G. K. Brown

1.0k total citations
18 papers, 801 citations indexed

About

G. K. Brown is a scholar working on Molecular Biology, Clinical Biochemistry and Biochemistry. According to data from OpenAlex, G. K. Brown has authored 18 papers receiving a total of 801 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Molecular Biology, 12 papers in Clinical Biochemistry and 10 papers in Biochemistry. Recurrent topics in G. K. Brown's work include Metabolism and Genetic Disorders (12 papers), Biochemical Acid Research Studies (10 papers) and Biochemical and Molecular Research (4 papers). G. K. Brown is often cited by papers focused on Metabolism and Genetic Disorders (12 papers), Biochemical Acid Research Studies (10 papers) and Biochemical and Molecular Research (4 papers). G. K. Brown collaborates with scholars based in United Kingdom, Australia and Canada. G. K. Brown's co-authors include R. M. Brown, Wendy Hutchison, Lucy J. Otero, H H Dahl, H Dahl, R. D. Scholem, Carol Wicking, Paul M. Matthews, M. V. Squier and David R. Marchington and has published in prestigious journals such as Journal of Biological Chemistry, Brain and Neurology.

In The Last Decade

G. K. Brown

18 papers receiving 784 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
G. K. Brown United Kingdom	13	541	416	324	130	90	18	801
R. M. Brown United Kingdom	18	663 1.2×	561 1.3×	384 1.2×	164 1.3×	102 1.1×	27	1.0k
Alan S. Lidsky United States	9	582 1.1×	577 1.4×	94 0.3×	142 1.1×	106 1.2×	10	855
A Ponzone Italy	16	366 0.7×	468 1.1×	132 0.4×	92 0.7×	98 1.1×	56	729
Toshinobu Matsuura Japan	17	854 1.6×	386 0.9×	199 0.6×	668 5.1×	53 0.6×	44	1.3k
C. Aulehla‐Scholz Germany	14	344 0.6×	312 0.8×	73 0.2×	96 0.7×	46 0.5×	27	703
Niels Gregersen Denmark	14	630 1.2×	535 1.3×	70 0.2×	65 0.5×	176 2.0×	28	935
Maja Di Rocco Italy	12	212 0.4×	122 0.3×	124 0.4×	69 0.5×	131 1.5×	20	459
James G. Coldwell United States	13	357 0.7×	222 0.5×	34 0.1×	177 1.4×	125 1.4×	17	620
Jorge Asin-Cayuela Sweden	11	669 1.2×	157 0.4×	40 0.1×	48 0.4×	77 0.9×	16	764
Catherine Brunel‐Guitton Canada	14	454 0.8×	203 0.5×	47 0.1×	38 0.3×	66 0.7×	28	621

Countries citing papers authored by G. K. Brown

Since Specialization

Citations

This map shows the geographic impact of G. K. Brown's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by G. K. Brown with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites G. K. Brown more than expected).

Fields of papers citing papers by G. K. Brown

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by G. K. Brown. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by G. K. Brown. The network helps show where G. K. Brown may publish in the future.

Co-authorship network of co-authors of G. K. Brown

This figure shows the co-authorship network connecting the top 25 collaborators of G. K. Brown. A scholar is included among the top collaborators of G. K. Brown based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with G. K. Brown. G. K. Brown is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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18 of 18 papers shown

Yapıcı, Zühal, Gülçin Benbir Şenel, Sema Saltık, et al.. (2009). Two Cases with Progressive Cystic Leukoencephalopathy. Neuropediatrics. 40(1). 47–51. 2 indexed citations

Ridout, Cheryl K., et al.. (2008). A putative exonic splicing enhancer in exon 7 of thePDHA1 gene affects splicing of adjacent exons. Human Mutation. 29(3). 451–451. 11 indexed citations

Brown, R. M., et al.. (2007). Pyruvate dehydrogenase E3 binding protein (protein X) deficiency. Developmental Medicine & Child Neurology. 48(9). 756–760. 6 indexed citations

Brown, R. M., et al.. (2006). Pyruvate dehydrogenase E3 binding protein (protein X) deficiency. Developmental Medicine & Child Neurology. 48(9). 756–756. 22 indexed citations

Brown, G. K.. (2005). Congenital brain malformations in mitochondrial disease. Journal of Inherited Metabolic Disease. 28(3). 393–401. 16 indexed citations

Matthews, Paul M., M. V. Squier, L. V. B. Nicholson, et al.. (1995). Muscle X-inactivation patterns and dystrophin expression in Duchenne muscular dystrophy carriers. Neuromuscular Disorders. 5(3). 209–220. 45 indexed citations

Matthews, Paul M., R. M. Brown, Lucy J. Otero, et al.. (1994). Pyruvate dehydrogenase deficiency. Clinical presentation and molecular genetic characterization of five new patients. Brain. 117(3). 435–443. 30 indexed citations

Brown, R. M. & G. K. Brown. (1994). Prenatal diagnosis of pyruvate dehydrogenase E1α subunit deficiency. Prenatal Diagnosis. 14(6). 435–441. 13 indexed citations

Brown, G. K., et al.. (1994). Pyruvate dehydrogenase deficiency.. Journal of Medical Genetics. 31(11). 875–879. 139 indexed citations

10.

Dahl, H H & G. K. Brown. (1994). Pyruvate dehydrogenase deficiency in a male caused by a point mutation (F205L) in the E1α subunit. Human Mutation. 3(2). 152–155. 11 indexed citations

11.

Matthews, Paul M., et al.. (1994). Isolated capillary proliferation in Leigh's syndrome.. PubMed. 13(3). 139–41. 4 indexed citations

12.

Matthews, Paul M., et al.. (1993). Molecular genetic characterization of an X‐linked form of Leigh's syndrome. Annals of Neurology. 33(6). 652–655. 51 indexed citations

13.

Matthews, Paul M., R. M. Brown, Lucy J. Otero, et al.. (1993). Neurodevelopmental abnormalities and lactic acidosis in a girl with a 20‐bp deletion in the X‐linked pyruvate dehydrogenase E1α subunit gene. Neurology. 43(10). 2025–2025. 19 indexed citations

14.

Brown, R. M. & G. K. Brown. (1993). X chromosome inactivation and the diagnosis of X linked disease in females.. Journal of Medical Genetics. 30(3). 177–184. 50 indexed citations

15.

Dahl, H, et al.. (1990). A testis-specific form of the human pyruvate dehydrogenase E1α subunit is coded for by an intronless gene on chromosome 4. Genomics. 8(2). 225–232. 167 indexed citations

16.

Dahl, H H, et al.. (1987). The human pyruvate dehydrogenase complex. Isolation of cDNA clones for the E1 alpha subunit, sequence analysis, and characterization of the mRNA.. Journal of Biological Chemistry. 262(15). 7398–7403. 115 indexed citations

17.

Wicking, Carol, et al.. (1986). Immunochemical analysis of normal and mutant forms of human pyruvate dehydrogenase. Biochemical Journal. 239(1). 89–96. 80 indexed citations

18.

Scholem, R. D. & G. K. Brown. (1983). Metabolism of malonic semialdehyde in man. Biochemical Journal. 216(1). 81–85. 20 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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