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🐜
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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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|
🐜
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Newly identified genetic risk variants for celiac disease related to the immune response
38 auth.
K. Hunt,
A. Zhernakova,
Graham Turner,
Graham A. R. Heap,
L. Franke,
M. Bruinenberg,
J. Romanos,
L. Dinesen,
A. Ryan,
Davinder Panesar,
R. Gwilliam,
F. Takeuchi,
W. McLaren,
G. Holmes,
P. Howdle,
...
J. Walters,
D. Sanders,
R. Playford,
G. Trynka,
C. Mulder,
M. Mearin,
W. Verbeek,
V. Trimble,
F. Stevens,
C. O'Morain,
N. Kennedy,
Dermot Kelleher,
D. Pennington,
D. Strachan,
W. McArdle,
C. Mein,
M. Wapenaar,
P. Deloukas,
R. McGinnis,
R. McManus,
C. Wijmenga,
C. Wijmenga,
D. Heel
|
9 |
2008 |
9
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|
🐜
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Mutations in ABCA12 underlie the severe congenital skin disease harlequin ichthyosis.
27 auth.
D. Kelsell,
E. Norgett,
Harriet C Unsworth,
M. Teh,
T. Cullup,
C. Mein,
P. Dopping-Hepenstal,
B. Dale,
G. Tadini,
P. Fleckman,
K. Stephens,
V. Sybert,
S. Mallory,
B. North,
D. Witt,
...
E. Sprecher,
A. Taylor,
A. Ilchyshyn,
C. Kennedy,
H. Goodyear,
C. Moss,
D. Paige,
J. Harper,
B. Young,
I. Leigh,
R. Eady,
E. O’Toole
|
8 |
2005 |
8
🐜
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|
🦁
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A search for type 1 diabetes susceptibility genes in families from the United Kingdom
15 auth.
C. Mein,
L. Esposito,
M. G. Dunn,
G. Johnson,
A. Timms,
J. V. Goy,
Annabel N. Smith,
L. Sebag-Montefiore,
M. Merriman,
Amanda J. Wilson,
...
L. E. Pritchard,
F. Cucca,
A. Barnett,
S. Bain,
J. Todd
|
8 |
1998 |
8
🦁
|
|
🐜
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Yes-associated protein (YAP) functions as a tumor suppressor in breast
16 auth.
Ming Yuan,
V. Tomlinson,
R. Lara,
D. Holliday,
C. Chelala,
T. Harada,
R. Gangeswaran,
C. Manson-Bishop,
P. Smith,
S. Danovi,
...
O. Pardo,
T. Crook,
C. Mein,
N. Lemoine,
L. Jones,
S. Basu
|
8 |
2008 |
8
🐜
|
|
🐜
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Genetic interaction of BBS1 mutations with alleles at other BBS loci can result in non-Mendelian Bardet-Biedl syndrome.
12 auth.
P. Beales,
José L. Badano,
A. Ross,
S. J. Ansley,
B. Hoskins,
Brigitta Kirsten,
...
C. Mein,
P. Froguel,
P. Scambler,
R. Lewis,
J. Lupski,
N. Katsanis
|
7 |
2003 |
7
🐜
|
|
🦁
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Evaluation of single nucleotide polymorphism typing with invader on PCR amplicons and its automation.
14 auth.
C. Mein,
B. J. Barratt,
M. G. Dunn,
Thorsten Siegmund,
Annabel N. Smith,
L. Esposito,
S. Nutland,
H. Stevens,
A. Wilson,
M. Phillips,
...
Nancy Jarvis,
Scott M. Law,
Monika de Arruda,
J. Todd
|
7 |
2000 |
7
🦁
|
|
🐜
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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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Blood pressure loci identified with a gene-centric array.
104 auth.
T. Johnson,
Tom R. Gaunt,
S. Newhouse,
S. Padmanabhan,
M. Tomaszewski,
M. Kumari,
R. Morris,
I. Tzoulaki,
E. O’Brien,
N. Poulter,
P. Sever,
D. Shields,
Simon A Thom,
S. G. Wannamethee,
P. Whincup,
...
Morris J. Brown,
J. Connell,
R. Dobson,
Philip J Howard,
C. Mein,
Abiodun K Onipinla,
S. Shaw-Hawkins,
Yun Zhang,
G. Davey Smith,
I. Day,
D. Lawlor,
A. Goodall,
F. Fowkes,
G. Abecasis,
P. Elliott,
Vesela Gateva,
P. Braund,
P. Burton,
C. Nelson,
M. Tobin,
P. van der Harst,
N. Glorioso,
Hani Neuvrith,
E. Salvi,
J. Staessen,
A. Stucchi,
N. Devos,
X. Jeunemaître,
P. Plouin,
J. Tichet,
Peeter Juhanson,
E. Org,
Margus Putku,
S. Sõber,
G. Veldre,
M. Viigimaa,
Anna Levinsson,
A. Rosengren,
D. Thelle,
C. Hastie,
T. Hedner,
W. Lee,
O. Melander,
B. Wahlstrand,
R. Hardy,
A. Wong,
J. Cooper,
J. Palmen,
Li Chen,
A. Stewart,
G. Wells,
H. Westra,
M. Wolfs,
R. Clarke,
M. Franzosi,
A. Goel,
A. Hamsten,
M. Lathrop,
J. Peden,
U. Seedorf,
H. Watkins,
W. Ouwehand,
J. Sambrook,
J. Stephens,
J. Casas,
F. Drenos,
M. Holmes,
M. Kivimaki,
Sonia H. Shah,
T. Shah,
P. Talmud,
J. Whittaker,
C. Wallace,
C. Delles,
M. Laan,
D. Kuh,
S. Humphries,
F. Nyberg,
D. Cusi,
R. Roberts,
C. Newton‐Cheh,
L. Franke,
A. Stanton,
A. Dominiczak,
M. Farrall,
A. Hingorani,
N. Samani,
M. Caulfield,
P. Munroe
|
7 |
2011 |
7
🐜
|
|
🐜
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Harlequin ichthyosis: a review of clinical and molecular findings in 45 cases.
24 auth.
S. Rajpopat,
C. Moss,
J. Mellerio,
A. Vahlquist,
A. Gånemo,
M. Hellstrom-Pigg,
A. Ilchyshyn,
N. Burrows,
G. Lestringant,
A. Taylor,
...
C. Kennedy,
D. Paige,
J. Harper,
M. Glover,
P. Fleckman,
D. Everman,
M. Fouani,
H. Kayserili,
D. Purvis,
E. Hobson,
C. Chu,
C. Mein,
D. Kelsell,
E. O’Toole
|
7 |
2011 |
7
🐜
|
|
🐜
|
A variation in the ghrelin gene increases weight and decreases insulin secretion in tall, obese children.
9 auth.
M. Korbonits,
M. Gueorguiev,
E. O'Grady,
C. Lecoeur,
D. Swan,
C. Mein,
...
J. Weill,
A. Grossman,
P. Froguel
|
7 |
2002 |
7
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