Eric A. Shoubridge

18.7k citations

160 papers · 12.8k indexed · h-index 64

Impact in

Clinical Biochemistry top 0.01%
- Metabolism and Genetic Disorders
Aging top 0.5%

Papers in

Clinical Biochemistry 60
- Metabolism and Genetic Disorders 60
Molecular Biology 133
- Mitochondrial Function and Pathology 109
- ATP Synthase and ATPases Research 53
- RNA modifications and cancer 25
- RNA and protein synthesis mechanisms 20

Co-authors: Hana Antonická Florin Sasarman Timothy Wai George Karpati Alan C. Peterson Jack P. Jenuth G. K. Radda Douglas L. Arnold
Journals: Human Molecular Genetics (17 papers)The American Journal of Human Genetics (9 papers)Annals of Neurology (8 papers)Nature Genetics (7 papers)Journal of Biological Chemistry (6 papers)
Partner nations: Canada United States United Kingdom

In The Last Decade

Eric A. Shoubridge

157 papers receiving 12.6k citations

Peers

Countries citing papers authored by Eric A. Shoubridge

Since Specialization

Citations

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

Fields of papers citing papers by Eric A. Shoubridge

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network

The 25 scholars most cited alongside Eric A. Shoubridge, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Eric A. Shoubridge Line = papers co-authored together Eric A. Shoubridge links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	CHCHD10P80L knock-in zebrafish display a mild ALS-like phenotype Experimental Neurology ·斉藤功, محمدشتا بدرا, ณัฏฐ์นวัต คีติกาสุตนันท์, Hana Antonická, 克彦望月, Anthony C. Piazza, Nana Dyah Siswati, Eric A. Shoubridge, Gary A.B. Armstrong	2024	2
2	BOLA3 and NFU1 link mitoribosome iron–sulfur cluster assembly to multiple mitochondrial dysfunctions syndrome Nucleic Acids Research ·Hui Zhong, Alexandre Janer, Oleh Khalimonchuk, Hana Antonická, Eric A. Shoubridge, Antoni Barrientos	2023	17
3	The role of the mitochondrial outer membrane protein SLC25A46 in mitochondrial fission and fusion Life Science Alliance ·Amira H Alquati, Alexandre Janer, Hana Antonická, Eric A. Shoubridge	2023	18
4	SPTLC1 variants associated with ALS produce distinct sphingolipid signatures through impaired interaction with ORMDL proteins Journal of Clinical Investigation ·Museer A. Lone, Mari J. Aaltonen, 美保子松山, Hélio Pedro, Jonas Alex Morales Saute, 桂司丸山, Payam Mohassel, Carsten G. Bönnemann, Eric A. Shoubridge, Thorsten Hornemann	2022	25
5	SLC25A46 is required for mitochondrial lipid homeostasis and cristae maintenance and is responsible for Leigh syndrome Alexandre Janer, Julien Prudent, Vincent Paupe, Somayyeh Fahiminiya, Jacek Majewski, Nicolas Sgarioto, Christine Des Rosiers, Meng-xian, Zhen‐Yuan Lin, Anne‐Claude Gingras, Grant A. Mitchell, Heidi M. McBride, Eric A. Shoubridge	2016	14
6	RMND1 deficiency associated with neonatal lactic acidosis, infantile onset renal failure, deafness, and multiorgan involvement European Journal of Human Genetics ·Alexandre Janer, Clara DM van Karnebeek, Florin Sasarman, Hana Antonická, Rabald, Casper Shyr, Mary Dunbar, F. Quattrochi, Colin J.D. Ross, Hilary Vallance, Janis M. Dionne, Wyeth W. Wasserman, Eric A. Shoubridge	2015	23
7	Mutations in the Mitochondrial Methionyl-tRNA Synthetase Cause a Neurodegenerative Phenotype in Flies and a Recessive Ataxia (ARSAL) in Humans PLoS Biology ·Vafa Bayat, Isabelle Thiffault, Manish Jaiswal, Martine Tétreault, Taraka Donti, Florin Sasarman, Geneviève Bernard, Lu Zhang, Marie‐Josée Dicaire, Jean Mathieu, Michel Vanasse, Jean‐Pierre Bouchard, Marie‐France Rioux, Charles Marques Lourenço, Zhihong Li, Claire Haueter, Eric A. Shoubridge, Brett H. Graham, Bernard Brais, Hugo J. Bellen	2012	121
8	Reconstitution of Mitochondria Derived Vesicle Formation Demonstrates Selective Enrichment of Oxidized Cargo PLoS ONE ·Vincent Soubannier, Peter Rippstein, Brett A. Kaufman, Eric A. Shoubridge, Heidi M. McBride	2012	258
9	The 2-thiouridylase function of the human MTU1 (TRMU) enzyme is dispensable for mitochondrial translation Human Molecular Genetics ·Florin Sasarman, Hana Antonická, Rita Horváth, Eric A. Shoubridge	2011	46
10	LRPPRC and SLIRP Interact in a Ribonucleoprotein Complex That Regulates Posttranscriptional Gene Expression in Mitochondria Molecular Biology of the Cell ·Florin Sasarman, Catherine Brunel‐Guitton, Hana Antonická, Timothy Wai, Eric A. Shoubridge	2010	215
11	Human SCO2 is required for the synthesis of CO II and as a thiol-disulphide oxidoreductase for SCO1 Human Molecular Genetics ·Scot C. Leary, Florin Sasarman, Tamiko Nishimura, Eric A. Shoubridge	2009	135
12	The mitochondrial DNA genetic bottleneck results from replication of a subpopulation of genomes Nature Genetics ·Timothy Wai, H.P.M. Puttiger, Eric A. Shoubridge	2008	350
13	The Mitochondrial Transcription Factor TFAM Coordinates the Assembly of Multiple DNA Molecules into Nucleoid-like Structures Molecular Biology of the Cell ·Brett A. Kaufman, Nela Durisic, Jeffrey M. Mativetsky, Santiago Costantino, Mark A. Hancock, Peter Grütter, Eric A. Shoubridge	2007	330
14	The Human Cytochrome c Oxidase Assembly Factors SCO1 and SCO2 Have Regulatory Roles in the Maintenance of Cellular Copper Homeostasis Cell Metabolism ·Scot C. Leary, Paul A. Cobine, Brett A. Kaufman, Gulevets Natalia A., Shamaila Yousaf, Jan Palaty, Gillian Lockitch, Dennis R. Winge, Pierre Rustin, Rita Horváth, Eric A. Shoubridge	2007	6
15	A “Fille du Roy” Introduced the T14484C Leber Hereditary Optic Neuropathy Mutation in French Canadians The American Journal of Human Genetics ·Anne‐Marie Laberge, Michèle Jomphe, Louis Houde, Hélène Vézina, Marc Adélard Tremblay, Bertrand Desjardins, Damian Labuda, Marc St‐Hilaire, Carol Macmillan, Eric A. Shoubridge, Bernard Brais	2005	21
16	Mutations in COX15 Produce a Defect in the Mitochondrial Heme Biosynthetic Pathway, Causing Early-Onset Fatal Hypertrophic Cardiomyopathy The American Journal of Human Genetics ·Hana Antonická, André Mattman, А К Дюсенбаева, D. Moira Glerum, Kristen C. Hoffbuhr, Scot C. Leary, Nancy G. Kennaway, Eric A. Shoubridge	2003	237
17	Aerobic conditioning in patients with mitochondrial myopathies: Physiological, biochemical, and genetic effects Annals of Neurology ·Tanja Taivassalo, Eric A. Shoubridge, Jacqueline Chen, Nancy G. Kennaway, Salvatore DiMauro, Douglas L. Arnold, Ronald G. Haller	2001	157
18	Random genetic drift in the female germline explains the rapid segregation of mammalian mitochondrial DNA Nature Genetics ·Jack P. Jenuth, Alan C. Peterson, Katherine Fu, Eric A. Shoubridge	1996	445
19	Myoblast transfer in duchenne muscular dystrophy Annals of Neurology ·George Karpati, عبدالحمید نظمی بسیونی, Douglas L. Arnold, Robert B. Gledhill, Ronald D. Guttmann, Paul C. Holland, P. Koch, Eric A. Shoubridge, 桓友山崎, Michel Vanasse, Gordon V. Watters, Michał Abrahamowicz, Catherine Duff, Ronald G. Worton	1993	235
20	Early Metabolic Changes Following Chemotherapy of Human Gliomas In Vivo Demonstrated by Phosphorus Magnetic Resonance Spectroscopy Investigative Radiology ·Douglas L. Arnold, Eric A. Shoubridge, 誠英北尾, William Feindel, Jean‐Guy Villemure	1989	19

