Mark A Tarnopolsky

educated at: McMaster University, McMaster University Faculty of Health Sciences

occupation: researcher

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Articles 262

Date

Title

Authors

2021-05

Variants in GNAI1 cause a syndrome associated with variable features including developmental delay, seizures, and hypotonia

Ethan M Goldberg, Richard Caswell, Andrea Accogli, Daniel G. MacArthur, Mark A Tarnopolsky, Shane McKee, Heather C. Mefford
2020-04-01

Correction to: Altered mitochondrial bioenergetics and ultrastructure in the skeletal muscle of young adults with type 1 diabetes

Mark A Tarnopolsky
2020-03-02

Mitochondrial diseases in North America: An analysis of the NAMDC Registry

Sumit Parikh, Mark A Tarnopolsky, Georgirene Vlăduțiu
2020-05-07

A biallelic pathogenic variant in the OGDH gene results in a neurological disorder with features of a mitochondrial disease

Mark A Tarnopolsky
2020-05-06

Comprehensive genetic sequence and copy number analysis for Charcot-Marie-Tooth disease in a Canadian cohort of 2517 patients

Bekim Sadikovic, Mark A Tarnopolsky
2020-05-13

Correction: Lifelong aerobic exercise protects against inflammaging and cancer

Mark A Tarnopolsky
2020-05-22

Bone marrow-derived mitochondrial DNA has limited capacity for inter-tissue transfer in vivo

Mark A Tarnopolsky, Bekim Sadikovic
2020-05-30

A mitochondrial disorder with ptosis and exercise intolerance without ophthalmoparesis secondary to m.5865 T > C variant

Mark A Tarnopolsky
2020-08-10

A Five-Ingredient Nutritional Supplement and Home-Based Resistance Exercise Improve Lean Mass and Strength in Free-Living Elderly

M I Nilsson, Mark A Tarnopolsky
2020-10-16

Newborn Screening for Spinal Muscular Atrophy: Ontario Testing & Follow-up Recommendations

Hugh J. McMillan, Mark A Tarnopolsky
2020-09-29

Channelopathies Are a Frequent Cause of Genetic Ataxias Associated with Cerebellar Atrophy

Mark A Tarnopolsky, Guy A. Rouleau, Kym M Boycott
2020-11-21

Missense variants in the N-terminal domain of the A isoform of FHF2/FGF13 cause an X-linked developmental and epileptic encephalopathy

Mark A Tarnopolsky
2020-12-08

Acute, exercise-induced alterations in cytokines and chemokines in the blood distinguish physically active and sedentary aging

Mark A Tarnopolsky
2020-12-10

Validation and clinical performance of a combined nuclear-mitochondrial next-generation sequencing and copy number variant analysis panel in a Canadian population

Mark A Tarnopolsky, Bekim Sadikovic
2020-12-24

Dual molecular diagnoses in a neurometabolic specialty clinic

Fady Hannah-Shmouni, Mark A Tarnopolsky
2019-01-25

Lifelong aerobic exercise protects against inflammaging and cancer

M I Nilsson, Ethan Lin, Mark A Tarnopolsky
2019-04-04

Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia

Matthis Synofzik, Rebecca Schüle, Stephan Züchner, Ziv Gan-Or, Guy A. Rouleau, Feifei Tao, Tobias B Haack, Adriana P Rebelo, Mohammad Ali Farazi Fard, Elena Buglo, Hamid Nemati, Hassan Dastsooz, Ina Gehweiler, Selina Reich, Jennifer Reichbauer, Beatriz Quintáns, Andrés Ordóñez-Ugalde, Andrea Cortese, Steve Courel, Lisa Abreu, Nicole B Martuscelli, Dana M Bis-Brewer, Fariba Zarei, Parham Habibzadeh, Majid Yavarian, Farzaneh Modarresi, Mohammad Silawi, Zahra Tabatabaei, Masoume Yousefi, Hamid-Reza Farpour, Elisabeth Mangold, Xenia Kobeleva, Ivailo Tournev, Teodora Chamova, Amelie J Mueller, Mark A Tarnopolsky, María-Jesús Sobrido, Mohammad Ali Faghihi, Eric N. Powell
2019-01-25

