Farrer, Matt: search on Z-Library

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1

Doubts about TMEM230 as a gene for parkinsonism

Farrer, Matt J.

Journal:

Nature Genetics

Year:

2019

Language:

english

File:

PDF, 818 KB

english, 2019

2

Lewy bodies and parkinsonism in families with parkin mutations

Matt Farrer, Piu Chan, Rong Chen, Louis Tan, Sarah Lincoln, Dena Hernandez, Lysia Forno, Katrina Gwinn-Hardy, Leonard Petrucelli, Jennifer Hussey, Andrew Singleton, Caroline Tanner, John Hardy, J. Wil

Journal:

Annals of Neurology

Year:

2001

Language:

english

File:

PDF, 5.08 MB

english, 2001

3

Parkinson’s Genetics: Molecular Insights for the New Millennium

Lisa Skipper, Matt Farrer

Journal:

NeuroToxicology

Year:

2002

Language:

english

File:

PDF, 261 KB

english, 2002

4

Parkin Mutations and Early-Onset Parkinsonism in a Taiwanese Cohort

Wu, Ruey-Meei, Bounds, Rebecca, Lincoln, Sarah, Hulihan, Mary, Lin, Chin-Hsien, Hwu, Wuh-Liang, Chen, Judy, Gwinn-Hardy, Katrina, Farrer, Matt

Journal:

Archives of Neurology

Year:

2005

Language:

english

File:

PDF, 118 KB

english, 2005

5

Ethnic differences in the expression of neurodegenerative disease: Machado-Joseph disease in Africans and Caucasians

S.H. Subramony, Dena Hernandez, Amanda Adam, Stephanie Smith-Jefferson, Jennifer Hussey, Katrina Gwinn-Hardy, Timothy Lynch, Olga McDaniel, John Hardy, Matt Farrer, Andrew Singleton

Journal:

Movement Disorders

Year:

2002

Language:

english

File:

PDF, 65 KB

english, 2002

6

A family with a tau P301L mutation presenting with parkinsonism

Ruth H Walker, Joseph Friedman, Jill Wiener, Ronald Hobler, Katrina Gwinn-Hardy, Amanda Adam, Jennifer DeWolfe, Rebecca Gibbs, Matt Baker, Matt Farrer, Mike Hutton, John Hardy

Journal:

Parkinsonism & Related Disorders

Year:

2002

Language:

english

File:

PDF, 62 KB

english, 2002

7

P1-106: LRRK2 as a common link between tauopathies and synucleinopathies

Sarah Miles, Heather Melrose, Joshua Knight, Sarah Lincoln, Matt Farrer, Jada Lewis

Journal:

Alzheimer's & Dementia

Year:

2008

Language:

english

File:

PDF, 68 KB

english, 2008

8

NEUROGENETICS: A GUIDE FOR CLINICIANS. 2012. Edited byWood Nicholas W.. Published by Cambridge University Press. 241 pages. C$70.00 approx.

Journal:

Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques

Year:

2013

Language:

english

File:

PDF, 58 KB

english, 2013

9

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

10

Origin of the Mutations in the parkin Gene in Europe: Exon Rearrangements Are Independent Recurrent Events, whereas Point Mutations May Result from Founder Effects

Magali Periquet, Christoph B. Lücking, Jenny R. Vaughan, Vincenzo Bonifati, Alexandra Dürr, Giuseppe De Michele, Martin W. Horstink, Matt Farrer, Sergei N. Illarioshkin, Pierre Pollak, Michel Borg, Ch

Journal:

The American Journal of Human Genetics

Year:

2001

Language:

english

File:

PDF, 249 KB

english, 2001

11

Tau neurotoxicity without the lesions: a fly challenges a tangled web

Rohan de Silva, Matt Farrer

Journal:

Trends in Neurosciences

Year:

2002

Language:

english

File:

PDF, 29 KB

english, 2002

12

LRRK2: a common pathway for parkinsonism, pathogenesis and prevention?

