Nancy G. Kennaway

2.6k citations

37 papers · 2.0k indexed · h-index 22

Clinical Biochemistry top 0.2%
- Metabolism and Genetic Disorders 22
Biochemistry top 2%
- Amino Acid Enzymes and Metabolism 5
Molecular Biology top 5%
- Mitochondrial Function and Pathology 17
- ATP Synthase and ATPases Research 10
- Biochemical and Molecular Research 3
- RNA modifications and cancer 3
- Retinal Development and Disorders 3
- RNA and protein synthesis mechanisms 3
Hepatology top 10%
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
Cited by: Clinical Biochemistry Biochemistry Molecular Biology
Journals: Journal of Biological Chemistry (2 papers)Nature Genetics (2 papers)The Journal of Clinical Endocrinology & Metabolism (1 paper)
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

The 25 scholars most cited alongside Nancy G. Kennaway, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Nancy G. Kennaway Line = papers co-authored together Nancy G. Kennaway links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

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

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