N. MacKay

740 total citations
15 papers, 552 citations indexed

About

N. MacKay is a scholar working on Biochemistry, Clinical Biochemistry and Molecular Biology. According to data from OpenAlex, N. MacKay has authored 15 papers receiving a total of 552 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Biochemistry, 9 papers in Clinical Biochemistry and 7 papers in Molecular Biology. Recurrent topics in N. MacKay's work include Metabolism and Genetic Disorders (9 papers), Biochemical Acid Research Studies (9 papers) and Mitochondrial Function and Pathology (4 papers). N. MacKay is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Biochemical Acid Research Studies (9 papers) and Mitochondrial Function and Pathology (4 papers). N. MacKay collaborates with scholars based in Canada, United States and Australia. N. MacKay's co-authors include B. H. Robinson, Kathy Chun, Roumyana Petrova-Benedict, Linda De Meırleır, M Lambert, Grant A. Mitchell, Rachel Laframboise, C Morin, R. Gagné and Brian H. Robinson and has published in prestigious journals such as Journal of Biological Chemistry, Journal of Clinical Investigation and Biochemical and Biophysical Research Communications.

In The Last Decade

N. MacKay

15 papers receiving 546 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
N. MacKay Canada	13	373	315	222	58	50	15	552
Valeriy Levandovskiy Canada	14	493 1.3×	279 0.9×	130 0.6×	41 0.7×	75 1.5×	17	668
Nevena MacKay Canada	9	388 1.0×	152 0.5×	59 0.3×	19 0.3×	34 0.7×	9	514
Elena Martín‐Hernández Spain	16	408 1.1×	331 1.1×	52 0.2×	34 0.6×	77 1.5×	41	596
Jaak Jaeken Belgium	9	236 0.6×	123 0.4×	132 0.6×	25 0.4×	64 1.3×	11	350
Nanna Cornelius Denmark	8	423 1.1×	341 1.1×	71 0.3×	34 0.6×	98 2.0×	10	551
Christoph Korenke Germany	14	343 0.9×	329 1.0×	70 0.3×	18 0.3×	178 3.6×	21	757
Yoichi Wada Japan	13	209 0.6×	113 0.4×	39 0.2×	19 0.3×	43 0.9×	27	372
Devorah Soiferman Israel	10	426 1.1×	173 0.5×	26 0.1×	30 0.5×	49 1.0×	10	531
R. Nair Finland	10	265 0.7×	84 0.3×	54 0.2×	15 0.3×	41 0.8×	12	380
Aisha Al‐Shamsi United Arab Emirates	13	268 0.7×	107 0.3×	47 0.2×	31 0.5×	29 0.6×	29	466

Countries citing papers authored by N. MacKay

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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 of co-authors of N. MacKay

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

All Works

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15 of 15 papers shown

Cameron, Jessie M., Mary C. Maj, Valeriy Levandovskiy, et al.. (2009). Pyruvate dehydrogenase phosphatase 1 (PDP1) null mutation produces a lethal infantile phenotype. Human Genetics. 125(3). 319–326. 25 indexed citations

Tam, Emily, Annette Feigenbaum, Jane Addis, et al.. (2008). A Novel Mitochondrial DNA Mutation inCOX1Leads to Strokes, Seizures, and Lactic Acidosis. Neuropediatrics. 39(6). 328–334. 35 indexed citations

Lambert, M, Bruno Maranda, Rachel Laframboise, et al.. (2008). Pyruvate Dehydrogenase Deficiency Presenting as Intermittent Isolated Acute Ataxia. Neuropediatrics. 39(1). 20–23. 27 indexed citations

MacKay, N. & Brian H. Robinson. (2007). Measurement of the Ratio of Lactate to Pyruvate in Skin Fibroblast Cultures. Methods in cell biology. 80. 173–178. 6 indexed citations

Tarnopolsky, Mark A., Jacqueline M. Bourgeois, Г. В. Катаева, et al.. (2003). Novel SCO2 mutation (G1521A) presenting as a spinal muscular atrophy type I phenotype. American Journal of Medical Genetics Part A. 125A(3). 310–314. 45 indexed citations

Carbone, Mary Anna, N. MacKay, Mingfu Ling, et al.. (1998). Amerindian Pyruvate Carboxylase Deficiency Is Associated with Two Distinct Missense Mutations. The American Journal of Human Genetics. 62(6). 1312–1319. 38 indexed citations

Robinson, B. H., et al.. (1996). Disorders of pyruvate carboxylase and the pyruvate dehydrogenase complex. Journal of Inherited Metabolic Disease. 19(4). 452–462. 42 indexed citations

Chun, Kathy, N. MacKay, Roumyana Petrova-Benedict, et al.. (1995). 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.. PubMed. 56(3). 558–69. 47 indexed citations

MacKay, N., et al.. (1994). cDNA Cloning of Human Kidney Pyruvate Carboxylase. Biochemical and Biophysical Research Communications. 202(2). 1009–1014. 19 indexed citations

10.

Merante, Frank, Roumyana Petrova-Benedict, N. MacKay, et al.. (1993). A biochemically distinct form of cytochrome oxidase (COX) deficiency in the Saguenay-Lac-Saint-Jean region of Quebec.. PubMed. 53(2). 481–7. 78 indexed citations

11.

Dahl, H H, Garry K. Brown, R. M. Brown, et al.. (1992). Mutations and polymorphisms in the pyruvate dehydrogenase E1α gene. Human Mutation. 1(2). 97–102. 60 indexed citations

12.

Chun, Kathy, N. MacKay, Roumyana Petrova-Benedict, & B. H. Robinson. (1991). Pyruvate dehydrogenase deficiency due to a 20-bp deletion in exon II of the pyruvate dehydrogenase (PDH) E1 alpha gene.. PubMed. 49(2). 414–20. 16 indexed citations

13.

Robinson, B. H., et al.. (1990). Defects in the E2 lipoyl transacetylase and the X-lipoyl containing component of the pyruvate dehydrogenase complex in patients with lactic acidemia.. Journal of Clinical Investigation. 85(6). 1821–1824. 44 indexed citations

14.

Chun, Kathy, N. MacKay, Huntington F. Willard, & Brian H. Robinson. (1990). Isolation, characterization and chromosomal localization of cDNA clones for the E₁β subunit of the pyruvate dehydrogenase complex. European Journal of Biochemistry. 194(2). 587–592. 6 indexed citations

15.

Meırleır, Linda De, et al.. (1988). Isolation of a full-length complementary DNA coding for human E1 alpha subunit of the pyruvate dehydrogenase complex.. Journal of Biological Chemistry. 263(4). 1991–1995. 64 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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