2023 - Research.com Genetics in United Kingdom Leader Award
Douglass M. Turnbull spends much of his time researching Mitochondrial DNA, Genetics, Mutation, Mitochondrion and Mitochondrial disease. Douglass M. Turnbull combines subjects such as Respiratory chain and Disease, Pathology with his study of Mitochondrial DNA. The Mutation study combines topics in areas such as Somatic cell, Mutant, DNA, mitochondrial fusion and Molecular biology.
His Mitochondrion research incorporates elements of Multiple sclerosis, Transfer RNA and Central nervous system. His Mitochondrial disease research is multidisciplinary, incorporating elements of Epidemiology, Polymorphism, Bioinformatics, Intensive care medicine and Nuclear DNA. His research investigates the connection between Heteroplasmy and topics such as Mitochondrial myopathy that intersect with issues in Skeletal muscle.
Douglass M. Turnbull mainly investigates Mitochondrial DNA, Genetics, Mitochondrion, Mitochondrial disease and Mutation. His Mitochondrial DNA research integrates issues from Molecular biology, Disease and Point mutation. Gene, Genome, Mitochondrial myopathy, Mutation and Phenotype are subfields of Genetics in which his conducts study.
His work investigates the relationship between Mitochondrion and topics such as Skeletal muscle that intersect with problems in Cytochrome c oxidase. His Mitochondrial disease research includes elements of Bioinformatics, Pathology, Internal medicine, Chronic progressive external ophthalmoplegia and Pediatrics. His Mutation study integrates concerns from other disciplines, such as Mutant and Somatic cell.
His primary areas of study are Mitochondrial disease, Mitochondrial DNA, Mitochondrion, Genetics and Internal medicine. His Mitochondrial disease study incorporates themes from Neurodegeneration, Cohort, Pathology, Ataxia and Disease burden. His Mitochondrial DNA research is multidisciplinary, relying on both Mutation, Disease, Mitochondrial respiratory chain and Skeletal muscle.
The concepts of his Mutation study are interwoven with issues in Mitochondrial myopathy, Bioinformatics and Somatic cell. His studies in Mitochondrion integrate themes in fields like Oxidative phosphorylation, Neuroscience and Function. His Internal medicine research is multidisciplinary, incorporating perspectives in Endocrinology, Oncology and Cardiology.
The scientist’s investigation covers issues in Mitochondrial DNA, Mitochondrial disease, Mitochondrion, Genetics and Skeletal muscle. His Mitochondrial DNA research includes themes of Mutation, Computational biology, Disease and Mitochondrial respiratory chain. Douglass M. Turnbull has included themes like Internal medicine, Epilepsy, Genome and Pathology in his Mitochondrial disease study.
His work carried out in the field of Mitochondrion brings together such families of science as Chronic progressive external ophthalmoplegia and Endocrinology. He performs integrative study on Genetics and Reproductive technology. His research integrates issues of Molecular biology, Mitochondrial myopathy and Mitochondrial biogenesis in his study of Skeletal muscle.
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Reanalysis and revision of the Cambridge reference sequence for human mitochondrial DNA
Richard M. Andrews;Iwona Kubacka;Patrick F. Chinnery;Robert N. Lightowlers.
Nature Genetics (1999)
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)
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)
Ageing and Parkinson's disease: why is advancing age the biggest risk factor?
Amy V. Reeve;Eve Simcox;Doug Turnbull.
Ageing Research Reviews (2014)
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)
Reduced-Median-Network Analysis of Complete Mitochondrial DNA Coding-Region Sequences for the Major African, Asian, and European Haplogroups
Corinna Herrnstadt;Joanna L. Elson;Eoin Fahy;Gwen Preston.
American Journal of Human Genetics (2002)
Leber hereditary optic neuropathy
P Y W Man;D M Turnbull;D M Turnbull;P F Chinnery;P F Chinnery.
Journal of Medical Genetics (2002)
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