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Colin Freeman
Colin Freeman
Wellcome Centre for Human Genetics, University of Oxford
Adresse e-mail validée de well.ox.ac.uk
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A haplotype map of the human genome
International HapMap Consortium Altshuler David altshuler@ molbio. mgh ...
Nature 437 (7063), 1299-1320, 2005
6139*2005
The UK Biobank resource with deep phenotyping and genomic data
C Bycroft, C Freeman, D Petkova, G Band, LT Elliott, K Sharp, A Motyer, ...
Nature 562 (7726), 203-209, 2018
60272018
A second generation human haplotype map of over 3.1 million SNPs
IHM Consortium
Nature 449 (7164), 851, 2007
5383*2007
Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis
Nature 476 (7359), 214-219, 2011
29842011
Analysis of immune-related loci identifies 48 new susceptibility variants for multiple sclerosis
International IBD Genetics Consortium (IIBDGC), C Agliardi, L Alfredsson, ...
Nature genetics 45 (11), 1353-1360, 2013
13372013
A fine-scale map of recombination rates and hotspots across the human genome
S Myers, L Bottolo, C Freeman, G McVean, P Donnelly
Science 310 (5746), 321-324, 2005
12572005
Interaction between ERAP1 and HLA-B27 in ankylosing spondylitis implicates peptide handling in the mechanism for HLA-B27 in disease susceptibility
Australo-Anglo-American Spondyloarthritis Consortium (TASC), ...
Nature genetics 43 (8), 761-767, 2011
9662011
Drive against hotspot motifs in primates implicates the PRDM9 gene in meiotic recombination
S Myers, R Bowden, A Tumian, RE Bontrop, C Freeman, TS MacFie, ...
Science 327 (5967), 876-879, 2010
7552010
Genome-wide genetic data on~ 500,000 UK Biobank participants
C Bycroft, C Freeman, D Petkova, G Band, LT Elliott, K Sharp, A Motyer, ...
BioRxiv, 166298, 2017
7202017
Genome-wide association study of ulcerative colitis identifies three new susceptibility loci, including the HNF4A region
Data and Analysis Group: Spencer Chris CA chris. spencer@ well. ox. ac. uk 5 ...
Nature genetics 41 (12), 1330-1334, 2009
6272009
The fine-scale genetic structure of the British population
S Leslie, B Winney, G Hellenthal, D Davison, A Boumertit, T Day, K Hutnik, ...
Nature 519 (7543), 309-314, 2015
5432015
A common sequence motif associated with recombination hot spots and genome instability in humans
S Myers, C Freeman, A Auton, P Donnelly, G McVean
Nature genetics 40 (9), 1124-1129, 2008
5282008
Genomic dissection of bipolar disorder and schizophrenia, including 28 subphenotypes
DM Ruderfer, S Ripke, A McQuillin, J Boocock, EA Stahl, JMW Pavlides, ...
Cell 173 (7), 1705-1715. e16, 2018
5182018
Common variants near ATM are associated with glycemic response to metformin in type 2 diabetes
LW Harries, AT Hattersley, ASF Doney, H Colhoun, AD Morris, ...
Nature genetics 43 (2), 117-120, 2011
4962011
Novel insights into the genetics of smoking behaviour, lung function, and chronic obstructive pulmonary disease (UK BiLEVE): a genetic association study in UK Biobank
LV Wain, N Shrine, S Miller, VE Jackson, I Ntalla, MS Artigas, ...
The Lancet Respiratory Medicine 3 (10), 769-781, 2015
4512015
Genome-wide association study identifies a variant in HDAC9 associated with large vessel ischemic stroke
International Stroke Genetics Consortium (ISGC), ...
Nature genetics 44 (3), 328-333, 2012
4322012
Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins
I Postmus, S Trompet, HA Deshmukh, MR Barnes, X Li, HR Warren, ...
Nature communications 5 (1), 5068, 2014
2792014
Dissection of the genetics of Parkinson's disease identifies an additional association 5′ of SNCA and multiple associated haplotypes at 17q21
Human molecular genetics 20 (2), 345-353, 2011
2222011
Common variants at the MHC locus and at chromosome 16q24. 1 predispose to Barrett's esophagus
Esophageal Adenocarcinoma Genetics Consortium, ...
Nature genetics 44 (10), 1131-1136, 2012
2082012
Sequencing of human genomes with nanopore technology
R Bowden, RW Davies, A Heger, AT Pagnamenta, M de Cesare, ...
Nature communications 10 (1), 1869, 2019
2062019
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