: 39222823
Stereotactic body radiation therapy (SBRT) is an innovative modality for the treatment of refractory ventricular arrhythmias (VAs). Phase 1/2 clinical trials have demonstrated the remarkable efficacy of SBRT at reducing...
8.
Lau C, Flood E, Hunter M, Williams-Noonan B, Corbett K, Ng C, et al.
Nat Commun . 2024 Aug; 15(1):7470. PMID: 39209832
The fine tuning of biological electrical signaling is mediated by variations in the rates of opening and closing of gates that control ion flux through different ion channels. Human ether-a-go-go...
9.
Lim S, Mangala M, Holliday M, Cserne Szappanos H, Barratt-Ross S, Li S, et al.
Dis Model Mech . 2024 Aug; 17(8). PMID: 39189070
Hypertrophic cardiomyopathy (HCM) is an inherited heart muscle disease that is characterised by left ventricular wall thickening, cardiomyocyte disarray and fibrosis, and is associated with arrhythmias, heart failure and sudden...
10.
Ma J, ONeill M, Richardson E, Thomson K, Ingles J, Muhammad A, et al.
Circ Genom Precis Med . 2024 Jul; 17(4):e004569. PMID: 38953211
Background: Brugada syndrome is an inheritable arrhythmia condition that is associated with rare, loss-of-function variants in . Interpreting the pathogenicity of missense variants is challenging, and ≈79% of missense variants...