John W. Yarham

1.5k total citations
10 papers, 518 citations indexed

About

John W. Yarham is a scholar working on Molecular Biology, Clinical Biochemistry and Genetics. According to data from OpenAlex, John W. Yarham has authored 10 papers receiving a total of 518 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 4 papers in Clinical Biochemistry and 1 paper in Genetics. Recurrent topics in John W. Yarham's work include Mitochondrial Function and Pathology (9 papers), RNA modifications and cancer (6 papers) and RNA and protein synthesis mechanisms (6 papers). John W. Yarham is often cited by papers focused on Mitochondrial Function and Pathology (9 papers), RNA modifications and cancer (6 papers) and RNA and protein synthesis mechanisms (6 papers). John W. Yarham collaborates with scholars based in United Kingdom, United States and Australia. John W. Yarham's co-authors include Robert W. Taylor, Robert McFarland, Emma L. Blakely, Joanna L. Elson, Charlotte L. Alston, Mazhor Aldosary, Langping He, Francesco Bruni, Enrico Baruffini and Tek N. Lamichhane and has published in prestigious journals such as PLoS Genetics, Journal of Neuropathology & Experimental Neurology and Journal of the Neurological Sciences.

In The Last Decade

John W. Yarham

10 papers receiving 514 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
John W. Yarham United Kingdom	8	486	170	53	39	17	10	518
Daniela Fornůsková Czechia	6	353 0.7×	110 0.6×	26 0.5×	26 0.7×	20 1.2×	8	398
Jeannette Gootjes Netherlands	12	446 0.9×	129 0.8×	25 0.5×	40 1.0×	13 0.8×	17	497
Sarah L. Stenton Germany	9	316 0.7×	210 1.2×	82 1.5×	12 0.3×	21 1.2×	14	369
Camilla Koolmeister Sweden	11	427 0.9×	172 1.0×	37 0.7×	30 0.8×	20 1.2×	15	473
Anna Vincent Germany	2	330 0.7×	93 0.5×	92 1.7×	8 0.2×	18 1.1×	3	345
Takashi Ohsato Japan	7	317 0.7×	102 0.6×	17 0.3×	30 0.8×	29 1.7×	11	372
Sarah Groves United Kingdom	4	250 0.5×	89 0.5×	55 1.0×	9 0.2×	31 1.8×	8	334
Jose Carlo United States	6	260 0.5×	195 1.1×	20 0.4×	8 0.2×	23 1.4×	6	287
Morten J. Corydon Denmark	7	387 0.8×	365 2.1×	35 0.7×	12 0.3×	11 0.6×	9	489
William Lee Australia	7	261 0.5×	67 0.4×	29 0.5×	46 1.2×	4 0.2×	11	295

Countries citing papers authored by John W. Yarham

Since Specialization

Citations

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

Fields of papers citing papers by John W. Yarham

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by John W. Yarham. 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 John W. Yarham. The network helps show where John W. Yarham may publish in the future.

Co-authorship network of co-authors of John W. Yarham

This figure shows the co-authorship network connecting the top 25 collaborators of John W. Yarham. A scholar is included among the top collaborators of John W. Yarham 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 John W. Yarham. John W. Yarham 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

Yarham, John W., Tek N. Lamichhane, Angela Pyle, et al.. (2014). Defective i6A37 Modification of Mitochondrial and Cytosolic tRNAs Results from Pathogenic Mutations in TRIT1 and Its Substrate tRNA. PLoS Genetics. 10(6). e1004424–e1004424. 102 indexed citations

Lax, Nichola Z., Sharmilee Gnanapavan, Charlotte L. Alston, et al.. (2013). Early-Onset Cataracts, Spastic Paraparesis, and Ataxia Caused by a Novel Mitochondrial tRNA^Glu(MT-TE) Gene Mutation Causing Severe Complex I Deficiency: A Clinical, Molecular, and Neuropathologic Study. Journal of Neuropathology & Experimental Neurology. 72(2). 164–175. 13 indexed citations

Zamzami, Mazin A., John A. Duley, Gareth Price, et al.. (2013). Inosine Triphosphate Pyrophosphohydrolase (ITPA) polymorphic sequence variants in adult hematological malignancy patients and possible association with mitochondrial DNA defects. Journal of Hematology & Oncology. 6(1). 24–24. 17 indexed citations

Blakely, Emma L., John W. Yarham, Charlotte L. Alston, et al.. (2013). Pathogenic Mitochondrial t RNA Point Mutations: Nine Novel Mutations Affirm Their Importance as a Cause of Mitochondrial Disease. Human Mutation. 34(9). 1260–1268. 61 indexed citations

Tuppen, Helen, K Naess, Nancy G. Kennaway, et al.. (2012). Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy. European Journal of Human Genetics. 20(8). 897–904. 11 indexed citations

Yarham, John W., Robert McFarland, Robert W. Taylor, & Joanna L. Elson. (2012). A proposed consensus panel of organisms for determining evolutionary conservation of mt-tRNA point mutations. Mitochondrion. 12(5). 533–538. 27 indexed citations

Elson, Joanna L., M G Sweeney, Vincent Procaccio, et al.. (2012). Toward a mtDNA locus-specific mutation database using the LOVD platform. Human Mutation. 33(9). 1352–1358. 7 indexed citations

Yarham, John W., Emma L. Blakely, Charlotte L. Alston, et al.. (2012). The m.3291T>C mt-tRNALeu(UUR) mutation is definitely pathogenic and causes multisystem mitochondrial disease. Journal of the Neurological Sciences. 325(1-2). 165–169. 5 indexed citations

Yarham, John W., Mazhor Aldosary, Emma L. Blakely, et al.. (2011). A comparative analysis approach to determining the pathogenicity of mitochondrial tRNA mutations. Human Mutation. 32(11). 1319–1325. 136 indexed citations

10.

Yarham, John W., Joanna L. Elson, Emma L. Blakely, Robert McFarland, & Robert W. Taylor. (2010). Mitochondrial tRNA mutations and disease. Wiley Interdisciplinary Reviews - RNA. 1(2). 304–324. 139 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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