Julie P. Taylor, Ignacio F. Mata, Matt J. Farrer

Journal:

Trends in Molecular Medicine

Year:

2006

Language:

english

File:

PDF, 206 KB

english, 2006

13

P4-158 Tau H1 haplotype disease association and splice mutations: investigations into mutational mechanisms

Pickering-Brown, Stuart M., Crook, Richard, Skipper, Lisa, Mann, David, Farrer, Matt, Hutton, Michael

Journal:

Neurobiology of Aging

Year:

2004

Language:

english

File:

PDF, 158 KB

english, 2004

14

Accurate Determination of Ataxin-2 Polyglutamine Expansion in Patients with Intermediate-Range Repeats

Hussey, Jennifer, Lockhart, Paul J., Seltzer, William, Wszolek, Zbigniew K., Payami, Haydeh, Hanson, Melissa, Gwinn-Hardy, Katrina, Farrer, Matt

Journal:

Genetic Testing

Year:

2002

Language:

english

File:

PDF, 114 KB

english, 2002

15

Advances in the genetics of Parkinson disease

Trinh, Joanne, Farrer, Matt

Journal:

Nature Reviews Neurology (formerly Nature Clinical Practice Neurology)

Year:

2013

Language:

english

File:

PDF, 521 KB

english, 2013

16

Mutations in LRRK2 increase phosphorylation of peroxiredoxin 3 exacerbating oxidative stress-induced neuronal death

Dario C. Angeles, Bong-Hwa Gan, Luisa Onstead, Yi Zhao, Kah-Leong Lim, Justus Dachsel, Heather Melrose, Matt Farrer, Zbigniew K. Wszolek, Dennis W. Dickson, Eng-King Tan

Journal:

Year:

2011

Language:

english

File:

PDF, 422 KB

english, 2011

17

Exclusion of genetic linkage to 4q21-23 and 17q21 in a family with lewy body parkinsonism

Hardy, John, P�rez-Tur, Jordi, Baker, Matt, Farrer, Matt, Crook, Richard, Hutton, Mike, Johnson, William G., Gwinn, Katrina, Muenter, Manfred, Rocca, Walter A., Maraganore, Demetrius

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 122 KB

english, 1998

18

Linkage exclusion in French families with probable Parkinson's disease

Matt Farrer, Alain Destée, Estelle Becquet, Fabienne Wavrant-De Vrièze, Vincent Mouroux, Florence Richard, Luc Defebvre, Sarah Lincoln, John Hardy, Philippe Amouyel, Marie-Christine Chartier-Harlin

Journal:

Movement Disorders

Year:

2000

Language:

english

File:

PDF, 143 KB

english, 2000

19

The Tau H1 Haplotype is associated with Parkinson's disease in the Norwegian population

Matt Farrer, Lisa Skipper, Marianne Berg, Gina Bisceglio, Melissa Hanson, John Hardy, Amanda Adam, Katrina Gwinn-Hardy, Jan Aasly

Journal:

Neuroscience Letters

Year:

2002

Language:

english

File:

PDF, 76 KB

english, 2002

20

α-Synuclein Gene May Interact with Environmental Factors in Increasing Risk of Parkinson’s Disease

Gatto, Nicole M., Rhodes, Shannon L., Manthripragada, Angelika D., Bronstein, Jeff, Cockburn, Myles, Farrer, Matt, Ritz, Beate

Journal:

Neuroepidemiology

Year:

2010

Language:

english

File:

PDF, 108 KB

english, 2010

21

Low frequency of α-synuclein mutations in familial Parkinson's disease

Matt Farrer, Fabienne Wavrant-De Vrieze, Richard Crook, Lizzie Boles, Jordi Perez-Tur, John Hardy, William G. Johnson, John Steele, Demetrius Maraganore, Dr Katrina Gwinn, Tim Lynch

Journal:

Annals of Neurology

Year:

1998

Language:

english

File:

PDF, 404 KB

english, 1998

22

Parkinson's genetics: An embarrassment of riches

Katrina Gwinn-Hardy, Matt Farrer

Journal:

Annals of Neurology

Year:

2002

Language:

english

File:

PDF, 107 KB

english, 2002

23

Comparison of kindreds with parkinsonism and α-synuclein genomic multiplications

Matt Farrer, Jennifer Kachergus, Lysia Forno, Sarah Lincoln, Deng-Shun Wang, Mary Hulihan, Demetrius Maraganore, Katrina Gwinn-Hardy, Zbigniew Wszolek, Dennis Dickson, J. William Langston

Journal:

Annals of Neurology

Year:

2004

Language:

english

File:

PDF, 211 KB

english, 2004

24

Dopamine receptors and BDNF -haplotypes predict dyskinesia in Parkinson's disease

Kusters, Cynthia D.J., Paul, Kimberly C., Guella, Ilaria, Bronstein, Jeff M., Sinsheimer, Janet S., Farrer, Matt J., Ritz, Beate R.

