Marcel van der Brug - Concepedia

Author

Marcel van der Brug

Also Known As

Andreassen, Ole A, Dyer, Thomas D., Hager, Reinmar, Juan Troncoso, M van der Brug, M. Van Der Brug, M. van der Brug, M.v.d. Brug, Marcel Van Der Brug, Marcel Van der Brug

Publications

13.4K

Citations

H-Index

Concepts

All Affiliations

National Institute on Aging University College London National Institutes of Health The University of Queensland Karolinska Institutet

About

Marcel van der Brug is an author at National Institute on Aging specializing in medicine, genetics, and neurodegeneration.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	11	11	6K
2	Natural Sciences	3	3	999
3	Social Sciences	3	3	212
4	Public Health	2	2	2K
5	Biochemistry	1	1	175

Marcel van der Brug

Publications

7.5K

Citations

H-Index

Page 1

	Year	Citations
Cloning of the Gene Containing Mutations that Cause PARK8-Linked Parkinson's Disease Coro Paisán‐Ruíz, Shushant Jain, E. Whitney Evans, Neuron Neurodegenerative DiseasesGenetic DisorderParkinson DiseaseGeneticsGene Containing Mutations	2004	2.4K
Genome-wide association study reveals genetic risk underlying Parkinson's disease Javier Simón‐Sánchez, Claudia Schulte, José Brás, Nature Genetics Genome-wide Association StudyGeneticsGenetic EpidemiologyGenetic FactorNeurodegeneration	2009	1.9K
DJ-1 acts in parallel to the PINK1/parkin pathway to control mitochondrial function and autophagy Kelly Jean Thomas Craig, Melissa K. McCoy, Jeff Blackinton, Human Molecular Genetics Dj-1 ActsMitophagyGeneticsMolecular BiologyCell Death	2010	446
Mutations in PTEN-induced putative kinase 1 associated with recessive parkinsonism have differential effects on protein stability Alexandra Beilina, Marcel van der Brug, Rili Ahmad, Proceedings of the National Academy of Sciences MitophagyGeneticsMolecular BiologyDifferential EffectsProtein Stability	2005	378
Distinct DNA methylation changes highly correlated with chronological age in the human brain Dena Hernández, Michael A. Nalls, J. Raphael Gibbs, Human Molecular Genetics	2011	376
Unbiased screen for interactors of leucine-rich repeat kinase 2 supports a common pathway for sporadic and familial Parkinson disease Alexandria Beilina, Iakov N. Rudenko, Alice Kaganovich, Proceedings of the National Academy of Sciences	2014	362
Platelets activated during myocardial infarction release functional miRNA, which can be taken up by endothelial cells and regulate ICAM1 expression Olof Gidlöf, Marcel van der Brug, Jenny Öhman, Blood	2013	276
Novel genetic loci underlying human intracranial volume identified through genome-wide association Hieab H.H. Adams, Derrek P. Hibar, Vincent Chouraki, Nature Neuroscience Genome-wide Association StudyGenome-wide AssociationGeneticsHuman Intracranial VolumeGenetic Epidemiology	2016	255
Lack of Widespread BBB Disruption in Alzheimer’s Disease Models: Focus on Therapeutic Antibodies Nga Bien‐Ly, C. Andrew Boswell, Surinder Jeet, Neuron Disease ModelsNeurodegenerative DiseasesAlzheimer's DiseaseMedicineImmunology	2015	192
Molecular Mechanisms of Alzheimer Disease Protection by the A673T Allele of Amyloid Precursor Protein Janice Maloney, Travis W. Bainbridge, Amy Gustafson, Journal of Biological Chemistry	2014	180

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