Gavin Brown
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Scottish-Australian mathematician and university administrator
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Gavin Brown mathematics Degrees
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Mathematics
Why Is Gavin Brown Influential?
(Suggest an Edit or Addition)According to Wikipedia, Gavin Brown AO FAA CorrFRSE was a Scottish-born mathematician and long-serving Vice-Chancellor and Principal of the University of Sydney between 1996 and 2008. Early career After attending secondary school at Madras College in St Andrews, Brown graduated with a Master of Arts degree from the University of St Andrews , and a Doctor of Philosophy degree from the University of Newcastle upon Tyne . His academic career began at the University of Liverpool, where he became a senior lecturer in mathematics.
Gavin Brown 's Published Works
Number of citations in a given year to any of this author's works
Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author
Published Works
- A prospective study of children with head injures: III. Psychiatric sequelae (1981) (355)
- A prospective study of children with head injuries: II. Cognitive sequelae (1981) (261)
- Glucose transporters: Structure, function and consequences of deficiency (2000) (202)
- A testis-specific form of the human pyruvate dehydrogenase E1 alpha subunit is coded for by an intronless gene on chromosome 4. (1990) (197)
- Pyruvate dehydrogenase deficiency. (1994) (175)
- Models of Metal Binding Structures in Fulvic Acid from the Suwannee River, Georgia (1998) (166)
- Families of mtDNA re-arrangements can be detected in patients with mtDNA deletions: duplications may be a transient intermediate form. (1993) (151)
- X-chromosome localization of the functional gene for the E1 alpha subunit of the human pyruvate dehydrogenase complex. (1989) (130)
- A new point mutation associated with mitochondrial encephalomyopathy. (1993) (129)
- The human pyruvate dehydrogenase complex. Isolation of cDNA clones for the E1 alpha subunit, sequence analysis, and characterization of the mRNA. (1987) (120)
- Deficiency of respiratory chain complex I is a common cause of leigh disease (1996) (117)
- A prospective study of children with head injuries: I. Design and methods (1980) (113)
- beta-hydroxyisobutyryl coenzyme A deacylase deficiency: a defect in valine metabolism associated with physical malformations. (1982) (106)
- Potential endocrine disrupting organic chemicals in treated municipal wastewater and river water (2000) (99)
- Arthroscopic Treatment of Lateral Epicondylitis: Clinical and Cadaveric Studies (2005) (95)
- Comparison of the relative levels of the 3243 (A-->G) mtDNA mutation in heteroplasmic adult and fetal tissues. (1994) (94)
- Immunochemical analysis of normal and mutant forms of human pyruvate dehydrogenase. (1986) (91)
- Differential methylation of the hypervariable locus DXS255 on active and inactive X chromosomes correlates with the expression of a human X-linked gene. (1990) (79)
- Are duplications of mitochondrial DNA characteristic of Kearns-Sayre syndrome? (1994) (77)
- Molecular genetic characterization of an X‐linked form of Leigh's syndrome (1993) (75)
- Cerebral dysgenesis and lactic acidemia: an MRI/MRS phenotype associated with pyruvate dehydrogenase deficiency. (1994) (74)
- Mutations and polymorphisms in the pyruvate dehydrogenase E1α gene (1992) (74)
- X chromosome inactivation and the diagnosis of X linked disease in females. (1993) (72)
- Urinary organic acids in succinic semialdehyde dehydrogenase deficiency: Evidence of α-oxidation of 4-hydroxybutyric acid, interaction of succinic semialdehyde with pyruvate dehydrogenase and possible secondary inhibition of mitochondrial β-oxidation (1987) (67)
- The Clinical and Biochemical Spectrum of Human Pyruvate Dehydrogenase Complex Deficiency (1989) (67)
- An RMND1 Mutation causes encephalopathy associated with multiple oxidative phosphorylation complex deficiencies and a mitochondrial translation defect. (2012) (65)
- “Cerebral” lactic acidosis: defects in pyruvate metabolism with profound brain damage and minimal systemic acidosis (2004) (64)
- Functional and genetic studies demonstrate that mutation in the COX15 gene can cause Leigh syndrome (2004) (63)
- Reversible infantile respiratory chain deficiency is a unique, genetically heterogenous mitochondrial disease (2011) (61)
- Characterization and diagenesis of strong-acid carboxyl groups in humic substances (2003) (60)
- Molecular weight differences between human platelet and placental monoamine oxidase. (1980) (59)
