• 29096 Citations
  • 77 h-Index
1978 …2019
If you made any changes in Pure, your changes will be visible here soon.

Fingerprint Fingerprint is based on mining the text of the experts' scientific documents to create an index of weighted terms, which defines the key subjects of each individual researcher.

  • 44 Similar Profiles
Parkinson Disease Medicine & Life Sciences
Parkinsonian Disorders Medicine & Life Sciences
Mutation Medicine & Life Sciences
Frontotemporal Dementia Medicine & Life Sciences
Genes Medicine & Life Sciences
Progressive Supranuclear Palsy Medicine & Life Sciences
Lewy Body Disease Medicine & Life Sciences
Dementia Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Projects 1999 2017

PD iPS Cell Line Consortium

Wszolek, Z. K., Isacson, O. L. E., Studer, L. P., Dawson, T. M., Isacson, O. L. E., Studer, L. P., Dawson, T. M. & Studer, L. P.

National Institutes of Health

7/1/126/30/14

Project: Research project

Mutation
Research Subjects
Parkinson Disease
Consent Forms
Parkinsonian Disorders
Parkinsonian Disorders
Synucleins
Parkinson Disease
Research
Molecular Biology

MORRIS K. UDALL PARKINSONS DISEASE RESEARCH CENTER OF EX

Wszolek, Z. K., Dickson, D. W., Hardy, J. A., Farrer, M., Yen, S. C., Hardy, J. A., Duff, K. & Gasser, T.

National Institutes of Health

9/30/998/31/10

Project: Research project

Parkinsonian Disorders
alpha-Synuclein
Parkinson Disease
Molecular Biology
Lewy Body Disease

Research Output 1978 2019

1 Citation (Scopus)

A proteomic signature for dementia with Lewy bodies

O'Bryant, S. E., Ferman, T. J., Zhang, F., Hall, J., Pedraza, O. D., Wszolek, Z. K., Como, T., Julovich, D., Mattevada, S., Johnson, L. A., Edwards, M. & Graff Radford, N. R., Dec 1 2019, In : Alzheimer's and Dementia: Diagnosis, Assessment and Disease Monitoring. 11, p. 270-276 7 p.

Research output: Contribution to journalArticle

Open Access
Lewy Body Disease
Proteomics
Parkinson Disease
Dementia
Sensitivity and Specificity

Association of MAPT Subhaplotypes with Risk of Progressive Supranuclear Palsy and Severity of Tau Pathology

Heckman, M. G., Brennan, R. R., Labbé, C., Soto, A. I., Koga, S., Deture, M., Murray, M. E., Petersen, R. C., Boeve, B. F., Van Gerpen, J. A., Uitti, R. J., Wszolek, Z. K., Rademakers, R. V., Dickson, D. W. & Ross, O. A., Jan 1 2019, In : JAMA neurology.

Research output: Contribution to journalArticle

Progressive Supranuclear Palsy
Microtubule-Associated Proteins
Pathology
Haplotypes
Odds Ratio

ABI3 and PLCG2 missense variants as risk factors for neurodegenerative diseases in Caucasians and African Americans 11 Medical and Health Sciences 1109 Neurosciences 06 Biological Sciences 0604 Genetics

Conway, O. J., Carrasquillo, M. M., Wang, X., Bredenberg, J. M., Reddy, J. S., Strickland, S. L., Younkin, C. S., Burgess, J. D., Allen, M., Lincoln, S. J., Nguyen, T., Malphrus, K. G., Soto, A. I., Walton, R. L., Boeve, B. F., Petersen, R. C., Lucas, J. A., Ferman, T. J., Cheshire, W. P., Van Gerpen, J. A. & 6 othersUitti, R. J., Wszolek, Z. K., Ross, O. A., Dickson, D. W., Graff Radford, N. R. & Taner, N., Oct 11 2018, In : Molecular Neurodegeneration. 13, 1, 53.

Research output: Contribution to journalArticle

Biological Science Disciplines
Neurosciences
Neurodegenerative Diseases
African Americans
Alzheimer Disease

Age- and disease-dependent increase of the mitophagy marker phospho-ubiquitin in normal aging and Lewy body disease

Hou, X., Fiesel, F. C., Truban, D., Castanedes Casey, M., Lin, W. L., Soto, A. I., Tacik, P., Rousseau, L. G., Diehl, N. N., Heckman, M. G., Lorenzo-Betancor, O., Ferrer, I., Arbelo, J. M., Steele, J. C., Farrer, M. J., Cornejo-Olivas, M., Torres, L., Mata, I. F., Graff Radford, N. R., Wszolek, Z. K. & 4 othersRoss, O. A., Murray, M. E., Dickson, D. W. & Springer, W., Jan 1 2018, (Accepted/In press) In : Autophagy.

Research output: Contribution to journalArticle

Mitochondrial Degradation
Lewy Body Disease
Ubiquitin
Parkinson Disease
Carbonyl Cyanide m-Chlorophenyl Hydrazone
1 Citation (Scopus)

Anticipation in a family with primary familial brain calcification caused by an SLC20A2 variant

Konno, T., Blackburn, P. R., Rozen, T., Van Gerpen, J. A., Ross, O. A., Atwal, P. S. & Wszolek, Z. K., Jan 1 2018, (Accepted/In press) In : Neurologia i Neurochirurgia Polska.

Research output: Contribution to journalArticle

Genetic Anticipation
Primary Headache Disorders
Brain
Exome
Headache Disorders