|
๐
|
Moderate-to-severe asthma in individuals of European ancestry: a genome-wide association study
43 auth.
N. Shrine,
M. Portelli,
C. John,
M. Soler Artigas,
N. Bennett,
R. Hall,
J. Lewis,
A. Henry,
C. Billington,
Azaz Ahmad,
R. Packer,
D. Shaw,
Z. Pogson,
A. Fogarty,
T. McKeever,
...
A. Singapuri,
L. Heaney,
A. Mansur,
R. Chaudhuri,
N. Thomson,
J. Holloway,
G. Lockett,
P. Howarth,
R. Djukanoviฤ,
J. Hankinson,
R. Niven,
A. Simpson,
K. Chung,
P. Sterk,
J. Blakey,
I. Adcock,
Sile Hu,
Yike Guo,
M. Obeidat,
D. Sin,
M. van den Berge,
D. Nickle,
Y. Bossรฉ,
M. Tobin,
I. Hall,
C. Brightling,
L. Wain,
I. Sayers
|
7 |
2019 |
7
๐
|
|
๐
|
Identification and characterisation of a rare MTTP variant underlying hereditary non-alcoholic fatty liver disease
25 auth.
J. Grove,
P. Lo,
N. Shrine,
J. Barwell,
L. Wain,
M. Tobin,
A. Salter,
Aditi N. Borkar,
Sara Cuevas-Ocaรฑa,
N. Bennett,
C. John,
I. Ntalla,
Gabriela E. Jones,
Christopher P. Neal,
Mervyn G. Thomas,
...
H. Kuht,
Pankaj Gupta,
V. Vemala,
A. Grant,
A. Adewoye,
K. Shenoy,
L. Balakumaran,
E. Hollox,
N. Hannan,
G. Aithal
|
3 |
2023 |
3
๐
|
|
๐
|
238th ENMC International Workshop: Updating management recommendations of cardiac dystrophinopathyHoofddorp, The Netherlands, 30 November - 2 December 2018
24 auth.
J. Bourke,
M. Guglieri,
D. Duboc,
A. Aartsma-Rus,
A. Bandali,
N. Bennett,
B. Cools,
L. Cripe,
I. Groot,
S. Dittrich,
...
A. Florian,
P. Furlong,
N. Goemans,
K. Hor,
Frank van Leperen,
G. MacGowan,
Elizabeth McNally,
E. Pegoraro,
L. Politano,
M. ล edivรก,
V. Starรก,
J. Timmermans,
E. Vroom,
K. Wahbi
|
3 |
2019 |
3
๐
|
|
๐
|
Familial hypereosinophilia associated with eosinophilic gastrointestinal symptoms in individuals with a missense mutation in CKLFโlike MARVEL transmembrane domain containing 3
13 auth.
A. Wardlaw,
J. Barwell,
C. Hitchman,
N. Shrine,
N. Bennett,
A. Adewoye,
H. Ozturk,
T. Ntereke,
P. Wurm,
M. Tobin,
...
B. Gooptu,
E. Hollox,
L. Wain
|
2 |
2021 |
2
๐
|
|
๐
|
A Genome Wide Association Study of Moderate-Severe Asthma in subjects from the United Kingdom
33 auth.
N. Shrine,
Maria Soler-Artigas,
M. Portelli,
N. Bennett,
I. Ntalla,
A. Henry,
C. Billington,
D. Shaw,
Z. Pogson,
Andrew Fogerty,
T. McKeever,
L. Jonker,
A. Singapuri,
L. Heaney,
A. Mansur,
...
R. Chaudhuri,
N. Thomson,
J. Holloway,
G. Lockett,
P. Howarth,
R. Djukanoviฤ,
J. Hankinson,
R. Niven,
A. Simpson,
K. Chung,
P. Sterk,
J. Blakey,
I. Adcock,
M. Tobin,
I. Hall,
C. Brightling,
L. Wain,
I. Sayers
|
1 |
2017 |
1
๐
|
|
๐
|
FP.30 TREAT-NMD FSHD Global Registry Network: A collaboration of neuromuscular and FSHD patient registries
7 auth.
B. Porter,
N. Bennett,
D. Allison,
C. Campbell,
M. Guglieri,
A. Ambrosini,
...
R. Tupler
|
0 |
2022 |
0
๐
|
|
๐
|
Title : Identification and functional characterisation of a rare MTTP variant underlying hereditary non-alcoholic fatty liver disease
17 auth.
J. Barwell,
L. Wain,
M. Tobin,
A. Salter,
N. Bennett,
C. John,
I. Ntalla,
Gabriela E. Jones,
C. P. Neal,
Mervyn G. Thomas,
...
H. Kuht,
P. Gupta,
V. Vemala,
A. Grant,
A. Adewoye,
K. Shenoy,
L. Balakumaran
|
0 |
2021 |
0
๐
|
