Paul Flicek
Paul Flicek
EMBL, European Bioinformatics Institute, Wellcome Sanger Institute
Verified email at ebi.ac.uk
Title
Cited by
Cited by
Year
An integrated encyclopedia of DNA elements in the human genome
ENCODE Project Consortium
Nature 489 (7414), 57, 2012
118452012
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68, 2015
7807*2015
A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
73692010
Initial sequencing and comparative analysis of the mouse genome
RH Waterston, L Pachter
Nature 420 (6915), 520-562, 2002
73642002
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56, 2012
69142012
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project
ENCODE Project Consortium
nature 447 (7146), 799, 2007
52772007
The NHGRI GWAS Catalog, a curated resource of SNP-trait associations
D Welter, J MacArthur, J Morales, T Burdett, P Hall, H Junkins, A Klemm, ...
Nucleic acids research 42 (D1), D1001-D1006, 2014
27242014
The ensembl variant effect predictor
W McLaren, L Gil, SE Hunt, HS Riat, GRS Ritchie, A Thormann, P Flicek, ...
Genome biology 17 (1), 1-14, 2016
25322016
Sequence and comparative analysis of the chicken genome provide unique perspectives on vertebrate evolution
LDW Hillier, W Miller, E Birney, W Warren, RC Hardison, CP Ponting, ...
Nature 432 (7018), 695-716, 2004
24282004
Ensembl 2018
DR Zerbino, P Achuthan, W Akanni, MR Amode, D Barrell, J Bhai, K Billis, ...
Nucleic acids research 46 (D1), D754-D761, 2018
21052018
International network of cancer genome projects
International Cancer Genome Consortium
Nature 464 (7291), 993, 2010
17612010
Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor
W McLaren, B Pritchard, D Rios, Y Chen, P Flicek, F Cunningham
Bioinformatics 26 (16), 2069-2070, 2010
15772010
Ensembl 2015
F Cunningham, MR Amode, D Barrell, K Beal, K Billis, S Brent, ...
Nucleic acids research 43 (D1), D662-D669, 2015
15432015
Transcriptome and genome sequencing uncovers functional variation in humans
T Lappalainen, M Sammeth, MR Friedlšnder, P Ac‘t Hoen, J Monlong, ...
Nature 501 (7468), 506-511, 2013
15432013
The IPD and IMGT/HLA database: allele variant databases
J Robinson, JA Halliwell, JD Hayhurst, P Flicek, P Parham, SGE Marsh
Nucleic acids research 43 (D1), D423-D431, 2015
15142015
The new NHGRI-EBI Catalog of published genome-wide association studies (GWAS Catalog)
J MacArthur, E Bowler, M Cerezo, L Gil, P Hall, E Hastings, H Junkins, ...
Nucleic acids research 45 (D1), D896-D901, 2017
15052017
Ensembl 2014
P Flicek, MR Amode, D Barrell, K Beal, K Billis, S Brent, D Carvalho-Silva, ...
Nucleic acids research 42 (D1), D749-D755, 2014
14632014
An integrated map of structural variation in 2,504 human genomes
PH Sudmant, T Rausch, EJ Gardner, RE Handsaker, A Abyzov, ...
Nature 526 (7571), 75-81, 2015
14502015
Ensembl 2016
A Yates, W Akanni, MR Amode, D Barrell, K Billis, D Carvalho-Silva, ...
Nucleic acids research 44 (D1), D710-D716, 2016
14182016
Genetic effects on gene expression across human tissues
GTEx Consortium
Nature 550 (7675), 204, 2017
13682017
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