Samantha Barratt Ross
Overview
Explore the profile of Samantha Barratt Ross including associated specialties, affiliations and a list of published articles.
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Articles
14
Citations
167
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0
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Recent Articles
1.
Cserne Szappanos H, Viola H, Ito D, Lim S, Mangala M, Holliday M, et al.
Sci Rep
. 2023 Jul;
13(1):11296.
PMID: 37438479
Familial hypertrophic cardiomyopathy (FHC) patients are advised to avoid strenuous exercise due to increased risk of arrhythmias. Mice expressing the human FHC-causing mutation R403Q in the myosin heavy chain gene...
2.
Barratt Ross S, Barratt A, Semsarian C
Heart Lung Circ
. 2021 Nov;
31(3):301-303.
PMID: 34838455
No abstract available.
3.
Semsarian C, Ingles J, Barratt Ross S, Dunwoodie S, Bagnall R, Kovacic J
J Am Coll Cardiol
. 2021 May;
77(20):2517-2530.
PMID: 34016265
Our understanding of the genetic basis of cardiovascular diseases (CVDs) has evolved rapidly. This has resulted from a combination of dedicated research in well phenotyped CVD patients, the sequencing of...
4.
Barratt Ross S, Singer E, Driscoll E, Nowak N, Yeates L, Puranik R, et al.
Hum Genome Var
. 2020 Oct;
7:33.
PMID: 33082984
The genetic etiology and heritability of left ventricular noncompaction (LVNC) in adults is unclear. This study sought to assess the value of genetic testing in adults with LVNC. Adults diagnosed...
5.
Holliday M, Barratt Ross S, Lim S, Mangala M, Hill A, Cserne Szappanos H, et al.
Stem Cell Res
. 2018 Dec;
33:269-273.
PMID: 30508693
Hypertrophic cardiomyopathy (HCM) is an inherited cardiomyopathy characterized by left ventricular hypertrophy ≥15 mm in the absence of loading conditions. HCM has a prevalence of up to one in 200,...
6.
Holliday M, Barratt Ross S, Lim S, Semsarian C
Stem Cell Res
. 2018 Oct;
33:56-59.
PMID: 30316040
Hypertrophic cardiomyopathy is an inherited cardiomyopathy with a prevalence of up to 1 in 200, which can result in significant morbidity and mortality. An iPSC line was generated from peripheral...
7.
Barratt Ross S, Semsarian C
JAMA Cardiol
. 2018 Aug;
3(11):1033-1034.
PMID: 30140926
No abstract available.
8.
Bagnall R, Ingles J, Dinger M, Cowley M, Barratt Ross S, Minoche A, et al.
J Am Coll Cardiol
. 2018 Jul;
72(4):419-429.
PMID: 30025578
Background: Whole genome sequencing (WGS) is a comprehensive genetic testing approach that reports most types of nucleotide variants. Objectives: This study sought to assess WGS for hypertrophic cardiomyopathy (HCM) in...
9.
Barratt Ross S, Bagnall R, Yeates L, Sy R, Semsarian C
HeartRhythm Case Rep
. 2018 May;
4(4):146-151.
PMID: 29755943
No abstract available.
10.
Barratt Ross S, Fraser S, Semsarian C
Heart Rhythm
. 2017 Aug;
15(1):137-144.
PMID: 28823602
Inherited arrhythmia syndromes, including familial long QT syndrome, catecholaminergic polymorphic ventricular tachycardia, and Brugada syndrome, can cause life-threatening arrhythmias and are responsible for a significant proportion of sudden deaths in...