D-Index & Metrics Best Publications

D-Index & Metrics D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines.

Discipline name D-index D-index (Discipline H-index) only includes papers and citation values for an examined discipline in contrast to General H-index which accounts for publications across all disciplines. Citations Publications World Ranking National Ranking
Biology and Biochemistry D-index 67 Citations 22,571 180 World Ranking 3522 National Ranking 1794

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Internal medicine
  • Genetics

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 most cited work include:

  • Missense mutations in the rod domain of the lamin A/C gene as causes of dilated cardiomyopathy and conduction-system disease. (1045 citations)
  • Genome-wide association of early-onset myocardial infarction with single nucleotide polymorphisms and copy number variants. (939 citations)
  • Alpha-tropomyosin and cardiac troponin T mutations cause familial hypertrophic cardiomyopathy: a disease of the sarcomere. (883 citations)

What are the main themes of his work throughout his whole career to date?

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.

He most often published in these fields:

  • Internal medicine (34.29%)
  • Cardiology (23.33%)
  • Zebrafish (24.76%)

What were the highlights of his more recent work (between 2018-2021)?

  • Disease (15.48%)
  • Heart failure (13.81%)
  • Internal medicine (34.29%)

In recent papers he was focusing on the following fields of study:

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.

Between 2018 and 2021, his most popular works were:

  • Lysosomal Storage and Albinism Due to Effects of a De Novo CLCN7 Variant on Lysosomal Acidification. (22 citations)
  • Expanding the Spectrum of BAF-Related Disorders: De Novo Variants in SMARCC2 Cause a Syndrome with Intellectual Disability and Developmental Delay (18 citations)
  • De Novo Variants in WDR37 Are Associated with Epilepsy, Colobomas, Dysmorphism, Developmental Delay, Intellectual Disability, and Cerebellar Hypoplasia. (16 citations)

In his most recent research, the most cited papers focused on:

  • Gene
  • Internal medicine
  • Mutation

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.

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.
The New England Journal of Medicine (1999)

1512 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.
Cell (1994)

1395 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.
Nature Genetics (2009)

1113 Citations

Variants conferring risk of atrial fibrillation on chromosome 4q25

Daniel F Gudbjartsson;David O Arnar;Anna Helgadottir;Solveig Gretarsdottir.
Nature (2007)

936 Citations

Primary contribution to zebrafish heart regeneration by gata4+ cardiomyocytes

Kazu Kikuchi;Jennifer E. Holdway;Andreas A. Werdich;Ryan M. Anderson.
Nature (2010)

931 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.
Nature Genetics (2004)

882 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.
Nature Genetics (1995)

766 Citations

Zebrafish as tools for drug discovery

Calum A. MacRae;Randall T. Peterson.
Nature Reviews Drug Discovery (2015)

655 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.
Journal of the American College of Cardiology (2006)

626 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.
Nature Genetics (2010)

486 Citations

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