|
๐
|
Meta-analysis of genome scans and replication identify CD6, IRF8 and TNFRSF1A as new multiple sclerosis susceptibility loci
33 auth.
P. D. Jager,
Xiaoming Jia,
Joanne Wang,
P. D. Bakker,
L. Ottoboni,
N. Aggarwal,
L. Piccio,
S. Raychaudhuri,
Dong Tran,
C. Aubin,
R. Briskin,
S. Romano,
S. Baranzini,
J. McCauley,
M. Pericak-Vance,
...
J. Haines,
R. Gibson,
Yvonne Naeglin,
B. Uitdehaag,
P. Matthews,
L. Kappos,
C. Polman,
W. McArdle,
D. Strachan,
Denis A. Evans,
A. Cross,
M. Daly,
Alastair Compston,
S. Sawcer,
H. Weiner,
S. Hauser,
D. Hafler,
J. Oksenberg
|
9 |
2009 |
9
๐
|
|
๐
|
Candidate single-nucleotide polymorphisms from a genomewide association study of Alzheimer disease.
48 auth.
Hao Li,
S. Wetten,
Li Li,
P. S. St Jean,
R. Upmanyu,
L. Surh,
D. Hosford,
M. Barnes,
J. D. Briley,
M. Borrie,
Natalie Coletta,
Richard Delisle,
Daniella Dhalla,
M. Ehm,
H. Feldman,
...
L. Fornazzari,
S. Gauthier,
Neil Goodgame,
D. Guzman,
Sandra Hammond,
P. Hollingworth,
G. Hsiung,
Joan Johnson,
Devon Kelly,
R. Keren,
A. Kertesz,
K. King,
S. Lovestone,
Inge Loy-English,
P. Matthews,
M. Owen,
M. Plumpton,
W. Pryse-Phillips,
R. Prinjha,
J. Richardson,
A. Saunders,
A. J. Slater,
P. S. St George-Hyslop,
S. Stinnett,
J. Swartz,
R. Taylor,
J. Wherrett,
Julie Williams,
D. Yarnall,
R. Gibson,
M. Irizarry,
L. Middleton,
A. Roses
|
9 |
2008 |
9
๐
|
|
๐
|
Genome-wide association analysis of susceptibility and clinical phenotype in multiple sclerosis.
37 auth.
S. Baranzini,
Joanne Wang,
R. Gibson,
N. Galwey,
Y. Naegelin,
F. Barkhof,
E. Radue,
R. Lindberg,
B. Uitdehaag,
Michael R. Johnson,
A. Angelakopoulou,
L. Hall,
J. Richardson,
R. Prinjha,
A. Gass,
...
J. Geurts,
J. Kragt,
M. Sombekke,
H. Vrenken,
P. Qualley,
R. Lincoln,
R. Gomez,
S. Caillier,
Michaela F. George,
H. Mousavi,
R. Guerrero,
D. Okuda,
B. Cree,
A. Green,
E. Waubant,
D. Goodin,
D. Pelletier,
P. Matthews,
S. Hauser,
L. Kappos,
C. Polman,
J. Oksenberg
|
8 |
2009 |
8
๐
|
|
๐
|
Pathway and network-based analysis of genome-wide association studies in multiple sclerosis
15 auth.
S. Baranzini,
N. Galwey,
Joanne Wang,
Pouya Khankhanian,
R. Lindberg,
D. Pelletier,
Wen Wu,
B. Uitdehaag,
L. Kappos,
C. Polman,
...
P. Matthews,
S. Hauser,
R. Gibson,
J. Oksenberg,
M. Barnes
|
8 |
2009 |
8
๐
|
|
๐
|
Age at onset in two common neurodegenerative diseases is genetically controlled.
32 auth.
Yi-Ju Li,
W. Scott,
D. Hedges,
Fengyu Zhang,
P. Gaskell,
M. Nance,
R. Watts,
J. Hubble,
W. Koller,
R. Pahwa,
M. Stern,
B. Hiner,
J. Jankovic,
F. H. Allen,
C. Goetz,
...
F. Mastaglia,
J. Stajich,
R. Gibson,
L. Middleton,
A. Saunders,
B. Scott,
G. Small,
K. Nicodemus,
Allison D Reed,
D. Schmechel,
K. Welsh-Bohmer,
P. Conneally,
A. Roses,
J. Gilbert,
J. Vance,
J. Haines,
M. Pericak-Vance
|
8 |
2002 |
8
๐
|
|
๐
|
Translation initiator EIF4G1 mutations in familial Parkinson disease.
50 auth.
M. Chartier-Harlin,
J. Dachsel,
C. Vilariรฑo-Gรผell,
S. Lincoln,
F. Lepreฬtre,
M. Hulihan,
J. Kachergus,
A. Milnerwood,
L. Tapia,
M. Song,
ร. Le Rhun,
E. Mutez,
L. Larvor,
A. Duflot,
C. Vanbesien-Mailliot,
...
A. Kreisler,
O. Ross,
K. Nishioka,
A. Soto-Ortolaza,
S. A. Cobb,
H. Melrose,
B. Behrouz,
B. Keeling,
Justin A. Bacon,
E. Hentati,
L. Williams,
Akiko Yanagiya,
N. Sonenberg,
P. Lockhart,
A. Zubair,
R. Uitti,
J. Aasly,
A. Krygowska-Wajs,
G. Opala,
Z. Wszolek,
R. Frigerio,
D. Maraganore,
D. Gosal,
T. Lynch,
Michael K. Hutchinson,
A. Bentivoglio,
E. Valente,
W. Nichols,
N. Pankratz,
T. Foroud,
R. Gibson,
F. Hentati,
D. Dickson,
A. Destรฉe,
M. Farrer
|
8 |
2011 |
8
๐
|
|
๐
|
Positional cloning of the Fanconi anaemia group A gene
35 auth.
