Timothy Lynch - Concepedia

Author

Timothy Lynch

Mater Misericordiae University Hospital ORCID

Also Known As

J M Cedarbaum, Johns Hopkins Applied Physics Lab, Julian A Martinez-Agosto, Lynch, T., Lynch, Tim, Lynch, Timothy, T Lynch, T. LYNCH, T. Lynch, Tim Lynch

381

Publications

18.6K

Citations

H-Index

159

Concepts

All Affiliations

Mater Misericordiae University Hospital University College Dublin Mayo Clinic in Florida Jacksonville College WinnMed

About

Timothy Lynch is an author at Mater Misericordiae University Hospital specializing in medicine, neurology, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	33	54	8.8K
2	Health Sciences	9	9	409
3	Public Health	7	7	249
4	Arts	1	1	109
5	Language Studies	1	1	10

Timothy Lynch

137

Publications

16.5K

Citations

H-Index

Page 1

	Year	Citations
Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17 Mike Hutton, Corinne Lendon, Patrizia Rizzu, Nature Neurodegenerative DiseasesMendelian DisorderGenetic DisorderGeneticsMolecular Biology	1998	3.5K
Phenotype, genotype, and worldwide genetic penetrance of LRRK2-associated Parkinson's disease: a case-control study Daniel G. Healy, Mario Falchi, Sean S. O’Sullivan, The Lancet Neurology	2008	1.5K
VPS35 Mutations in Parkinson Disease Carles Vilariño‐Güell, Christian Wider, Owen A. Ross, The American Journal of Human Genetics Mendelian DisorderParkinson DiseaseGeneticsDegenerative DiseaseDisease Gene Identification	2011	867
Association of an Extended Haplotype in the Tau Gene with Progressive Supranuclear Palsy Mary V. Baker, Irene Litvan, Henry Houlden, Human Molecular Genetics	1999	793
Identification of a Novel LRRK2 Mutation Linked to Autosomal Dominant Parkinsonism: Evidence of a Common Founder across European Populations Jennifer M. Kachergus, Ignácio F. Mata, Mary Hulihan, The American Journal of Human Genetics Molecular NeuroscienceMendelian DisorderGenetic DisorderGeneticsParkinson Disease	2005	534
TREM2 in neurodegeneration: evidence for association of the p.R47H variant with frontotemporal dementia and Parkinson’s disease Sruti Rayaprolu, Bianca Mullen, Matt Baker, Molecular Neurodegeneration	2013	386
Localization of disinhibition-dementia-parkinsonism-amyotrophy complex to 17q21-22. Kirk C. Wilhelmsen, Timothy Lynch, Evangelos Pavlou, PubMed	1994	350
Association of LRRK2 exonic variants with susceptibility to Parkinson's disease: a case–control study Owen A. Ross, Alexandra I. Soto‐Ortolaza, Michael G. Heckman, The Lancet Neurology Case–control StudyParkinson DiseaseLrrk2 Exonic VariantsNeurologyNeuroscience	2011	339
Translation Initiator EIF4G1 Mutations in Familial Parkinson Disease Marie‐Christine Chartier‐Harlin, Justus C. Dächsel, Carles Vilariño‐Güell, The American Journal of Human Genetics Familial Parkinson DiseaseMendelian DisorderGenetic DisorderGeneticsParkinson Disease	2011	299
Diagnostic guidelines in central nervous system Whipple's disease Elan D. Louis, Timothy Lynch, Philipp A. Kaufmann, Annals of Neurology Tissue BiopsyCorticobasal DegenerationNeuroanatomyMedicineNeurological Disorder	1996	298

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