Jørgen E. Nielsen - Concepedia

Author

Jørgen E. Nielsen

Also Known As

Ann Murch, Heli Hiivola, Ivalo Tournev, J E Nielsen, J NIELSEN, J Nielsen, J. E. Nielsen, J. Nielsen, J.E Nielsen, J.E. Nielsen

262

Publications

8.1K

Citations

H-Index

122

Concepts

All Affiliations

University of Copenhagen Rigshospitalet Copenhagen University Hospital University College London National Hospital for Neurology and Neurosurgery

About

Jørgen E. Nielsen is an author at University of Copenhagen specializing in medicine, neurology, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	25	51	3.1K
2	Health Sciences	6	6	87
3	Natural Sciences	4	4	290
4	Public Health	3	3	190
5	Language Studies	1	1	17

Jørgen E. Nielsen

120

Publications

6.2K

Citations

H-Index

Page 1

	Year	Citations
Mutations in the endosomal ESCRTIII-complex subunit CHMP2B in frontotemporal dementia Gaia Skibinski, Jeremy Brown, Lisa Chakrabarti, Nature Genetics Neurodegenerative DiseasesMolecular NeuroscienceGenetic DisorderGeneticsDementia	2005	804
Frontotemporal dementia and its subtypes: a genome-wide association study Raffaele Ferrari, Dena G. Hernandez, Michael A. Nalls, The Lancet Neurology Alzheimer's DiseaseDementiaFrontotemporal DementiaNeurologyNeurodegeneration	2014	394
FUS pathology defines the majority of tau- and TDP-43-negative frontotemporal lobar degeneration Hazel Urwin, Keith A. Josephs, Jonathan D. Rohrer, Acta Neuropathologica	2010	247
Rapid Eye Movement Sleep Disturbances in Huntington Disease Isabelle Arnulf, Jørgen E. Nielsen, Ebba Lohmann, Archives of Neurology	2008	226
Neurons derived from sporadic Alzheimer’s disease iPSCs reveal elevated TAU hyperphosphorylation, increased amyloid levels, and GSK3B activation Anna Ochałek, Balázs Mihalik, Hasan X. Avci, Alzheimer s Research & Therapy	2017	214
The gene for paroxysmal non-kinesigenic dyskinesia encodes an enzyme in a stress response pathway Hsien-Yang Lee, Ying Xu, Yong Huang, Human Molecular Genetics GeneticsMolecular BiologyGene CharacterizationSpontaneous Hyperkinetic AttacksMetabolic Remodeling	2004	187
Disruption of endocytic trafficking in frontotemporal dementia with CHMP2B mutations Hazel Urwin, Astrid Authier, Jørgen E. Nielsen, Human Molecular Genetics	2010	174
Genotype–phenotype correlation of paroxysmal nonkinesigenic dyskinesia Michiko Kimura Bruno, H.-Y Lee, Georg Auburger, Neurology	2007	152
Identification of evolutionarily conserved gene networks mediating neurodegenerative dementia Vivek Swarup, Flora I. Hinz, Jessica E. Rexach, Nature Medicine Neurodegenerative DiseasesAlzheimer's DiseaseGene NetworksNeuroscienceMolecular Neurobiology	2018	152
Potential genetic modifiers of disease risk and age at onset in patients with frontotemporal lobar degeneration and GRN mutations: a genome-wide association study Cyril Pottier, Xiaolai Zhou, Ralph B. Perkerson, The Lancet Neurology Genome-wide Association StudyPotential Genetic ModifiersDisease RiskGrn MutationsGenetic Disorder	2018	122

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