|
🐜
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Identification of multiple risk variants for ankylosing spondylitis through high-density genotyping of immune-related loci
65 auth.
A. Cortes,
J. Hadler,
J. Pointon,
P. Robinson,
T. Karaderi,
P. Leo,
K. Cremin,
Karena Pryce,
J. Harris,
Seunghun Lee,
K. Joo,
S. Shim,
M. Weisman,
Michael D. Ward,
Xiaodong Zhou,
...
H. Garchon,
G. Chiocchia,
J. Nossent,
B. Lie,
Ø. Førre,
J. Tuomilehto,
K. Laiho,
Lei Jiang,
Yu Liu,
Xin Wu,
L. Bradbury,
D. Elewaut,
R. Burgos-Vargas,
S. Stebbings,
L. Appleton,
C. Farrah,
Jonathan Lau,
T. Kenna,
N. Haroon,
M. Ferreira,
Jian Yang,
J. Mulero,
J. Fernández-Sueiro,
M. González-Gay,
C. López-Larrea,
P. Deloukas,
P. Donnelly,
P. Bowness,
K. Gafney,
H. Gaston,
D. Gladman,
P. Rahman,
W. Maksymowych,
Huji Xu,
J. Crusius,
I. E. van der Horst-Bruinsma,
C. Chou,
R. Valle-Oñate,
C. Romero-Sánchez,
I. M. Hansen,
F. Pimentel-Santos,
R. Inman,
V. Videm,
Javier Martín,
M. Breban,
J. Reveille,
David M. Evans,
Tae-Hwan Kim,
Bryan Paul Wordsworth,
M. Brown
|
9 |
2013 |
9
🐜
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|
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Genome-wide association meta-analyses combining multiple risk phenotypes provides insights into the genetic architecture of cutaneous melanoma susceptibility
152 auth.
M. Landi,
D. Bishop,
S. Macgregor,
M. Machiela,
A. Stratigos,
P. Ghiorzo,
M. Brossard,
D. Calista,
Jiyeon Choi,
M. Fargnoli,
Tongwu Zhang,
M. Rodolfo,
A. Trower,
C. Menin,
Jacobo Martinez,
...
A. Hadjisavvas,
L. Song,
I. Stefanaki,
R. Scolyer,
Rose Yang,
A. Goldstein,
M. Potrony,
K. Kypreou,
L. Pastorino,
P. Queirolo,
C. Pellegrini,
L. Cattaneo,
M. Zawistowski,
P. Giménez-Xavier,
Arantxa Rodriguez,
L. Elefanti,
S. Manoukian,
L. Rivoltini,
Blair H. Smith,
M. Loizidou,
L. Del Regno,
D. Massi,
M. Mandalà,
K. Khosrotehrani,
L. Akslen,
C. Amos,
P. A. Andresen,
M. Avril,
E. Azizi,
H. Soyer,
V. Bataille,
B. Dalmasso,
L. Bowdler,
K. Burdon,
W. Chen,
V. Codd,
J. Craig,
T. Dębniak,
M. Falchi,
S. Fang,
E. Friedman,
Sara Simi,
P. Galan,
Z. García-Casado,
E. Gillanders,
S. Gordon,
A. Green,
N. Gruis,
J. Hansson,
M. Harland,
J. Harris,
P. Helsing,
A. Henders,
M. Hočevar,
V. Höiom,
D. Hunter,
C. Ingvar,
Rajiv Kumar,
J. Lang,
G. Lathrop,
Jeffrey E. Lee,
Xin Li,
J. Lubiński,
R. MacKie,
M. Malt,
J. Malvehy,
K. McAloney,
H. Mohamdi,
A. Molven,
E. Moses,
R. Neale,
S. Novaković,
D. Nyholt,
H. Olsson,
N. Orr,
L. Fritsche,
J. Puig-Butillé,
A. Qureshi,
G. Radford-Smith,
J. Randerson-Moor,
C. Requena,
C. Rowe,
N. Samani,
Marianna Sanna,
D. Schadendorf,
H. Schulze,
L. Simms,
M. Smithers,
F. Song,
A. Swerdlow,
N. van der Stoep,
N. Kukutsch,
A. Visconti,
L. Wallace,
S. Ward,
L. Wheeler,
R. Sturm,
A. Hutchinson,
K. Jones,
Michael J Malasky,
A. Vogt,
Weiyin Zhou,
K. Pooley,
D. Elder,
Jiali Han,
B. Hicks,
N. Hayward,
P. Kanetsky,
C. Brummett,
G. Montgomery,
C. Olsen,
C. Hayward,
A. Dunning,
N. Martin,
E. Evangelou,
G. Mann,
G. Long,
P. Pharoah,
D. Easton,
J. Barrett,
A. Cust,
G. Abecasis,
D. Duffy,
D. Whiteman,
H. Gogas,
A. De Nicolo,
M. Tucker,
J. Newton-Bishop,
K. Peris,
S. Chanock,
F. Demenais,
K. Brown,
S. Puig,
E. Nagore,
Jianxin Shi,
M. Iles,
M. Law
|
7 |
2020 |
7
🐜
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|
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Genetic Dissection of Acute Anterior Uveitis Reveals Similarities and Differences in Associations Observed With Ankylosing Spondylitis
31 auth.
P. Robinson,
T. Claushuis,
A. Cortes,
T. Martin,
David M. Evans,
P. Leo,
P. Mukhopadhyay,
L. Bradbury,
K. Cremin,
J. Harris,
W. Maksymowych,
R. Inman,
P. Rahman,
N. Haroon,
L. Gensler,
...
