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Aaron G. Day-Williams
Aaron G. Day-Williams
Matterhorn Biosciences
Verified email at matterhornbiosciences.com - Homepage
Title
Cited by
Cited by
Year
The genetic architecture of type 2 diabetes
C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ...
Nature 536 (7614), 41-47, 2016
12362016
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
Science, 2015
9872015
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1268-1283. e6, 2018
5762018
Identification of new susceptibility loci for osteoarthritis (arcOGEN): a genome-wide association study
arcOGEN Consortium, arcOGEN Collaborators
The Lancet 380 (9844), 815-823, 2012
4442012
Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel
J Huang, B Howie, S McCarthy, Y Memari, K Walter, JL Min, P Danecek, ...
Nature communications 6 (1), 8111, 2015
3992015
Diagnosis of Parkinson's disease on the basis of clinical and genetic classification: a population-based modelling study
MA Nalls, CY McLean, J Rick, S Eberly, SJ Hutten, K Gwinn, M Sutherland, ...
The Lancet Neurology 14 (10), 1002-1009, 2015
2142015
A variant in MCF2L is associated with osteoarthritis
AG Day-Williams, L Southam, K Panoutsopoulou, NW Rayner, T Esko, ...
The American Journal of Human Genetics 89 (3), 446-450, 2011
1782011
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip
E Evangelou, HJ Kerkhof, U Styrkarsdottir, EE Ntzani, SD Bos, T Esko, ...
Annals of the rheumatic diseases 73 (12), 2130-2136, 2014
1692014
Insights into the genetic architecture of osteoarthritis from stage 1 of the arcOGEN study
K Panoutsopoulou, L Southam, KS Elliott, N Wrayner, G Zhai, C Beazley, ...
Annals of the rheumatic diseases 70 (5), 864-867, 2011
1682011
Phenome-wide association studies across large population cohorts support drug target validation
D Diogo, C Tian, CS Franklin, M Alanne-Kinnunen, M March, ...
Nature communications 9 (1), 1-13, 2018
1492018
Genetic risk of Parkinson disease and progression: an analysis of 13 longitudinal cohorts
H Iwaki, C Blauwendraat, HL Leonard, G Liu, J Maple-Grødem, JC Corvol, ...
Neurology: Genetics 5 (4), e348, 2019
1362019
Genome-wide association study in a Chinese population identifies a susceptibility locus for type 2 diabetes at 7q32 near PAX4
RCW Ma, C Hu, CH Tam, R Zhang, P Kwan, TF Leung, GN Thomas, ...
Diabetologia 56, 1291-1305, 2013
1172013
Genomewide association study of Parkinson's disease clinical biomarkers in 12 longitudinal patients' cohorts
H Iwaki, C Blauwendraat, HL Leonard, JJ Kim, G Liu, J Maple‐Grødem, ...
Movement Disorders 34 (12), 1839-1850, 2019
1132019
Whole-genome sequence-based analysis of thyroid function
PN Taylor, E Porcu, S Chew, PJ Campbell, M Traglia, SJ Brown, ...
Nature communications 6 (1), 5681, 2015
1122015
A whole-genome sequence study identifies genetic risk factors for neuromyelitis optica
K Estrada, CW Whelan, F Zhao, P Bronson, RE Handsaker, C Sun, ...
Nature communications 9 (1), 1929, 2018
952018
A rare variant in APOC3 is associated with plasma triglyceride and VLDL levels in Europeans
NJ Timpson, K Walter, JL Min, I Tachmazidou, G Malerba, SY Shin, ...
Nature communications 5 (1), 4871, 2014
792014
The effect of next‐generation sequencing technology on complex trait research
AG Day‐Williams, E Zeggini
European journal of clinical investigation 41 (5), 561-567, 2011
792011
ARIEL and AMELIA: testing for an accumulation of rare variants using next-generation sequencing data
JL Asimit, AG Day-Williams, AP Morris, E Zeggini
Human heredity 73 (2), 84-94, 2012
732012
Large-scale association analysis of TNF/LTA gene region polymorphisms in type 2 diabetes
V Boraska, NW Rayner, CJ Groves, TM Frayling, M Diakite, KA Rockett, ...
BMC medical genetics 11, 1-7, 2010
732010
Differences in the presentation and progression of Parkinson's disease by sex
H Iwaki, C Blauwendraat, HL Leonard, MB Makarious, JJ Kim, G Liu, ...
Movement Disorders 36 (1), 106-117, 2021
662021
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