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Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
193 auth.
Ashley H. Beecham,
N. Patsopoulos,
Dionysia K. Xifara,
Mary F. Davis,
A. Kemppinen,
C. Cotsapas,
T. Shah,
C. Spencer,
D. Booth,
An Goris,
A. Oturai,
Janna Saarela,
B. Fontaine,
Bernhard Hemmer,
Claes Martin,
...
F. Zipp,
Sandra D’Alfonso,
F. Martinelli-Boneschi,
Bruce Taylor,
H. Harbo,
I. Kockum,
J. Hillert,
T. Olsson,
M. Ban,
J. Oksenberg,
R Q Hintzen,
Lisa F Barcellos,
C. Agliardi,
L. Alfredsson,
Mehdi Alizadeh,
Carl A. Anderson,
Robert Andrews,
H. Søndergaard,
A. Baker,
G. Band,
S. Baranzini,
N. Barizzone,
J. Barrett,
C. Bellenguez,
L. Bergamaschi,
L. Bernardinelli,
A. Berthele,
V. Biberacher,
Thomas M C Binder,
H. Blackburn,
I. Bomfim,
P. Brambilla,
S. Broadley,
B. Brochet,
Lou Brundin,
D. Buck,
H. Butzkueven,
S. Caillier,
William Camu,
W. Carpentier,
Paola Cavalla,
E. Celius,
Irène Coman,
G. Comi,
L. Corrado,
Leentje Cosemans,
I. Cournu-Rebeix,
B. Cree,
D. Cusi,
V. Damotte,
Gilles Defer,
Silvia R Delgado,
P. Deloukas,
A. Di Sapio,
A. Dilthey,
Peter Donnelly,
B. Dubois,
M. Duddy,
S. Edkins,
Irina Elovaara,
F. Esposito,
N. Evangelou,
B. Fiddes,
J. Field,
A. Franke,
C. Freeman,
I. Frohlich,
Daniela Galimberti,
C. Gieger,
P. Gourraud,
Christiane Graetz,
Andrew Graham,
V. Grummel,
C. Guaschino,
Athena Hadjixenofontos,
H. Hakonarson,
Christopher Halfpenny,
Gillian Hall,
Per Hall,
Anders Hamsten,
James Harley,
Tim Harrower,
Clive Hawkins,
G. Hellenthal,
Charles Hillier,
Jeremy Hobart,
Muni Hoshi,
Sarah E. Hunt,
M. Jagodic,
I. Jelcic,
A. Jochim,
Brian Kendall,
Allan G. Kermode,
Trevor Kilpatrick,
Keijo Koivisto,
I. Konidari,
Thomas Korn,
Helena Kronsbein,
C. Langford,
Malin Larsson,
Mark Lathrop,
C. Lebrun-Frénay,
J. Lechner-Scott,
Michelle H. Lee,
Maurizio Leone,
V. Leppä,
G. Liberatore,
Benedicte A. Lie,
C. Lill,
M. Lindén,
J. Link,
F. Luessi,
J. Lycke,
Fabio Macciardi,
Satu Männistö,
C. Manrique,
Roland Martin,
V. Martinelli,
Deborah Mason,
Gordon Mazibrada,
C. McCabe,
Inger‐Lise Mero,
J. Mescheriakova,
L. Moutsianas,
K. Myhr,
Guy Nagels,
Richard Nicholas,
Petra Nilsson,
Fredrik Piehl,
Matti Pirinen,
Siân E Price,
H. Quach,
M. Reunanen,
Wim Robberecht,
Neil P Robertson,
M. Rodegher,
D. Rog,
M. Salvetti,
N. Schnetz-Boutaud,
F. Sellebjerg,
Rebecca C. Selter,
Catherine Schaefer,
Sandip Shaunak,
Ling Shen,
Simon Shields,
Volker Siffrin,
M. Slee,
P. S. Sørensen,
M. Sorosina,
M. Sospedra,
Anne Spurkland,
A. Strange,
E. Sundqvist,
Vincent Thijs,
John Thorpe,
A. Ticca,
P. Tienari,
C. V. van Duijn,
Elizabeth M Visser,
S. Vucic,
Helga Westerlind,
James S. Wiley,
Alastair Wilkins,
James F. Wilson,
J. Winkelmann,
John Zajicek,
Eva Zindler,
Jonathan L. Haines,
M. Pericak-Vance,
A. Ivinson,
Graeme Stewart,
David Hafler,
S. L. Hauser,
Alastair Compston,
G. McVean,
P. D. de Jager,
S. Sawcer,
J. McCauley
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9 |
2013 |
9
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Germline mutations in the proof-reading domains of POLE and POLD1 predispose to colorectal adenomas and carcinomas
37 auth.
