What is he best known for?
The fields of study he is best known for:
Brian H. Robinson spends much of his time researching Biochemistry, Internal medicine, Respiratory chain, Molecular biology and Endocrinology.
His studies in Superoxide, Radical, Mitochondrion, Leigh disease and Reactive oxygen species are all subfields of Biochemistry research.
His Internal medicine study integrates concerns from other disciplines, such as Pyruvate dehydrogenase deficiency, Pyruvate dehydrogenase complex and Mitochondrial Encephalomyopathies, Mitochondrial myopathy.
His work deals with themes such as Adenosine triphosphate, Mitochondrial disease, Mitochondrial respiratory chain, Fibroblast and Metabolism, which intersect with Respiratory chain.
His research integrates issues of Genetics, Polymerase chain reaction, Gene, Biotin and Genomic library in his study of Molecular biology.
His Endocrinology study combines topics from a wide range of disciplines, such as Pyruvate Dehydrogenase Complex Deficiency Disease, Oxoglutarate dehydrogenase complex, Physiology and Proportionate short stature.
His most cited work include:
- Mitochondria, oxygen free radicals, disease and ageing (897 citations)
- Approaches to DNA Mutagenesis: An Overview (459 citations)
- Heteroplasmic mtDNA mutation (T----G) at 8993 can cause Leigh disease when the percentage of abnormal mtDNA is high. (442 citations)
What are the main themes of his work throughout his whole career to date?
Brian H. Robinson focuses on Biochemistry, Molecular biology, Internal medicine, Pyruvate dehydrogenase complex and Endocrinology.
His Biochemistry research focuses on Mitochondrion, Pyruvate carboxylase, Pyruvate dehydrogenase kinase, Oxoglutarate dehydrogenase complex and Pyruvate decarboxylation.
His studies in Mitochondrion integrate themes in fields like Citrate synthase, Enzyme and Pathology.
His Molecular biology research incorporates elements of Complementary DNA, Genetics, Gene, Mutation and Cytochrome c oxidase.
His study focuses on the intersection of Cytochrome c oxidase and fields such as Respiratory chain with connections in the field of Mitochondrial respiratory chain.
His Endocrinology research is multidisciplinary, relying on both Hypotonia and Dihydrolipoamide dehydrogenase.
He most often published in these fields:
- Biochemistry (49.25%)
- Molecular biology (33.67%)
- Internal medicine (25.13%)
What were the highlights of his more recent work (between 2004-2015)?
- Mitochondrion (24.62%)
- Molecular biology (33.67%)
- Mitochondrial DNA (12.06%)
In recent papers he was focusing on the following fields of study:
His primary areas of study are Mitochondrion, Molecular biology, Mitochondrial DNA, Biochemistry and Internal medicine.
The Mitochondrion study combines topics in areas such as Citrate synthase and Bioinformatics.
He interconnects Missense mutation, Pyruvate dehydrogenase phosphatase, Mutant and Cytochrome c oxidase in the investigation of issues within Molecular biology.
The various areas that Brian H. Robinson examines in his Mitochondrial DNA study include Mutation, Respiratory chain and Skeletal muscle.
Brian H. Robinson has included themes like Gastroenterology, Congenital lactic acidosis, Endocrinology and Pathology in his Internal medicine study.
His work on Lactic acidosis as part of general Endocrinology research is often related to Scad, thus linking different fields of science.
Between 2004 and 2015, his most popular works were:
- Inhibition of Mitochondrial Translation as a Therapeutic Strategy for Human Acute Myeloid Leukemia (369 citations)
- Mutations in Iron-Sulfur Cluster Scaffold Genes NFU1 and BOLA3 Cause a Fatal Deficiency of Multiple Respiratory Chain and 2-Oxoacid Dehydrogenase Enzymes (188 citations)
- Long-term outcome and clinical spectrum of 73 pediatric patients with mitochondrial diseases. (127 citations)
In his most recent research, the most cited papers focused on:
His scientific interests lie mostly in Mitochondrion, Molecular biology, Internal medicine, Biochemistry and Respiratory chain.
His study in Mitochondrion is interdisciplinary in nature, drawing from both Leukemia, Cancer research, BCL2-related protein A1 and Citrate synthase.
His work focuses on many connections between Molecular biology and other disciplines, such as Missense mutation, that overlap with his field of interest in Point mutation, Mutant and Heteroplasmy.
His Internal medicine research includes themes of Gastroenterology, Congenital lactic acidosis, Endocrinology and Pathology.
His Biochemistry study is mostly concerned with Pyruvate dehydrogenase phosphatase, Pyruvate dehydrogenase complex, Gene product and Pyruvate decarboxylation.
His Respiratory chain study contributes to a more complete understanding of Genetics.
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