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Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes
40 auth.
J. Todd,
N. Walker,
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39 auth.
B. Javierre,
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H. Stunnenberg,
J. Todd,
D. Zerbino,
O. Stegle,
W. Ouwehand,
M. Frontini,
C. Wallace,
M. Spivakov,
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2016 |
9
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A genome-wide association study of nonsynonymous SNPs identifies a type 1 diabetes locus in the interferon-induced helicase (IFIH1) region
14 auth.
D. Smyth,
J. Cooper,
Rebecca Bailey,
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9 |
2006 |
9
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Fine mapping of type 1 diabetes susceptibility loci and evidence for colocalization of causal variants with lymphoid gene enhancers
26 auth.
S. Onengut-Gumuscu,
Wei-Min Chen,
O. Burren,
N. Cooper,
A. Quinlan,
J. Mychaleckyj,
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9 |
2015 |
9
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Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls
217 auth.
N. Craddock,
M. Hurles,
Niall J. Cardin,
R. Pearson,
V. Plagnol,
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Damjan Vukcevic,
Chris P. Barnes,
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Jake K. Byrnes,
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2010 |
9
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Widespread seasonal gene expression reveals annual differences in human immunity and physiology
15 auth.
X. C. Dopico,
M. Evangelou,
R. Ferreira,
Hui Guo,
M. Pekalski,
D. Smyth,
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O. Burren,
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2015 |
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Whole-genome sequencing of patients with rare diseases in a national health system
452 auth.
E. Turro,
W. Astle,
K. Megy,
S. Gräf,
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H. L. Allen,
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2020 |
8
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The International Human Epigenome Consortium: A Blueprint for Scientific Collaboration and Discovery
230 auth.
H. Stunnenberg,
M. Hirst,
S. Abrignani,
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Genome-wide association study of copy number variation in 16,000 cases of eight common diseases and 3,000 shared controls
217 auth.
N. Craddock,
M. Hurles,
Niall J. Cardin,
R. Pearson,
V. Plagnol,
S. Robson,
Damjan Vukcevic,
Chris P. Barnes,
D. Conrad,
E. Giannoulatou,
Chris Holmes,
J. Marchini,
K. Stirrups,
M. Tobin,
L. Wain,
...
C. Yau,
J. Aerts,
T. Ahmad,
T. Andrews,
Hazel Arbury,
A. Attwood,
A. Auton,
S. Ball,
A. Balmforth,
J. Barrett,
I. Barroso,
A. Barton,
A. Bennett,
S. Bhaskar,
K. Błaszczyk,
J. Bowes,
O. Brand,
P. Braund,
F. Bredin,
G. Breen,
Morris J. Brown,
I. Bruce,
J. Bull,
O. Burren,
J. Burton,
Jake K. Byrnes,
S. Caesar,
C. Clee,
A. Coffey,
J. Connell,
J. Cooper,
A. Dominiczak,
K. Downes,
H. Drummond,
D. Dudakia,
A. Dunham,
Bernadette Ebbs,
D. Eccles,
S. Edkins,
C. Edwards,
Anna Elliot,
P. Emery,
David M. Evans,
G. Evans,
S. Eyre,
A. Farmer,
I. Ferrier,
L. Feuk,
Tomas W. Fitzgerald,
E. Flynn,
A. Forbes,
L. Forty,
J. Franklyn,
R. Freathy,
P. Gibbs,
Paul D. Gilbert,
O. Gokumen,
K. Gordon-Smith,
Emma V. Gray,
E. Green,
C. Groves,
D. Grozeva,
R. Gwilliam,
A. Hall,
Naomi Hammond,
Matthew Hardy,
Pille Harrison,
N. Hassanali,
H. Hebaishi,
Sarah Hines,
A. Hinks,
