Calum A. MacRae

Overview

Best Publications

• 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

  1532
  Citations

• 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

  1446
  Citations

• 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

  1232
  Citations

• Zebrafish as tools for drug discovery

  Calum A. MacRae;Randall T. Peterson

  1144
  Citations

• Primary contribution to zebrafish heart regeneration by gata4+ cardiomyocytes

  Kazu Kikuchi;Jennifer E. Holdway;Andreas A. Werdich;Ryan M. Anderson

  1140
  Citations

• Variants conferring risk of atrial fibrillation on chromosome 4q25

  Daniel F Gudbjartsson;David O Arnar;Anna Helgadottir;Solveig Gretarsdottir

  1062
  Citations

• 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

  990
  Citations

• 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

  789
  Citations

• 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

  724
  Citations

• RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

  Wei Guo;Sebastian Schafer;Marion L Greaser;Michael H Radke

  588
  Citations

• Rapid behavior-based identification of neuroactive small molecules in the zebrafish

  David Kokel;Jennifer Bryan;Christian Laggner;Rick White

  553
  Citations

• Common variants in KCNN3 are associated with lone atrial fibrillation

  Patrick T. Ellinor;Kathryn L. Lunetta;Kathryn L. Lunetta;Nicole L. Glazer;Arne Pfeufer

  548
  Citations

• Drugs That Induce Repolarization Abnormalities Cause Bradycardia in Zebrafish

  David J. Milan;Travis A. Peterson;Jeremy N. Ruskin;Randall T. Peterson

  491
  Citations

• Chemical suppression of a genetic mutation in a zebrafish model of aortic coarctation.

  Randall T Peterson;Stanley Y Shaw;Stanley Y Shaw;Travis A Peterson;David J Milan

  443
  Citations

• High-throughput assay for small molecules that modulate zebrafish embryonic heart rate

  C Geoffrey Burns;David J Milan;Eric J Grande;Eric J Grande;Wolfgang Rottbauer;Wolfgang Rottbauer

  438
  Citations

• C/EBPβ controls exercise-induced cardiac growth and protects against pathological cardiac remodeling

  Pontus Boström;Nina Mann;Jun Wu;Pablo A. Quintero

  429
  Citations

• The regenerative capacity of zebrafish reverses cardiac failure caused by genetic cardiomyocyte depletion

  Jinhu Wang;Daniela Panáková;Kazu Kikuchi;Jennifer E. Holdway

  387
  Citations

• Klf2 Is an Essential Regulator of Vascular Hemodynamic Forces In Vivo

  John S. Lee;Qing Yu;Jordan T. Shin;Eric Sebzda

  345
  Citations

• Familial aggregation in lone atrial fibrillation.

  Patrick T. Ellinor;Danita M. Yoerger;Jeremy N. Ruskin;Calum A. MacRae

  341
  Citations

• Risk stratification in the long-QT syndrome.

  Patrick T Ellinor;David J Milan;Calum A MacRae

  6
  Citations