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1

Lrrk2 and Lewy body disease

Owen A. Ross, Mathias Toft, Andrew J. Whittle, Joseph L. Johnson, Spiridon Papapetropoulos, Deborah C. Mash, Irene Litvan, Mark F. Gordon, Zbigniew K. Wszolek, Matthew J. Farrer, Dennis W. Dickson

Journal:

Annals of Neurology

Year:

2006

Language:

english

File:

PDF, 217 KB

english, 2006

2

Pathogenicity of the Lrrk2 R1514Q substitution in Parkinson's disease

Mathias Toft, Ignacio F. Mata, Owen A. Ross, Jennifer Kachergus, Mary M. Hulihan, Kristoffer Haugarvoll, Jeremy T. Stone, Marta Blazquez, J. Mark Gibson, Jan O. Aasly, Linda R. White, Timothy Lynch, C

Journal:

Movement Disorders

Year:

2007

Language:

english

File:

PDF, 92 KB

english, 2007

3

ELAVL4, PARK10, and the Celts

Kristoffer Haugarvoll, Mathias Toft, Owen A. Ross, Jeremy T. Stone, Michael G. Heckman, Linda R. White, Timothy Lynch, John Mark Gibson, Zbigniew K. Wszolek, Ryan J. Uitti, Jan O. Aasly, Matthew J. Fa

Journal:

Movement Disorders

Year:

2007

Language:

english

File:

PDF, 64 KB

english, 2007

4

Lrrk2 G2019S substitution in frontotemporal lobar degeneration with ubiquitin-immunoreactive neuronal inclusions

Justus C. Dächsel, Owen A. Ross, Ignacio F. Mata, Jennifer Kachergus, Mathias Toft, Ashley Cannon, Matt Baker, Jennifer Adamson, Mike Hutton, Dennis W. Dickson, Matthew J. Farrer

Journal:

Acta Neuropathologica

Year:

2007

Language:

english

File:

PDF, 372 KB

english, 2007

5

Fine-mapping and candidate gene investigation within the PARK10 locus

Haugarvoll, Kristoffer, Toft, Mathias, Skipper, Lisa, Heckman, Michael G, Crook, Julia E, Soto, Alexandra, Ross, Owen A, Hulihan, Mary M, Kachergus, Jennifer M, Sando, Sigrid B

Journal:

European Journal of Human Genetics

Year:

2008

Language:

english

File:

PDF, 142 KB

english, 2008

6

LRRK2 mutations are not common in Alzheimer's disease

Mathias Toft, Sigrid Botne Sando, Stacey Melquist, Owen A. Ross, Linda R. White, Jan O. Aasly, Matthew J. Farrer

Journal:

Mechanisms of Ageing and Development

Year:

2005

Language:

english

File:

PDF, 120 KB

english, 2005

7

Variants in the LRRK1 gene and susceptibility to Parkinson's disease in Norway

Kristoffer Haugarvoll, Mathias Toft, Owen A. Ross, Linda R. White, Jan O. Aasly, Matthew J. Farrer

Journal:

Neuroscience Letters

Year:

2007

Language:

english

File:

PDF, 102 KB

english, 2007

8

Clinical traits of LRRK2-associated Parkinson's disease in Ireland: A link between familial and idiopathic PD

David Gosal, Owen A. Ross, Joe Wiley, G. Brent Irvine, Janet A. Johnston, Mathias Toft, Ignacio F. Mata, Jennifer Kachergus, Mary Hulihan, Julie P. Taylor, Sarah J. Lincoln, Matthew J. Farrer, Timothy

Journal:

Parkinsonism & Related Disorders

Year:

2005

Language:

english

File:

PDF, 133 KB

english, 2005

9

LRRK2 mutations and Parkinsonism

Mathias Toft, Ignacio F Mata, Jennifer M Kachergus, Owen A Ross, Matthew J Farrer

Journal:

Year:

2005

Language:

english

File:

PDF, 79 KB

english, 2005

10

Linkage Disequilibrium and Association of MAPT H1 in Parkinson Disease

Lisa Skipper, Kristen Wilkes, Mathias Toft, Matthew Baker, Sarah Lincoln, Mary Hulihan, Owen A. Ross, Mike Hutton, Jan Aasly, Matthew Farrer

Journal:

The American Journal of Human Genetics

Year:

2004

Language:

english

File:

PDF, 817 KB

english, 2004

11

Copy number variation in Parkinson's disease

Mathias Toft,Owen A Ross

Journal:

Genome Medicine

Year:

2010

Language:

english

File:

PDF, 909 KB

english, 2010

12

Exome Variant Mining in Familial Parkinson Disease

Toft, Mathias, Ross, Owen A.

Journal:

Year:

2016

Language:

english

File:

PDF, 117 KB

english, 2016

13

Clinical Heterogeneity of the LRRK2 G2019S Mutation

Papapetropoulos, Spiridon, Singer, Carlos, Ross, Owen A., Toft, Mathias, Johnson, Joseph L., Farrer, Matthew J., Mash, Deborah C.

Journal:

Archives of Neurology

Year:

2006

Language:

english

File:

PDF, 164 KB

english, 2006

14

Evaluation of the Role of SNCA Variants in Survival without Neurological Disease

Heckman, Michael G., Soto-Ortolaza, Alexandra I., Diehl, Nancy N., Carrasquillo, Minerva M., Uitti, Ryan J., Wszolek, Zbigniew K., Graff-Radford, Neill R., Ross, Owen A., Toft, Mathias

Journal:

Year:

2012

Language:

english

File:

PDF, 344 KB

english, 2012

15

Genetic modifier of LRRK2-parkinsonism is not transferable to idiopathic disease No evidence for DNM3 as genetic modifier of age at onset in idiopathic Parkinson's disease

Berge-Seidl, Victoria, Pihlstrøm, Lasse, Wszolek, Zbigniew K., Ross, Owen A., Toft, Mathias

Journal:

Neurobiology of Aging

Year:

2018

Language:

english

File:

PDF, 317 KB

english, 2018