Grant A. Mitchell

17.5k total citations · 2 hit papers
206 papers, 11.8k citations indexed

About

Grant A. Mitchell is a scholar working on Molecular Biology, Clinical Biochemistry and Physiology. According to data from OpenAlex, Grant A. Mitchell has authored 206 papers receiving a total of 11.8k indexed citations (citations by other indexed papers that have themselves been cited), including 112 papers in Molecular Biology, 102 papers in Clinical Biochemistry and 63 papers in Physiology. Recurrent topics in Grant A. Mitchell's work include Metabolism and Genetic Disorders (102 papers), Mitochondrial Function and Pathology (39 papers) and Diet and metabolism studies (30 papers). Grant A. Mitchell is often cited by papers focused on Metabolism and Genetic Disorders (102 papers), Mitochondrial Function and Pathology (39 papers) and Diet and metabolism studies (30 papers). Grant A. Mitchell collaborates with scholars based in Canada, United States and China. Grant A. Mitchell's co-authors include Shupei Wang, Mélanie Fortier, Saverio Cinti, Incoronata Murano, E Ceresi, Andrew S. Greenberg, Giorgio Barbatelli, Emanuela Faloia, Martin S. Obin and Toshiyuki Fukao and has published in prestigious journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and The Lancet.

In The Last Decade

Grant A. Mitchell

200 papers receiving 11.6k citations

Hit Papers

align trajectories sort by overperformance

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Adipocyte death defines macrophage localization and function in adipose tissue of obese mice and humans

2005 1.9k citations Grant A. Mitchell, Shupei Wang et al. profile →
A combined syndrome of juvenile polyposis and hereditary haemorrhagic telangiectasia associated with mutations in MADH4 ( SMAD4)

2004 534 citations Grant A. Mitchell, Éric Drouin et al. profile →

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author						Papers	Cites
Grant A. Mitchell	5.8k	3.7k	2.9k	2.0k	1.9k	206	11.8k
Paul A. Watkins	7.7k 1.3×	2.3k 0.6×	2.5k 0.9×	1.1k 0.5×	1.4k 0.7×	181	10.7k
Orian S. Shirihai	11.2k 1.9×	3.9k 1.1×	1.9k 0.6×	4.4k 2.2×	862 0.5×	163	16.8k
Frédéric M. Vaz	6.0k 1.0×	2.1k 0.6×	2.5k 0.9×	998 0.5×	839 0.5×	257	9.5k
Jerry Vockley	7.0k 1.2×	3.1k 0.8×	5.8k 2.0×	743 0.4×	694 0.4×	318	11.3k
Arnold W. Strauss	6.4k 1.1×	1.6k 0.4×	3.4k 1.2×	1.1k 0.5×	511 0.3×	220	10.5k
Jean E. Schaffer	6.3k 1.1×	3.9k 1.1×	622 0.2×	2.2k 1.1×	2.4k 1.3×	108	12.1k
Hans R. Waterham	12.8k 2.2×	2.1k 0.6×	3.7k 1.3×	1.0k 0.5×	1.3k 0.7×	300	15.8k
Anne N. Murphy	8.3k 1.4×	2.5k 0.7×	966 0.3×	1.8k 0.9×	588 0.3×	130	13.2k
Godfrey S. Getz	5.1k 0.9×	2.5k 0.7×	780 0.3×	1.4k 0.7×	690 0.4×	221	11.6k
Marc Liesa	6.5k 1.1×	2.8k 0.8×	1.1k 0.4×	2.2k 1.1×	678 0.4×	83	9.4k

Countries citing papers authored by Grant A. Mitchell

Since Specialization

Citations

This map shows the geographic impact of Grant A. Mitchell'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 Grant A. Mitchell with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Grant A. Mitchell more than expected).

Fields of papers citing papers by Grant A. Mitchell

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Grant A. Mitchell. 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 Grant A. Mitchell. The network helps show where Grant A. Mitchell may publish in the future.

Co-authorship network of co-authors of Grant A. Mitchell

This figure shows the co-authorship network connecting the top 25 collaborators of Grant A. Mitchell. A scholar is included among the top collaborators of Grant A. Mitchell 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 Grant A. Mitchell. Grant A. Mitchell 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

Lamari, Foudil, Francis Rossignol, & Grant A. Mitchell. (2025). Glycerophospholipids: Roles in Cell Trafficking and Associated Inborn Errors. Journal of Inherited Metabolic Disease. 48(2). e70019–e70019. 6 indexed citations

Rossignol, Francis, Foudil Lamari, & Grant A. Mitchell. (2025). Phosphoinositide Metabolism: Biochemistry, Physiology and Genetic Disorders. Journal of Inherited Metabolic Disease. 48(2). e70008–e70008. 4 indexed citations

Demaret, Tanguy, Philippe Ovetchkine, Fatima Kakkar, et al.. (2024). 150 From pancytopenia to hyperleukocytosis, an unexpected presentation of immune reconstitution inflammatory syndrome in an infant with methylmalonic acidemia. Clinical Immunology. 262. 110092–110092.

