D-Index & Metrics Best Publications
Genetics
UK
2023

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
Medicine D-index 103 Citations 40,624 857 World Ranking 4327 National Ranking 417
Genetics D-index 100 Citations 38,145 708 World Ranking 475 National Ranking 73

Research.com Recognitions

Awards & Achievements

2023 - Research.com Genetics in United Kingdom Leader Award

Overview

What is he best known for?

The fields of study he is best known for:

  • Gene
  • Internal medicine
  • Mutation

His primary areas of study are Mitochondrial DNA, Genetics, Mutation, Mitochondrial disease and Mitochondrion. His Mitochondrial DNA research includes elements of Molecular biology and Disease. His study in Point mutation, Gene, Respiratory chain, Genome and Mitochondrial respiratory chain are all subfields of Genetics.

His work carried out in the field of Mutation brings together such families of science as Polymerase, Phenotype, Southern blot, Mutant and Mitochondrial Encephalomyopathies. His Mitochondrial disease research is multidisciplinary, relying on both Mutation, Pathology, Mitochondrial encephalomyopathy, Genetic counseling and Nuclear DNA. The Mitochondrion study combines topics in areas such as Neuropathology, Transfer RNA and Pathogenesis.

His most cited work include:

  • MITOCHONDRIAL DNA MUTATIONS IN HUMAN DISEASE (1295 citations)
  • High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease. (1114 citations)
  • Recombinant Human Interleukin 1 Receptor Antagonist in the Treatment of Patients With Sepsis Syndrome: Results From a Randomized, Double-blind, Placebo-Controlled Trial (815 citations)

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

His primary areas of investigation include Mitochondrial DNA, Genetics, Mitochondrial disease, Mutation and Internal medicine. Robert W. Taylor usually deals with Mitochondrial DNA and limits it to topics linked to Pathology and Ataxia. His study in Gene, Respiratory chain, Mitochondrial respiratory chain, Phenotype and Human mitochondrial genetics falls within the category of Genetics.

His Mitochondrial disease research incorporates elements of Bioinformatics, Myopathy, Disease, Cytochrome c oxidase and Genetic heterogeneity. His research in Internal medicine intersects with topics in Diabetes mellitus, Endocrinology and Gastroenterology. His study ties his expertise on Mitochondrial myopathy together with the subject of Heteroplasmy.

He most often published in these fields:

  • Mitochondrial DNA (42.11%)
  • Genetics (35.32%)
  • Mitochondrial disease (32.40%)

What were the highlights of his more recent work (between 2017-2021)?

  • Mitochondrial disease (32.40%)
  • Mitochondrial DNA (42.11%)
  • Genetics (35.32%)

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

His main research concerns Mitochondrial disease, Mitochondrial DNA, Genetics, Mitochondrion and Gene. His Mitochondrial disease research includes themes of Pathology, Myopathy, Cytochrome c oxidase, Skeletal muscle and Respiratory chain. Robert W. Taylor has included themes like Muscle biopsy and Chronic progressive external ophthalmoplegia in his Cytochrome c oxidase study.

His study focuses on the intersection of Skeletal muscle and fields such as Mitochondrial myopathy with connections in the field of Mitochondrial biogenesis. His research integrates issues of Mutation, Molecular biology and Cell biology in his study of Mitochondrial DNA. His study in Heteroplasmy is interdisciplinary in nature, drawing from both Disease and Point mutation.

Between 2017 and 2021, his most popular works were:

  • mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease (76 citations)
  • mtDNA heteroplasmy level and copy number indicate disease burden in m.3243A>G mitochondrial disease (76 citations)
  • Going beyond prescription pain relievers to understand the opioid epidemic: the role of illicit fentanyl, new psychoactive substances, and street heroin. (62 citations)

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

  • Gene
  • Internal medicine
  • Enzyme

Robert W. Taylor spends much of his time researching Mitochondrial disease, Mitochondrial DNA, Genetics, Mitochondrion and Internal medicine. The concepts of his Mitochondrial disease study are interwoven with issues in Exome sequencing, Transcriptome, Asymptomatic carrier, Hypotonia and Genetic heterogeneity. His Mitochondrial DNA research integrates issues from Mitochondrial respiratory chain and Skeletal muscle.

His research related to Gene, Allele, TOP3A, Mutation and Deep sequencing might be considered part of Genetics. His studies deal with areas such as Molecular biology, Membrane protein and Nicotinamide, Enzyme as well as Mitochondrion. Robert W. Taylor has researched Internal medicine in several fields, including Endocrinology, Oncology and Medical 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

MITOCHONDRIAL DNA MUTATIONS IN HUMAN DISEASE

Robert W. Taylor;Doug M. Turnbull.
Nature Reviews Genetics (2005)

1924 Citations

High levels of mitochondrial DNA deletions in substantia nigra neurons in aging and Parkinson disease.

Andreas Bender;Kim J Krishnan;Christopher M Morris;Geoffrey A Taylor.
Nature Genetics (2006)

1606 Citations

Recombinant human interleukin 1 receptor antagonist in the treatment of patients with sepsis syndrome. Results from a randomized, double-blind, placebo-controlled trial. Phase III rhIL-1ra Sepsis Syndrome Study Group.

Fisher Cj;Dhainaut Jf;Opal Sm;Pribble Jp.
JAMA (1994)

1513 Citations

Mitochondrial DNA mutations in human colonic crypt stem cells

Robert W. Taylor;Martin J. Barron;Gillian M. Borthwick;Amy Gospel.
Journal of Clinical Investigation (2003)

741 Citations

Prevalence of nuclear and mitochondrial DNA mutations related to adult mitochondrial disease.

Gráinne S. Gorman;Andrew M. Schaefer;Yi Ng;Nicholas Gomez.
Annals of Neurology (2015)

722 Citations

Mitochondrial DNA mutations and human disease

Helen A.L. Tuppen;Emma L. Blakely;Douglass M. Turnbull;Robert W. Taylor.
Biochimica et Biophysica Acta (2010)

702 Citations

Prevalence of mitochondrial DNA disease in adults

Andrew M. Schaefer;Robert McFarland;Emma L. Blakely;Langping He.
Annals of Neurology (2008)

683 Citations

Large-scale discovery of novel genetic causes of developmental disorders

T.W. Fitzgerald;S.S. Gerety;W.D. Jones;M. van Kogelenberg.
Nature (2015)

661 Citations

The epidemiology of pathogenic mitochondrial DNA mutations.

P. F. Chinnery;M. A. Johnson;T. M. Wardell;R. Singh-Kler.
Annals of Neurology (2000)

531 Citations

Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease

Lyndsey Craven;Helen A. Tuppen;Gareth D. Greggains;Stephen J. Harbottle.
Nature (2010)

518 Citations

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