Robert G Weintraub
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Explore the profile of Robert G Weintraub including associated specialties, affiliations and a list of published articles.
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101
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Recent Articles
1.
Austin R, Brown J, Casauria S, Madelli E, Mattiske T, Boughtwood T, et al.
Genet Med Open
. 2024 Dec;
2:101842.
PMID: 39669597
Purpose: The Australian Genomics Cardiovascular Disorders Flagship was a national multidisciplinary collaboration. It aimed to investigate the feasibility of genome sequencing (GS) and functional genomics to resolve variants of uncertain...
2.
Wadey C, Tomlinson O, Barker A, Stuart A, Tran D, Laohachai K, et al.
J Am Heart Assoc
. 2024 Aug;
13(17):e034035.
PMID: 39189612
Background: Peak oxygen consumption (peak ) is routinely measured in people who have congenital heart disease and is reported as a percentage of predicted value, based upon age- and sex-matched...
3.
Ishigami S, King G, Buratto E, Fricke T, Weintraub R, Brizard C, et al.
J Thorac Cardiovasc Surg
. 2024 Jun;
169(2):400-410.e7.
PMID: 38897544
Objective: The study objective was to evaluate the outcomes of the extracardiac Fontan operation at a single institution. Methods: We conducted a retrospective study of 398 patients from a single...
4.
Chowdhuri K, Buratto E, Ishigami S, Moscoso B, Davies B, Brizard C, et al.
Heart Lung Circ
. 2024 Jun;
33(8):1193-1200.
PMID: 38871532
Aim: Heart transplantation (HT) in patients with failing univentricular circulation is often challenging. This is compounded by the ever-increasing number of patients with prior Norwood-type reconstruction of the aorta, large...
5.
Sholler AM G, Selbie L, Tallon M, Keating J, Ayer J, Burchill L, et al.
Heart Lung Circ
. 2024 Mar;
33(2):153-196.
PMID: 38453293
These first Australian National Standards of Care for Childhood-onset Heart Disease (CoHD Standards) have been developed to inform the healthcare requirements for CoHD services and enable all Australian patients, families...
6.
Singer E, Crowe J, Holliday M, Isbister J, Lal S, Nowak N, et al.
NPJ Genom Med
. 2023 Oct;
8(1):29.
PMID: 37821546
There is an incomplete understanding of the burden of splice-disrupting variants in definitively associated inherited heart disease genes and whether these genes can amplify from blood RNA to support functional...
7.
Chang Y, Wacker J, Ingles J, Macciocca I, King I, Semsarian C, et al.
J Med Genet
. 2023 Sep;
61(2):171-175.
PMID: 37657916
encodes a cardiac transcription factor that is associated with atrial septal defects. Recent studies implicate loss-of-function variants with left ventricular non-compaction cardiomyopathy (LVNC), although clinical and genetic data in families...
8.
Lynch A, Tatangelo M, Ahuja S, Steve Fan C, Min S, Lafreniere-Roula M, et al.
J Am Coll Cardiol
. 2023 Mar;
81(11):1035-1045.
PMID: 36922089
Background: Genetic defects in the RAS/mitogen-activated protein kinase pathway are an important cause of hypertrophic cardiomyopathy (RAS-HCM). Unlike primary HCM (P-HCM), the risk of sudden cardiac death (SCD) and long-term...
9.
Conway J, Min S, Villa C, Weintraub R, Nakano S, Godown J, et al.
Circulation
. 2022 Nov;
147(9):718-727.
PMID: 36335467
Background: Hypertrophic cardiomyopathy (HCM) can be associated with an abnormal exercise response. In adults with HCM, abnormal results on exercise stress testing are predictive of heart failure outcomes. Our goal...
10.
Bagnall R, Singer E, Wacker J, Nowak N, Ingles J, King I, et al.
Circ Genom Precis Med
. 2022 Oct;
15(6):e003686.
PMID: 36252119
Background: The causes of cardiomyopathy in children are less well described than in adults. We evaluated the clinical diagnoses and genetic causes of childhood cardiomyopathy and outcomes of cascade genetic...