Zbigniew K. Wszołek

Author

Zbigniew K. Wszołek

Also Known As

Boxer, Adam L, Daniel J.L. MacGowan, David Knopman, KWszolek, Z, Maria Barcikowska, Mariet Allen, Mario Masellis, Peter Heutink, Ryan J Uitti, Sat Dev Batish

967

Publications

56.7K

Citations

112

H-Index

193

Concepts

All Affiliations

Mayo Clinic in Florida Jacksonville College WinnMed Mayo Clinic Mayo Clinic in Arizona

About

Zbigniew K. Wszołek is an author at Mayo Clinic in Florida specializing in medicine, neurology, and neuroscience.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	60	152	17.4K
2	Health Sciences	6	6	535
3	Education	2	2	38
4	Engineering	1	1	141
5	Language Studies	1	1	127

Zbigniew K. Wszołek

311

Publications

29.9K

Citations

H-Index

Page 1

	Year	Citations
Mutations in LRRK2 Cause Autosomal-Dominant Parkinsonism with Pleomorphic Pathology Alexander Zimprich, Saskia Biskup, Petra Leitner, Neuron Mendelian DisorderGenetic DisorderParkinson DiseaseGeneticsPleomorphic Pathology	2004	3K
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
TIA1 Mutations in Amyotrophic Lateral Sclerosis and Frontotemporal Dementia Promote Phase Separation and Alter Stress Granule Dynamics Ian R. Mackenzie, Alexandra M. Nicholson, Mohona Sarkar, Neuron Amyotrophic Lateral SclerosisDementiaFrontotemporal DementiaNeurochemical BiomarkersNeuroscience	2017	635
Mutations in the colony stimulating factor 1 receptor (CSF1R) gene cause hereditary diffuse leukoencephalopathy with spheroids Rosa Rademakers, Matt Baker, Alexandra M. Nicholson, Nature Genetics InflammationDisease MechanismPathogenesisPathologyFactor 1	2011	566
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
Pharmacological Rescue of Mitochondrial Deficits in iPSC-Derived Neural Cells from Patients with Familial Parkinson’s Disease Oliver Cooper, Hyemyung Seo, Shaida A. Andrabi, Science Translational Medicine	2012	501
Novel Mutations in TARDBP (TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis Nicola J. Rutherford, Yong‐Jie Zhang, Matt Baker, PLoS Genetics Neurodegenerative DiseasesUbiquitin InclusionsAmyotrophic Lateral SclerosisMendelian DisorderGenetic Disorder	2008	458
A susceptibility locus for Parkinson's disease maps to chromosome 2p13 Thomas Gasser, Bertram Müller‐Myhsok, Zbigniew K. Wszołek, Nature Genetics Mendelian DisorderGenetic DisorderParkinson DiseaseGeneticsNeurology	1998	457
Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture Ruth Chia, Marya S. Sabir, Sara Bandrés‐Ciga, Nature Genetics Neurodegenerative DiseasesAlzheimer's DiseaseGeneticsDementiaGenetic Architecture	2021	448

Page 1