|
๐
|
Somatic SF3B1 mutation in myelodysplasia with ring sideroblasts.
51 auth.
E. Papaemmanuil,
M. Cazzola,
J. Boultwood,
L. Malcovati,
P. Vyas,
D. Bowen,
A. Pellagatti,
J. Wainscoat,
E. Hellstrรถm-Lindberg,
C. Gambacorti-Passerini,
A. Godfrey,
I. Rapado,
A. Cvejic,
A. Cvejic,
Richard Rance,
...
C. McGee,
P. Ellis,
L. Mudie,
P. Stephens,
Stuart Mclaren,
C. Massie,
P. Tarpey,
I. Varela,
S. Nik-Zainal,
Helen R Davies,
A. Shlien,
David A. Jones,
K. Raine,
Jonathon Hinton,
A. Butler,
J. Teague,
E. Baxter,
J. Score,
A. Gallรฌ,
M. D. Porta,
E. Travaglino,
M. Groves,
S. Tauro,
Nikhil C. Munshi,
Kym Anderson,
A. El-Naggar,
Andrej Fischer,
Andrej Fischer,
Ville Mustonen,
A. Warren,
N. Cross,
A. Green,
P. Futreal,
Michael R. Stratton,
P. Campbell,
P. Campbell
|
10 |
2011 |
10
๐
|
|
๐
|
Identification of somatically acquired rearrangements in cancer using genome-wide massively parallel paired-end sequencing
24 auth.
P. Campbell,
P. Stephens,
E. Pleasance,
Sarah O 'meara,
Heng Li,
T. Santarius,
L. Stebbings,
Catherine Leroy,
S. Edkins,
Claire W. Hardy,
...
J. Teague,
A. Menzies,
I. Goodhead,
D. Turner,
C. Clee,
Michael A. Quail,
Antony V. Cox,
Clive Brown,
R. Durbin,
M. Hurles,
Paul A. Edwards,
G. Bignell,
M. Stratton,
A. Futreal
|
9 |
2008 |
9
๐
|
|
๐
|
A systematic, large-scale resequencing screen of X-chromosome coding exons in mental retardation
80 auth.
P. Tarpey,
Raffaella Smith,
E. Pleasance,
A. Whibley,
S. Edkins,
Claire W. Hardy,
S. OโMeara,
Calli Latimer,
E. Dicks,
A. Menzies,
P. Stephens,
M. Blow,
Christopher Greenman,
Yali Xue,
C. Tyler-Smith,
...
Deborah J. Thompson,
K. Gray,
J. Andrews,
S. Barthorpe,
G. Buck,
J. Cole,
R. Dunmore,
David Jones,
M. Maddison,
T. Mironenko,
Rachel Turner,
K. Turrell,
J. Varian,
S. West,
S. Widaa,
P. Wray,
J. Teague,
A. Butler,
A. Jenkinson,
Mingming Jia,
David Richardson,
Rebecca Shepherd,
R. Wooster,
Isabel Tejada,
F. Martรญnez,
G. Carvill,
R. Goliath,
M. ArjanP,
de Brouwer,
H. Bokhoven,
H. Esch,
J. Chelly,
M. Raynaud,
H. Ropers,
F. Abidi,
A. Srivastava,
J. Cox,
Ying Luo,
U. Mallya,
Jenny Moon,
Josef Parnau,
S. Mohammed,
J. Tolmie,
C. Shoubridge,
M. Corbett,
A. Gardner,
E. Haan,
Sinitdhorn Rujirabanjerd,
M. Shaw,
Lucianne Vandeleur,
T. Fullston,
D. Easton,
Jackie Boyle,
M. Partington,
A. Hackett,
M. Field,
C. Skinner,
R. Stevenson,
M. Bobrow,
G. Turner,
C. Schwartz,
Jozef Gecz,
Lucy Raymond,
P. Futreal,
M. Stratton
|
9 |
2009 |
9
๐
|
|
๐
|
Constitutional translocation breakpoint mapping by genome-wide paired-end sequencing identifies HACE1 as a putative Wilms tumour susceptibility gene
13 auth.
I. Slade,
P. Stephens,
J. Douglas,
K. Barker,
L. Stebbings,
K. Pritchard-Jones,
R. Cole,
B. Pizer,
C. Stiller,
G. Vujaniฤ,
...
R. Scott,
Michael R. Stratton,
N. Rahman
|
5 |
2009 |
5
๐
|
|
๐
|
Somatic structural rearrangements in genetically engineered mouse mammary tumors
17 auth.
I. Varela,
Christiaan Klijn,
Christiaan Klijn,
P. Stephens,
L. Mudie,
L. Stebbings,
Danushka Galappaththige,
H. Gulden,
Eva Schut,
S. Klarenbeek,
...
P. Campbell,
L. Wessels,
L. Wessels,
M. Stratton,
J. Jonkers,
P. Futreal,
D. Adams
|
4 |
2010 |
4
๐
|
|
๐
|
An integrated map of human 6q22.3-q24 including a 3-Mb high-resolution BAC/PAC contig encompassing a QTL for fetal hemoglobin.
16 auth.
L. Game,
J. Close,
P. Stephens,
J. Mitchell,
S. Best,
J. Rochette,
C. Louis-dit-Sully,
J. Riley,
C. G. See,
P. Sanseau,
...
L. Kearney,
G. Bethel,
S. Humphray,
I. Dunham,
A. Mungall,
S. Thein
|
3 |
2000 |
3
๐
|
