Jennifer R. Toone

1.8k total citations
39 papers, 1.2k citations indexed

About

Jennifer R. Toone is a scholar working on Clinical Biochemistry, Molecular Biology and Biochemistry. According to data from OpenAlex, Jennifer R. Toone has authored 39 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 25 papers in Clinical Biochemistry, 22 papers in Molecular Biology and 11 papers in Biochemistry. Recurrent topics in Jennifer R. Toone's work include Metabolism and Genetic Disorders (25 papers), Amino Acid Enzymes and Metabolism (10 papers) and Lysosomal Storage Disorders Research (8 papers). Jennifer R. Toone is often cited by papers focused on Metabolism and Genetic Disorders (25 papers), Amino Acid Enzymes and Metabolism (10 papers) and Lysosomal Storage Disorders Research (8 papers). Jennifer R. Toone collaborates with scholars based in Canada, United States and Australia. Jennifer R. Toone's co-authors include Derek A. Applegarth, Marion B. Coulter-Mackie, Johan L.K. Van Hove, Siddharth Shah, Julie Hoover‐Fong, Ada Hamosh, A. P. Sims, Harvey L. Levy, Peter Brophy and Dennis E. Vance and has published in prestigious journals such as Neurology, PEDIATRICS and Annals of Neurology.

In The Last Decade

Jennifer R. Toone

39 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jennifer R. Toone Canada 17 627 600 314 306 157 39 1.2k
Mark Korson United States 19 616 1.0× 553 0.9× 243 0.8× 121 0.4× 139 0.9× 38 1.1k
M Tuchman United States 20 567 0.9× 503 0.8× 153 0.5× 228 0.7× 186 1.2× 52 1.1k
Hélène Ogier de Baulny France 24 968 1.5× 1.2k 2.0× 290 0.9× 276 0.9× 168 1.1× 45 1.9k
F. Güttler Denmark 21 917 1.5× 681 1.1× 346 1.1× 141 0.5× 143 0.9× 67 1.2k
K. Bartholomé Germany 16 636 1.0× 441 0.7× 181 0.6× 162 0.5× 108 0.7× 27 931
Philip P. Dembure United States 16 606 1.0× 403 0.7× 200 0.6× 256 0.8× 304 1.9× 26 1.0k
Diane S. Roe United States 19 913 1.5× 811 1.4× 365 1.2× 99 0.3× 151 1.0× 27 1.2k
Sara Boenzi Italy 20 524 0.8× 539 0.9× 263 0.8× 101 0.3× 136 0.9× 43 1.0k
C. Jakobs Netherlands 17 621 1.0× 680 1.1× 223 0.7× 106 0.3× 116 0.7× 39 1.1k
Shigeaki Miyabayashi Japan 20 708 1.1× 1.0k 1.7× 131 0.4× 111 0.4× 59 0.4× 62 1.3k

Countries citing papers authored by Jennifer R. Toone

Since Specialization
Citations

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

Fields of papers citing papers by Jennifer R. Toone

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Jennifer R. Toone. 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 Jennifer R. Toone. The network helps show where Jennifer R. Toone may publish in the future.

