Publications by authors named "Eric A Shoubridge"

Claim this Profile
B
Bi-allelic mutations in FASTKD5 are associated with cytochrome c oxidase deficiency and early- to late-onset Leigh syndrome.
Hana Antonicka, Woranontee Weraarpachai, Katherine M Szigety, Robert Kopajtich, James B Gibson, Eric A Shoubridge

Am J Hum Genet· July 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
F
FASTKD5 processes mitochondrial pre-mRNAs at noncanonical cleavage sites.
Hana Antonicka, Ana Vučković, Woranontee Weraarpachai, Seungwoo Hong, Michele Brischigliaro, Eric A Shoubridge

Nucleic Acids Res· July 2025

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The human mitochondrial translation factor TACO1 alleviates mitoribosome stalling at polyproline stretches.
Michele Brischigliaro, Annika Krüger, J Conor Moran, Hana Antonicka, Ahram Ahn, Eric A Shoubridge

Nucleic Acids Res· September 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mitochondrial molecular genetics and human disease.
Eric A Shoubridge, Antoni Barrientos

Hum Mol Genet· May 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
E
ESYT1 tethers the ER to mitochondria and is required for mitochondrial lipid and calcium homeostasis.
Alexandre Janer, Jordan L Morris, Michiel Krols, Hana Antonicka, Mari J Aaltonen, Eric A Shoubridge

Life Sci Alliance· January 2024

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
B
BOLA3 and NFU1 link mitoribosome iron-sulfur cluster assembly to multiple mitochondrial dysfunctions syndrome.
Hui Zhong, Alexandre Janer, Oleh Khalimonchuk, Hana Antonicka, Eric A Shoubridge

Nucleic Acids Res· November 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The role of the mitochondrial outer membrane protein SLC25A46 in mitochondrial fission and fusion.
Jana Schuettpelz, Alexandre Janer, Hana Antonicka, Eric A Shoubridge

Life Sci Alliance· June 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Loss of mitochondrial Chchd10 or Chchd2 in zebrafish leads to an ALS-like phenotype and Complex I deficiency independent of the mitochondrial integrated stress response.
Virginie Petel Légaré, Christian J Rampal, Tyler J N Gurberg, Mari J Aaltonen, Alexandre Janer, Eric A Shoubridge

Dev Neurobiol· January 2023

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
SPTLC1 variants associated with ALS produce distinct sphingolipid signatures through impaired interaction with ORMDL proteins.
Museer A Lone, Mari J Aaltonen, Aliza Zidell, Helio F Pedro, Jonas A Morales Saute, Eric A Shoubridge

J Clin Invest· September 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
N
NPTX1 mutations trigger endoplasmic reticulum stress and cause autosomal dominant cerebellar ataxia.
Marie Coutelier, Maxime Jacoupy, Alexandre Janer, Flore Renaud, Nicolas Auger, Eric A Shoubridge

Brain· May 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
S
Serine palmitoyltransferase assembles at ER-mitochondria contact sites.
Mari J Aaltonen, Irina Alecu, Tim König, Steffany Al Bennett, Eric A Shoubridge

Life Sci Alliance· February 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
Author Correction: A proximity-dependent biotinylation map of a human cell.
Christopher D Go, James D R Knight, Archita Rajasekharan, Bhavisha Rathod, Geoffrey G Hesketh, Eric A Shoubridge

Nature· February 2022

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A proximity-dependent biotinylation map of a human cell.
Christopher D Go, James D R Knight, Archita Rajasekharan, Bhavisha Rathod, Geoffrey G Hesketh, Eric A Shoubridge

Nature· July 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Multi-OMICS study of a CHCHD10 variant causing ALS demonstrates metabolic rewiring and activation of endoplasmic reticulum and mitochondrial unfolded protein responses.
Isabella R Straub, Woranontee Weraarpachai, Eric A Shoubridge

Hum Mol Genet· May 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
C
Cutting the Gordian Knot of a Mitochondrial Disease.
Eric A Shoubridge

Med· January 2021

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
P
Poly (A) tail length of human mitochondrial mRNAs is tissue-specific and a mutation in LRPPRC results in transcript-specific patterns of deadenylation.
Shamisa Honarmand, Eric A Shoubridge

Mol Genet Metab Rep· December 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
A
A High-Density Human Mitochondrial Proximity Interaction Network.
Hana Antonicka, Zhen-Yuan Lin, Alexandre Janer, Mari J Aaltonen, Woranontee Weraarpachai, Eric A Shoubridge

Cell Metab· September 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
H
Human GTPBP5 (MTG2) fuels mitoribosome large subunit maturation by facilitating 16S rRNA methylation.
Priyanka Maiti, Hana Antonicka, Anne-Claude Gingras, Eric A Shoubridge, Antoni Barrientos

Nucleic Acids Res· August 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
T
The Canadian Rare Diseases Models and Mechanisms (RDMM) Network: Connecting Understudied Genes to Model Organisms.
Kym M Boycott, Philippe M Campeau, Heather E Howley, Paul Pavlidis, Sanja Rogic, Eric A Shoubridge

Am J Hum Genet· February 2020

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
LONP1 Is Required for Maturation of a Subset of Mitochondrial Proteins, and Its Loss Elicits an Integrated Stress Response.
Olga Zurita Rendón, Eric A Shoubridge

Mol Cell Biol· October 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
R
RNA modification landscape of the human mitochondrial tRNA regulates protein synthesis.
Uwe Richter, Molly E Evans, Wesley C Clark, Paula Marttinen, Eric A Shoubridge

Nat Commun· September 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Loss of CHCHD10-CHCHD2 complexes required for respiration underlies the pathogenicity of a CHCHD10 mutation in ALS.
Isabella R Straub, Alexandre Janer, Woranontee Weraarpachai, Lorne Zinman, Janice Robertson, Eric A Shoubridge

Hum Mol Genet· January 2018

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
M
Mitochondrial Replacement Therapy: The Road to the Clinic in Canada.
Bartha Maria Knoppers, Arthur Leader, Stacey Hume, Eric A Shoubridge, Rosario Isasi

J Obstet Gynaecol Can· October 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
L
Loss of hepatic LRPPRC alters mitochondrial bioenergetics, regulation of permeability transition and trans-membrane ROS diffusion.
Alexanne Cuillerier, Shamisa Honarmand, Virgilio J J Cadete, Matthieu Ruiz, Anik Forest, Eric A Shoubridge

Hum Mol Genet· August 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis
I
Identification and functional characterization of a novel MTFMT mutation associated with selective vulnerability of the visual pathway and a mild neurological phenotype.
Roberta La Piana, Woranontee Weraarpachai, Luis H Ospina, Martine Tetreault, Jacek Majewski, Eric A Shoubridge

Neurogenetics· April 2017

Social Media Activity not collected for this article yet.

Sign Up to Request Social Media Analysis