N. G. Kennaway

2.1k total citations
34 papers, 1.2k citations indexed

About

N. G. Kennaway is a scholar working on Molecular Biology, Clinical Biochemistry and Biochemistry. According to data from OpenAlex, N. G. Kennaway has authored 34 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 22 papers in Clinical Biochemistry and 10 papers in Biochemistry. Recurrent topics in N. G. Kennaway's work include Metabolism and Genetic Disorders (21 papers), Mitochondrial Function and Pathology (15 papers) and Amino Acid Enzymes and Metabolism (10 papers). N. G. Kennaway is often cited by papers focused on Metabolism and Genetic Disorders (21 papers), Mitochondrial Function and Pathology (15 papers) and Amino Acid Enzymes and Metabolism (10 papers). N. G. Kennaway collaborates with scholars based in United States, Netherlands and Canada. N. G. Kennaway's co-authors include Neil R.M. Buist, Roderick Capaldi, T. Burlingame, Victor Darley‐Usmar, Philippe Soriano, Markus Grompe, Milton J. Finegold, C N Ou, Richard G. Weleber and William Bank and has published in prestigious journals such as Proceedings of the National Academy of Sciences, The Lancet and Journal of Biological Chemistry.

In The Last Decade

N. G. Kennaway

34 papers receiving 1.2k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
N. G. Kennaway United States 18 838 520 174 137 110 34 1.2k
Nancy G. Kennaway United States 22 1.5k 1.8× 906 1.7× 179 1.0× 166 1.2× 93 0.8× 37 2.0k
Uta Lichter‐Konecki United States 20 608 0.7× 717 1.4× 201 1.2× 223 1.6× 39 0.4× 35 1.1k
E. Holme Sweden 22 1.1k 1.3× 926 1.8× 262 1.5× 303 2.2× 17 0.2× 45 1.7k
Kathryn E. Kronquist United States 15 675 0.8× 120 0.2× 89 0.5× 135 1.0× 26 0.2× 20 987
Michael S. DeBuysere United States 17 350 0.4× 257 0.5× 223 1.3× 260 1.9× 44 0.4× 23 750
Audrey Boutron France 21 1.2k 1.4× 627 1.2× 230 1.3× 228 1.7× 15 0.1× 47 1.6k
Hélène Ogier de Baulny France 24 1.2k 1.4× 968 1.9× 276 1.6× 290 2.1× 22 0.2× 45 1.9k
Yanling Yang China 19 857 1.0× 505 1.0× 101 0.6× 117 0.9× 14 0.1× 138 1.5k
H. F. Teutsch Germany 19 340 0.4× 162 0.3× 48 0.3× 176 1.3× 238 2.2× 32 1000
Kurt Amsler United States 17 639 0.8× 62 0.1× 117 0.7× 73 0.5× 25 0.2× 34 974

Countries citing papers authored by N. G. Kennaway

Since Specialization
Citations

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

Fields of papers citing papers by N. G. Kennaway

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by N. G. Kennaway. 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 N. G. Kennaway. The network helps show where N. G. Kennaway may publish in the future.

