Nancy G. Kennaway

2.6k citations

37 papers · 2.0k indexed · h-index 22

Molecular Biology top 5%
Clinical Biochemistry top 0.2%
Biochemistry top 2%
Physiology
Cellular and Molecular Neuroscience top 10%

Co-authors: Neil R.M. Buist Eric A. Shoubridge Hana Antonická Kristen C. Hoffbuhr Richard G. Weleber Miriam D. Burton Tanja Taivassalo Ronald G. Haller
Topics: Metabolism and Genetic Disorders (22 papers)Mitochondrial Function and Pathology (17 papers)ATP Synthase and ATPases Research (10 papers)
Cited by: Clinical Biochemistry Biochemistry Molecular Biology
Journals: Journal of Biological Chemistry Nature Genetics The Journal of Clinical Endocrinology & Metabolism
Partner nations: United States Canada Japan

In The Last Decade

Nancy G. Kennaway

37 papers receiving 1.9k citations

Peers

Countries citing papers authored by Nancy G. Kennaway

Since Specialization

Citations

This map shows the geographic impact of Nancy 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 Nancy 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 Nancy G. Kennaway more than expected).

Fields of papers citing papers by Nancy G. Kennaway

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Mutations in the mitochondrial tRNASer(AGY) gene are associated with deafness, retinal degeneration, myopathy and epilepsy 2012 ·European Journal of Human Genetics ·Helen Tuppen,K Naess,Nancy G. Kennaway,Mazhor Aldosary,Nicole Lesko,John W. Yarham,Helene Bruhn,Rolf Wibom,Inger Nennesmo,Richard G. Weleber,Emma L. Blakely,Robert W. Taylor,Robert McFarland	11
2	The molecular basis for tissue specificity of the oxidative phosphorylation deficiencies in patients with mutations in the mitochondrial translation factor EFG1 2006 ·Human Molecular Genetics ·Hana Antonická,Florin Sasarman,Nancy G. Kennaway,Eric A. Shoubridge	111
3	Contrasting phenotypes in three patients with novel mutations in mitochondrial tRNA genes 2004 ·Molecular Genetics and Metabolism ·Roberto P. Anitori,(unknown),Franklin Quan,Richard G. Weleber,Neil R.M. Buist,Eric A. Shoubridge,Nancy G. Kennaway	35
4	Mutations in COX15 Produce a Defect in the Mitochondrial Heme Biosynthetic Pathway, Causing Early-Onset Fatal Hypertrophic Cardiomyopathy 2003 ·The American Journal of Human Genetics ·Hana Antonická,André Mattman,(unknown),D. Moira Glerum,Kristen C. Hoffbuhr,Scot C. Leary,Nancy G. Kennaway,Eric A. Shoubridge	237
5	Identification and Characterization of a Common Set of Complex I Assembly Intermediates in Mitochondria from Patients with Complex I Deficiency 2003 ·Journal of Biological Chemistry ·Hana Antonická,Isla Ogilvie,Tanja Taivassalo,Roberto P. Anitori,Ronald G. Haller,John Vissing,Nancy G. Kennaway,Eric A. Shoubridge	158
6	Aerobic conditioning in patients with mitochondrial myopathies: Physiological, biochemical, and genetic effects 2001 ·Annals of Neurology ·Tanja Taivassalo,Eric A. Shoubridge,Jacqueline Chen,Nancy G. Kennaway,Salvatore DiMauro,Douglas L. Arnold,Ronald G. Haller	157
7	Mitochondrial Encephalomyopathy and Complex III Deficiency Associated with a Stop-Codon Mutation in the Cytochrome b Gene 2000 ·The American Journal of Human Genetics ·J. Andrew Keightley,Roberto P. Anitori,Miriam D. Burton,Franklin Quan,Neil R.M. Buist,Nancy G. Kennaway	96
8	A Pathogenic 15-Base Pair Deletion in Mitochondrial DNA-encoded Cytochrome c Oxidase Subunit III Results in the Absence of Functional Cytochrome c Oxidase 2000 ·Journal of Biological Chemistry ·Kristen C. Hoffbuhr,Edgar Davidson,(unknown),Mercy M. Davidson,Nancy G. Kennaway,Michael P. King	44
9	Genotype-phenotype correlation of a pyridoxine-responsive form of gyrate atrophy 1999 ·Ophthalmic Genetics ·Yukihiko Mashima,Richard G. Weleber,Nancy G. Kennaway,George Inana	16