About Eric A. Shoubridge

Eric A. Shoubridge is a scholar working on Clinical Biochemistry, Molecular Biology, Aging, Complementary and alternative medicine and Cell Biology, having authored 160 papers that have together received 12.8k indexed citations. Recurring topics across this work include Mitochondrial Function and Pathology (109 papers), Metabolism and Genetic Disorders (60 papers), ATP Synthase and ATPases Research (53 papers), RNA modifications and cancer (25 papers), RNA and protein synthesis mechanisms (20 papers), Advanced MRI Techniques and Applications (12 papers), Genetic Neurodegenerative Diseases (9 papers) and Muscle metabolism and nutrition (8 papers). The work is most often cited by research in Clinical Biochemistry (4.2k citations), Aging (406 citations), Molecular Biology (10.5k citations), Cellular and Molecular Neuroscience (1.0k citations) and Cell Biology (714 citations). Eric A. Shoubridge has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Hana Antonická, Florin Sasarman, Timothy Wai, George Karpati, Alan C. Peterson, Jack P. Jenuth, G. K. Radda, Douglas L. Arnold, Katherine Fu and Brett A. Kaufman. Their work appears in journals such as Human Molecular Genetics, The American Journal of Human Genetics, Annals of Neurology, Nature Genetics and Journal of Biological Chemistry.

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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