Steve Bevan
Steve Bevan
Head, School of Life Sciences, University of Lincoln
Verified email at
Cited by
Cited by
Analysis of shared heritability in common disorders of the brain
Brainstorm Consortium, V Anttila, B Bulik-Sullivan, HK Finucane, ...
Science 360 (6395), eaap8757, 2018
Multiancestry genome-wide association study of 520,000 subjects identifies 32 loci associated with stroke and stroke subtypes
R Malik, G Chauhan, M Traylor, M Sargurupremraj, Y Okada, A Mishra, ...
Nature genetics 50 (4), 524-537, 2018
Mutations in the SMAD4/DPC4 Gene in Juvenile Polyposis
JR Howe, S Roth, JC Ringold, RW Summers, HJ Järvinen, P Sistonen, ...
Science 280 (5366), 1086-1088, 1998
A sequence variant in ZFHX3 on 16q22 associates with atrial fibrillation and ischemic stroke
DF Gudbjartsson, H Holm, S Gretarsdottir, G Thorleifsson, GB Walters, ...
Nature genetics 41 (8), 876-878, 2009
Genetic risk factors for ischaemic stroke and its subtypes (the METASTROKE collaboration): a meta-analysis of genome-wide association studies
M Traylor, M Farrall, EG Holliday, C Sudlow, JC Hopewell, YC Cheng, ...
The Lancet Neurology 11 (11), 951-962, 2012
Genetic heritability of ischemic stroke and the contribution of previously reported candidate gene and genomewide associations
S Bevan, M Traylor, P Adib-Samii, R Malik, NLM Paul, C Jackson, ...
Stroke 43 (12), 3161-3167, 2012
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
Shared genetic susceptibility to ischemic stroke and coronary artery disease: a genome-wide analysis of common variants
M Dichgans, R Malik, IR König, J Rosand, R Clarke, S Gretarsdottir, ...
Stroke 45 (1), 24-36, 2014
Risk variants for atrial fibrillation on chromosome 4q25 associate with ischemic stroke
S Gretarsdottir, G Thorleifsson, A Manolescu, U Styrkarsdottir, ...
Annals of neurology 64 (4), 402-409, 2008
Sequence variants on chromosome 9p21. 3 confer risk for atherosclerotic stroke
A Gschwendtner, S Bevan, JW Cole, A Plourde, M Matarin, ...
Annals of Neurology: Official Journal of the American Neurological …, 2009
Meta-analysis of genome-wide association studies from the CHARGE consortium identifies common variants associated with carotid intima media thickness and plaque
JC Bis, M Kavousi, N Franceschini, A Isaacs, GR Abecasis, U Schminke, ...
Nature genetics 43 (10), 940-947, 2011
The influence of genetic and cardiovascular risk factors on the CADASIL phenotype
S Singhal, S Bevan, T Barrick, P Rich, HS Markus
Brain 127 (9), 2031-2038, 2004
Common variants at 6p21. 1 are associated with large artery atherosclerotic stroke
EG Holliday, JM Maguire, TJ Evans, SA Koblar, J Jannes, JW Sturm, ...
Nature genetics 44 (10), 1147-1151, 2012
The role of genetic variants of matrix metalloproteinases in coronary and carotid atherosclerosis
S Abilleira, S Bevan, HS Markus
Journal of medical genetics 43 (12), 897-901, 2006
Investigating the causal relationship of C-reactive protein with 32 complex somatic and psychiatric outcomes: a large-scale cross-consortium Mendelian randomization study
BP Prins, A Abbasi, A Wong, A Vaez, I Nolte, N Franceschini, PE Stuart, ...
PLoS medicine 13 (6), e1001976, 2016
Ischemic stroke is associated with the ABO locus: The EuroCLOT study
FMK Williams, AM Carter, PG Hysi, G Surdulescu, D Hodgkiss, N Soranzo, ...
Annals of neurology 73 (1), 16-31, 2013
Loci associated with ischaemic stroke and its subtypes (SiGN): a genome-wide association study
SL Pulit, PF McArdle, Q Wong, R Malik, K Gwinn, S Achterberg, A Algra, ...
The Lancet Neurology 15 (2), 174-184, 2016
Multiethnic meta-analysis of genome-wide association studies in> 100 000 subjects identifies 23 fibrinogen-associated Loci but no strong evidence of a causal association …
M Sabater-Lleal, J Huang, D Chasman, S Naitza, A Dehghan, ...
Circulation 128 (12), 1310-1324, 2013
Low-frequency and common genetic variation in ischemic stroke: the METASTROKE collaboration
R Malik, M Traylor, SL Pulit, S Bevan, JC Hopewell, EG Holliday, W Zhao, ...
Neurology 86 (13), 1217-1226, 2016
Common variation in COL4A1/COL4A2 is associated with sporadic cerebral small vessel disease
K Rannikmäe, G Davies, PA Thomson, S Bevan, WJ Devan, GJ Falcone, ...
Neurology 84 (9), 918-926, 2015
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