N. MacKay
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders 9
- Biochemistry top 2%
- Biochemical Acid Research Studies 9
- Amino Acid Enzymes and Metabolism 3
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- Mitochondrial Function and Pathology 4
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- Skin and Cellular Biology Research 1
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- Electrolyte and hormonal disorders 2
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- Pancreatic function and diabetes 2
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- Cancer, Hypoxia, and Metabolism 1
- Co-authors
- B. H. RobinsonKathy ChunRoumyana Petrova-BenedictLinda De MeırleırM LambertGrant A. MitchellRachel LaframboiseBrian H. Robinson
- Journals
- Neuropediatrics (2 papers)Human Mutation (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- CanadaUnited StatesAustralia
In The Last Decade
N. MacKay
15 papers receiving 546 citations
Peers
Comparison fields: 5 of 56
- Clinical Biochemistry 315
- Biochemistry 222
- Molecular Biology 373
- Cell Biology 58
- Neurology 39
Countries citing papers authored by N. MacKay
This map shows the geographic impact of N. MacKay'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. MacKay with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites N. MacKay more than expected).
Fields of papers citing papers by N. MacKay
This network shows the impact of papers produced by N. MacKay. 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. MacKay. The network helps show where N. MacKay may publish in the future.
Co-authorship network
The 25 scholars most cited alongside N. MacKay, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2009 | 25 | |
| 2 | 2008 | 27 | |
| 3 | 2008 | 35 | |
| 4 | 2007 | 6 | |
| 5 | 2003 | 45 | |
| 6 | 1998 | 38 | |
| 7 | 1996 | 42 | |
| 8 | Mutations in the X-linked E1 alpha subunit of pyruvate dehydrogenase: exon skipping, insertion of duplicate sequence, and missense mutations leading to the deficiency of the pyruvate dehydrogenase complex. | 1995 | 47 |
| 9 | 1994 | 19 | |
| 10 | A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of Quebec. | 1993 | 78 |
| 11 | 1992 | 60 | |
| 12 | Pyruvate dehydrogenase deficiency due to a 20-bp deletion in exon II of the pyruvate dehydrogenase (PDH) E1 alpha gene. | 1991 | 16 |
| 13 | 1990 | 44 | |
| 14 | 1990 | 6 | |
| 15 | 1988 | 64 |
About N. MacKay
N. MacKay is a scholar working on Biochemistry, Clinical Biochemistry and Cell Biology, having authored 15 papers that have together received 552 indexed citations. Recurring topics across this work include Metabolism and Genetic Disorders (9 papers), Biochemical Acid Research Studies (9 papers), Mitochondrial Function and Pathology (4 papers), Amino Acid Enzymes and Metabolism (3 papers), Electrolyte and hormonal disorders (2 papers), Pancreatic function and diabetes (2 papers), Skin and Cellular Biology Research (1 paper) and Cancer, Hypoxia, and Metabolism (1 paper). The work is most often cited by research in Clinical Biochemistry (315 citations), Biochemistry (222 citations) and Molecular Biology (373 citations). N. MacKay has collaborated with scholars based in Canada, United States and Australia. Frequent co-authors include B. H. Robinson, Kathy Chun, Roumyana Petrova-Benedict, Linda De Meırleır, M Lambert, Grant A. Mitchell, Rachel Laframboise, Brian H. Robinson, R. Gagné and Frank Merante. Their work appears in journals such as Neuropediatrics, Human Mutation, The American Journal of Human Genetics, Journal of Inherited Metabolic Disease and European Journal of Biochemistry.
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.