Co-authorship network of co-authors of N. G. Kennaway

This figure shows the co-authorship network connecting the top 25 collaborators of N. G. Kennaway. A scholar is included among the top collaborators of N. G. Kennaway 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 N. G. Kennaway. N. G. Kennaway 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.
Gibson, K. Michael, Suzanne B. Cassidy, Laurie H. Seaver, et al.. (1994). Fatal cardiomyopathy associated with 3‐hydroxy‐3‐methylglutaryl‐CoA lyase deficiency. Journal of Inherited Metabolic Disease. 17(3). 291–294. 30 indexed citations
2.
Henriksson, K. G., et al.. (1993). Mitochondrial myopathy with succinate dehydrogenase and aconitase deficiency. Abnormalities of several iron-sulfur proteins.. Journal of Clinical Investigation. 92(6). 2660–2666. 68 indexed citations
3.
Ibel, H., W. Endres, Thomas Deufel, et al.. (1993). Multiple respiratory chain abnormalities associated with hypertrophic cardiomyopathy and 3-methylglutaconic aciduria. European Journal of Pediatrics. 152(8). 665–670. 27 indexed citations
4.
Grompe, Markus, Milton J. Finegold, C N Ou, et al.. (1993). Loss of fumarylacetoacetate hydrolase is responsible for the neonatal hepatic dysfunction phenotype of lethal albino mice.. Genes & Development. 7(12a). 2298–2307. 287 indexed citations
5.
Mashima, Yukihiko, et al.. (1992). A single-base change at a splice acceptor site in the ornithine aminotransferase gene causes abnormal RNA splicing in gyrate atrophy. Human Genetics. 90(3). 305–7. 8 indexed citations
6.
Elliot, Diane L., Berkley R. Powell, Neil R.M. Buist, N. G. Kennaway, & L. Goldberg. (1992). CARNITINE RESPONSIVE LIPID MYOPATHY. Medicine & Science in Sports & Exercise. 24(Supplement). S56–S56. 1 indexed citations
7.
Inana, George, et al.. (1989). Molecular basis of ornithine aminotransferase defect in gyrate atrophy.. PubMed. 314. 191–111. 7 indexed citations
8.
Hotta, Yoshihiro, N. G. Kennaway, Richard G. Weleber, & George Inana. (1989). Inheritance of ornithine aminotransferase gene, mRNA, and enzyme defect in a family with gyrate atrophy of the choroid and retina.. PubMed. 44(3). 353–7. 11 indexed citations
9.
Inana, George, Yoshihiro Hotta, Carmelann Zintz, et al.. (1988). Expression defect of ornithine aminotransferase gene in gyrate atrophy.. PubMed. 29(7). 1001–5. 28 indexed citations
10.
Smith, Margaret L., N. G. Kennaway, Neil R.M. Buist, et al.. (1987). Prenatal diagnosis of cystinosis utilizing chorionic villus sampling. Prenatal Diagnosis. 7(1). 23–26. 8 indexed citations
11.
12.
Chance, B., Donald Younkin, Richard I. Kelley, et al.. (1986). Magnetic resonance spectroscopy of normal and diseased muscles. American Journal of Medical Genetics. 25(4). 659–679. 25 indexed citations
13.
Eleff, Scott M., N. G. Kennaway, Neil R.M. Buist, et al.. (1984). 31P NMR study of improvement in oxidative phosphorylation by vitamins K3 and C in a patient with a defect in electron transport at complex III in skeletal muscle.. Proceedings of the National Academy of Sciences. 81(11). 3529–3533. 206 indexed citations
14.
Tongue, Andrea Cibis, et al.. (1984). Ophthalmic Manifestations of Infantile Phytanic Acid Storage Disease. Archives of Ophthalmology. 102(9). 1317–1321. 33 indexed citations
15.
Wirtz, Markus, N. G. Kennaway, & Richard G. Weleber. (1984). Heterogeneity and complementation analysis of fibroblasts from vitamin B6 responsive and non‐responsive patients with gyrate atrophy of the choroid and retina. Journal of Inherited Metabolic Disease. 8(2). 71–74. 5 indexed citations
16.
Giardini, O, A Cantani, N. G. Kennaway, & P D’Eufemia. (1983). Chronic Tyrosinemia Associated with 4-Hydroxyphenylpyruvate Dioxygenase Deficiency with Acute Intermittent Ataxia and without Visceral and Bone Involvement. Pediatric Research. 17(1). 25–29. 36 indexed citations
17.
Kennaway, N. G., Richard G. Weleber, & Neil R.M. Buist. (1980). Gyrate atrophy of the choroid and retina with hyperornithinemia: biochemical and histologic studies and response to vitamin B6.. PubMed. 32(4). 529–41. 43 indexed citations
18.
Kennaway, N. G., et al.. (1980). Complementation analysis in fibroblasts from eight patients with clinically different forms of citrullinaemia. Journal of Inherited Metabolic Disease. 4(1). 23–25. 4 indexed citations
19.
Spector, Elaine, et al.. (1977). Citrullinemia, argininosuccinate synthetase deficiency. Cytogenetic and Genome Research. 19(1). 51–52. 6 indexed citations
20.
Fellman, J.H., Neil R.M. Buist, & N. G. Kennaway. (1977). Pitfalls in metabolic studies: the origin of urinary p-Tyramine. Clinical Biochemistry. 10(5). 168–170. 3 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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