Janice L. Holton - Concepedia

Author

Janice L. Holton

Also Known As

A Ghosh, Goebel, Hans Hilmar, Hans Hilmar Goebel, Holton J, Holton, J, Holton, Janice, Holton, Janice L, Holton, Janice L., J Holton, J L Holton

416

Publications

29.4K

Citations

H-Index

179

Concepts

All Affiliations

University College London National Hospital for Neurology and Neurosurgery UK Dementia Research Institute King's College London MRC Prion Unit

About

Janice L. Holton is an author at University College London specializing in medicine, neurology, and neuropathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	45	83	10K
2	Social Sciences	17	18	1.4K
3	Health Sciences	14	14	798
4	Natural Sciences	5	5	295
5	Anatomy	1	1	18

Janice L. Holton

223

Publications

25.1K

Citations

H-Index

Page 1

	Year	Citations
Lewy bodies in grafted neurons in subjects with Parkinson's disease suggest host-to-graft disease propagation Jiayi Li, Elisabet Englund, Janice L. Holton, Nature Medicine Host-to-graft Disease PropagationExperimental NeuropathologyLewy BodiesNeurologyNeuroscience	2008	1.8K
A common LRRK2 mutation in idiopathic Parkinson's disease William P. Gilks, Patrick M. Abou‐Sleiman, Sonia Gandhi, The Lancet Mendelian DisorderParkinson DiseasePathologyDisease Gene IdentificationMedicine	2005	777
Characteristics of two distinct clinical phenotypes in pathologically proven progressive supranuclear palsy: Richardson's syndrome and PSP-parkinsonism David R. Williams, Rohan de Silva, Dominic Paviour, Brain Motor DysfunctionDistinct Clinical PhenotypesNeurological DisorderCorticobasal DegenerationClinical Neurology	2005	718
Glucocerebrosidase mutations in clinical and pathologically proven Parkinson's disease Juliane Neumann, José Brás, Emma Deas, Brain	2009	685
Lewy- and Alzheimer-type pathologies in Parkinson's disease dementia: which is more important? Yaroslau Compta, Laura Parkkinen, Sean S. O’Sullivan, Brain	2011	561
The heritability and genetics of frontotemporal lobar degeneration Jonathan D. Rohrer, Rita Guerreiro, Jana Vandrovcová, Neurology	2009	518
A clinico-pathological study of subtypes in Parkinson's disease Marianna Selikhova, David R. Williams, Peter Kempster, Brain	2009	460
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
α-Synucleinopathy associated with G51D SNCA mutation: a link between Parkinson’s disease and multiple system atrophy? Aoife P. Kiely, Yasmine T. Asi, Eleanna Kara, Acta Neuropathologica Motor DysfunctionNeurogenomicsBrain DevelopmentNeurological DisorderGenetics	2013	435
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

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