G. Hitman,
L. Hocking,
E. Howard,
Philip N. Howard,
J. Howson,
D. Hughes,
S. Hunt,
J. Isaacs,
Mahim Jain,
D. Jewell,
T. Johnson,
J. Jolley,
I. Jones,
L. Jones,
G. Kirov,
C. Langford,
H. Lango-Allen,
G. Lathrop,
James Lee,
Kate L. Lee,
C. Lees,
Kevin Lewis,
C. Lindgren,
Meeta Maisuria-Armer,
J. Maller,
J. Mansfield,
Paul Martin,
D. Massey,
W. McArdle,
P. McGuffin,
K. McLay,
A. Mentzer,
M. Mimmack,
A. Morgan,
A. Morris,
C. Mowat,
S. Myers,
W. Newman,
E. Nimmo,
M. O’Donovan,
Abiodun K Onipinla,
Ifejinelo Onyiah,
Nigel R. Ovington,
M. Owen,
Kimmo Palin,
K. Parnell,
D. Pernet,
J. Perry,
A. Phillips,
D. Pinto,
N. Prescott,
I. Prokopenko,
M. Quail,
S. Rafelt,
N. W. Rayner,
R. Redon,
D. Reid,
Renwick,
S. Ring,
N. Robertson,
E. Russell,
D. St. Clair,
J. Sambrook,
J. Sanderson,
Helen Schuilenburg,
C. Scott,
R. Scott,
S. Seal,
S. Shaw-Hawkins,
B. Shields,
M. Simmonds,
D. Smyth,
Elilan Somaskantharajah,
Katarina Spanova,
S. Steer,
J. Stephens,
H. Stevens,
M. Stone,
Z. Su,
D. Symmons,
J. Thompson,
W. Thomson,
M. Travers,
C. Turnbull,
A. Valsesia,
M. Walker,
N. Walker,
C. Wallace,
M. Warren-Perry,
N. Watkins,
J. Webster,
M. Weedon,
A. Wilson,
Matt Woodburn,
B. P. Wordsworth,
A. Young,
E. Zeggini,
N. Carter,
T. Frayling,
Charles Lee,
G. McVean,
P. Munroe,
A. Palotie,
S. Sawcer,
S. Scherer,
D. Strachan,
C. Tyler-Smith,
M. Brown,
P. Burton,
M. Caulfield,
Alastair Compston,
M. Farrall,
S. Gough,
A. Hall,
A. Hattersley,
A. Hill,
C. Mathew,
M. Pembrey,
J. Satsangi,
M. Stratton,
Jane Worthington,
P. Deloukas,
A. Duncanson,
D. Kwiatkowski,
M. McCarthy,
W. Ouwehand,
M. Parkes,
N. Rahman,
J. Todd,
N. Samani,
P. Donnelly
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8 |
2010 |
8
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Rare variant contribution to human disease in 281,104 UK Biobank exomes
59 auth.
Quanli Wang,
R. Dhindsa,
K. Carss,
A. Harper,
A. Nag,
I. Tachmazidou,
D. Vitsios,
Sri V. V. Deevi,
A. Mackay,
D. Muthas,
M. Hühn,
S. Monkley,
H. Olsson,
B. Angermann,
Ronen Artzi,
...
Carl Barrett,
Maria G. Belvisi,
M. Bohlooly-y,
O. Burren,
L. Buvall,
B. Challis,
Sophia R. Cameron-Christie,
Suzanne Cohen,
Andrew Davis,
R. F. Danielson,
B. Dougherty,
B. Georgi,
Z. Ghazoui,
Pernille B L Hansen,
Fengyuan Hu,
Magdalena Jeznach,
Xiao Jiang,
C. Kumar,
Z. Lai,
G. Lassi,
Samuel H. Lewis,
B. Linghu,
Kieren T. Lythgow,
P. Maccallum,
Carla Martins,
A. Matakidou,
E. Michaëlsson,
S. Moosmang,
Sean E. O'Dell,
Y. Ohne,
J. Okae,
A. O'neill,
D. Paul,
A. Reznichenko,
M. A. Snowden,
A. Walentinsson,
J. Zerón,
M. Pangalos,
Sebastian Wasilewski,
Katherine R. Smith,
R. March,
A. Platt,
C. Haefliger,
S. Petrovski
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8 |
2021 |
8
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|
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Cell-specific protein phenotypes for the autoimmune locus IL2RA using a genotype-selectable human bioresource
19 auth.
C. Dendrou,
V. Plagnol,
E. Fung,
Jennie H. M. Yang,
K. Downes,
J. Cooper,
S. Nutland,
Gillian Coleman,
M. Himsworth,
Matthew Hardy,
...
O. Burren,
B. Healy,
N. Walker,
K. Koch,
W. Ouwehand,
J. Bradley,
N. Wareham,
J. Todd,
L. Wicker
|
8 |
2009 |
8
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Inherited Variation in Vitamin D Genes Is Associated With Predisposition to Autoimmune Disease Type 1 Diabetes
15 auth.
J. Cooper,
D. Smyth,
N. Walker,
H. Stevens,
O. Burren,
C. Wallace,
C. Greissl,
E. Ramos‐Lopez,
E. Hyppönen,
D. Dunger,
...
T. Spector,
W. Ouwehand,
Thomas J. Wang,
K. Badenhoop,
J. Todd
|
8 |
2011 |
8
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