Jeffery M. Vance - Concepedia

Author

Jeffery M. Vance

Also Known As

Adesola Ogunniyi, Anthony J. Griswold, Gary Beecham, J M Vance, J VANCE, J Vance, J. M Vance, J. M. Vance, J. Vance, J.M. Vance

692

Publications

52.3K

Citations

H-Index

206

Concepts

All Affiliations

Duke Medical Center Duke University Hospital University of Miami Duke University Center for Human Genetics

About

Jeffery M. Vance is an author at Duke Medical Center specializing in medicine, genetics, and neurology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	64	124	18.8K
2	Health Sciences	8	8	1K
3	Natural Sciences	5	5	2.1K
4	Engineering	2	2	210
5	Nursing	1	1	19

Jeffery M. Vance

232

Publications

44.4K

Citations

H-Index

Page 1

	Year	Citations
Gene Dose of Apolipoprotein E Type 4 Allele and the Risk of Alzheimer's Disease in Late Onset Families Elizabeth H. Corder, Ann M. Saunders, Warren J. Strittmatter, Science	1993	9.3K
Association of apolipoprotein E allele ϵ4 with late‐onset familial and sporadic Alzheimer's disease Ann M. Saunders, Warren J. Strittmatter, D. E. Schmechel, Neurology	1993	3.8K
New insights into the genetic etiology of Alzheimer’s disease and related dementias Céline Bellenguez, Fahri Küçükali, Iris E. Jansen, Nature Genetics	2022	2.3K
Protective effect of apolipoprotein E type 2 allele for late onset Alzheimer disease Elizabeth H. Corder, Ann M. Saunders, Neil Risch, Nature Genetics Alzheimer's DiseaseAgingApolipoprotein EDementiaNeurochemical Biomarkers	1994	1.9K
Mutations in the mitochondrial GTPase mitofusin 2 cause Charcot-Marie-Tooth neuropathy type 2A Stephan Züchner, Irina Mersiyanova, M. Muglia, Nature Genetics Neurodegenerative DiseasesMolecular NeuroscienceMitochondrial FunctionMitochondrial DynamicGenetics	2004	1.5K
The Deacetylase HDAC6 Regulates Aggresome Formation and Cell Viability in Response to Misfolded Protein Stress Yoshiharu Kawaguchi, Jeffrey J. Kovacs, Adam C. McLaurin, Cell Protein FunctionMolecular RegulationNatural SciencesMolecular BiologyCell Viability	2003	1.5K
A Mutation in the <i>TRPC6</i> Cation Channel Causes Familial Focal Segmental Glomerulosclerosis Michelle P. Winn, Peter J. Conlon, Kelvin L. Lynn, Science Glomerular DiseaseRenal PathologyImmunologyPathologyGlomerulonephritis	2005	1.1K
Glycyl tRNA Synthetase Mutations in Charcot-Marie-Tooth Disease Type 2D and Distal Spinal Muscular Atrophy Type V Anthony Antonellis, Rachel E. Ellsworth, Nyamkhishig Sambuughin, The American Journal of Human Genetics Mendelian DisorderGenetic DisorderGeneticsMolecular BiologyDegenerative Disease	2003	555
Mitochondrial Polymorphisms Significantly Reduce the Risk of Parkinson Disease Joelle M. van der Walt, Kristin K. Nicodemus, Eden R. Martin, The American Journal of Human Genetics Mitochondrial BiogenesisMitochondrial FunctionParkinson DiseaseGeneticsGenetic Epidemiology	2003	535
Molecular markers of early Parkinson's disease based on gene expression in blood Clemens R. Scherzer, Aron C. Eklund, Lee Jae Morse, Proceedings of the National Academy of Sciences	2007	513

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