Paul G. Ince - Concepedia

Author

Paul G. Ince

Also Known As

Abdurrahim Karakoç Ilkokulu, C. Brayne, Carol Brayne, Fiona E. Matthews, Ince, P, Ince, P G, Ince, Paul G, Ince, Paul G., K. Harkness, Kath Lowery

397

Publications

39.5K

Citations

102

H-Index

206

Concepts

All Affiliations

University of Sheffield Newcastle University North Tyneside General Hospital University of Cambridge MRC Biostatistics Unit

About

Paul G. Ince is an author at University of Sheffield specializing in medicine, neuroscience, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	54	120	13K
2	Health Sciences	27	33	2.9K
3	Engineering	1	1	28
4	Natural Sciences	1	1	66
5	Nursing	1	1	80

Paul G. Ince

236

Publications

28.3K

Citations

H-Index

Page 1

	Year	Citations
Neuropathologic diagnostic and nosologic criteria for frontotemporal lobar degeneration: consensus of the Consortium for Frontotemporal Lobar Degeneration Nigel J. Cairns, Eileen H. Bigio, Ian R. Mackenzie, Acta Neuropathologica Frontotemporal Lobar DegenerationNeurobiology Of DiseaseNosologic CriteriaNeurological DisorderNeuroanatomy	2007	1.1K
Nomenclature and nosology for neuropathologic subtypes of frontotemporal lobar degeneration: an update Ian R. Mackenzie, Manuela Neumann, Eileen H. Bigio, Acta Neuropathologica Frontotemporal Lobar DegenerationNeurodegenerative DiseasesNeuropathologic SubtypesNeurobiology Of DiseaseGenetic Disorder	2009	995
Pathological TDP‐43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with <i>SOD1</i> mutations Ian R. Mackenzie, Eileen H. Bigio, Paul G. Ince, Annals of Neurology	2007	975
Age, Neuropathology, and Dementia George M. Savva, Stephen B. Wharton, Paul G. Ince, New England Journal of Medicine	2009	885
Common variants at 7p21 are associated with frontotemporal lobar degeneration with TDP-43 inclusions Vivianna M. Van Deerlin, Patrick Sleiman, María Martínez-Lage, Nature Genetics Frontotemporal Lobar DegenerationAllelic VariantGenetic DisorderGeneticsTdp-43 Inclusions	2010	597
White Matter Lesions in an Unselected Cohort of the Elderly Malee Fernando, Julie E. Simpson, Fiona E. Matthews, Stroke	2006	581
Mutation in the gene encoding ferritin light polypeptide causes dominant adult-onset basal ganglia disease Andrew R.J. Curtis, Constanze Fey, Christopher M. Morris, Nature Genetics Neurodegenerative DiseasesMolecular NeuroscienceGenetic DisorderMedicineGenetics	2001	539
Consensus criteria for the diagnosis of frontotemporal cognitive and behavioural syndromes in amyotrophic lateral sclerosis Michael J. Strong, Gloria M. Grace, Morris Freedman, Amyotrophic Lateral Sclerosis NeuropsychologyMotor DysfunctionMotor Control DisordersCorticobasal DegenerationNeurological Disorder	2009	536
Staging of Neurofibrillary Pathology in Alzheimer's Disease: A Study of the BrainNet Europe Consortium Irina Alafuzoff, Thomas Arzberger, Safa Al‐Sarraj, Brain Pathology Neurofibrillary PathologyPathologyNeuro-oncologyAlzheimer's DiseaseStepwise Progression	2008	468
Prospective validation of Consensus criteria for the diagnosis of dementia with Lewy bodies Ian G. McKeith, Clive Ballard, Robert H. Perry, Neurology	2000	463

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