J. Powell,
I. E. van der Horst-Bruinsma,
A. Hewitt,
J. Craig,
L. Lim,
D. Wakefield,
P. McCluskey,
V. Voigt,
P. Fleming,
M. Degli-Esposti,
Jennifer J. Pointon,
M. Weisman,
Bryan Paul Wordsworth,
J. Reveille,
J. Rosenbaum,
M. Brown
|
6 |
2015 |
6
🐜
|
|
🐜
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Cross-ethnic meta-analysis identifies association of the GPX3-TNIP1 locus with amyotrophic lateral sclerosis
64 auth.
Beben Benyamin,
Ji He,
Qiongyi Zhao,
J. Gratten,
F. Garton,
P. Leo,
Zhijun Liu,
M. Mangelsdorf,
A. Al-Chalabi,
L. Anderson,
Tim J. Butler,
Lu Chen,
Xiangding Chen,
K. Cremin,
H. Deng,
...
Matthew S. Devine,
J. Edson,
J. Fifita,
S. Furlong,
Yingying Han,
J. Harris,
A. Henders,
R. Jeffree,
Zi‐Bing Jin,
Zhongshan Li,
Ting Li,
Mengmeng Li,
Yong Lin,
Xiao-lu Liu,
M. Marshall,
E. McCann,
B. Mowry,
S. Ngo,
R. Pamphlett,
S. Ran,
D. Reutens,
D. Rowe,
P. Sachdev,
Sonia H. Shah,
Sharon Song,
L. Tan,
Lu Tang,
L. H. van den Berg,
W. van Rheenen,
J. Veldink,
R. Wallace,
L. Wheeler,
K. Williams,
Jinyu Wu,
Xin Wu,
Jian Yang,
W. Yue,
Zong-Hong Zhang,
Dai Zhang,
P. G. Noakes,
I. Blair,
R. Henderson,
P. Mccombe,
P. Visscher,
Huji Xu,
P. Bartlett,
M. Brown,
N. Wray,
D. Fan
|
6 |
2017 |
6
🐜
|
|
🐜
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Multiple Endocrine Tumors Associated with Germline MAX Mutations: Multiple Endocrine Neoplasia Type 5?
20 auth.
Amanda Seabrook,
J. Harris,
Sofia B Velosa,
Edward J. Kim,
A. McInerney-Leo,
T. Dwight,
Jason I Hockings,
Nicholas G Hockings,
J. Kirk,
P. Leo,
...
Amanda J Love,
C. Luxford,
M. Marshall,
O. Mete,
David Pennisi,
M. Brown,
A. Gill,
G. I. Hockings,
R. Clifton-Bligh,
E. Duncan
|
5 |
2020 |
5
🐜
|
|
🐜
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Mutations in LTBP3 cause acromicric dysplasia and geleophysic dysplasia
14 auth.
A. McInerney-Leo,
Carine Le Goff,
P. Leo,
T. Kenna,
P. Keith,
J. Harris,
R. Steer,
C. Bôle-Feysot,
P. Nitschké,
C. Kielty,
...
M. Brown,
A. Zankl,
E. Duncan,
V. Cormier-Daire
|
5 |
2016 |
5
🐜
|
|
🐜
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Whole exome sequencing is an efficient, sensitive and specific method for determining the genetic cause of short‐rib thoracic dystrophies
14 auth.
A. McInerney-Leo,
J. Harris,
P. Leo,
M. Marshall,
B. Gardiner,
E. Kinning,
H. Leong,
F. McKenzie,
W. Ong,
J. Vodopiutz,
...
C. Wicking,
M. Brown,
A. Zankl,
E. Duncan
|
5 |
2015 |
5
🐜
|
|
🐜
|
Genome-wide association study in Turkish and Iranian populations identify rare familial Mediterranean fever gene (MEFV) polymorphisms associated with ankylosing spondylitis
30 auth.
Zhixiu Li,
S. Akar,
H. Yarkan,
Sau Kuen Lee,
P. Çetin,
G. Can,
G. Kenar,
Fernur Çapa,
O. Pamuk,
Y. Pehlivan,
K. Cremin,
Erika De Guzman,
J. Harris,
L. Wheeler,
A. Jamshidi,
...
Mahdi Vojdanian,
E. Farhadi,
N. Ahmadzadeh,
Z. Yüce,
E. Dalkılıç,
D. Solmaz,
Berrin Akın,
S. Dönmez,
I. Sari,
P. Leo,
T. Kenna,
F. Önen,
M. Mahmoudi,
M. Brown,
N. Akkoç
|
5 |
2019 |
5
🐜
|
|
🐜
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Fryns Syndrome Associated with Recessive Mutations in PIGN in two Separate Families
14 auth.
A. McInerney-Leo,
J. Harris,
M. Gattas,
Elizabeth E. Peach,
S. Sinnott,
T. Dudding-Byth,
S. Rajagopalan,
C. Barnett,
L. Anderson,
L. Wheeler,
...
M. Brown,
P. Leo,
C. Wicking,
E. Duncan
|
5 |
2016 |
5
🐜
|
|
🐜
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Compound heterozygous mutations in RIPPLY2 associated with vertebral segmentation defects.
12 auth.
A. McInerney-Leo,
D. Sparrow,
J. Harris,
B. Gardiner,
M. Marshall,
V. O'Reilly,
...
Hongjun Shi,
M. Brown,
P. Leo,
A. Zankl,
S. Dunwoodie,
E. Duncan
|
5 |
2015 |
5
🐜
|
