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1

Sporadic SCA8 mutation resembling corticobasal degeneration

Yasuhiko Baba, Ryan J. Uitti, Matthew J. Farrer, Zbigniew K. Wszolek

Journal:

Parkinsonism & Related Disorders

Year:

2005

Language:

english

File:

PDF, 76 KB

english, 2005

2

A Novel DCTN1 mutation with late-onset parkinsonism and frontotemporal atrophy

Araki, Eiichi, Tsuboi, Yoshio, Daechsel, Justus, Milnerwood, Austen, Vilarino-Guell, Carles, Fujii, Naoki, Mishima, Takayasu, Oka, Takayuki, Hara, Hideo, Fukae, Jiro, Farrer, Matthew J.

Journal:

Movement Disorders

Year:

2014

Language:

english

File:

PDF, 293 KB

english, 2014

3

Parkinson's disease, genetic variability and the Faroe Islands

Petersen, Maria Skaalum, Guella, Ilaria, Bech, Sara, Gustavsson, Emil, Farrer, Matthew J.

Journal:

Parkinsonism & Related Disorders

Year:

2015

Language:

english

File:

PDF, 206 KB

english, 2015

4

Multi-instrument characterization of five nanodiamond samples: a thorough example of nanomaterial characterization

Singh, Bhupinder, Smith, Stacey J., Jensen, David S., Jones, Hodge F., Dadson, Andrew E., Farnsworth, Paul B., Vanfleet, Richard, Farrer, Jeffrey K., Linford, Matthew R.

Journal:

Analytical and Bioanalytical Chemistry

Year:

2016

Language:

english

File:

PDF, 2.96 MB

english, 2016

5

Whole Exome Sequencing of an Exceptional Longevity Cohort

Nygaard, Haakon B, Erson-Omay, E Zeynep, Wu, Xiujuan, Kent, Brianne A, Bernales, Cecily Q, Evans, Daniel M, Farrer, Matthew J, Vilariño-Güell, Carles, Strittmatter, Stephen M

Journal:

The Journals of Gerontology Series A Biological Sciences and Medical Sciences

Year:

2018

Language:

english

File:

PDF, 484 KB

english, 2018

6

Neuron-autonomous susceptibility to induced synuclein aggregation is exacerbated by endogenous Lrrk2 mutations and ameliorated by Lrrk2 genetic knock-out

MacIsaac, Sarah, Quevedo Melo, Thaiany, Zhang, Yuting, Volta, Mattia, Farrer, Matthew J, Milnerwood, Austen J

Journal:

Brain Communications

Year:

2020

File:

PDF, 1.08 MB

2020

7

Case-control study of debrisoquine 4-hydroxylase, n-acetyltransferase 2, and apolipoprotein e gene polymorphisms in Parkinson's disease

Demetrius M. Maraganore, Matthew J. Farrer, John A. Hardy, Shannon K. McDonnell, Daniel J. Schaid, Walter A. Rocca

Journal:

Movement Disorders

Year:

2000

Language:

english

File:

PDF, 54 KB

english, 2000

8

Apolipoprotein E4 is probably responsible for the chromosome 19 linkage peak for Parkinson's disease

Maria Martinez, Alexis Brice, Jenny R. Vaughan, Alexander Zimprich, Monique M.B. Breteler, Giuseppe Meco, Alessandro Filla, Matthew J. Farrer, Christine Bétard, Andrew Singleton, John Hardy, Giuseppe

Journal:

American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Year:

2005

Language:

english

File:

PDF, 51 KB

english, 2005

9

Case-control study of the extended tau gene haplotype in Parkinson's disease

Demetrius M. Maraganore, Dena G. Hernandez, Andrew B. Singleton, Matthew J. Farrer, Shannon K. McDonnell, Michael L. Hutton, John A. Hardy, Walter A. Rocca

Journal:

Annals of Neurology

Year:

2001

Language:

english

File:

PDF, 12.19 MB

english, 2001

10

Interaction of α-synuclein and tau genotypes in Parkinson's disease

Catherine E. Mamah, Timothy G. Lesnick, Sarah J. Lincoln, Kari J. Strain, Mariza de Andrade, James H. Bower, J. Eric Ahlskog, Walter A. Rocca, Matthew J. Farrer, Demetrius M. Maraganore

Journal:

Annals of Neurology

Year:

2005

Language:

english

File:

PDF, 87 KB

english, 2005

11

Clinical features of LRRK2-associated Parkinson's disease in central Norway

Jan O. Aasly, Mathias Toft, Ignacio Fernandez-Mata, Jennifer Kachergus, Mary Hulihan, Linda R. White, Matthew Farrer

Journal:

Annals of Neurology

Year:

2005

Language:

english

File:

PDF, 73 KB

english, 2005

12

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

13

Clinical heterogeneity of α-synuclein gene duplication in Parkinson's disease

Kenya Nishioka, Shin Hayashi, Matthew J. Farrer, Andrew B. Singleton, Hiroyo Yoshino, Hisamasa Imai, Toshiaki Kitami, Kenichi Sato, Ryu Kuroda, Hiroyuki Tomiyama, Koichi Mizoguchi, Miho Murata, Tatsus

Journal:

Annals of Neurology

Year:

2006

Language:

english

File:

PDF, 2.23 MB

english, 2006

14

Tau kinases and Parkinson's disease: Guilt by association?

