N. MacKay
Impact in
- Clinical Biochemistry top 1%
- Metabolism and Genetic Disorders
- Biochemistry top 2%
- Biochemical Acid Research Studies
- Amino Acid Enzymes and Metabolism
Papers in
- Biochemistry 10
- Biochemical Acid Research Studies 9
- Amino Acid Enzymes and Metabolism 3
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- Metabolism and Genetic Disorders 9
- Co-authors
- B. H. Robinson (9 shared papers)Kathy Chun (5 shared papers)Roumyana Petrova-Benedict (4 shared papers)Linda De Meırleır (2 shared papers)Rachel Laframboise (2 shared papers)Grant A. Mitchell (2 shared papers)M Lambert (2 shared papers)Marc De Braekeleer (1 shared paper)
- Journals
- Neuropediatrics (2 papers)Human Mutation (1 paper)The American Journal of Human Genetics (1 paper)Journal of Inherited Metabolic Disease (1 paper)European Journal of Biochemistry (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-authors
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 | A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of Quebec. | 1993 | 78 |
| 2 | 1988 | 64 | |
| 3 | 1992 | 60 | |
| 4 | 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 |
| 5 | 2003 | 45 | |
| 6 | 1990 | 44 | |
| 7 | 1996 | 42 | |
| 8 | 1998 | 38 | |
| 9 | 2008 | 35 | |
| 10 | 2008 | 27 | |
| 11 | 2009 | 25 | |
| 12 | 1994 | 19 | |
| 13 | Pyruvate dehydrogenase deficiency due to a 20-bp deletion in exon II of the pyruvate dehydrogenase (PDH) E1 alpha gene. | 1991 | 16 |
| 14 | 1990 | 6 | |
| 15 | 2007 | 6 |
About N. MacKay
N. MacKay is a scholar working on Biochemistry, Clinical Biochemistry, Molecular Biology, Cell Biology and Surgery, 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), Pancreatic function and diabetes (2 papers), Electrolyte and hormonal disorders (2 papers), Viral Infectious Diseases and Gene Expression in Insects (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), Molecular Biology (373 citations), Cell Biology (58 citations) and Neurology (39 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, Rachel Laframboise, Grant A. Mitchell, M Lambert, Marc De Braekeleer, R. Gagné and C Morin. 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.