Mitchell, Grant A., et al.. (2023). TUFM variants lead to white matter abnormalities mimicking multiple sclerosis. European Journal of Neurology. 30(10). 3400–3403. 3 indexed citations

Morin, Charles, et al.. (2017). Premature Ovarian Failure in French Canadian Leigh Syndrome. The Journal of Pediatrics. 184. 227–229.e1. 13 indexed citations

Janer, Alexandre, Julien Prudent, Vincent Paupe, et al.. (2016). SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome. 5. 14 indexed citations

Attané, Camille, Marie‐Line Peyot, Roxane Lussier, et al.. (2016). A beta cell ATGL-lipolysis/adipose tissue axis controls energy homeostasis and body weight via insulin secretion in mice. Diabetologia. 59(12). 2654–2663. 43 indexed citations

Soni, Krishnakant G., Richard Lehner, Pavel Metalnikov, et al.. (2004). Carboxylesterase 3 (EC 3.1.1.1) Is a Major Adipocyte Lipase. Journal of Biological Chemistry. 279(39). 40683–40689. 127 indexed citations

Mootha, Vamsi K., Patricia Lepage, Kathleen A. Miller, et al.. (2003). Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics. Proceedings of the National Academy of Sciences. 100(2). 605–610. 452 indexed citations

10.

Corzo, Deyanira, William T. Gibson, Grant A. Mitchell, et al.. (2002). Contiguous Deletion of the X-Linked Adrenoleukodystrophy Gene (ABCD1) and DXS1357E: A Novel Neonatal Phenotype Similar to Peroxisomal Biogenesis Disorders. The American Journal of Human Genetics. 70(6). 1520–1531. 50 indexed citations

11.

Chagnon, Pierre, Jacques L. Michaud, Grant A. Mitchell, et al.. (2002). A Missense Mutation (R565W) in Cirhin (FLJ14728) in North American Indian Childhood Cirrhosis. The American Journal of Human Genetics. 71(6). 1443–1449. 69 indexed citations

12.

Lahjouji, Karim, Christiane Malo, Grant A. Mitchell, & Ijaz A. Qureshi. (2002). L-Carnitine transport in mouse renal and intestinal brush-border and basolateral membrane vesicles. Biochimica et Biophysica Acta (BBA) - Biomembranes. 1558(1). 82–93. 26 indexed citations

13.

Lee, Nana, Mark J. Daly, Terrye Delmonte, et al.. (2001). A Genomewide Linkage-Disequilibrium Scan Localizes the Saguenay–Lac-Saint-Jean Cytochrome Oxidase Deficiency to 2p16. The American Journal of Human Genetics. 68(2). 397–409. 31 indexed citations

14.

Drouin, Éric, Pierre Russo, Béatriz Tuchweber, Grant A. Mitchell, & Andrée Rasquin‐Weber. (2000). North American Indian Cirrhosis in Children: A Review of 30 Cases. Journal of Pediatric Gastroenterology and Nutrition. 31(4). 395–404. 4 indexed citations

15.

Bétard, Christine, Andrée Rasquin‐Weber, Carl G. Brewer, et al.. (2000). Localization of a Recessive Gene for North American Indian Childhood Cirrhosis to Chromosome Region 16q22—and Identification of a Shared Haplotype. The American Journal of Human Genetics. 67(1). 222–228. 26 indexed citations

16.

Mérouani, Aïcha, Jacques Genest, Rima Rozen, et al.. (1999). Cerebral vascular complication and hyperhomocysteinemia in a cystinotic uremic child. Pediatric Nephrology. 13(1). 73–76. 2 indexed citations

17.

Lee, Nana, et al.. (1998). Saguenay Lac Saint Jean cytochrome oxidase deficiency: sequence analysis of nuclear encoded COX subunits, chromosomal localization and a sequence anomaly in subunit VIc. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1406(1). 1–4. 8 indexed citations

18.

Song, Xiang‐Qian, Toshiyuki Fukao, Grant A. Mitchell, et al.. (1997). Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): Development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1360(2). 151–156. 19 indexed citations

19.

Lemay, Jacinthe, Marie Lambert, Grant A. Mitchell, et al.. (1992). Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: Neurologic, ophthalmologic, and neuropsychologic examination of six patients. The Journal of Pediatrics. 121(5). 725–730. 25 indexed citations

20.

Mitchell, Grant A., Lawrence C. Brody, James E. Looney, et al.. (1988). An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina.. Journal of Clinical Investigation. 81(2). 630–633. 77 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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