D. T. Brown

1.4k total citations
10 papers, 747 citations indexed

About

D. T. Brown is a scholar working on Molecular Biology, Clinical Biochemistry and Biotechnology. According to data from OpenAlex, D. T. Brown has authored 10 papers receiving a total of 747 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 6 papers in Clinical Biochemistry and 2 papers in Biotechnology. Recurrent topics in D. T. Brown's work include Mitochondrial Function and Pathology (8 papers), Metabolism and Genetic Disorders (6 papers) and Cassava research and cyanide (2 papers). D. T. Brown is often cited by papers focused on Mitochondrial Function and Pathology (8 papers), Metabolism and Genetic Disorders (6 papers) and Cassava research and cyanide (2 papers). D. T. Brown collaborates with scholars based in United Kingdom, Italy and Germany. D. T. Brown's co-authors include Patrick F. Chinnery, Douglass M. Turnbull, Mark Johnson, T. M. Wardell, Christine Hayes, Laurence A. Bindoff, Neil Howell, David C. Samuels, Richard M. Andrews and Paul Riordan‐Eva and has published in prestigious journals such as Brain, Neurology and Annals of Neurology.

In The Last Decade

D. T. Brown

10 papers receiving 726 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
D. T. Brown United Kingdom	9	677	408	71	55	46	10	747
R.N. Lightowlers United Kingdom	11	624 0.9×	280 0.7×	45 0.6×	35 0.6×	70 1.5×	14	723
Mina Pellegrini Sweden	7	734 1.1×	270 0.7×	52 0.7×	43 0.8×	37 0.8×	7	791
H Poláková Slovakia	11	221 0.3×	153 0.4×	18 0.3×	60 1.1×	30 0.7×	29	450
Erik Hagström Sweden	5	495 0.7×	177 0.4×	39 0.5×	20 0.4×	60 1.3×	8	569
Angela Schmidt Germany	9	201 0.3×	110 0.3×	24 0.3×	25 0.5×	101 2.2×	21	426
Viktoriya Peeva Germany	10	488 0.7×	177 0.4×	61 0.9×	8 0.1×	28 0.6×	15	588
Cristina Dallabona Italy	14	703 1.0×	258 0.6×	79 1.1×	25 0.5×	48 1.0×	41	809
Marris G. Dibley Australia	4	502 0.7×	132 0.3×	31 0.4×	10 0.2×	38 0.8×	4	585
Marina A. Schwab Germany	6	339 0.5×	323 0.8×	36 0.5×	10 0.2×	18 0.4×	6	453
M. Isabel G. Lopez Sanchez Australia	15	565 0.8×	99 0.2×	25 0.4×	8 0.1×	42 0.9×	24	696

Countries citing papers authored by D. T. Brown

Since Specialization

Citations

This map shows the geographic impact of D. T. 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 D. T. Brown with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites D. T. Brown more than expected).

Fields of papers citing papers by D. T. Brown

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by D. T. 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 D. T. Brown. The network helps show where D. T. Brown may publish in the future.

Co-authorship network of co-authors of D. T. Brown

This figure shows the co-authorship network connecting the top 25 collaborators of D. T. Brown. A scholar is included among the top collaborators of D. T. 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 D. T. Brown. D. T. 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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10 of 10 papers shown

1.

Durham, Steve E., D. T. Brown, Douglass M. Turnbull, & Patrick F. Chinnery. (2006). Progressive depletion of mtDNA in mitochondrial myopathy. Neurology. 67(3). 502–504. 10 indexed citations

2.

Man, Patrick Yu Wai, D. T. Brown, Manfred Wehnert, et al.. (2002). NDUFA-1 is not a nuclear modifier gene in Leber hereditary optic neuropathy. Neurology. 58(12). 1861–1862. 11 indexed citations

3.

Chinnery, Patrick F., Geoffrey A. Taylor, Neil Howell, et al.. (2001). Point Mutations of the mtDNA Control Region in Normal and Neurodegenerative Human Brains. The American Journal of Human Genetics. 68(2). 529–532. 71 indexed citations

4.

Chinnery, Patrick F., D. T. Brown, Richard M. Andrews, et al.. (2001). The mitochondrial ND6 gene is a hot spot for mutations that cause Leber's hereditary optic neuropathy. Brain. 124(1). 209–218. 140 indexed citations

5.

Brown, D. T., et al.. (2001). Random Genetic Drift Determines the Level of Mutant mtDNA in Human Primary Oocytes. The American Journal of Human Genetics. 68(2). 533–536. 118 indexed citations

6.

Chinnery, Patrick F., Doris J. Taylor, D. T. Brown, et al.. (2000). Very low levels of the mtDNA A3243G mutation associated with mitochondrial dysfunction in vivo. Annals of Neurology. 47(3). 381–384. 5 indexed citations

7.

Chinnery, Patrick F., Doris J. Taylor, D. T. Brown, et al.. (2000). Very low levels of the mtDNA A3243G mutation associated with mitochondrial dysfunction in vivo. Annals of Neurology. 47(3). 381–384. 55 indexed citations

8.

Chinnery, Patrick F., Mark Johnson, T. M. Wardell, et al.. (2000). The epidemiology of pathogenic mitochondrial DNA mutations. Annals of Neurology. 48(2). 188–193. 270 indexed citations

9.

Brown, D. T., Peter D. Turner, & Catherine O’Reilly. (1995). Expression of the cyanide hydratase enzyme fromFusarium lateritiuminEscherichia coliand identification of an essential cysteine residue. FEMS Microbiology Letters. 134(2-3). 143–146. 9 indexed citations

10.

Turner, Phil, et al.. (1993). Purification and properties of cyanide hydratase from Fusarium lateritium and analysis of the corresponding chy1 gene. Journal of General Microbiology. 139(8). 1807–1815. 58 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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