Journal:

Parkinsonism & Related Disorders

Year:

2017

Language:

english

File:

PDF, 262 KB

english, 2017

25

A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1

Crook, Richard, Verkkoniemi, Auli, Perez-Tur, Jordi, Mehta, Nitin, Baker, Matt, Houlden, Henry, Farrer, Matt, Hutton, Mike, Lincoln, Sarah, Hardy, John

Journal:

Nature Medicine

Year:

1998

File:

PDF, 586 KB

1998

26

Identification and characterization of the human parkin gene promoter

Andrew West, Matt Farrer, Leonard Petrucelli, Mark Cookson, Paul Lockhart, John Hardy

Journal:

Journal of Neurochemistry

Year:

2001

Language:

english

File:

PDF, 528 KB

english, 2001

27

Transfected synphilin-1 forms cytoplasmic inclusions in HEK293 cells

Casey O’Farrell, Diane D Murphy, Leonard Petrucelli, Andrew B Singleton, Jennifer Hussey, Matt Farrer, John Hardy, Dennis W Dickson, Mark R Cookson

Journal:

Molecular Brain Research

Year:

2001

Language:

english

File:

PDF, 1.86 MB

english, 2001

28

Dopa-responsive dystonia presenting with prominent isolated bilateral resting leg tremor: Evidence for a role of parkin?

Ronald B. Postuma, Yoshiaki Furukawa, Ekaterina Rogaeva, Peter H. St. George-Hyslop, Matt J. Farrer, Anthony E. Lang

Journal:

Movement Disorders

Year:

2003

Language:

english

File:

PDF, 725 KB

english, 2003

29

Lack of Nigral Pathology in Transgenic Mice Expressing Human α-Synuclein Driven by the Tyrosine Hydroxylase Promoter

Yasuji Matsuoka, Miquel Vila, Sarah Lincoln, Alison McCormack, Melanie Picciano, John LaFrancois, Xin Yu, Dennis Dickson, William J. Langston, Eileen McGowan, Matt Farrer, John Hardy, Karen Duff, Serg

Journal:

Neurobiology of Disease

Year:

2001

Language:

english

File:

PDF, 120 KB

english, 2001

30

α-Synuclein promoter confers susceptibility to Parkinson's disease

Philippe Pals, Sarah Lincoln, Jonathan Manning, Michael Heckman, Lisa Skipper, Mary Hulihan, Marleen Van den Broeck, Tim De Pooter, Patrick Cras, Julia Crook, Christine Van Broeckhoven, Matt J. Farrer

Journal:

Annals of Neurology

Year:

2004

Language:

english

File:

PDF, 164 KB

english, 2004

31

Clinical, 18F-dopa PET, and genetic analysis of an ethnic Chinese kindred with early-onset parkinsonism and parkin gene mutations

Ruey-Meei Wu, Din-E Shan, Chen-Ming Sun, Ren-Shyan Liu, Wuh-Liang Hwu, Chun-Hwei Tai, Jennifer Hussey, Andrew West, Katrina Gwinn-Hardy, John Hardy, Judy Chen, Matt Farrer, Sarah Lincoln

Journal:

Movement Disorders

Year:

2002

Language:

english

File:

PDF, 276 KB

english, 2002

32

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

33

Low frequency of pathogenic mutations in the ubiquitin carboxyterminal hydrolase gene in familial Parkinsonʼs disease

Lincoln, Sarah, Vaughan, Jenny, Wood, Nick, Baker, Matt, Adamson, Jennifer, Gwinn-Hardy, Katrina, Lynch, Tim, Hardy, John, Farrer, Matt

Journal:

Year:

1999

Language:

english

File:

PDF, 129 KB

english, 1999

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