Ruth M. Brown

2.5k total citations
31 papers, 1.6k citations indexed

About

Ruth M. Brown is a scholar working on Molecular Biology, Clinical Biochemistry and Biochemistry. According to data from OpenAlex, Ruth M. Brown has authored 31 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 15 papers in Clinical Biochemistry and 12 papers in Biochemistry. Recurrent topics in Ruth M. Brown's work include Metabolism and Genetic Disorders (15 papers), Biochemical Acid Research Studies (12 papers) and Mitochondrial Function and Pathology (5 papers). Ruth M. Brown is often cited by papers focused on Metabolism and Genetic Disorders (15 papers), Biochemical Acid Research Studies (12 papers) and Mitochondrial Function and Pathology (5 papers). Ruth M. Brown collaborates with scholars based in United Kingdom, United States and Australia. Ruth M. Brown's co-authors include Garry K. Brown, Hans‐Henrik M. Dahl, Eric A. Shoubridge, William Chester Jordan, Andrew Cuthbert, Jianbo Yao, Katherine Fu, Zhiqing Zhu, Robert F. Newbold and Mario Chevrette and has published in prestigious journals such as Nature, Nature Genetics and PLoS ONE.

In The Last Decade

Ruth M. Brown

30 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ruth M. Brown United Kingdom	19	1.0k	795	316	282	162	31	1.6k
Brendan J. Battersby Finland	22	1.7k 1.6×	570 0.7×	37 0.1×	157 0.6×	40 0.2×	38	2.0k
Paweł Golik Poland	25	1.9k 1.9×	303 0.4×	16 0.1×	530 1.9×	58 0.4×	54	2.5k
Dimitra Chalkia United States	11	1.1k 1.1×	413 0.5×	16 0.1×	333 1.2×	47 0.3×	16	1.5k
Carmen Díez‐Sánchez Spain	15	840 0.8×	332 0.4×	14 0.0×	248 0.9×	40 0.2×	21	1.4k
Gavin Stewart Ireland	18	712 0.7×	229 0.3×	143 0.5×	76 0.3×	16 0.1×	46	1.2k
Gemma Gadaleta Italy	12	1.0k 1.0×	245 0.3×	14 0.0×	336 1.2×	48 0.3×	25	1.2k
Akitsugu Sato Japan	16	789 0.8×	383 0.5×	19 0.1×	122 0.4×	19 0.1×	24	968
Isha H. Jain United States	13	844 0.8×	175 0.2×	45 0.1×	151 0.5×	14 0.1×	24	1.1k
Hironori Ueda Japan	22	384 0.4×	63 0.1×	26 0.1×	410 1.5×	20 0.1×	86	1.6k
Maxim V. Gerashchenko United States	19	1.2k 1.2×	18 0.0×	38 0.1×	131 0.5×	41 0.3×	27	1.7k

Countries citing papers authored by Ruth M. Brown

Since Specialization

Citations

This map shows the geographic impact of Ruth M. 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 Ruth M. Brown with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ruth M. Brown more than expected).

Fields of papers citing papers by Ruth M. Brown

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ruth M. Brown

This figure shows the co-authorship network connecting the top 25 collaborators of Ruth M. Brown. A scholar is included among the top collaborators of Ruth M. 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 Ruth M. Brown. Ruth M. 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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20 of 20 papers shown

Horga, Alejandro, Isabel Pareés, Iain P. Hargreaves, et al.. (2019). Differential phenotypic expression of a novel PDHA1 mutation in a female monozygotic twin pair. Human Genetics. 138(11-12). 1313–1322. 9 indexed citations

Brown, Ruth M., et al.. (2015). Hybridization and Back-Crossing in Giant Petrels (Macronectes giganteus and M. halli) at Bird Island, South Georgia, and a Summary of Hybridization in Seabirds. PLoS ONE. 10(3). e0121688–e0121688. 24 indexed citations

Brown, Ruth M., et al.. (2014). Thiamine-Responsive and Non-responsive Patients with PDHC-E1 Deficiency: A Retrospective Assessment. JIMD Reports. 15. 13–27. 30 indexed citations

Wedatilake, Yehani, Ruth M. Brown, Robert McFarland, et al.. (2013). SURF1 deficiency: a multi-centre natural history study. Orphanet Journal of Rare Diseases. 8(1). 96–96. 91 indexed citations

