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, E Ceresi, Martin S. Obin, Emanuela Faloia, Giorgio Barbatelli, Incoronata Murano, Andrew S. Greenberg 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

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 →

Peers

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

#	Work	Indexed citations
1	Phosphoinositide Metabolism: Biochemistry, Physiology and Genetic Disorders 2025 ·Journal of Inherited Metabolic Disease ·Francis Rossignol, Foudil Lamari, Grant A. Mitchell	4
2	150 From pancytopenia to hyperleukocytosis, an unexpected presentation of immune reconstitution inflammatory syndrome in an infant with methylmalonic acidemia 2024 ·Clinical Immunology ·(unknown), (unknown), Tanguy Demaret, Philippe Ovetchkine, Fatima Kakkar, (unknown), Caroline Laverdière, François Proulx, (unknown), (unknown), Grant A. Mitchell, (unknown), Hélène Decaluwe	0
3	Cardiac-specific deficiency of 3-hydroxy-3-methylglutaryl coenzyme A lyase in mice causes cardiomyopathy and a distinct pattern of acyl-coenzyme A-related biomarkers 2022 ·Molecular Genetics and Metabolism ·Hao Yang, Youlin Wang, (unknown), Paula J. Waters, Shupei Wang, Pierre Allard, Robert O. Ryan, Anne Monique Nuyt, Pierre Paradis, Ernesto L. Schiffrin, Alexandra Fürtös, Grant A. Mitchell	3
4	Premature Ovarian Failure in French Canadian Leigh Syndrome 2017 ·The Journal of Pediatrics ·(unknown), Charles Morin, Catherine Brunel‐Guitton, Grant A. Mitchell, Guy Van Vliet, Céline Huot	13
5	Epistatic interaction between the lipase-encoding genes Pnpla2 and Lipe causes liposarcoma in mice 2017 ·PLoS Genetics ·Jiang Wei Wu, Christoph Preuß, Shu Pei Wang, Hao Yang, Bo Ji, Gregory W. Carter, Rebecca A. Gladdy, Grégor Andelfinger, Grant A. Mitchell	37
6	Mildly elevated succinylacetone and normal liver function in compound heterozygotes with pathogenic and pseudodeficient FAH alleles 2017 ·Molecular Genetics and Metabolism Reports ·Hao Yang, Francis Rossignol, Denis Cyr, Rachel Laframboise, Shu Pei Wang, (unknown), (unknown), Yves Giguère, Paula J. Waters, Grant A. Mitchell	7
7	SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome 2016 ·Alexandre Janer, Julien Prudent, Vincent Paupe, Somayyeh Fahiminiya, Jacek Majewski, Nicolas Sgarioto, Christine Des Rosiers, (unknown), Zhen‐Yuan Lin, Anne‐Claude Gingras, Grant A. Mitchell, Heidi M. McBride, Eric A. Shoubridge	14
8	A beta cell ATGL-lipolysis/adipose tissue axis controls energy homeostasis and body weight via insulin secretion in mice 2016 ·Diabetologia ·Camille Attané, Marie‐Line Peyot, Roxane Lussier, Pegah Poursharifi, Shangang Zhao, Dongwei Zhang, (unknown), Marco Pineda, Shupei Wang, Olivier Dumortier, Neil B. Ruderman, Grant A. Mitchell, Brigitte Simons, S.R. Murthy Madiraju, Érik Joly, Marc Prentki	43
9	Liver specific inactivation of carboxylesterase 3/triacylglycerol hydrolase decreases blood lipids without causing severe steatosis in mice 2012 ·Hepatology ·Jihong Lian, En‐Hui Wei, Shu Pei Wang, Ariel D. Quiroga, Lena Li, Alba Di Pardo, (unknown), Simonetta Sipione, Grant A. Mitchell, Richard Lehner	55
10	Deficiency of liver adipose triglyceride lipase in mice causes progressive hepatic steatosis 2011 ·Hepatology ·Jiang Wei Wu, Shu Pei Wang, Fernando Alvarez, (unknown), Nicolas Gauthier, (unknown), Krishnakant G. Soni, Gongshe Yang, Grant A. Mitchell	198
