J. V. Leonard

671 total citations
13 papers, 379 citations indexed

About

J. V. Leonard is a scholar working on Clinical Biochemistry, Molecular Biology and Physiology. According to data from OpenAlex, J. V. Leonard has authored 13 papers receiving a total of 379 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Clinical Biochemistry, 6 papers in Molecular Biology and 4 papers in Physiology. Recurrent topics in J. V. Leonard's work include Metabolism and Genetic Disorders (7 papers), Biochemical and Molecular Research (3 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). J. V. Leonard is often cited by papers focused on Metabolism and Genetic Disorders (7 papers), Biochemical and Molecular Research (3 papers) and Glycogen Storage Diseases and Myoclonus (2 papers). J. V. Leonard collaborates with scholars based in United Kingdom, India and Australia. J. V. Leonard's co-authors include J. K. Lloyd, M A Preece, David B. Dunger, Olaf A. Bodamer, Douglass M. Turnbull, D. Halliday, A. A. M. Morris, S. E. Olpin, Morteza Pourfarzam and N. Herschkowitz and has published in prestigious journals such as The Lancet, The Journal of Pediatrics and Journal of Inherited Metabolic Disease.

In The Last Decade

J. V. Leonard

13 papers receiving 353 citations

Peers

J. V. Leonard

CB

MB

PHYSI

EDM

SURGE

Richard J. Hodach United States

D. Novak United States

Uwe Stave Germany

F. X. Coudé France

Mahoko Furujo Japan

Ference J. Loupatty Netherlands

Marilyn M Lusk United States

İlyas Okur Türkiye

Valentina Colonna Italy

Jacob L. Zaidman Israel

Richard J. Hodach United States

J. V. Leonard

167 ×1.1

CB

259 ×1.9

MB

86 ×0.9

PHYSI

21 ×0.2

EDM

32 ×0.4

SURGE

Citations per year, relative to J. V. Leonard J. V. Leonard (= 1×) peers Richard J. Hodach

Countries citing papers authored by J. V. Leonard

Since Specialization

Citations

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

Fields of papers citing papers by J. V. Leonard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by J. V. Leonard. 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 J. V. Leonard. The network helps show where J. V. Leonard may publish in the future.

Co-authorship network of co-authors of J. V. Leonard

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

All Works

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13 of 13 papers shown

1.

Olpin, S. E., N. J. Manning, James R. Bonham, et al.. (2003). Mutation and biochemical analysis in carnitine palmitoyltransferase type II (CPT II) deficiency. Journal of Inherited Metabolic Disease. 26(6). 543–557. 43 indexed citations

2.

Wilson, Callum, P. J. Lee, & J. V. Leonard. (2001). Plasma glutamine and ammonia concentrations in ornithine carbamoyltransferase deficiency and citrullinaemia. Journal of Inherited Metabolic Disease. 24(7). 691–695. 7 indexed citations

3.

Morris, A. A. M., S. E. Olpin, M. Brivet, et al.. (1998). A patient with carnitine-acylcarnitine translocase deficiency with a mild phenotype. The Journal of Pediatrics. 132(3). 514–516. 34 indexed citations

4.

Morris, Andrew A. M., et al.. (1998). N‐Acetylglutamate synthetase deficiency: Favourable experience with carbamylglutamate. Journal of Inherited Metabolic Disease. 21(8). 867–868. 32 indexed citations

5.

Bodamer, Olaf A., J. V. Leonard, & D. Halliday. (1997). Dietary treatment in late-onset acid maltase deficiency. European Journal of Pediatrics. 156(S1). S39–S42. 28 indexed citations

6.

Bodamer, Olaf A., Ertan Mayatepek, & J. V. Leonard. (1997). Leucine and glucose kinetics in glycogen storage disease type IIIa. Journal of Inherited Metabolic Disease. 20(6). 847–847. 2 indexed citations

7.

Leonard, J. V., et al.. (1995). Ketonuria and medium‐chain acyl‐CoA dehydrogenase deficiency. Journal of Inherited Metabolic Disease. 18(1). 98–99. 7 indexed citations

8.

Rajagopalan, B., et al.. (1987). STUDY OF HEREDITARY FRUCTOSE INTOLERANCE BY USE OF 31P MAGNETIC RESONANCE SPECTROSCOPY. The Lancet. 330(8565). 931–934. 67 indexed citations

9.

Walter, J H, Peter T. Clayton, & J. V. Leonard. (1986). 3‐Hydroxy‐3‐methylglutaryl‐CoA lyase deficiency. Journal of Inherited Metabolic Disease. 9(3). 287–288. 13 indexed citations

10.

Lloyd, J. K., et al.. (1980). LONG-TERM FOLLOW-UP OF CHILDREN WITH FAMILIAL HYPERCHOLESTEROLÆMIA TREATED WITH CHOLESTYRAMINE. The Lancet. 316(8200). 873–875. 65 indexed citations

11.

Dunger, David B., et al.. (1980). EFFECT OF NALOXONE IN A PREVIOUSLY UNDESCRIBED HYPOTHALAMIC SYNDROME. The Lancet. 315(8181). 1277–1281. 57 indexed citations

12.

Milla, Peter J., et al.. (1978). Disordered intestinal function in glycogen storage disease. Journal of Inherited Metabolic Disease. 1(4). 155–157. 22 indexed citations

13.

Leonard, J. V.. (1975). An Assessment of the Performance of the SMA 12/micro Autoanalyser in Clinical Use. Annals of Clinical Biochemistry International Journal of Laboratory Medicine. 12(1-6). 70–77. 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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