Dennis W. Dickson, Matthew J. Farrer

Journal:

Annals of Neurology

Year:

2005

Language:

english

File:

PDF, 46 KB

english, 2005

15

Biochemical and pathological characterization of Lrrk2

Benoit I. Giasson, Jason P. Covy, Nancy M. Bonini, Howard I. Hurtig, Matthew J. Farrer, John Q. Trojanowski, Vivianna M. Van Deerlin

Journal:

Annals of Neurology

Year:

2006

Language:

english

File:

PDF, 1011 KB

english, 2006

16

Reply to: SNCA variants are associated with increased risk of multiple system atrophy

Owen A. Ross, Carles Vilariño-Güell, Zbigniew K. Wszolek, Matthew J. Farrer, Dennis W. Dickson

Journal:

Annals of Neurology

Year:

2010

Language:

english

File:

PDF, 78 KB

english, 2010

17

Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21–22

Matt Baker, John B. J. Kwok, Steve Kucera, Richard Crook, Matthew Farrer, Henry Houlden, Adrian Isaacs, Sarah Lincoln, Luisa Onstead, John Hardy, Leonie Wittenberg, Peter Dodd, Sonja Webb, Nick Haywar

Journal:

Annals of Neurology

Year:

1997

Language:

english

File:

PDF, 511 KB

english, 1997

18

Molecular mapping of alzheimer-type dementia in Down's syndrome

Dr V. P. Prasher, Matthew J. Farrer, Anna M. Kessling, Elizabeth M. C. Fisher, R. J. West, P. C. Barber, A. C. Butler

Journal:

Annals of Neurology

Year:

1998

Language:

english

File:

PDF, 887 KB

english, 1998

19

MAPK-pathway activity, Lrrk2 G2019S, and Parkinson's disease

Linda R. White, Mathias Toft, Sylvia N. Kvam, Matthew J. Farrer, Jan O. Aasly

Journal:

Journal of Neuroscience Research

Year:

2007

Language:

english

File:

PDF, 238 KB

english, 2007

20

Case-Control study of dopamine transporter-1, monoamine oxidase-B, and catechol-O-methyl transferase polymorphisms in Parkinson's disease

John L. Goudreau, Demetrius M. Maraganore, Matthew J. Farrer, Timothy G. Lesnick, Andrew B. Singleton, James H. Bower, John A. Hardy, Walter A. Rocca

Journal:

Movement Disorders

Year:

2002

Language:

english

File:

PDF, 73 KB

english, 2002

21

Marked variation in clinical presentation and age of onset in a family with a heterozygous parkin mutation

Louis C. Tan, Caroline M. Tanner, Rong Chen, Piu Chan, Matthew Farrer, John Hardy, J. William Langston

Journal:

Movement Disorders

Year:

2003

Language:

english

File:

PDF, 66 KB

english, 2003

22

Complex interactions in Parkinson's disease: A two-phased approach

Demetrius M. Maraganore, Mariza de Andrade, Timothy G. Lesnick, Matthew J. Farrer, James H. Bower, John A. Hardy, Walter A. Rocca

Journal:

Movement Disorders

Year:

2003

Language:

english

File:

PDF, 78 KB

english, 2003

23

Case-control study of the α-synuclein interacting protein gene and Parkinson's disease

Demetrius M. Maraganore, Matthew J. Farrer, Timothy G. Lesnick, Mariza De Andrade, James H. Bower, Dena Hernandez, John A. Hardy, Walter A. Rocca

Journal:

Movement Disorders

Year:

2003

Language:

english

File:

PDF, 71 KB

english, 2003

24

Parkin variants in North American Parkinson's disease: Cases and controls

Sarah J. Lincoln, Demetrius M. Maraganore, Timothy G. Lesnick, Rebecca Bounds, Mariza de Andrade, James H. Bower, John A. Hardy, Matthew J. Farrer

Journal:

Movement Disorders

Year:

2003

Language:

english

File:

PDF, 69 KB

english, 2003

25

Parkinson's disease in Ireland: Clinical presentation and genetic heterogeneity in patients with parkin mutations

Joseph Wiley, Timothy Lynch, Sarah Lincoln, Lisa Skipper, Mary Hulihan, David Gosal, Gina Bisceglio, Jennifer Kachergus, John Hardy, Matthew J. Farrer