- Pyruvate dehydrogenase deficiency caused by deletion of a 7-bp repeat sequence in the E1 alpha gene. (1990) (56)
- Structural organization of the gene for the E1 alpha subunit of the human pyruvate dehydrogenase complex. (1989) (54)
- Clinical diversity of pyruvate dehydrogenase deficiency. (1994) (52)
- Neuropathology and pathogenesis of mitochondrial diseases (1996) (51)
- Interconversion of different molecular weight forms of human erythrocyte orotidylate decarboxylase. (1975) (50)
- Pyruvate dehydrogenase deficiency. Clinical presentation and molecular genetic characterization of five new patients. (1994) (43)
- Variation in mitochondrial DNA levels in muscle from normal controls. Is depletion of mtDNA in patients with mitochondrial myopathy a distinct clinical syndrome? (1995) (41)
- Simultaneous determination of Ca, Cu, Ni, Zn and Cd binding strengths with fulvic acid fractions by Schubert's method (1999) (41)
- Malonyl coenzyme a decarboxylase deficiency (1984) (38)
- Pyruvate dehydrogenase deficiency presenting as dystonia in childhood. (2004) (35)
- Malonyl coenzyme A decarboxylase deficiency. Clinical and biochemical findings in a second child with a more severe enzyme defect (1986) (34)
- Cu(II) binding by a pH-fractionated fulvic acid (1999) (33)
- Atypical pyroglutamic aciduria: possible role of paracetamol (1990) (32)
- Neurodevelopmental abnormalities and lactic acidosis in a girl with a 20‐bp deletion in the X‐linked pyruvate dehydrogenase E1α subunit gene (1993) (30)
- Pyruvate dehydrogenase E3 binding protein (protein X) deficiency. (2006) (30)
- Alteration of quaternary structural behaviour of an hepatic orotate phosphoribosyltransferase-orotidine-5'-phosphate decarboxylase complex in rats following allopurinol therapy. (1972) (30)
- Rupture of the biceps brachii tendon sheath in two dogs. (2004) (28)
- X-linked pyruvate dehydrogenase E1α subunit deficiency in heterozygous females: Variable manifestation of the same mutation (1992) (28)
- Inhibition of human erythrocyte orotidylate decarboxylase. (1977) (27)
- Platelet monoamine oxidase: specific activity and turnover number in headache. (1982) (26)
- Subunit structure of the orotate phosphoribosyltransferase--orotidylate decarboxylase complex from human erythrocytes. (1977) (25)
- Transfection screening for primary defects in the pyruvate dehydrogenase E1alpha subunit gene. (1997) (24)
- Arginine 302 mutations in the pyruvate dehydrogenase E1α subunit gene: Identification of further patients and in vitro demonstration of pathogenicity (1998) (23)
- Pyruvate dehydrogenase E1α subunit genes in the mouse: Mapping and comparison with human homologs (1990) (23)
- Hyperammonaemia and lactic acidosis in a patient with pyruvate dehydrogenase deficiency (1987) (22)
- Intracellular heteroplasmy for disease-associated point mutations in mtDNA: implications for disease expression and evidence for mitotic segregation of heteroplasmic units of mtDNA (1995) (22)
- Pyruvate dehydrogenase E1α deficiency (1992) (20)
- Dichloroacetate stabilizes the mutant E1α subunit in pyruvate dehydrogenase deficiency (1999) (20)
- Mutations and polymorphisms in the pyruvate dehydrogenase E1 alpha gene. (1992) (20)
- Lactic acidosis and developmental delay due to deficiency of E3 binding protein (protein X) of the pyruvate dehydrogenase complex (2004) (19)
- Toxicity screening in a large municipal wastewater system (1989) (19)
- Prenatal diagnosis of pyruvate dehydrogenase E1α subunit deficiency (1994) (18)
- Leigh syndrome resulting from de novo mutation at position 8993 of mitochodrial DNA (1997) (18)
- Metabolism of malonic semialdehyde in man. (1983) (17)
- Traumatic fracture of the patella in 11 cats (2008) (17)
- Mitochondrial DNA does not appear to influence the congenital onset type of myotonic dystrophy. (1995) (17)
- Congenital brain malformations in mitochondrial disease (2005) (16)
- Client-assessed long-term outcome in dogs with surgical site infection following tibial plateau levelling osteotomy (2016) (16)
- Characterization of the mutations in three patients with pyruvate dehydrogenase E1α deficiency (1991) (16)
- Succinic semialdehyde dehydrogenase deficiency—A further case (1985) (15)
- The use of muscle stimulation for inducing scoliotic curves. A preliminary report. (1975) (15)
- Pyruvate dehydrogenase deficiency in a male caused by a point mutation (F205L) in the E1α subunit (1994) (15)
- Synthesis of mitochondrial DNA in permeabilised human cultured cells. (2001) (13)
- Fluorometric determination of "albumin-titratable bilirubin" in the jaundiced neonate. (1975) (13)
