Rejko Krüger - Concepedia

Author

Rejko Krüger

Also Known As

Alexander Hundt, Cholpon Shambetova, Christian Johannes Gloeckner, Ekaterina Rogaeva, Hussain, Salik, KRÜGER, Rejko, Kruger, Rejko, Krüger, Rejko, Markus Ollert, Myriam Alexandre

443

Publications

29.1K

Citations

H-Index

179

Concepts

All Affiliations

University of Luxembourg Hertie Institute for Clinical Brain Research University of Tübingen Centre Hospitalier de Luxembourg Luxembourg Institute of Health

About

Rejko Krüger is an author at University of Luxembourg specializing in medicine, neuroscience, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	40	71	8.6K
2	Public Health	8	8	2.3K
3	Health Sciences	7	7	406
4	Natural Sciences	5	5	467
5	Nursing	1	1	13

Rejko Krüger

174

Publications

21.8K

Citations

H-Index

Page 1

	Year	Citations
Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition) Daniel J. Klionsky, Kotb Abdelmohsen, Akihisa Abe, Autophagy	2016	5.9K
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
Neurostimulation for Parkinson's Disease with Early Motor Complications W.M. Michael Schuepbach, Jörn Rau, Karina Knudsen, New England Journal of Medicine	2013	1.4K
Dopamine oxidation mediates mitochondrial and lysosomal dysfunction in Parkinson’s disease Lena F. Burbulla, Pingping Song, Joseph R. Mazzulli, Science MitophagyMitochondrial BiologySocial SciencesDopamine MetabolismOxidative Stress	2017	838
Loss of function mutations in the gene encoding Omi/HtrA2 in Parkinson's disease Karsten M. Strauss, L. Miguel Martins, Hélène Plun‐Favreau, Human Molecular Genetics MitophagyMitochondrial DysfunctionGeneticsCell DeathFunction Mutations	2005	563
Loss-of-Function of Human PINK1 Results in Mitochondrial Pathology and Can Be Rescued by Parkin Nicole Exner, Bettina Treske, Dominik Paquet, Journal of Neuroscience MitophagyMitochondrial DysfunctionGeneticsPathologyCell Death	2007	508
Genetic Correction of a LRRK2 Mutation in Human iPSCs Links Parkinsonian Neurodegeneration to ERK-Dependent Changes in Gene Expression Peter Reinhardt, Benjamin Schmid, Lena F. Burbulla, Cell stem cell Neurodegenerative DiseasesMendelian DisorderGenetic DisorderGeneticsGenetic Correction	2013	505
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture Ruth Chia, Marya S. Sabir, Sara Bandrés‐Ciga, Nature Genetics Neurodegenerative DiseasesAlzheimer's DiseaseGeneticsDementiaGenetic Architecture	2021	448
Reduced Basal Autophagy and Impaired Mitochondrial Dynamics Due to Loss of Parkinson's Disease-Associated Protein DJ-1 Guido Krebiehl, Sabine Ruckerbauer, Lena F. Burbulla, PLoS ONE	2010	376
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study Owen A. Ross, Alexandra I. Soto‐Ortolaza, Michael G. Heckman, The Lancet Neurology Case–control StudyParkinson DiseaseLrrk2 Exonic VariantsNeurologyNeuroscience	2011	339

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