C
Christian Turner
Researcher at Children's Hospital at Westmead
Publications - 26
Citations - 809
Christian Turner is an academic researcher from Children's Hospital at Westmead. The author has contributed to research in topics: Catecholaminergic polymorphic ventricular tachycardia & Population. The author has an hindex of 12, co-authored 22 publications receiving 587 citations. Previous affiliations of Christian Turner include University of Sydney & Boston Children's Hospital.
Papers
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Journal ArticleDOI
Whole Genome Sequencing Improves Outcomes of Genetic Testing in Patients With Hypertrophic Cardiomyopathy
Richard D. Bagnall,Jodie Ingles,Marcel E. Dinger,Mark J. Cowley,Samantha Barratt Ross,André E. Minoche,Sean Lal,Christian Turner,Alison Colley,Sulekha Rajagopalan,Yemima Berman,Anne Ronan,Diane Fatkin,Christopher Semsarian +13 more
TL;DR: WGS identified additional genetic causes of HCM over targeted gene sequencing approaches and extended genetic screening to deep intronic regions identified pathogenic variants in 9% of gene-elusive HCM.
Journal ArticleDOI
Long-Term Outcomes of Dilated Cardiomyopathy Diagnosed During Childhood: Results from a National Population-Based Study of Childhood Cardiomyopathy
Peta M. A. Alexander,Piers E.F. Daubeney,Alan Nugent,Katherine J Lee,Christian Turner,Steven D. Colan,Terry Robertson,Andrew M. Davis,J. Ramsay,Robert N. Justo,Gary F. Sholler,Ingrid King,Robert G. Weintraub +12 more
TL;DR: In this paper, a population-based study examined long-term outcomes for children with dilated cardiomyopathy based on clinical, echocardiographic, and pathological findings.
Journal ArticleDOI
Sudden death in childhood cardiomyopathy: Results from a long-term national population-based study
Tara Bharucha,Katherine J Lee,Piers E.F. Daubeney,Alan Nugent,Christian Turner,Gary F. Sholler,Terry Robertson,Robert N. Justo,J. Ramsay,John B. Carlin,Steven D. Colan,Ingrid King,Robert G. Weintraub,Robert G. Weintraub,Andrew M. Davis,Andrew M. Davis +15 more
TL;DR: Predictors of SCD include CM phenotype, family history of CM ( DCM), severity of systolic dysfunction (DCM), and extent of LV hypertrophy (HCM).
Journal ArticleDOI
Long-term outcomes of hypertrophic cardiomyopathy diagnosed during childhood: results from a national population-based study
Peta M. A. Alexander,Alan Nugent,Piers E.F. Daubeney,Katherine J Lee,Lynn A. Sleeper,Lynn A. Sleeper,Tibor Schuster,Christian Turner,Christian Turner,Andrew M. Davis,Andrew M. Davis,Christopher Semsarian,Steven D. Colan,Steven D. Colan,Terry Robertson,J. Ramsay,Robert N. Justo,Gary F. Sholler,Gary F. Sholler,Ingrid King,Robert G. Weintraub,Robert G. Weintraub +21 more
TL;DR: The highest risk of death or transplantation for children with hypertrophic cardiomyopathy is within 1 year after diagnosis, with low attrition rates thereafter.
Journal ArticleDOI
A novel heterozygous mutation in cardiac calsequestrin causes autosomal dominant catecholaminergic polymorphic ventricular tachycardia.
Belinda Gray,Belinda Gray,Belinda Gray,Richard D. Bagnall,Richard D. Bagnall,Lien Lam,Lien Lam,Jodie Ingles,Jodie Ingles,Jodie Ingles,Christian Turner,Eric Haan,Andrew M. Davis,Pei Chi Yang,Colleen E. Clancy,Raymond W. Sy,Raymond W. Sy,Christopher Semsarian,Christopher Semsarian,Christopher Semsarian +19 more
TL;DR: It is shown for the first time that a variant in CASQ2 causes autosomal dominant CPVT, a lethal inherited arrhythmia syndrome characterized by adrenergically stimulated ventricular tachycardia.