- Immunological Studies of Human Monoamine Oxidases (1982) (12)
- Association of cerebral dysgenesis and lactic acidemia with X-linked PDH E1 alpha subunit mutations in females. (1995) (12)
- Diagnostic difficulties with common SURF1 mutations in patients with cytochrome oxidase-deficient Leigh syndrome (2004) (12)
- Bottlenecks and beyond: mitochondrial DNA segregation in health and disease (1997) (12)
- Sequence variations in the NDUFA1 gene encoding a subunit of complex I of the respiratory chain (2001) (11)
- A putative exonic splicing enhancer in exon 7 of the PDHA1 gene affects splicing of adjacent exons (2008) (10)
- Properties of succinic semialdehyde dehydrogenase in cultured human lymphoblasts. (1985) (8)
- Pyruvate dehydrogenase E1 alpha deficiency. (1992) (8)
- Investigation of mitochondrial disease. (1995) (8)
- Episodes of severe metabolic acidosis in a patient with 3-methylglutaconic aciduria (1987) (8)
- Complementation analysis of systemic cytochrome oxidase deficiency presenting as Leigh syndrome (1996) (7)
- Mitochondrial cytopathies, phenotypic heterogeneity and a high incidence. (2006) (7)
- Localization of human liver 6-phosphofructo-2-kinase/fructose-2,6-bisphosphatase (PFKFB1) within a YAC contig in Xp11.21. (1997) (7)
- Cytochrome c oxidase deficiency in subacute necrotizing encephalopathy (Leigh syndrome) (1989) (6)
- Arginine 302 mutations in the pyruvate dehydrogenase E1alpha subunit gene: identification of further patients and in vitro demonstration of pathogenicity. (1998) (6)
- Avulsion fragmentation of the tibial tuberosity apophysis and associated patellar tendon enthesopathy in a skeletally immature dog (2013) (5)
- Pyruvate dehydrogenase deficiency in a male caused by a point mutation (F205L) in the E1 alpha subunit. (1994) (5)
- Neonatal seizures and limb malformations associated with liver-specific complex IV respiratory chain deficiency. (2004) (5)
- A pathogenic glutamate‐to‐aspartate substitution (D296E) in the pyruvate dehydrogenase E1 subunit gene PDHA1 (2003) (5)
- Isolated capillary proliferation in Leigh's syndrome. (1994) (5)
- Prenatal diagnosis of pyruvate dehydrogenase E1 alpha subunit deficiency. (1994) (5)
- Pyruvate dehydrogenase deficiency presenting as dystonia in childhood (2004) (5)
- Characterization of the mutations in three patients with pyruvate dehydrogenase E1 alpha deficiency. (1991) (5)
- Pyruvate dehydrogenase deficiency caused by a 5 base pair duplication in the E1 alpha subunit. (1993) (5)
- A novel mutation (P316L) in a female with pyruvate dehydrogenase E1α deficiency (1995) (5)
- Metabolic disorders of embryogenesis (1994) (4)
- Pyruvate dehydrogenase E3 binding protein (protein X) deficiency (2006) (4)
- Syndrome of the month Pyruvate dehydrogenase deficiency (3)
- Two cases with progressive cystic leukoencephalopathy. (2009) (2)
- Striatal degeneration in glutaric acidaemia type II (2004) (2)
- Is mild deficiency of mitochondrial malonyl CoA decarboxylase a risk factor for hyperlipidemia? (1988) (2)
- Radioimmunological assay of placental monoamine oxidase [proceedings]. (1979) (2)
- Properties of human monoamine oxidases. (1982) (2)
- A novel mutation (P316L) in a female with pyruvate dehydrogenase E1 alpha deficiency. (1995) (1)
- TO JMG Functional and genetic studies demonstrate that mutation in the COX 15 gene can cause Leigh syndrome (2004) (0)
- Recombinant DNA techniques in medicine. (1988) (0)
- Profound neurological illness, relieved by protein restriction, in a baby with a transient disturbance in the metabolism of ingested isoleucine (1987) (0)
- CRASH INJURY BIOMECHANICS: PROCEEDINGS OF A CONFERENCE HELD IN ADELAIDE, SOUTH AUSTRALIA, 19-21 JULY 1992 (1993) (0)
- FETAL BRAIN MRI FINDINGS IN TWO CASES OF PYRUVATE DEHYDROGENASE DEFICIENCY (2006) (0)
- “Cerebral” lactic acidosis and cerebrospinal fluid pH (1988) (0)
- oxidase isoforms in regenerating rat skeletal muscle c Developmentally regulated expression of cytochrome (2015) (0)
- Patient outcomes following traumatic fracture of the femoral shaft. Does surgical approach influence outcomes? (2012) (0)
- Book review (1996) (0)
- TRAUMATIC SUBTROCHANTERIC FRACTURES. CLASSIFICATION, INTERVENTION, COMPLICATIONS AND PATIENT OUTCOMES (2012) (0)
- P55 Reversible infantile respiratory chain deficiency is a genetically heterogenous mitochondrial disease (2011) (0)
- Deoxyribose-5-phosphate aldolase deficiency — A harmless inborn error of metabolism (1983) (0)
- M14 Biallelic mutations in Oxa1l cause a mitochondrial encephalopathy and combined oxidative phosphorylation dysfunction (2018) (0)
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