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), 57-74, 2012
10503*2012
Initial sequencing and comparative analysis of the mouse genome
RH Waterston, K Lindblad-Toh, E Birney, J Rogers, JF Abril, P Agarwal, ...
Nature 420 (6915), 520-562, 2002
70652002
A map of human genome variation from population-scale sequencing
1000 Genomes Project Consortium
Nature 467 (7319), 1061, 2010
70382010
An integrated map of genetic variation from 1,092 human genomes
1000 Genomes Project Consortium
Nature 491 (7422), 56-65, 2012
65062012
A global reference for human genetic variation
1000 Genomes Project Consortium
Nature 526 (7571), 68-74, 2015
60632015
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
50692007
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
25052014
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
23262004
The ensembl variant effect predictor
W McLaren, L Gil, SE Hunt, HS Riat, GRS Ritchie, A Thormann, P Flicek, ...
Genome biology 17 (1), 122, 2016
17262016
International network of cancer genome projects
International Cancer Genome Consortium
Nature 464 (7291), 993, 2010
16082010
Ensembl 2018
DR Zerbino, P Achuthan, W Akanni, MR Amode, D Barrell, J Bhai, K Billis, ...
Nucleic acids research 46 (D1), D754-D761, 2018
15822018
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
14792010
Ensembl 2015
F Cunningham, MR Amode, D Barrell, K Beal, K Billis, S Brent, ...
Nucleic acids research 43 (D1), D662-D669, 2015
14482015
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
13932014
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
13832015
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
13752013
Ensembl 2016
A Yates, W Akanni, MR Amode, D Barrell, K Billis, D Carvalho-Silva, ...
Nucleic acids research 44 (D1), D710-D716, 2016
13002016
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
12332017
Population genomics of human gene expression
BE Stranger, AC Nica, MS Forrest, A Dimas, CP Bird, C Beazley, CE Ingle, ...
Nature genetics 39 (10), 1217-1224, 2007
12172007
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
11902015
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