10	GYRATE ATROPHY-LIKE PHENOTYPE WITH NORMAL PLASMA ORNITHINE 1997 ·Retina ·Ulrich Kellner,Richard G. Weleber,Nancy G. Kennaway,Gerald A. Fishman,Michael Foerster	6
11	Diabetes and Mitochondrial Encephalomyopathy with Lactic Acidosis and Stroke-Like Episodes (MELAS): Radiolabeled Polymerase Chain Reaction Is Necessary for Accurate Detection of Low Percentages of Mutation¹ 1997 ·The Journal of Clinical Endocrinology & Metabolism ·Margaret L. Smith,(unknown),Deborah Marsden,Dou Liu,Nancy G. Kennaway,(unknown),Richard Haas	24
12	Subunit specific monoclonal antibodies show different steady-state levels of various cytochrome-c oxidase subunits in chronic progressive external ophthalmoplegia 1996 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Jan‐Willem Taanman,Miriam D. Burton,Michael F. Marusich,Nancy G. Kennaway,Roderick Capaldi	52
13	Pharmacological correction of neonatal lethal hepatic dysfunction in a murine model of hereditary tyrosinaemia type I 1995 ·Nature Genetics ·Markus Grompe,Sven Lindstedt,Muhsen Al-Dhalimy,Nancy G. Kennaway,John Papaconstantinou,Carlos A. Torres‐Ramos,(unknown),Milton J. Finegold	238
14	Effect of ascorbate or N-acetylcysteine treatment in a patient with hereditary glutathione synthetase deficiency 1994 ·The Journal of Pediatrics ·(unknown),Neil R.M. Buist,Nancy G. Kennaway,Berkley R. Powell,Peter A.M. Auld,Johan Mårtensson	22
15	Human cytochrome c oxidase subunit VIb: characterization and mapping of a multigene family 1991 ·Gene ·(unknown),Franklin Quan,Robert N. Lightowlers,Nancy G. Kennaway,M. Litt,Michael Forte	16
16	Defects in the cytochromebc 1 complex in mitochondrial diseases 1988 ·Journal of Bioenergetics and Biomembranes ·Nancy G. Kennaway	26
17	Normal α-L-Fucosidase and Other Lysosomal Enzyme Activities in Progressive Cone Dystrophy 1988 ·American Journal of Ophthalmology ·(unknown),Richard G. Weleber,Nancy G. Kennaway	4
18	Dysmorphic syndrome with phytanic acid oxidase deficiency, abnormal very long chain fatty acids, and pipecolic acidemia: Studies in four children 1986 ·The Journal of Pediatrics ·Sarojini Budden,Nancy G. Kennaway,Neil R.M. Buist,A. Poulos,Richard G. Weleber	55
19	Lactic Acidosis and Mitochondrial Myopathy Associated with Deficiency of Several Components of Complex III of the Respiratory Chain 1984 ·Pediatric Research ·Nancy G. Kennaway,Neil R.M. Buist,Victor Darley‐Usmar,(unknown),Salvatore DiMauro,Richard I. Kelley,Roderick Capaldi,Nathan K. Blank,Anthony N. D’Agostino	2
20	Lactic Acidosis and Mitochondrial Myopathy Associated with Deficiency of Several Components of Complex III of the Respiratory Chain 1984 ·Pediatric Research ·Nancy G. Kennaway,Neil R.M. Buist,Victor Darley‐Usmar,(unknown),Salvatore DiMauro,Richard I. Kelley,Roderick Capaldi,Nathan K. Blank,Anthony N. D’Agostino	68

About Nancy G. Kennaway

Nancy G. Kennaway is a scholar working on Clinical Biochemistry, Biochemistry and Molecular Biology, having authored 37 papers that have together received 2.0k indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (22 papers), Mitochondrial Function and Pathology (17 papers) and ATP Synthase and ATPases Research (10 papers). The work is most often cited by research in Clinical Biochemistry (906 citations), Biochemistry (179 citations) and Molecular Biology (1.5k citations). Nancy G. Kennaway has collaborated with scholars based in United States, Canada and Japan. Frequent co-authors include Neil R.M. Buist, Eric A. Shoubridge, Hana Antonická, Kristen C. Hoffbuhr, Richard G. Weleber, Miriam D. Burton, Tanja Taivassalo, Ronald G. Haller, Roberto P. Anitori and J. Andrew Keightley. Their work appears in journals such as Journal of Biological Chemistry, Nature Genetics and The Journal of Clinical Endocrinology & Metabolism.

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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