Co-authorship network of co-authors of Jennifer R. Toone

This figure shows the co-authorship network connecting the top 25 collaborators of Jennifer R. Toone. A scholar is included among the top collaborators of Jennifer R. Toone 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 Jennifer R. Toone. Jennifer R. Toone 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.
Coulter-Mackie, Marion B., et al.. (2008). Mutation-based diagnostic testing for primary hyperoxaluria type 1: Survey of results. Clinical Biochemistry. 41(7-8). 598–602. 12 indexed citations
2.
Coulter-Mackie, Marion B., et al.. (2005). The major allele of the alanine:glyoxylate aminotransferase gene: Nine novel mutations and polymorphisms associated with primary hyperoxaluria type 1. Molecular Genetics and Metabolism. 86(1-2). 172–178. 19 indexed citations
3.
Applegarth, Derek A. & Jennifer R. Toone. (2005). Glycine encephalopathy (nonketotic hyperglycinemia): Comments and speculations. American Journal of Medical Genetics Part A. 140A(2). 186–188. 29 indexed citations
4.
Toone, Jennifer R., Derek A. Applegarth, Harvey L. Levy, Marion B. Coulter-Mackie, & Gary Lee. (2003). Molecular genetic and potential biochemical characteristics of patients with T-protein deficiency as a cause of glycine encephalopathy (NKH). Molecular Genetics and Metabolism. 79(4). 272–280. 12 indexed citations
5.
Coulter-Mackie, Marion B., et al.. (2003). The AGT gene in Africa: a distinctive minor allele haplotype, a polymorphism (V326I), and a novel PH1 mutation (A112D) in black Africans. Molecular Genetics and Metabolism. 78(1). 44–50. 19 indexed citations
6.
Toone, Jennifer R., Derek A. Applegarth, Shigeo Kure, et al.. (2002). Novel mutations in the P-protein (glycine decarboxylase) gene in patients with glycine encephalopathy (non-ketotic hyperglycinemia). Molecular Genetics and Metabolism. 76(3). 243–249. 14 indexed citations
7.
Coulter-Mackie, Marion B., et al.. (2002). Isolated Peripheral Neuropathy in Atypical Metachromatic Leukodystrophy: A Recurrent Mutation. Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 29(2). 159–163. 8 indexed citations
8.
Applegarth, Derek A. & Jennifer R. Toone. (2001). Nonketotic Hyperglycinemia (Glycine Encephalopathy): Laboratory Diagnosis. Molecular Genetics and Metabolism. 74(1-2). 139–146. 96 indexed citations
9.
Ham, Luc Van, et al.. (2000). Pyruvate dehydrogenase deficiency in Clumber and Sussex spaniels in the United States and Belgium. Ghent University Academic Bibliography (Ghent University). 9 indexed citations
10.
Applegarth, Derek A., et al.. (2000). Incidence of Inborn Errors of Metabolism in British Columbia, 1969–1996. PEDIATRICS. 105(1). e10–e10. 312 indexed citations
11.
Toone, Jennifer R., Derek A. Applegarth, Marion B. Coulter-Mackie, & E. James. (2000). Biochemical and Molecular Investigations of Patients with Nonketotic Hyperglycinemia. Molecular Genetics and Metabolism. 70(2). 116–121. 38 indexed citations
12.
13.
Jackson, Anthony H., Derek A. Applegarth, Jennifer R. Toone, Shigeo Kure, & Harvey L. Levy. (1999). Atypical Nonketotic Hyperglycinemia With Normal Cerebrospinal Fluid to Plasma Glycine Ratio. Journal of Child Neurology. 14(7). 464–467. 14 indexed citations
14.
Coulter-Mackie, Marion B., Derek A. Applegarth, Jennifer R. Toone, & Liane Gagnier. (1998). A protocol for detection of mitochondrial DNA deletions: characterization of a novel deletion. Clinical Biochemistry. 31(8). 627–632. 18 indexed citations
15.
Alroy, Joseph, M. Z. Jones, John W. Taylor, et al.. (1997). The ultrastructure of skin from a patient with mucopolysaccharidosis IIID. Acta Neuropathologica. 93(2). 210–213. 5 indexed citations
16.
Coulter-Mackie, Marion B., et al.. (1997). DNA-based diagnosis of arylsulfatase A deficiencies as a supplement to enzyme assay: A case in point. Clinical Biochemistry. 30(1). 57–61. 4 indexed citations
17.
Clarke, L., Jamal Nasir, Hanfang Zhang, et al.. (1994). Murine α-l-Iduronidase: cDNA Isolation and Expression. Genomics. 24(2). 311–316. 25 indexed citations
18.
Vallance, Hilary, Jennifer R. Toone, & Derek A. Applegarth. (1994). Measurement of pyruvate dehydrogenase complex (PDHC) in interleukin‐2 (IL‐2) stimulated lymphocytes. Journal of Inherited Metabolic Disease. 17(5). 627–628. 1 indexed citations
19.
Applegarth, Derek A., James E. Dimmick, & Jennifer R. Toone. (1989). Laboratory Detection of Metabolic Disease. Pediatric Clinics of North America. 36(1). 49–65. 8 indexed citations
20.

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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Mark Korson Breakdown of academic impact, for papers by M Tuchman Breakdown of academic impact, for papers by Hélène Ogier de Baulny Breakdown of academic impact, for papers by F. Güttler Breakdown of academic impact, for papers by K. Bartholomé Breakdown of academic impact, for papers by Philip P. Dembure Breakdown of academic impact, for papers by Diane S. Roe Breakdown of academic impact, for papers by Sara Boenzi Breakdown of academic impact, for papers by C. Jakobs Breakdown of academic impact, for papers by Shigeaki Miyabayashi
Rankless by CCL
2026