2023 - Research.com Genetics in United Kingdom Leader Award
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 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.
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.
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.
MITOCHONDRIAL DNA MUTATIONS IN HUMAN DISEASE
Robert W. Taylor;Doug M. Turnbull.
Nature Reviews Genetics (2005)
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)
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.
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)
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)
Mitochondrial DNA mutations and human disease
Helen A.L. Tuppen;Emma L. Blakely;Douglass M. Turnbull;Robert W. Taylor.
Biochimica et Biophysica Acta (2010)
Prevalence of mitochondrial DNA disease in adults
Andrew M. Schaefer;Robert McFarland;Emma L. Blakely;Langping He.
Annals of Neurology (2008)
Large-scale discovery of novel genetic causes of developmental disorders
T.W. Fitzgerald;S.S. Gerety;W.D. Jones;M. van Kogelenberg.
The epidemiology of pathogenic mitochondrial DNA mutations.
P. F. Chinnery;M. A. Johnson;T. M. Wardell;R. Singh-Kler.
Annals of Neurology (2000)
Pronuclear transfer in human embryos to prevent transmission of mitochondrial DNA disease
Lyndsey Craven;Helen A. Tuppen;Gareth D. Greggains;Stephen J. Harbottle.
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below: