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Multiple common variants for celiac disease influencing immune gene expression
70 auth.
P. Dubois,
G. Trynka,
L. Franke,
L. Franke,
K. Hunt,
J. Romanos,
Alessandra Curtotti,
A. Zhernakova,
Graham A. R. Heap,
R. Ádány,
A. Aromaa,
M. Bardella,
L. H. Berg,
N. Bockett,
E. G. Concha,
...
B. Dema,
R. Fehrmann,
M. Fernández‐Arquero,
S. Fiatal,
S. Fiatal,
E. Grandone,
P. Green,
H. Groen,
R. Gwilliam,
R. Houwen,
S. Hunt,
K. Kaukinen,
Dermot Kelleher,
I. Korponay-Szabó,
K. Kurppa,
P. Macmathuna,
M. Mäki,
M. C. Mazzilli,
O. T. McCann,
M. Mearin,
C. Mein,
M. Mirza,
Vanisha Mistry,
B. Mora,
K. Morley,
C. Mulder,
J. Murray,
C. Núñez,
E. Oosterom,
R. Ophoff,
R. Ophoff,
I. Polanco,
L. Peltonen,
M. Platteel,
A. Rybak,
V. Salomaa,
J. Schweizer,
M. P. Sperandeo,
G. Tack,
Graham Turner,
J. Veldink,
W. Verbeek,
R. Weersma,
V. Wolters,
E. Urcelay,
B. Cukrowska,
L. Greco,
S. Neuhausen,
R. McManus,
D. Barisani,
P. Deloukas,
J. Barrett,
P. Saavalainen,
C. Wijmenga,
D. Heel
|
10 |
2010 |
10
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|
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Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease
92 auth.
G. Trynka,
K. Hunt,
N. Bockett,
J. Romanos,
Vanisha Mistry,
A. Szperl,
S. Bakker,
M. Bardella,
Leena Bhaw-Rosun,
G. Castillejo,
E. G. Concha,
R. Almeida,
Kerith-Rae Dias,
C. V. Diemen,
P. Dubois,
...
R. Duerr,
S. Edkins,
L. Franke,
K. Fransén,
Javier Gutiérrez,
Graham A. R. Heap,
B. Hrdličková,
S. Hunt,
Leticia Plaza Izurieta,
V. Izzo,
L. Joosten,
C. Langford,
M. C. Mazzilli,
C. Mein,
V. Midah,
M. Mitrovič,
B. Mora,
M. Morelli,
S. Nutland,
C. Núñez,
S. Onengut-Gumuscu,
K. Pearce,
M. Platteel,
I. Polanco,
Simon C. Potter,
C. Ribes-Koninckx,
I. Ricaño-Ponce,
S. Rich,
A. Rybak,
J. L. Santiago,
Sabyasachi Senapati,
A. Sood,
H. Szajewska,
R. Troncone,
J. Varadé,
C. Wallace,
V. Wolters,
A. Zhernakova,
B. K. Thelma,
B. Cukrowska,
E. Urcelay,
J. Bilbao,
M. Mearin,
D. Barisani,
J. Barrett,
V. Plagnol,
P. Deloukas,
C. Wijmenga,
D. Heel,
M. Alsina,
M. E. Comas,
Laura Pardo Grau,
L. Castaño,
P. Oliver,
J. C. Vitoria,
Luís Rodrigo,
C. López-Larrea,
A. López-Vázquez,
I. Hualde,
Z. García,
Blanca Hernández Charro,
M. Ramos-Arroyo,
F. Sánchez-Valverde,
C. Farré,
T. Marqués,
P. Vilar,
E. Arranz,
J. A. Garrote,
R. Auricchio,
C. Esch,
A. Chmielewska,
Gosia Piescik,
E. Martínez,
V. Varea,
F. M. Cerezo,
E. Donat-Aliaga,
J. Escribano
|
9 |
2011 |
9
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Health and population effects of rare gene knockouts in adult humans with related parents
36 auth.
Vagheesh M. Narasimhan,
K. Hunt,
D. Mason,
C. Baker,
K. Karczewski,
M. Barnes,
A. Barnett,
C. Bates,
S. Bellary,
N. Bockett,
Kristina M. Giorda,
Chris Griffiths,
H. Hemingway,
Zhilong Jia,
M. Kelly,
...
H. Khawaja,
M. Lek,
Shane A. McCarthy,
R. McEachan,
A. O’Donnell-Luria,
K. Paigen,
C. Parisinos,
E. Sheridan,
L. Southgate,
L. Tee,
Mark George Thomas,
Yali Xue,
Michael Schnall-Levin,
P. Petkov,
C. Tyler-Smith,
E. Maher,
R. Trembath,
D. MacArthur,
John Wright,
R. Durbin,
D. Heel
|
8 |
2015 |
8
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|
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Negligible impact of rare autoimmune-locus coding-region variants on missing heritability
37 auth.
K. Hunt,
Vanisha Mistry,
N. Bockett,
T. Ahmad,
M. Ban,
J. Barker,
J. Barrett,
H. Blackburn,
O. Brand,
O. Burren,
F. Capon,
Alastair Compston,
S. Gough,
L. Jostins,
Y. Kong,
...
James C. Lee,
M. Lek,
D. MacArthur,
J. Mansfield,
C. Mathew,
C. Mein,
M. Mirza,
S. Nutland,
S. Onengut-Gumuscu,
E. Papouli,
M. Parkes,
S. Rich,
S. Sawcer,
J. Satsangi,
M. Simmonds,
R. Trembath,
N. Walker,
E. Woźniak,
J. Todd,
M. Simpson,
V. Plagnol,
D. V. van Heel
|
7 |
2013 |
7
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|
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Genome-wide analysis of allelic expression imbalance in human primary cells by high-throughput transcriptome resequencing
16 auth.
Graham A. R. Heap,
Jennie H. M. Yang,
K. Downes,
B. Healy,
K. Hunt,
N. Bockett,
L. Franke,
P. Dubois,
C. Mein,
Richard J. B. Dobson,
...
T. Albert,
M. Rodesch,
D. Clayton,
J. Todd,
D. V. van Heel,
V. Plagnol
|
7 |
2009 |
7
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|
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A mutation of human cytochrome c enhances the intrinsic apoptotic pathway but causes only thrombocytopenia
20 auth.
I. Morison,
E. C. Bordé,
E. J. Cheesman,
P. Cheong,
A. Holyoake,
S. Fichelson,
R. Weeks,
Alexandra Lo,
S. Davies,
S. Wilbanks,
...
Robert D. Fagerlund,
M. Ludgate,
F. D. S. Tatley,
Melanie S A Coker,
N. Bockett,
G. Hughes,
Diana A Pippig,
Mark P Smith,
C. Capron,
E. Ledgerwood
|
7 |
2008 |
7
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|
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DNAJC21 Mutations Link a Cancer-Prone Bone Marrow Failure Syndrome to Corruption in 60S Ribosome Subunit Maturation.
16 auth.
H. Tummala,
A. Walne,
Mike Williams,
N. Bockett,
L. Collopy,
S. Cardoso,
A. Ellison,
R. Wynn,
T. Leblanc,
J. Fitzgibbon,
...
D. Kelsell,
D. V. van Heel,
Elspeth M. Payne,
V. Plagnol,
I. Dokal,
T. Vulliamy
|
6 |
2016 |
6
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|
🐜
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Meta-analysis of Immunochip data of four autoimmune diseases reveals novel single-disease and cross-phenotype associations
262 auth.
A. Márquez,
M. Kerick,
A. Zhernakova,
Javier Gutiérrez-Achury,
Wei-Min Chen,
S. Onengut-Gumuscu,
I. González-Álvaro,
L. Rodríguez-Rodríguez,
R. Ríos-Fernandez,
M. González-Gay,
G. Trynka,
K. Hunt,
N. Bockett,
J. Romanos,
Vanisha Mistry,
...
A. Szperl,
S. Bakker,
M. Bardella,
Leena Bhaw-Rosun,
G. Castillejo,
E. G. de la Concha,
R. C. de Almeida,
Kerith-Rae Dias,
C. V. van Diemen,
P. Dubois,
R. Duerr,
S. Edkins,
L. Franke,
K. Fransén,
Javier Gutiérrez,
Graham A. R. Heap,
B. Hrdličková,
Sarah E. Hunt,
Leticia Plaza Izurieta,
V. Izzo,
L. Joosten,
C. Langford,
M. C. Mazzilli,
C. Mein,
V. Midah,
M. Mitrovič,
B. Mora,
M. Morelli,
Sarah Nutlan,
K. Pearce,
M. Platteel,
I. Polanco,
Simon C. Potter,
C. Ribes-Koninckx,
I. Ricaño-Ponce,
A. Rybak,
J. L. Santiago,
Sabyasachi Senapati,
A. Sood,
H. Szajewska,
R. Troncone,
J. Varadé,
C. Wallace,
V. Wolters,
A. Zhernakova,
B. K. Thelma,
B. Cukrowska,
E. Urcelay,
J. Bilbao,
M. Luisa Mearin,
D. Barisani,
J. Barrett,
V. Plagnol,
C. Wijmenga,
D. V. van Heel,
S. Eyre,
J. Bowes,
D. Diogo,
Annette T. Lee,
A. Barton,
Paul Martin,
E. Stahl,
S. Viatte,
Kate Mcallister,
C. Amos,
L. Padyukov,
R. Toes,
T. Huizinga,
H. Westra,
L. Alfredsson,
Xinli Hu,
C. Sandor,
S. Davila,
C. Khor,
K. Heng,
Robert Andrews,
Sarah E. Hunt,
D. Symmons,
P. Concannon,
Stephen S. Rich,
M. González-Gay,
L. Rodríguez-Rodríguez,
Lisbeth Ärlsetig,
Javier Martín,
S. Rantapää-Dahlqvist,
R. Plenge,
Soumya Raychaudhuri,
Lars Klareskog,
P. Gregersen,
Jane Worthington,
Maureen D. Mayes,
L. Bossini‐Castillo,
O. Gorlova,
Xiaodong Zhou,
Wei V. Chen,
S. Assassi,
Jun Ying,
F. Tan,
F. Arnett,
J. Reveille,
S. Guerra,
Annette T. Lee,
C. Simeón,
P. Carreira,
I. Castellví,
M. González-Gay,
L. Beretta,
A. Voskuyl,
P. Airò,
C. Lunardi,
P. Shiels,
J. V. van Laar,
A. Herrick,
C. Denton,
J. Broen,
T. Radstake,
C. Fonseca,
B. Koeleman,
R. Ríos,
J. Callejas,
J. A. Vargas Hitos,
R. García Portales,
M. Camps,
A. Fernández-Nebro,
M. González-Escribano,
F. García-Hernández,
Marcelita Castillo,
M. Aguirre,
I. Gómez-Gracia,
L. Rodríguez-Rodríguez,
P. García de la Peña,
E. Vicente,
J. Andreu,
M. Fernández de Castro,
F. López-longo,
L. Martínez,
V. Fonollosa,
A. Guillén,
G. Espinosa,
C. Tolosa,
A. Pros,
M. Rodríguez Carballeira,
F. Narváez,
M. Rubio Rivas,
V. Ortiz-Santamaria,
A. Madroñero,
B. Díaz,
L. Trapiella,
A. Sousa,
M. Egurbide,
P. Fanlo Mateo,
L. Sáez-comet,
Federico Díaz,
V. Hernández,
E. Beltrán,
J. Román-Ivorra,
E. Grau,
J. Alegre-Sancho,
F. B. Blanco García,
N. Oreiro,
N. Ortego-Centeno,
M. Freire,
B. Fernández-Gutiérrez,
A. Balsa,
A. M. Ortiz,
J. D. de Vries-Bouwstra,
C. Magro-Checa,
A. Santaniello,
C. Bellocchi,
G. Moroncini,
A. Gabrielli,
E. Adlem,
James Allen,
J. Barrett,
Judy Brown,
O. Burren,
Pamela Clarke,
D. Clayton,
Gillian Coleman,
Jason Cooper,
F. Cucca,
L. Davison,
K. Downes,
Simon Duley,
D. Dunger,
L. Esposito,
Vincent H. Everett,
Sarah F. Field,
J. Hafler,
Matthew Hardy,
D. Harrison,
Inge Harrison,
Steve Hawkins,
B. Healy,
S. Hood,
S. Howell,
M. Maisuria,
William Meadows,
Trupti Mistry,
Sergey Nezhenstsev,
S. Nutland,
Nigel R. Ovington,
Daniel B. Rainbow,
Kara M. Rainbow,
S. Raj,
Helen Schuilenburg,
A. Simpson,
L. Smink,
D. Smyth,
H. Stevens,
N. Taylor,
J. Todd,
J. Tuomilehto,
N. Walker,
L. Wicker,
B. Widmer,
Mark Wilson,
H. Withers,
Jennie H. M. Yang,
Mark Brown,
Arnetta Crews,
J. Griffin,
M. Hall,
Teresa Harnish,
John Hepler,
J. Hilner,
Nancy King,
K. Lohman,
Lingyi Lu,
J. Mychaleckyj,
J. Nail,
Letitia H Perdue,
J. Pierce,
D. Reboussin,
S. Rushing,
M. Sale,
Elizabeth G. Sides,
B. Snively,
H. Teuschler,
Goodrich Theil,
Lynne M Wagenknecht,
Dustin Williams,
Maureen D. Mayes,
Soumya Raychaudhuri,
Stephen S. Rich,
C. Wijmenga,
Javier Martín
|
6 |
2018 |
6
🐜
|
|
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Rare and functional SIAE variants are not associated with autoimmune disease risk in up to 66,924 individuals of European ancestry
65 auth.
K. Hunt,
D. Smyth,
T. Balschun,
M. Ban,
Vanisha Mistry,
T. Ahmad,
Vidya Anand,
J. Barrett,
Leena Bhaw-Rosun,
N. Bockett,
O. Brand,
E. Brouwer,
P. Concannon,
J. Cooper,
Kerith-Rae Dias,
...
C. V. Diemen,
P. Dubois,
S. Edkins,
R. Fölster-Holst,
K. Fransén,
D. Glass,
G. Heap,
S. Hofmann,
T. Huizinga,
S. Hunt,
C. Langford,
James Lee,
J. Mansfield,
M. Marrosu,
C. Mathew,
C. Mein,
J. Müller‐Quernheim,
S. Nutland,
S. Onengut-Gumuscu,
W. Ouwehand,
K. Pearce,
N. Prescott,
M. Posthumus,
Simon C. Potter,
G. Rosati,
J. Sambrook,
J. Satsangi,
S. Schreiber,
Corina J Shtir,
M. Simmonds,
M. Sudman,
S. Thompson,
R. Toes,
G. Trynka,
T. Vyse,
N. Walker,
S. Weidinger,
A. Zhernakova,
M. Zoledziewska,
R. Weersma,
S. Gough,
S. Sawcer,
C. Wijmenga,
M. Parkes,
F. Cucca,
A. Franke,
P. Deloukas,
S. Rich,
J. Todd,
D. Heel
|
5 |
2011 |
5
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|
|
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The combination of transcriptomics and informatics identifies pathways targeted by miR-204 during neurogenesis and axon guidance
17 auth.
I. Conte,
S. Merella,
J. Garcia-Manteiga,
C. Migliore,
D. Lazarević,
S. Carrella,
Raquel Marco-Ferreres,
Raffaella Avellino,
N. P. Davidson,
W. Emmett,
...
R. Sanges,
N. Bockett,
David van Heel,
G. Meroni,
P. Bovolenta,
E. Stupka,
S. Banfi
|
5 |
2014 |
5
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|
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Identification of Cancer Stem Cell Subpopulations in Head and Neck Metastatic Malignant Melanoma
11 auth.
Vithushiya Yoganandarajah,
J. Patel,
Bede van Schaijik,
N. Bockett,
H. Brasch,
Erin Paterson,
...
D. Sim,
P. Davis,
I. Roth,
T. Itinteang,
S. Tan
|
4 |
2019 |
4
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