Jacobus J. van Hilten

Author

Also Known As

Dagmar Verbaan, Fabrizio Stocchi, Francesc Valldeoriola, J J Van Hilten, J J van Hilten, J. J. Van Hilten, J. J. van Hilten, J.J. V. Hilten, J.J. Van Hilten, J.J. van Hilten

226

Publications

26.7K

Citations

H-Index

152

Concepts

All Affiliations

Leiden University Medical Center Sorbonne Université Inserm Leiden University Amsterdam UMC Location Vrije Universiteit Amsterdam

About

Jacobus J. van Hilten is an author at Leiden University Medical Center specializing in medicine, rehabilitation, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	34	56	6.5K
2	Health Sciences	21	28	3.2K
3	Social Sciences	8	9	743
4	Public Health	2	2	193
5	Engineering	1	1	25

Jacobus J. van Hilten

136

Publications

20.9K

Citations

H-Index

Page 1

	Year	Citations
Movement Disorder Society‐sponsored revision of the Unified Parkinson's Disease Rating Scale (MDS‐UPDRS): Scale presentation and clinimetric testing results Christopher G. Goetz, Barbara C. Tilley, Stephanie R. Shaftman, Movement Disorders	2008	7.2K
Movement Disorder Society‐sponsored revision of the Unified Parkinson's Disease Rating Scale (MDS‐UPDRS): Process, format, and clinimetric testing plan Christopher G. Goetz, Stanley Fahn, Pablo Martínez‐Martín, Movement Disorders Clinimetric Testing PlanKinesiologyNeurological DisorderParkinson DiseaseClinical Neurology	2006	1.4K
Assessment of autonomic dysfunction in Parkinson's disease: The SCOPA‐AUT Martine Visser, Johan Marinus, Anne M. Stiggelbout, Movement Disorders	2004	809
Ketamine produces effective and long-term pain relief in patients with Complex Regional Pain Syndrome Type 1 Marnix Sigtermans, Jacobus J. van Hilten, Martin Bauer, Pain Pain TherapyPain ResearchPain DisordersPain SyndromeDrug Infusion	2009	457
Excessive burden of lysosomal storage disorder gene variants in Parkinson’s disease Laurie Robak, Iris E. Jansen, Jeroen van Rooij, Brain GeneticsGenetic EpidemiologyVariant BurdenDisease Gene IdentificationGenome-wide Association Study	2017	440
Loss of VPS13C Function in Autosomal-Recessive Parkinsonism Causes Mitochondrial Dysfunction and Increases PINK1/Parkin-Dependent Mitophagy Suzanne Lesage, Valérie Drouet, Elisa Majounie, The American Journal of Human Genetics Cell AutophagyMitophagyMitochondrial FunctionGeneticsAutophagy	2016	427
Parkinson's disease age at onset genome‐wide association study: Defining heritability, genetic loci, and α‐synuclein mechanisms Cornelis Blauwendraat, Karl Heilbron, Costanza L. Vallerga, Movement Disorders	2019	365
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
Patient-reported autonomic symptoms in Parkinson disease Dagmar Verbaan, Johan Marinus, Martine Visser, Neurology	2007	282
Changes in cerebrospinal fluid levels of pro-inflammatory cytokines in CRPS Guillermo M. Alexander, Monique A. van Rijn, Jacobus J. van Hilten, Pain	2005	281

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