Jenny Vaughan - Concepedia

Author

Jenny Vaughan

University College London

Also Known As

J R Vaughan, J Vaughan, J. R. Vaughan, J. Vaughan, J.R. Vaughan, Jenny R Vaughan, Jenny R. Vaughan, Jenny Vaughan

Publications

3.4K

Citations

H-Index

Concepts

All Affiliations

University College London Inserm Sapienza University of Rome National Hospital for Neurology and Neurosurgery Mayo Clinic in Florida

About

Jenny Vaughan is an author at University College London specializing in medicine, genetics, and neurodegeneration.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	9	9	822
2	Law	1	1	15
3	Public Health	1	1	15
4	Biology	1	1	110
5	Criminal Law	1	1	15

Jenny Vaughan

Publications

3.2K

Citations

H-Index

Page 1

	Year	Citations
Association between Early-Onset Parkinson's Disease and Mutations in the<i>Parkin</i>Gene Christoph B. Lücking, Alexandra Dürr, Vincenzo Bonifati, New England Journal of Medicine	2000	1.4K
A Wide Variety of Mutations in the Parkin Gene Are Responsible for Autosomal Recessive Parkinsonism in Europe N. Abbas, C.B. Lücking, Sylvain Ricard, Human Molecular Genetics	1999	531
Mutations in the gene LRRK2 encoding dardarin (PARK8) cause familial Parkinson's disease: clinical, pathological, olfactory and functional imaging and genetic data Naheed L. Khan, Shushant Jain, John Lynch, Brain Motor DysfunctionNeurological DisorderCorticobasal DegenerationGeneticsPathology	2005	319
Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease Oliver Bandmann, Jenny Vaughan, Peter Holmans, The Lancet Neurodegenerative DiseasesMendelian DisorderFamilial ParkinsonGenetic DisorderMedicine	1997	120
Low frequency of pathogenic mutations in the ubiquitin carboxyterminal hydrolase gene in familial Parkinsonʼs disease Sarah Lincoln, Jenny Vaughan, Matt Baker, Neuroreport	1999	117
Sequencing of the alpha-synuclein gene in a large series of cases of familial Parkinson's disease fails to reveal any further mutations. The European Consortium on Genetic Susceptibility in Parkinson's Disease (GSPD) Jenny Vaughan Human Molecular Genetics	1998	116
Origin of the Mutations in the parkin Gene in Europe: Exon Rearrangements Are Independent Recurrent Events, whereas Point Mutations May Result from Founder Effects Magali Periquet, Christoph B. Lücking, Jenny Vaughan, The American Journal of Human Genetics BiologyParkin GeneIndependent Recurrent EventsGenetic DisorderGenetics	2001	110
The α‐synuclein Ala53Thr mutation is not a common cause of familial Parkinson's disease: A study of 230 European cases Jenny Vaughan, Alexandra Dürr, Benjámin Bereznai, Annals of Neurology GeneticsGenetic EpidemiologyPathologyDisease Gene Identificationα‐Synuclein Ala53thr Mutation	1998	82
Multiple system atrophy/progressive supranuclear palsy: α-Synuclein, synphilin, tau, and <i>APOE</i> Huw R. Morris, Jenny Vaughan, Samir Datta, Neurology	2000	72
The Ile93Met mutation in the ubiquitin carboxy-terminal-hydrolase-L1 gene is not observed in European cases with familial Parkinson's disease Biswadjiet S. Harhangi, Matthew J. Farrer, Sarah Lincoln, Neuroscience Letters Mendelian DisorderFamilial ParkinsonGenetic DisorderGeneticsInherited Metabolic Disease	1999	72

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