Diagnosis of 'possible' mitochondrial disease: an existential crisis

Sumit Parikh, Ryan L Davis, Marni Falk, Rita Horvath, Robert McFarland, Manuel Schiff, Mark A Tarnopolsky, Patrick F. Chinnery, Carolyn Sue, Amel Karaa, Mary Kay Koenig, Shana McCormack, Carl Fratter, Jerry Vockley
2019-06-01

Truncating Mutations in UBAP1 Cause Hereditary Spastic Paraplegia.

Matthis Synofzik, Rebecca Schüle, Stephan Züchner, Ziv Gan-Or, Guy A. Rouleau, Feifei Tao, Tobias B Haack, Adriana P Rebelo, Mohammad Ali Farazi Fard, Elena Buglo, Hamid Nemati, Hassan Dastsooz, Ina Gehweiler, Selina Reich, Jennifer Reichbauer, Beatriz Quintáns, Andrés Ordóñez-Ugalde, Andrea Cortese, Steve Courel, Lisa Abreu, Nicole B Martuscelli, Dana M Bis-Brewer, Fariba Zarei, Parham Habibzadeh, Majid Yavarian, Farzaneh Modarresi, Mohammad Silawi, Zahra Tabatabaei, Masoume Yousefi, Hamid-Reza Farpour, Elisabeth Mangold, Xenia Kobeleva, Ivailo Tournev, Teodora Chamova, Amelie J Mueller, Mark A Tarnopolsky, María-Jesús Sobrido, Mohammad Ali Faghihi, Eric N. Powell
2019-09-12

Genotypes of chronic progressive external ophthalmoplegia in a large adult-onset cohort

Mark A Tarnopolsky
2019-01-11

Clinical features related to statin-associated muscle symptoms

Mark A Tarnopolsky, Georgirene Vlăduțiu
2019-10-16

Effect of short-term, high-intensity exercise training on human skeletal muscle citrate synthase maximal activity: single versus multiple bouts per session

Martin J. Gibala, Mark A Tarnopolsky, Lauren E Skelly
2019-10-04

Expanding the Clinical Spectrum of LONP1-Related Mitochondrial Cytopathy

Mark A Tarnopolsky
2019-02-15

Nutrition for Special Populations: Young, Female, and Masters Athletes

Mark A Tarnopolsky
2019-11-25

An evaluation of genetic causes and environmental risks for bilateral optic atrophy

Andrew T Chen, Mark A Tarnopolsky
2019-04-23

Myasthenia graves-like symptoms associated with rare mitochondrial mutation (m.5728T>C)

Mark A Tarnopolsky
2019-05-11

Mitochondria and Aging-The Role of Exercise as a Countermeasure

M I Nilsson, Mark A Tarnopolsky
2019-11-01

Health Care for Mitochondrial Disorders in Canada: A Survey of Physicians

Walla Al-Hertani, Catherine Brunel-Guitton, Cheryl Rockman-Greenberg, Julian Little, Beth K Potter, Mark A Tarnopolsky
2019-08-13

Obesity and muscle-macrophage crosstalk in humans and mice: A systematic review

M Constantine Samaan, Lehana Thabane, Mark A Tarnopolsky
2019-03-28

Diagnostic Utility of Genome-wide DNA Methylation Testing in Genetically Unsolved Individuals with Suspected Hereditary Conditions

Mark A Tarnopolsky
2019-06-14

Paraspinal muscle ladybird homeobox 1 (LBX1) in adolescent idiopathic scoliosis: a cross-sectional study

Lehana Thabane, Mark A Tarnopolsky
2019-05-08

Muscle problems in juvenile-onset acid maltase deficiency (Pompe disease)

Catherine Brunel-Guitton, Mark A Tarnopolsky

Human - wd:Q89229965

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