|
🐜
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Mutations in progranulin cause tau-negative frontotemporal dementia linked to chromosome 17
27 auth.
M. Baker,
I. Mackenzie,
S. Pickering-Brown,
J. Gass,
R. Rademakers,
C. Lindholm,
J. Snowden,
J. Adamson,
A. Sadovnick,
S. Rollinson,
A. Cannon,
E. Dwosh,
D. Neary,
S. Melquist,
A. Richardson,
...
Dennis W. Dickson,
Z. Berger,
J. Eriksen,
Todd Robinson,
C. Zehr,
C. Dickey,
R. Crook,
E. McGowan,
D. Mann,
B. Boeve,
H. Feldman,
M. Hutton
|
10 |
2006 |
10
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|
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Clinical, genetic, and neuropathologic characteristics of posterior cortical atrophy
9 auth.
D. Tang-Wai,
N. Graff-Radford,
B. Boeve,
D. Dickson,
J. Parisi,
R. Crook,
...
R. Caselli,
D. Knopman,
R. Petersen
|
9 |
2004 |
9
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|
🐜
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Mutations in progranulin are a major cause of ubiquitin-positive frontotemporal lobar degeneration.
30 auth.
J. Gass,
A. Cannon,
I. Mackenzie,
B. Boeve,
M. Baker,
J. Adamson,
R. Crook,
S. Melquist,
K. Kuntz,
Ron C. Petersen,
K. Josephs,
S. Pickering-Brown,
N. Graff-Radford,
R. Uitti,
D. Dickson,
...
Z. Wszolek,
John Gonzalez,
T. Beach,
E. Bigio,
N. Johnson,
S. Weintraub,
M. Mesulam,
C. White,
B. Woodruff,
R. Caselli,
G. Hsiung,
H. Feldman,
D. Knopman,
M. Hutton,
R. Rademakers
|
9 |
2006 |
9
🐜
|
|
🐜
|
The structure of the presenilin 1 (S182) gene and identification of six novel mutations in early onset AD families
64 auth.
Robert F. Clark,
Michael L Hutton,
M. Fuldner,
S. Froelich,
Eric Karran,
C. Talbot,
R. Crook,
C. Lendon,
G. Prihar,
C. He,
Kevin M. Korenblat,
Alonso Martínez,
Alonso Martínez,
M. Wragg,
F. Busfield,
...
M. Behrens,
Amanda J. Myers,
J. Norton,
John C. Morris,
N. Mehta,
Chad G. Pearson,
Sarah Lincoln,
M. Baker,
K. Duff,
C. Zehr,
Jordi Pérez-Tur,
H. Houlden,
A. Ruiz,
J. Ossa,
Francisco Lopera,
M. Arcos,
L. Madrigal,
John Collinge,
C. Humphreys,
Alan Ashworth,
S. Sarner,
Nick C. Fox,
Richard J. Harvey,
A. Kennedy,
P. Roques,
R. Cline,
C. A. Philips,
J. Venter,
L. Forsell,
K. Axelman,
L. Lilius,
Janet A. Johnston,
R. Cowburn,
Matti Viitanen,
Bengt Winblad,
Kenneth S. Kosik,
Matti Haltia,
Minna Pöyhönen,
D. W. Dickson,
D. Mann,
D. Neary,
J. Snowden,
Peter L. Lantos,
L. Lannfelt,
Martin N. Rossor,
G. Roberts,
Mark Raymond Adams,
J. Hardy,
Alison Goate
|
8 |
1995 |
8
🐜
|
|
🐜
|
Novel Mutations in TARDBP (TDP-43) in Patients with Familial Amyotrophic Lateral Sclerosis
31 auth.
Nicola J. Rutherford,
Yong-Jie Zhang,
M. Baker,
J. Gass,
N. Finch,
Ya-fei Xu,
H. Stewart,
B. Kelley,
K. Kuntz,
R. Crook,
J. Sreedharan,
C. Vance,
E. Sorenson,
C. Lippa,
E. Bigio,
...
D. Geschwind,
D. Knopman,
H. Mitsumoto,
R. Petersen,
N. Cashman,
M. Hutton,
C. Shaw,
K. Boylan,
B. Boeve,
N. Graff-Radford,
Z. Wszolek,
R. Caselli,
D. Dickson,
I. Mackenzie,
L. Petrucelli,
R. Rademakers
|
8 |
2008 |
8
🐜
|
|
🐜
|
Susceptibility locus for Alzheimer's disease on chromosome 10.
