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Natalie Nowak

Observed names: N Nowak, N. Nowak, Nowak, Natalie
ORCID: 0000-0001-7259-394X
Observed ORCID: 0000-0001-7259-394X
OpenAlex ID: A5058608343
Genetic Basis of Childhood Cardiomyopathy
2022 · Richard D. Bagnall, Emma S. Singer, et al. · Circulation Genomic and Precision Medicine · 67
Concealed Cardiomyopathy in Autopsy-Inconclusive Cases of Sudden Cardiac Death and Implications for Families
2022 · Julia C. Isbister, Natalie Nowak, et al. · Journal of the American College of Cardiology · 60
“Concealed cardiomyopathy” as a cause of previously unexplained sudden cardiac arrest
2020 · Julia C. Isbister, Natalie Nowak, et al. · International Journal of Cardiology · 58
Genetic architecture of left ventricular noncompaction in adults
2020 · Samantha Barratt Ross, Emma S. Singer, et al. · Human Genome Variation · 44
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The role of genetic testing in diagnosis and care of inherited cardiac conditions in a specialised multidisciplinary clinic
2022 · Fergus Stafford, Neesha Krishnan, et al. · Genome Medicine · 32
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Clinical Utility of a Phenotype-Enhanced MYH7 -Specific Variant Classification Framework in Hypertrophic Cardiomyopathy Genetic Testing
2020 · Connor L. Mattivi, J. Martijn Bos, et al. · Circulation Genomic and Precision Medicine · 20
Titin-related familial dilated cardiomyopathy: factors associated with disease onset
2025 · Renee Johnson, Robert A Fletcher, et al. · European Heart Journal · 19
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The burden of splice-disrupting variants in inherited heart disease and unexplained sudden cardiac death
2023 · Emma S. Singer, Joshua Crowe, et al. · npj Genomic Medicine · 15
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Generation of induced pluripotent stem cells (iPSCs) from a hypertrophic cardiomyopathy patient with the pathogenic variant p.Val698Ala in beta-myosin heavy chain ( MYH7 ) gene
2017 · Samantha Barratt Ross, Stuart T. Fraser, et al. · Stem Cell Research · 13
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A multitiered analysis platform for genome sequencing: Design and initial findings of the Australian Genomics Cardiovascular Disorders Flagship
2024 · Rachel Austin, Jaye S. Brown, et al. · Genetics in Medicine Open · 9
A rare splice-site variant in TNNT2: the need for ancestral diversity in genomic reference data sets
2025 · Alexandra Butters, Kate Thomson, et al. · European Heart Journal · 6
A rare splice-site variant in cardiac troponin-T ( TNNT2) : The need for ancestral diversity in genomic reference datasets
2024 · Alexandra Butters, Kate Thomson, et al. · medRxiv · 3
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A Rare Splice-Site Variant in Cardiac Troponin-T (TNNT2): The Need for Ancestral Diversity in Genomic Reference Datasets
2024 · A. Butters, K. Thomson, et al. · Heart Lung and Circulation · 1
Utility of genetic testing in athletes with suspected inherited cardiac conditions
2026 · Jasmine Follett, Charlotte Burns, et al. · European Journal of Preventive Cardiology
“Concealed cardiomyopathy” is an important cause of autopsy-inconclusive sudden cardiac death and diagnosis impacts care of surviving relatives
2022 · J C Isbister, N Nowak, et al. · European Heart Journal
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The Elusive Hearts Study: Seeking Genetic Diagnoses in Gene-elusive Cases of Rare Monogenic Cardiovascular Diseases
2022 · E. Richardson, N. Krishnan, et al. · Heart Lung and Circulation
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The Role of Genetic Testing in Diagnosis and Care of Inherited Cardiac Conditions in a Specialised Multidisciplinary Clinic
2022 · N. Krishnan, F. Stafford, et al. · Heart Lung and Circulation
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Genetic Basis of Childhood Cardiomyopathy
2022 · R. Bagnall, E. Singer, et al. · Heart Lung and Circulation
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Contribution and Functional Characterisation of Splice-Disrupting Variants in Inherited Heart Disease and Sudden Cardiac Death
2022 · E. Singer, N. Nowak, et al. · Heart Lung and Circulation
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NSW HEARTS: The NSW Inherited Cardiomyopathy Cohort Study protocol
2022 · A. Butters, J. Do, et al. · Heart Lung and Circulation
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Concealed Cardiomyopathy as a Cause of Sudden Cardiac Death
2021 · J. Isbister, N. Nowak, et al. · Heart Lung and Circulation
030 Improving the Yield of Genetic Testing in Sudden Cardiac Arrest Survivors: Clinical Predictors and Extended Genetic Assessment
2020 · J. Isbister, N. Nowak, et al. · Heart Lung and Circulation
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592 Using Phenotype and Genomics to Solve Undiagnosed Cardiac Diseases: A Family With Unsolved Conduction Disease and Sudden Cardiac Death
2020 · F. Stafford, V. Connell, et al. · Heart Lung and Circulation
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579 Absence of Pathogenic Variants in Patients With Isolated Left Ventricular Trabeculations After Deep Phenotyping
2020 · S. Ross, E. Singer, et al. · Heart Lung and Circulation
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591 The Australian Genetic Heart Disease Registry: 13 Years on
2020 · J. Do, L. Yeates, et al. · Heart Lung and Circulation
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Works count: 29
Citation count: 343
H-index: 9
I10-index: 9
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