Journal:

Movement Disorders

Year:

2004

Language:

english

File:

PDF, 71 KB

english, 2004

26

Case-control study of estrogen receptor gene polymorphisms in Parkinson's disease

Demetrius M. Maraganore, Matthew J. Farrer, Shannon K. McDonnell, Alexis Elbaz, Daniel J. Schaid, John A. Hardy, Walter A. Rocca

Journal:

Movement Disorders

Year:

2002

Language:

english

File:

PDF, 30 KB

english, 2002

27

It's a double knock-out! The quaking mouse is a spontaneous deletion of parkin and parkin co-regulated gene (PACRG)

Paul J. Lockhart, Casey A. O'Farrell, Matthew J. Farrer

Journal:

Movement Disorders

Year:

2004

Language:

english

File:

PDF, 201 KB

english, 2004

28

Lack of mutations in DJ-1 in a cohort of Taiwanese ethnic Chinese with early-onset parkinsonism

Paul J. Lockhart, Rebecca Bounds, Mary Hulihan, Jennifer Kachergus, Sarah Lincoln, Chin-Hsien Lin, Ruey-Meei Wu, Matthew J. Farrer

Journal:

Movement Disorders

Year:

2004

Language:

english

File:

PDF, 94 KB

english, 2004

29

Parkinsonism, FXTAS, and FMR1 premutations

Mathias Toft, Jan Aasly, Gina Bisceglio, Charles H. Adler, Ryan J. Uitti, Anna Krygowska-Wajs, Timothy Lynch, Zbigniew K. Wszolek, Matthew J. Farrer

Journal:

Movement Disorders

Year:

2005

Language:

english

File:

PDF, 83 KB

english, 2005

30

Global distribution and reduced penetrance: Lrrk2 R1441C in an Irish Parkinson's disease kindred

David Gosal, Timothy Lynch, Owen A. Ross, Kristoffer Haugarvoll, Matthew J. Farrer, J. Mark Gibson

Journal:

Movement Disorders

Year:

2007

Language:

english

File:

PDF, 106 KB

english, 2007

31

The ups and downs of α-synuclein mRNA expression

Justus C. Dächsel, Sarah J. Lincoln, John Gonzalez, Owen A. Ross, Dennis W. Dickson, Matthew J. Farrer

Journal:

Movement Disorders

Year:

2007

Language:

english

File:

PDF, 83 KB

english, 2007

32

Common variants in Parkinson's disease

Owen A. Ross, Matthew J. Farrer, Ruey-Meei Wu

Journal:

Movement Disorders

Year:

2007

Language:

english

File:

PDF, 48 KB

english, 2007

33

Genotype–phenotype correlates in Taiwanese patients with early-onset recessive parkinsonism

Ming-Jen Lee, Ignacio F. Mata, Chin-Hsien Lin, Kai-Yuan Tzen, Sarah J. Lincoln, Rebecca Bounds, Paul J. Lockhart, Mary M. Hulihan, Matthew J. Farrer, Ruey-Meei Wu

Journal:

Movement Disorders

Year:

2009

Language:

english

File:

PDF, 438 KB

english, 2009

34

Reported mutations in GIGYF2 are not a common cause of Parkinson's disease

Carles Vilariño-Güell, Owen A. Ross, Alexandra I. Soto, Matthew J. Farrer, Kristoffer Haugarvoll, Jan O. Aasly, Ryan J. Uitti, Zbigniew K. Wszolek

Journal:

Movement Disorders

Year:

2009

Language:

english

File:

PDF, 310 KB

english, 2009

35

Reply: GIGYF2 variants are not associated with Parkinson's disease in Italy

Carles Vilariño-Güell, Owen A. Ross, Matthew J. Farrer

Journal:

Movement Disorders

Year:

2009

Language:

english

File:

PDF, 47 KB

english, 2009

36

Alpha-synuclein polymorphisms are associated with Parkinson's disease in a Saskatchewan population

Alex Rajput, Carles Vilariño-Güell, Michele L. Rajput, Owen A. Ross, Alexandra I. Soto-Ortolaza, Sarah J. Lincoln, Stephanie A. Cobb, Michael G. Heckman, Matthew J. Farrer, Ali Rajput

Journal:

Movement Disorders

Year:

2009

Language:

english

File:

PDF, 369 KB

english, 2009

37

LRRK2 variation and Parkinson's disease in African Americans

Owen A. Ross, Greggory J. Wilhoite, Justin A. Bacon, Alexandra Soto-Ortolaza, Jennifer Kachergus, Stephanie A. Cobb, Andreas Puschmann, Carles Vilariño-Güell, Matthew J. Farrer, Neill Graff-Radford, J

Journal:

Movement Disorders

Year:

2010

Language:

english

File:

PDF, 639 KB

english, 2010

38

Dopamine turnover increases in asymptomatic LRRK2 mutations carriers

Vesna Sossi, Raul de la Fuente-Fernández, Ramachandiran Nandhagopal, Michael Schulzer, Jessamyn McKenzie, Thomas J. Ruth, Jan O. Aasly, Matthew J. Farrer, Zbigniew K. Wszolek, Jon A. Stoessl

Journal:

Movement Disorders

Year:

2010

Language:

english

File:

PDF, 271 KB

english, 2010

39

Common variants in PARK loci and related genes and Parkinson's disease

Sun Ju Chung, Sebastian M. Armasu, Joanna M. Biernacka, Timothy G. Lesnick, David N. Rider, Sarah J. Lincoln, Alexandra I. Ortolaza, Matthew J. Farrer, Julie M. Cunningham, Walter A. Rocca, Demetrius

Journal:

Movement Disorders

Year:

2011

Language:

english

File:

PDF, 327 KB

english, 2011

40

Genetic variants of α-synuclein are not associated with essential tremor

Owen A. Ross, Karen N. Conneely, Tao Wang, Carles Vilarino-Guell, Alexandra I. Soto-Ortolaza, Alex Rajput, Zbigniew K. Wszolek, Ryan J. Uitti, Elan D. Louis, Lorraine N. Clark, Matthew J. Farrer, Clau

Journal:

Movement Disorders

Year:

2011

Language:

english

File:

PDF, 264 KB

english, 2011

41

Effects of Brefeldin A on Galactosphingolipid Synthesis in an Immortalized Schwann Cell Line: Evidence for Different Intracellular Locations of Galactosylceramide Sulfotransferase and Ceramide Galactosyltransferase Activities

Robert G. Farrer, Matthew P. Warden, Richard H. Quarles

Journal:

Journal of Neurochemistry

Year:

1995

Language:

english

File:

PDF, 1012 KB

english, 1995

42

Sensitization of Neuronal Cells to Oxidative Stress with Mutated Human α-Synuclein

Li-wen Ko, Nitin D. Mehta, Matthew Farrer, Colin Easson, Jennifer Hussey, Samuel Yen, John Hardy, Shu-Hui C. Yen

Journal:

Journal of Neurochemistry

Year:

2000

Language:

english

File:

PDF, 225 KB

english, 2000

43

Co-ordinate transcriptional regulation of dopamine synthesis genes by α-synuclein in human neuroblastoma cell lines

Melisa J. Baptista, Casey O'Farrell, Sneha Daya, Rili Ahmad, David W. Miller, John Hardy, Matthew J. Farrer, Mark R. Cookson

Journal:

Journal of Neurochemistry

Year:

2003

Language:

english

File:

PDF, 224 KB

english, 2003

44

Nonsteroidal anti-inflammatory drug use and Alzheimer's disease risk: the MIRAGE Study

Agustín G Yip, Robert C Green, Matthew Huyck, L Adrienne Cupples, Lindsay A Farrer, for the MIRAGE Study Group

Journal:

Year:

2005

Language:

english

File:

PDF, 810 KB

english, 2005

45

Genetic association study ofsynphilin-1in idiopathic Parkinson's disease

Ronny Myhre, Helge Klungland, Matthew J Farrer, Jan O Aasly

Journal:

BMC Medical Genetics

Year:

2008

Language:

english

File:

PDF, 981 KB

english, 2008

46

Genetic association studies in Alzheimer's disease research: challenges and opportunities

Steven D. Edland, Susan Slager, Matthew Farrer

Journal:

Statistics in Medicine

Year:

2004

Language:

english

File:

PDF, 73 KB

english, 2004

47

Parkinson’s disease: a rethink of rodent models

Heather L. Melrose, Sarah J. Lincoln, Glenn M. Tyndall, Matthew J. Farrer

Journal:

Experimental Brain Research

Year:

2006

Language:

english

File:

PDF, 353 KB

english, 2006

48

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

49

Heterotrisomy, a significant contributing factor to ventricular septal defect associated with Down syndrome?

Melisa Baptista, Una Fairbrother, Catherine Howard, Matthew Farrer, Gail Davies, Dimitra Trikka, Klio Maratou, Andrew Redington, Gottfried Greve, Pål Njølstad, Anna Kessling

Journal:

Year:

2000

Language:

english

File:

PDF, 121 KB

english, 2000

50

Call for participation in the neurogenetics consortium within the Human Variome Project

Andrea Haworth, Lars Bertram, Paola Carrera, Joanna L. Elson, Corey D. Braastad, Diane W. Cox, Marc Cruts, Johann T. den Dunnen, Matthew J. Farrer, John K. Fink, Sherifa A. Hamed, Henry Houlden, Denni

Journal:

Year:

2011

Language:

english

File:

PDF, 529 KB

english, 2011