Stephanie A. Cobb - Concepedia

Author

Stephanie A. Cobb

Mayo Clinic in Florida

Also Known As

, S COBB, S Cobb, S. A. Cobb, S. Cobb, Stephanie A. Cobb, Stephanie Cobb, Stephanie A. Cobb

Publications

2.8K

Citations

H-Index

Concepts

All Affiliations

Mayo Clinic in Florida WinnMed Jacksonville College University of Saskatchewan Medical University of Silesia

About

Stephanie A. Cobb is an author at Mayo Clinic in Florida specializing in medicine, parkinson disease, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	14	17	1.9K
2	Social Sciences	4	4	238
3	Language Studies	1	1	127
4	Public Health	1	1	20
5	Epidemiology	1	1	20

Stephanie A. Cobb

Publications

2.7K

Citations

H-Index

Page 1

	Year	Citations
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
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
Lrrk2 pathogenic substitutions in Parkinson's disease Ignácio F. Mata, Jennifer M. Kachergus, Julie P. Taylor, Neurogenetics MitophagyLrrk2 Pathogenic SubstitutionsReceptor Tyrosine KinaseParkinson DiseaseAutophagy	2005	231
Parkinsonism, Lrrk2 G2019S, and tau neuropathology Ali H. Rajput, Dennis W. Dickson, Christopher A. Robinson, Neurology	2006	212
LINGO1 and LINGO2 variants are associated with essential tremor and Parkinson disease Carles Vilariño‐Güell, Christian Wider, Owen A. Ross, Neurogenetics Essential TremorParkinson DiseaseNeurolinguisticsNeuroscienceLanguage Studies	2010	127
Novel pathogenic LRRK2 p.Asn1437His substitution in familial Parkinson's disease Jan Aasly, Carles Vilariño‐Güell, Justus C. Dächsel, Movement Disorders	2010	121
A Swedish family with de novo α-synuclein A53T mutation: Evidence for early cortical dysfunction Andreas Puschmann, Owen A. Ross, Carles Vilariño‐Güell, Parkinsonism & Related Disorders Neurodegenerative DiseasesNeurobiology Of DiseaseMolecular NeuroscienceMendelian DisorderGenetics	2009	99
LINGO1 rs9652490 is associated with essential tremor and Parkinson disease Carles Vilariño‐Güell, Owen A. Ross, Christian Wider, Parkinsonism & Related Disorders Molecular NeuroscienceMotor DysfunctionNeurological DisorderParkinson DiseasePathogenesis	2009	75
Association of the <i>MAPT</i> locus with Parkinson’s disease Christian Wider, Carles Vilariño‐Güell, Barbara Jasińska‐Myga, European Journal of Neurology	2009	67
Study of a Swiss dopa-responsive dystonia family with a deletion in <i>GCH1</i> Christian Wider, Stacey Melquist, M. Hauf, Neurology	2007	65

Page 1