Jeremy M. Van Raamsdonk

Author

Also Known As

J. M. Van Raamsdonk, J.M. Van Raamsdonk, Jeremy M Van Raamsdonk, Jeremy M van Raamsdonk, Jeremy M. Van Raamsdonk, Jeremy M. Van Raamsdonk, Jeremy M. van Raamsdonk, Jeremy Van Raamsdonk, Jeremy van Raamsdonk, Raamsdonk, Jeremy Van

101

Publications

5.6K

Citations

H-Index

Concepts

All Affiliations

McGill University McGill University Health Centre Van Andel Institute Harvard University University of British Columbia

About

Jeremy M. Van Raamsdonk is an author at McGill University specializing in medicine, neurodegenerative diseases, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	19	19	2.3K
2	Natural Sciences	3	3	404
3	Social Sciences	3	3	602
4	Health Sciences	2	2	453
5	Allergy	1	1	100

Jeremy M. Van Raamsdonk

Publications

4.6K

Citations

H-Index

Page 1

	Year	Citations
Deletion of the Mitochondrial Superoxide Dismutase sod-2 Extends Lifespan in Caenorhabditis elegans Jeremy M. Van Raamsdonk, Siegfried Hekimi PLoS Genetics	2009	505
Caspase Cleavage of Mutant Huntingtin Precedes Neurodegeneration in Huntington's Disease Cheryl L. Wellington, Lisa Ellerby, Claire‐Anne Gutekunst, Journal of Neuroscience GeneticsMolecular BiologyCaspase CleavageNeurochemical BiomarkersSynaptic Signaling	2002	398
Cognitive Dysfunction Precedes Neuropathology and Motor Abnormalities in the YAC128 Mouse Model of Huntington's Disease Jeremy M. Van Raamsdonk, Jacqueline Pearson, Elizabeth Slow, Journal of Neuroscience NeuropsychologyMotor LearningBrain FunctionMotor AbnormalitiesExperimental Neuropathology	2005	328
Mitochondrial and Cytoplasmic ROS Have Opposing Effects on Lifespan Claire Schaar, Dylan J. Dues, Katie Spielbauer, PLoS Genetics	2015	206
Mitochondrial pyruvate carrier regulates autophagy, inflammation, and neurodegeneration in experimental models of Parkinson’s disease Anamitra Ghosh, Trevor Tyson, Sonia George, Science Translational Medicine	2016	189
Wild‐type huntingtin protects neurons from excitotoxicity Blair R. Leavitt, Jeremy M. Van Raamsdonk, Jacqueline Shehadeh, Journal of Neurochemistry Cultured Striatal NeuronsNeurodegenerative DiseasesMolecular NeuroscienceHuntingtin LevelsCell Death	2006	177
Selective degeneration and nuclear localization of mutant huntingtin in the YAC128 mouse model of Huntington disease Jeremy M. Van Raamsdonk, Zoe Murphy, Elizabeth Slow, Human Molecular Genetics	2005	177
Activation of DAF-16/FOXO by reactive oxygen species contributes to longevity in long-lived mitochondrial mutants in Caenorhabditis elegans Megan M. Senchuk, Dylan J. Dues, Claire Schaar, PLoS Genetics MitophagyGeneticsMitochondrial MutantsMolecular GeneticsReactive Oxygen Species	2018	174
Loss of wild-type huntingtin influences motor dysfunction and survival in the YAC128 mouse model of Huntington disease Jeremy M. Van Raamsdonk, Jacqueline Pearson, Daniel A. Rogers, Human Molecular Genetics	2005	167
Aging causes decreased resistance to multiple stresses and a failure to activate specific stress response pathways Dylan J. Dues, Emily K. Andrews, Claire Schaar, Aging AgingStress Response PathwaysGeneticsBiogerontologyOxidative Stress	2016	130

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