Calum A. MacRae spends much of his time researching Genetics, Internal medicine, Zebrafish, Endocrinology and Locus. His Genetics study incorporates themes from Titin and Hypertrophic cardiomyopathy. His studies examine the connections between Internal medicine and genetics, as well as such issues in Cardiology, with regards to Penetrance.
Calum A. MacRae combines subjects such as Myocyte, Regeneration, Cell biology, Computational biology and Drug discovery with his study of Zebrafish. His Endocrinology study combines topics in areas such as Regenerative medicine, Heart block, Torsades de pointes, Drug interaction and In vivo. The Missense mutation study which covers Molecular biology that intersects with TNNT2, Splice site mutation, Troponin T, TPM1 and Troponin complex.
His primary areas of study are Internal medicine, Cardiology, Zebrafish, Genetics and Cell biology. His research links Endocrinology with Internal medicine. His biological study spans a wide range of topics, including Family history and Cohort.
His Zebrafish course of study focuses on Computational biology and Model organism. Genetics is often connected to Disease in his work. His Disease research is multidisciplinary, incorporating perspectives in Precision medicine, Bioinformatics, Intensive care medicine, Genomics and Genetic testing.
The scientist’s investigation covers issues in Disease, Heart failure, Internal medicine, Intensive care medicine and Cell biology. The Disease study combines topics in areas such as Precision medicine, Arterial disease and Artificial intelligence. His Heart failure research includes elements of Stroke and Guideline.
His studies link Cardiology with Internal medicine. Calum A. MacRae focuses mostly in the field of Cell biology, narrowing it down to matters related to Zebrafish and, in some cases, Lamin, Cardiac conduction, LMNA, Cardiomyopathy and Cardiotoxicity. His Minor allele frequency study results in a more complete grasp of Genetics.
Calum A. MacRae mainly investigates Heart failure, Internal medicine, Stroke, Zebrafish and Emergency medicine. His research integrates issues of Genotype, Mutation and Cardiology in his study of Internal medicine. His work deals with themes such as Hypertrophic cardiomyopathy, Family medicine, Asymptomatic, Sudden cardiac death and Genetic testing, which intersect with Stroke.
The concepts of his Zebrafish study are interwoven with issues in Myocardial disease, Cardiotoxicity, In vivo and Bioinformatics. Calum A. MacRae is exploring Phenotype as part of his Genetics and Gene and Phenotype studies. He studies Hypotonia, a branch of Genetics.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease.
Diane Fatkin;Calum MacRae;Takeshi Sasaki;Matthew R. Wolff.
The New England Journal of Medicine (1999)
Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere.
Ludwig Thierfelder;Ludwig Thierfelder;Hugh Watkins;Hugh Watkins;Calum MacRae;Calum MacRae;Roger Lamas.
Cell (1994)
Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants.
Sekar Kathiresan;Benjamin F Voight;Shaun Purcell;Kiran Musunuru.
Nature Genetics (2009)
Variants conferring risk of atrial fibrillation on chromosome 4q25
Daniel F Gudbjartsson;David O Arnar;Anna Helgadottir;Solveig Gretarsdottir.
Nature (2007)
Primary contribution to zebrafish heart regeneration by gata4+ cardiomyocytes
Kazu Kikuchi;Jennifer E. Holdway;Andreas A. Werdich;Ryan M. Anderson.
Nature (2010)
Mutations in the desmosomal protein plakophilin-2 are common in arrhythmogenic right ventricular cardiomyopathy
Brenda Gerull;Brenda Gerull;Arnd Heuser;Arnd Heuser;Thomas Wichter;Matthias Paul.
Nature Genetics (2004)
Mutations in the cardiac myosin binding protein-C gene on chromosome 11 cause familial hypertrophic cardiomyopathy.
Hugh Watkins;Hugh Watkins;David Conner;Ludwig Thierfelder;John A. Jarcho.
Nature Genetics (1995)
Zebrafish as tools for drug discovery
Calum A. MacRae;Randall T. Peterson.
Nature Reviews Drug Discovery (2015)
Utility of Amino-Terminal Pro-Brain Natriuretic Peptide, Galectin-3, and Apelin for the Evaluation of Patients With Acute Heart Failure
Roland R. van Kimmenade;James L. Januzzi;Patrick T. Ellinor;Umesh C. Sharma.
Journal of the American College of Cardiology (2006)
Common variants in KCNN3 are associated with lone atrial fibrillation
Patrick T. Ellinor;Kathryn L. Lunetta;Kathryn L. Lunetta;Nicole L. Glazer;Arne Pfeufer.
Nature Genetics (2010)
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