Researcher
Jeffrey Barrett
Wellcome Trust Sanger Institute
Statistics
64 papers found
Papers authored by Jeffrey Barrett
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C. A. Anderson
optiCall: a robust genotype-calling algorithm for rare, low-frequency and common variants
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,
A. de Leiva,
P. de Bakker,
Nm Walker,
Cheung Pt,
Lee Yj,
P. Poh,
G. Price,
N. Ratnam,
C. Sanjeevi,
S. Sedimbi,
S. Shen,
B. Tait,
Deborah J. Smyth
and 538 other authors
Download from www.nature.com
Genetic risk prediction in complex disease
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Jeffrey C. Barrett
Imputation of low-frequency variants using the HapMap3 benefits from large, diverse reference sets
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Jeffrey C. Barrett ,
Eleftheria Zeggini
Synthetic associations in the context of genome-wide association scan signals
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Evoker: a visualization tool for genotype intensity data
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Karen A. Hunt,
Jihane Romanos,
Fehrmann Rs,
Alessandra Curtotti,
Alexandra Zhernakova,
Graham Ar R. Heap,
Róza Ádány,
A. Zhemakova,
Green Pm
and 88 other authors
Multiple common variants for celiac disease influencing immune gene expression
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Kai Wang,
Graham L. Radford-Smith,
Tariq Ahmad,
Charlie W. Lees,
Tobias Balschun,
James Lee,
Rebecca Roberts,
Luke Jostinm,
Carl A. Anderson,
Joshua C. Bis
and 90 other authors
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Lr Cardon,
Ap Morris,
Kt Zondervan
Marker selection for genetic case-control association studies.
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Natalie J. Prescott ,
Mark Tremelling,
Sheila A. Fisher,
Rhian Gwilliam,
Jemima Jacob,
Elaine R. Nimmo,
Hazel Drummond,
Charlie W. Lees,
Clive M. Onnie,
Catherine Hanson,
Katarzyna Blaszczyk,
Radhi Ravindrarajah
and 21 other authors
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Fisher Sa,
Mark Tremelling,
Er R. Nimmo,
Cw W. Lees,
Natalie J. Prescott,
Rhian Gwilliam,
Cm M. Onnie,
Ce E. Hanson,
Prescott Nj,
Lees Cw,
Dunecan Massey,
Nimmo Er,
Suzannah Bumpstead
and 41 other authors
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Dan L. Nicolae,
Richard H. Duerr,
Judy H. Cho,
John D. Rioux,
Lisa Wu Datta,
Mark S. Silverberg,
Steven R. Brant,
Kent D. Taylor,
Lw W. Datta,
Themistocles Dassopoulos,
Mm Michaël Barmada,
Genetics Consortium Niddk Ibd,
Alain Bitton
and 56 other authors
Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease
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Lon R. Cardon
To what extent do scans of non-synonymous SNPs complement denser genome-wide association studies?
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Rachel Cooney ,
Saad Pathan,
Carl A. Anderson,
Jeffrey C. Barrett ,
John Beckly,
Alessandra Geremia,
Laura Hancock,
Changcun Guo,
Tariq Ahmad,
Lon R. Cardon,
Derek P. Jewell
Confirmation of the role of ATG16l1 as a Crohnʼs disease susceptibility gene:
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