Roy W A Peake

666 total citations
42 papers, 438 citations indexed

About

Roy W A Peake is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, Roy W A Peake has authored 42 papers receiving a total of 438 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Clinical Biochemistry, 22 papers in Molecular Biology and 13 papers in Physiology. Recurrent topics in Roy W A Peake's work include Metabolism and Genetic Disorders (23 papers), Metabolomics and Mass Spectrometry Studies (10 papers) and Mitochondrial Function and Pathology (8 papers). Roy W A Peake is often cited by papers focused on Metabolism and Genetic Disorders (23 papers), Metabolomics and Mass Spectrometry Studies (10 papers) and Mitochondrial Function and Pathology (8 papers). Roy W A Peake collaborates with scholars based in United States, Saudi Arabia and United Kingdom. Roy W A Peake's co-authors include Mark D. Kellogg, Olaf A. Bodamer, Adam J. Spanier, Bin Huang, Robert S. Kahn, Hadley S. Sauers‐Ford, Lisa Crawford, Alexandra E. Irvine, T. C. M. Morris and Judie A. Howrylak and has published in prestigious journals such as PLoS ONE, PEDIATRICS and Scientific Reports.

In The Last Decade

Roy W A Peake

37 papers receiving 431 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roy W A Peake United States 12 145 117 73 69 68 42 438
Annalisa Sechi Italy 16 225 1.6× 133 1.1× 62 0.8× 74 1.1× 112 1.6× 38 631
Yiqiong Ma China 14 54 0.4× 276 2.4× 66 0.9× 79 1.1× 69 1.0× 19 596
Mustafa Vakur Bor Denmark 14 74 0.5× 176 1.5× 71 1.0× 28 0.4× 116 1.7× 39 595
Monia Elasmi Tunisia 15 93 0.6× 99 0.8× 79 1.1× 87 1.3× 36 0.5× 49 544
Samsul Arefin Sweden 11 76 0.5× 128 1.1× 47 0.6× 35 0.5× 26 0.4× 23 524
Hisato Shima Japan 11 140 1.0× 341 2.9× 71 1.0× 58 0.8× 22 0.3× 44 687
Deborah Ramini Italy 14 105 0.7× 156 1.3× 37 0.5× 53 0.8× 34 0.5× 25 454
Kensuke Asaba Japan 10 131 0.9× 130 1.1× 45 0.6× 26 0.4× 156 2.3× 20 602
Maria Wanic-Kossowska Poland 12 55 0.4× 83 0.7× 72 1.0× 47 0.7× 48 0.7× 47 452
Volker Richter Germany 15 97 0.7× 118 1.0× 148 2.0× 125 1.8× 32 0.5× 23 719

Countries citing papers authored by Roy W A Peake

Since Specialization
Citations

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

Fields of papers citing papers by Roy W A Peake

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Roy W A Peake. 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 Roy W A Peake. The network helps show where Roy W A Peake may publish in the future.

Co-authorship network of co-authors of Roy W A Peake

This figure shows the co-authorship network connecting the top 25 collaborators of Roy W A Peake. A scholar is included among the top collaborators of Roy W A Peake 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 Roy W A Peake. Roy W A Peake is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Almontashiri, Naif A. M., Mohammed Saleh, Mohamed Abu‐Farha, et al.. (2024). ME2 Deficiency Is Associated With Recessive Neurodevelopmental Disorder. Clinical Genetics. 107(2). 201–207.
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Kellogg, Mark D., et al.. (2024). A rare and underestimated cause of anion gap metabolic acidosis in a pediatric patient. American Journal of Clinical Pathology. 162(Supplement_1). S187–S187.
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Ptolemy, Adam S., Kung-Chia Young, Christopher MacDonald, et al.. (2023). B-201 Development of a Quantitative Gas Chromatography Tandem Mass Spectrometry Method for Metabolic Profiling of Urine Organic Acids. Clinical Chemistry. 69(Supplement_1).
6.
Shamsi, Monis Bilal, Mohamed Saleh, Roy W A Peake, et al.. (2021). Clinical characterization and further confirmation of the autosomal recessive SLC12A2 disease. Journal of Human Genetics. 66(7). 689–695. 9 indexed citations
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Peake, Roy W A, et al.. (2021). Progressive Ataxia and Neurologic Regression in RFXANK -Associated Bare Lymphocyte Syndrome. Neurology Genetics. 7(3). e586–e586. 2 indexed citations
9.
Peer‐Zada, Abdul Ali, Abdulrahman Al‐Hussaini, Sateesh Maddirevula, et al.. (2020). New paradigms of USP53 disease: normal GGT cholestasis, BRIC, cholangiopathy, and responsiveness to rifampicin. Journal of Human Genetics. 66(2). 151–159. 25 indexed citations
10.
Almontashiri, Naif A. M., Li Zha, Young Kim, et al.. (2020). Clinical Validation of Targeted and Untargeted Metabolomics Testing for Genetic Disorders: A 3 Year Comparative Study. Scientific Reports. 10(1). 9382–9382. 20 indexed citations
11.
Faqeih, Eissa, et al.. (2020). Metabolic Acidosis and Hypoglycemia in a Child with Leigh-Like Phenotype. Clinical Chemistry. 66(5). 739–741.
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Trommelen, Jorn, Jean Nyakayiru, Luc J. C. van Loon, et al.. (2018). Arginine does not rescue p.Q188R mutation deleterious effect in classic galactosemia. Orphanet Journal of Rare Diseases. 13(1). 212–212. 10 indexed citations
14.
Almontashiri, Naif A. M., Gerard T. Berry, Joseph A. Majzoub, & Roy W A Peake. (2018). Abnormal Glycerol Metabolism in a Child with Global Developmental Delay, Adrenal Insufficiency, and Intellectual Disability. Clinical Chemistry. 64(12). 1785–1787. 1 indexed citations
15.
Wojcik, Monica H., Klaas J. Wierenga, Lance H. Rodan, et al.. (2017). Beta-Ketothiolase Deficiency Presenting with Metabolic Stroke After a Normal Newborn Screen in Two Individuals. JIMD Reports. 39. 45–54. 7 indexed citations
16.
Morton, Sarah U., Edward Neilan, Roy W A Peake, et al.. (2016). Hyperammonemia as a Presenting Feature in Two Siblings with FBXL4 Variants. JIMD Reports. 35. 7–15. 10 indexed citations
17.
Rodan, Lance H., et al.. (2016). Now You See It, Now You Don't: Unidentified Plasma Amino Acid Peak. Clinical Chemistry. 62(5). 781–782. 3 indexed citations
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McDonald, Timothy J., Mandy H. Perry, Roy W A Peake, et al.. (2012). EDTA Improves Stability of Whole Blood C-Peptide and Insulin to Over 24 Hours at Room Temperature. PLoS ONE. 7(7). e42084–e42084. 39 indexed citations
20.
Turner, Helen, et al.. (2011). Seasonal pseudohyperkalaemia: no longer an issue?. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 49(1). 94–96. 14 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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