C. Palles,
J. Cazier,
K. Howarth,
Enric Domingo,
Angela M. Jones,
P. Broderick,
Zoe Kemp,
S. Spain,
Estrella Guarino Almeida,
Israel Salguero,
Amy Sherborne,
D. Chubb,
L. Carvajal-Carmona,
Yusanne Ma,
Kulvinder Kaur,
...
Sara E. Dobbins,
E. Barclay,
Maggie Gorman,
Lynn Martin,
Michal B Kovac,
S. Humphray,
Anneke Lucassen,
Christopher Holmes,
David Bentley,
Peter Donnelly,
Jenny C. Taylor,
C. Petridis,
R. Roylance,
E. Sawyer,
David J. Kerr,
S. Clark,
Jonathan M Grimes,
S. Kearsey,
H. J. Thomas,
G. McVean,
R. Houlston,
I. Tomlinson
|
9 |
2012 |
9
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|
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The DNA sequence and biological annotation of human chromosome 1
166 auth.
S. G. Gregory,
K. Barlow,
K. McLay,
R. Kaul,
D. Swarbreck,
A. Dunham,
C. P. Scott,
K. L. Howe,
K. Woodfine,
C. Spencer,
M. Jones,
C. Gillson,
S. Searle,
Y. Zhou,
F. Kokocinski,
...
L. McDonald,
R. Evans,
K. Phillips,
A. Atkinson,
R. Cooper,
C. Jones,
R. Hall,
T. Andrews,
C. Lloyd,
R. Ainscough,
J. Almeida,
K. Ambrose,
F. Anderson,
R. Andrew,
R. Ashwell,
K. Aubin,
A. Babbage,
C. L. Bagguley,
J. Bailey,
H. Beasley,
G. Bethel,
C. Bird,
S. Bray-Allen,
J. Brown,
A. Brown,
D. Buckley,
J. Burton,
J. Bye,
C. Carder,
J. Chapman,
S. Clark,
G. Clarke,
C. Clee,
V. Cobley,
R. Collier,
N. Corby,
G. Coville,
J. Davies,
R. Deadman,
M. Dunn,
M. Earthrowl,
A. Ellington,
H. Errington,
A. Frankish,
J. Frankland,
L. French,
P. Garner,
J. Garnett,
L. Gay,
M. Ghori,
R. Gibson,
L. M. Gilby,
W. Gillett,
R. Glithero,
D. Grafham,
C. Griffiths,
S. Griffiths-Jones,
R. Grocock,
S. Hammond,
E. Harrison,
E. Hart,
E. Haugen,
P. Heath,
S. Holmes,
K. Holt,
P. Howden,
A. R. Hunt,
S. Hunt,
G. Hunter,
J. Isherwood,
R. James,
C. Johnson,
D. Johnson,
A. Joy,
M. Kay,
J. K. Kershaw,
M. Kibukawa,
A. Kimberley,
A. King,
A. Knights,
H. Lad,
G. Laird,
S. Lawlor,
D. Leongamornlert,
D. Lloyd,
J. Loveland,
J. Lovell,
M. Lush,
R. Lyne,
S. Martin,
M. Mashreghi-mohammadi,
L. Matthews,
N. Matthews,
S. McLaren,
S. Milne,
S. Mistry,
M. J. F. M oore,
T. Nickerson,
C. O'Dell,
K. Oliver,
A. Palmeiri,
S. Palmer,
A. Parker,
D. Patel,
A. V. Pearce,
A. Peck,
S. Pelan,
K. Phelps,
B. Phillimore,
R. Plumb,
J. Rajan,
C. Raymond,
G. Rouse,
C. Saenphimmachak,
H. Sehra,
E. Sheridan,
R. Shownkeen,
S. Sims,
C. Skuce,
M. Smith,
C. Steward,
S. Subramanian,
N. Sycamore,
A. Tracey,
A. Tromans,
Z. Van Helmond,
M. Wall,
J. Wallis,
S. White,
S. Whitehead,
J. Wilkinson,
D. Willey,
H. Williams,
L. Wilming,
P. Wray,
Z. Wu,
A. Coulson,
M. Vaudin,
J. Sulston,
R. Durbin,
T. Hubbard,
R. Wooster,
I. Dunham,
N. P. Carter,
G. McVean,
M. T. Ross,
J. Harrow,
M. Olson,
S. Beck,
J. Rogers,
D. R. Bentley
|
7 |
2006 |
7
🐜
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|
🐜
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UK Biobank release and systematic evaluation of optimised polygenic risk scores for 53 diseases and quantitative traits
18 auth.
Deborah J Thompson,
Daniel Wells,
Saskia Selzam,
Iliana Peneva,
Rachel Moore,
Kevin Sharp,
William A. Tarran,
Edward J. Beard,
F. Riveros-Mckay,
Duncan,
...
Palmer,
Priyanka Seth,
James Harrison,
M. Futema,
G. McVean,
V. Plagnol,
Peter Donnelly,
M. Weale
|
6 |
2022 |
6
🐜
|
|
🐜
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Arabidopsis meiotic crossover hotspots overlap with H2A.Z nucleosomes at gene promoters
13 auth.
Kyuha Choi,
Xiaohui Zhao,
Krystyna A. Kelly,
Oliver Venn,
James D. Higgins,
Nataliya E. Yelina,
Thomas J. Hardcastle,
Piotr Ziółkowski,
Piotr Ziółkowski,
Gregory P Copenhaver,
...
F. C. H. Franklin,
G. McVean,
Ian R Henderson
|
6 |
2013 |
6
🐜
|
|
🐜
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Mutations in CDC 45 , Encoding an Essential Component of the Pre-initiation Complex , Cause Meier-Gorlin Syndrome and Craniosynostosis
41 auth.
John Bell,
David Bentley,
G. McVean,
Peter Ratcliffe,
Jenny C. Taylor,
Andrew Wilkie,
J. Broxholme,
David Buck,
J. Cazier,
R. Cornall,
L. Gregory,
Julian Knight,
G. Lunter,
Ian Tomlinson,
C. Allan,
...
M. Attar,
A. Green,
S. Humphray,
Z. Kingsbury,
S. Lamble,
L. Lonie,
A. Pagnamenta,
Paolo Piazza,
G. Polanco,
A. Trebes,
R. Copley,
S. Fiddy,
R. Grocock,
E. Hatton,
Chris Holmes,
Linda Hughes,
P. Humburg,
Alexander Kanapin,
S. Lise,
Hilary Martin,
L. Murray,
Davis J McCarthy,
A. Rimmer,
N. Sahgal,
Ben Wright,
Christopher Yau
|
3 |
2017 |
3
🐜
|
|
🐜
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Multi-level evidence of an allelic hierarchy of USH2A variants in hearing, auditory processing and speech/language outcomes
20 auth.
Peter Donnelly Chair,
John Bell,
David Bentley,
G. McVean,
Peter Ratcliffe,
Jenny C. Taylor,
Andrew Wilkie,
J. Broxholme,
David Buck,
J. Cazier,
...
R. Cornall,
L. Gregory,
Julian Knight,
G. Lunter,
Ian Tomlinson,
David Buck Lead,
C. Allan,
M. Attar,
A. Green,
S. Humphray
|
3 |
2020 |
3
🐜
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|
🦁
|
An introduction to population genetics
G. McVean,
Molly Prseworski,
Paul Fernhead,
Jonathan Pritchard
|
0 |
2001 |
0
🦁
|