11	Threshold for toxicity from hyperammonemia in critically ill children 2011 ·Journal of Hepatology ·(unknown), J. Craig Nelson, J.M. Cousineau, Marie Lambert, Véronique Phan, Grant A. Mitchell, Fernando Álvarez, Thiérry Ducruet, Philippe Jouvet	26
12	Pyruvate Dehydrogenase Deficiency Presenting as Intermittent Isolated Acute Ataxia 2008 ·Neuropediatrics ·(unknown), M Lambert, (unknown), Bruno Maranda, Rachel Laframboise, N. MacKay, Bruce H. Robinson, Grant A. Mitchell	27
13	Identification of a gene causing human cytochrome c oxidase deficiency by integrative genomics 2003 ·Proceedings of the National Academy of Sciences ·Vamsi K. Mootha, Patricia Lepage, Kathleen A. Miller, Jakob Bunkenborg, Michael Reich, Majbrit Hjerrild, Terrye Delmonte, (unknown), Robert Sladek, Fenghao Xu, Grant A. Mitchell, Charles Morin, Matthias Mann, Thomas J. Hudson, Brian Robinson, John D. Rioux, Eric S. Lander	452
14	A Missense Mutation (R565W) in Cirhin (FLJ14728) in North American Indian Childhood Cirrhosis 2002 ·The American Journal of Human Genetics ·Pierre Chagnon, Jacques L. Michaud, Grant A. Mitchell, Jocelyne Mercier, (unknown), Éric Drouin, Andrée Rasquin‐Weber, Thomas J. Hudson, Andréa Richter	69
15	The hormone-sensitive lipase gene is transcribed from at least five alternative first exons in mouse adipose tissue 2000 ·Mammalian Genome ·Nancy Laurin, Shu Pei Wang, Grant A. Mitchell	25
16	Cerebral vascular complication and hyperhomocysteinemia in a cystinotic uremic child 1999 ·Pediatric Nephrology ·Aïcha Mérouani, Jacques Genest, Rima Rozen, Marie Lambert, Grant A. Mitchell, Josée Dubois, Pierre Robitaille	2
17	Saguenay Lac Saint Jean cytochrome oxidase deficiency: sequence analysis of nuclear encoded COX subunits, chromosomal localization and a sequence anomaly in subunit VIc 1998 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Nana Lee, Charles Morin, Grant A. Mitchell, (unknown)	8
18	Succinyl-CoA:3-ketoacid coenzyme A transferase (SCOT): Development of an antibody to human SCOT and diagnostic use in hereditary SCOT deficiency 1997 ·Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease ·Xiang‐Qian Song, Toshiyuki Fukao, Grant A. Mitchell, Sacha Kassovska‐Bratinova, Magdalena Ugarte, Ronald J. A. Wanders, (unknown), Haruo Shintaku, Perry F. Churchill, (unknown), Tadao Orii, Naomi Kondo	19
19	Hyperammonemia-hyperornithinemia-homocitrullinuria syndrome: Neurologic, ophthalmologic, and neuropsychologic examination of six patients 1992 ·The Journal of Pediatrics ·Jacinthe Lemay, Marie Lambert, Grant A. Mitchell, Michel Vanasse, David Valle, (unknown), Johanne Dubé, (unknown), Marie Laberge, L Lafleur, (unknown), Insaf Ahmed Qureshi, Raynald Déry	25
20	An initiator codon mutation in ornithine-delta-aminotransferase causing gyrate atrophy of the choroid and retina. 1988 ·Journal of Clinical Investigation ·Grant A. Mitchell, Lawrence C. Brody, James E. Looney, Gary Steel, Maureen K. Suchanek, Carol E. Dowling, V Der Kaloustian, Muriel I. Kaiser‐Kupfer, David Valle	77

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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