Janer, Alexandre, Hana Antonická, Emilie Lalonde, et al.. (2012). An RMND1 Mutation Causes Encephalopathy Associated with Multiple Oxidative Phosphorylation Complex Deficiencies and a Mitochondrial Translation Defect. The American Journal of Human Genetics. 91(4). 737–743. 55 indexed citations

Brown, Ruth M., William Chester Jordan, Chris G. Faulkes, et al.. (2011). Phylogenetic Relationships in Pterodroma Petrels Are Obscured by Recent Secondary Contact and Hybridization. PLoS ONE. 6(5). e20350–e20350. 18 indexed citations

Brown, Ruth M., Richard A. Nichols, Chris G. Faulkes, et al.. (2010). Range expansion and hybridization in Round Island petrels (Pterodroma spp.): evidence from microsatellite genotypes. Molecular Ecology. 19(15). 3157–3170. 36 indexed citations

Ridout, Cheryl K., et al.. (2009). Pyruvate dehydrogenase E2 deficiency: A potentially treatable cause of episodic dystonia. European Journal of Paediatric Neurology. 14(4). 349–353. 36 indexed citations

Brown, Ruth M. & William Chester Jordan. (2009). Characterization of polymorphic microsatellite loci from Round Island Petrels (Pterodroma arminjoniana) and their utility in other seabird species. Journal für Ornithologie. 150(4). 925–929. 8 indexed citations

10.

Ridout, Cheryl K., Ruth M. Brown, John H. Walter, & Garry K. Brown. (2008). Somatic mosaicism for a PDHA1 mutation in a female with pyruvate dehydrogenase deficiency. Human Genetics. 124(2). 187–193. 12 indexed citations

11.

Brown, Ruth M., et al.. (2005). Clinical and genetic spectrum of pyruvate dehydrogenase deficiency: Dihydrolipoamide acetyltransferase (E2) deficiency. Annals of Neurology. 58(2). 234–241. 74 indexed citations

12.

López‐Vaamonde, Carlos, et al.. (2004). Social parasitism by male-producing reproductive workers in a eusocial insect. Nature. 430(6999). 557–560. 131 indexed citations

13.

Brown, Ruth M., Rosie Head, & Garry K. Brown. (2002). Pyruvate dehydrogenase E3 binding protein deficiency. Human Genetics. 110(2). 187–191. 22 indexed citations

14.

Brown, Ruth M., et al.. (2001). A SURF1 gene mutation presenting as isolated leukodystrophy. Annals of Neurology. 49(6). 797–800. 53 indexed citations

15.

Lissens, Willy, Linda De Meırleır, Sara Seneca, et al.. (2000). Mutations in the X-linked pyruvate dehydrogenase (E1) ? subunit gene (PDHA1) in patients with a pyruvate dehydrogenase complex deficiency. Human Mutation. 15(3). 209–219. 164 indexed citations

16.

Zhu, Zhiqing, Jianbo Yao, Timothy Johns, et al.. (1998). SURF1, encoding a factor involved in the biogenesis of cytochrome c oxidase, is mutated in Leigh syndrome. Nature Genetics. 20(4). 337–343. 474 indexed citations

17.

Thorburn, David R., et al.. (1995). A novel mutation (P316L) in a female with pyruvate dehydrogenase E1α deficiency. Human Mutation. 6(3). 274–275. 5 indexed citations

18.

Shevell, Michael, Paul M. Matthews, C R Scriver, et al.. (1994). Cerebral dysgenesis and lactic acidemia: An MRI/MRS phenotype associated with pyruvate dehydrogenase deficiency. Pediatric Neurology. 11(3). 224–229. 53 indexed citations

19.

Cross, J. Helen, Alan Connelly, David G. Gadian, et al.. (1994). Clinical diversity of pyruvate dehydrogenase deficiency. Pediatric Neurology. 10(4). 276–283. 39 indexed citations

20.

Brown, Ruth M., James Camakaris, & David M. Danks. (1984). Observations on the Menkes' and brindled mouse phenotypes in cell hybrids. Somatic Cell and Molecular Genetics. 10(4). 321–330. 2 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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