25 auth.
A. Myers,
P. Holmans,
Helen Marshall,
Jennifer Kwon,
D. Meyer,
Dzanan Ramic,
S. Shears,
J. Booth,
Fabienne Wavrant DeVriéze,
R. Crook,
M. Hamshere,
R. Abraham,
N. Tunstall,
Francis Rice,
S. Carty,
...
Sara Lillystone,
P. Kehoe,
V. Rudrasingham,
L. Jones,
S. Lovestone,
J. Pérez-Tur,
Julie Williams,
M. Owen,
John Hardy,
A. Goate
|
8 |
2000 |
8
🐜
|
|
🐜
|
A full genome scan for late onset Alzheimer's disease
23 auth.
P. Kehoe,
F. W. Vrièze,
R. Crook,
William S. Wu,
P. Holmans,
I. Fenton,
G. Spurlock,
N. Norton,
H. Williams,
N. Williams,
...
S. Lovestone,
J. Pérez-Tur,
M. Hutton,
M. Chartier-Harlin,
S. Shears,
K. Roehl,
J. Booth,
Wendy Van Voorst,
Dzanan Ramic,
Julie Williams,
A. Goate,
J. Hardy,
M. Owen
|
8 |
1999 |
8
🐜
|
|
🐜
|
Plasma progranulin levels predict progranulin mutation status in frontotemporal dementia patients and asymptomatic family members
16 auth.
N. Finch,
M. Baker,
R. Crook,
K. Swanson,
K. Kuntz,
R. Surtees,
G. Bisceglio,
A. Rovelet-Lecrux,
B. Boeve,
R. Petersen,
...
D. Dickson,
S. Younkin,
V. Deramecourt,
J. Crook,
N. Graff-Radford,
R. Rademakers
|
8 |
2009 |
8
🐜
|
|
🦁
|
A variant of Alzheimer's disease with spastic paraparesis and unusual plaques due to deletion of exon 9 of presenilin 1
18 auth.
R. Crook,
A. Verkkoniemi,
J. Pérez-Tur,
N. Mehta,
M. Baker,
H. Houlden,
M. Farrer,
M. Hutton,
S. Lincoln,
J. Hardy,
...
K. Gwinn,
M. Somer,
A. Paetau,
H. Kalimo,
R. Ylikoski,
M. Pöyhönen,
Steve Kucera,
M. Haltia
|
8 |
1998 |
8
🦁
|
|
🐜
|
Common variation in the miR-659 binding-site of GRN is a major risk factor for TDP43-positive frontotemporal dementia
22 auth.
R. Rademakers,
J. Eriksen,
M. Baker,
Todd Robinson,
Z. Ahmed,
S. Lincoln,
N. Finch,
Nicola J. Rutherford,
R. Crook,
K. Josephs,
...
B. Boeve,
D. Knopman,
R. Petersen,
J. Parisi,
R. Caselli,
Z. Wszolek,
R. Uitti,
H. Feldman,
M. Hutton,
I. Mackenzie,
N. Graff-Radford,
D. Dickson
|
8 |
2008 |
8
🐜
|
|
🐜
|
A mutation in Alzheimer's disease destroying a splice acceptor site in the presenilin-1 gene
26 auth.
J. Pérez-Tur,
S. Froelich,
G. Prihar,
R. Crook,
M. Baker,
K. Duff,
M. Wragg,
F. Busfield,
C. Lendon,
R. Clark,
P. Roques,
R. Fuldner,
J. Johnston,
R. Cowburn,
C. Forsell,
...
K. Axelman,
L. Lilius,
H. Houlden,
E. Karran,
G. Roberts,
M. Rossor,
M. Adams,
J. Hardy,
A. Goate,
L. Lannfelt,
M. Hutton
|
8 |
1995 |
8
🐜
|
|
🐜
|
A locus for familial early–onset Alzhelmer's disease on the long arm of chromosome 14, proximal to the α1–antichymotrypsin gene
11 auth.
M. Mullan,
H. Houlden,
M. Windelspecht,
L. Fidani,
Chris Lombardi,
P. Diaz,
...
M. Rossor,
R. Crook,
J. Hardy,
K. Duff,
F. Crawford
|
8 |
1992 |
8
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|