S. Apostolou,
S. Whitmore,
J. Crawford,
G. Lennon,
G. Sutherland,
D. Callen,
Leonarda lanzano,
M. Savino,
M. dโApolito,
Angelo Notarangeio,
E. Memeo,
M. R. Piemontese,
L. Zelante,
A. Savoia,
R. Gibson,
...
A. Tipping,
N. Morgan,
S. Hassock,
S. Jansen,
T. Ravel,
Carola Van Berkell,
J. Pronk,
D. Easton,
C. Mathew,
O. Levran,
P. Verlander,
S. Batish,
Tamar Erlich,
A. Auerbach,
A. Cleton-Jansen,
E. Moerland,
C. Cornelisse,
N. Doggett,
L. Deaven,
R. Moyzis
|
8 |
1996 |
8
๐
|
|
๐
|
Complete genomic screen in Parkinson disease: evidence for multiple genes.
31 auth.
W. Scott,
M. Nance,
R. Watts,
J. Hubble,
W. Koller,
Kelly E. Lyons,
R. Pahwa,
M. Stern,
A. Colcher,
B. Hiner,
J. Jankovic,
W. Ondo,
F. H. Allen,
C. Goetz,
G. Small,
...
Donna Masterman,
F. Mastaglia,
N. Laing,
J. Stajich,
B. Slotterbeck,
M. Booze,
R. Ribble,
E. Rampersaud,
S. West,
R. Gibson,
L. Middleton,
A. Roses,
J. Haines,
B. Scott,
J. Vance,
M. Pericak-Vance
|
8 |
2001 |
8
๐
|
|
๐
|
DNAJC13 mutations in Parkinson disease.
40 auth.
C. Vilariรฑo-Gรผell,
A. Rajput,
A. Milnerwood,
Brinda Shah,
C. SzuโTu,
J. Trinh,
Irene Yu,
M. Encarnacion,
Lise N. Munsie,
L. Tapia,
E. Gustavsson,
Patrick Chou,
Igor Tatarnikov,
Daniel M. Evans,
F. Pishotta,
...
Mattia Volta,
Dayne A Beccano-Kelly,
Christina Thompson,
Michelle K. Lin,
Holly E. Sherman,
Heather Han,
Bruce L. Guenther,
W. Wasserman,
V. Bernard,
C. Ross,
S. Appel-Cresswell,
A. Stoessl,
C. Robinson,
D. Dickson,
O. Ross,
Z. Wszolek,
J. Aasly,
R. Wu,
F. Hentati,
R. Gibson,
P. McPherson,
M. Girard,
M. Rajput,
A. Rajput,
M. Farrer
|
8 |
2014 |
8
๐
|
|
๐
|
Rare deletions at 16p13.11 predispose to a diverse spectrum of sporadic epilepsy syndromes.
51 auth.
E. Heinzen,
R. Radtke,
T. Urban,
G. Cavalleri,
C. Depondt,
A. Need,
N. Walley,
P. Nicoletti,
D. Ge,
C. Catarino,
J. Duncan,
Dalia Kasperaviฤiลซtฤ,
S. K. Tate,
L. Caboclo,
Josemir W Sander,
...
L. Clayton,
Kristen N. Linney,
K. Shianna,
C. Gumbs,
Jason P. Smith,
K. Cronin,
J. Maia,
C. Doherty,
M. Pandolfo,
D. Leppert,
L. Middleton,
R. Gibson,
Michael R. Johnson,
P. Matthews,
D. Hosford,
R. Kรคlviรคinen,
K. Eriksson,
Anne-Mari Kantanen,
T. Dorn,
J. Hansen,
G. Krรคmer,
B. Steinhoff,
H. Wieser,
D. Zumsteg,
Marcos Ortega,
N. Wood,
J. Huxley-Jones,
M. Mikati,
William B. Gallentine,
A. Husain,
P. Buckley,
R. Stallings,
M. Podgoreanu,
N. Delanty,
S. Sisodiya,
D. Goldstein
|
7 |
2010 |
7
๐
|
|
๐
|
Somatic Mosaicism in Fanconi Anemia: Molecular Basis and Clinical Significance
16 auth.
J. R. Foe,
M. Kwee,
M. Rooimans,
A. Oostra,
A. Veerman,
M. V. Weel,
R. Pauli,
N. Shahidi,
I. Dokal,
I. Roberts,
...
ร. Altay,
E. Gluckman,
R. Gibson,
C. Mathew,
F. Arwert,
H. Joenje
|
7 |
1997 |
7
๐
|
|
๐
|
Spontaneous functional correction of homozygous Fanconi anaemia alleles reveals novel mechanistic basis for reverse mosaicism
13 auth.
Q. Waisfisz,
N. Morgan,
M. Savino,
J. Winter,
C. V. Berkel,
M. Hoatlin,
L. Ianzano,
R. Gibson,
F. Arwert,
A. Savoia,
...
C. Mathew,
J. Pronk,
H. Joenje
|
7 |
1999 |
7
๐
|
